Patent Litigation 2026

Last Updated February 12, 2026

Switzerland

Law and Practice

Authors



Pestalozzi is a Swiss business law firm that has focused on high-end work for domestic and international clients since 1911. The firm guides and supports its clients in their strategic business decisions, anticipates their future challenges and helps them solve their critical issues. With over 100 professionals in Zurich and Geneva, the firm is at home in Switzerland’s two main commercial hubs. While being locally embedded, Pestalozzi has also developed sought-after expertise in dealing with multi-jurisdictional transactions and disputes. The firm has a long tradition in providing intellectual property services. Its IP practice group provides results-oriented, effective and pragmatic solutions for the protection and commercialisation of intangible assets, including representing clients from all industry sectors in enforcing and defending their intellectual property rights.

In Switzerland, inventions are primarily protected by patents. A patent with effect for the territory of Switzerland can either be applied for and granted as a Swiss national patent under the Swiss Patents Act (“PatA”) or as a European patent under the European Patent Convention (EPC) with the designation of Switzerland. According to the PatA and Swiss judicial practice, certain inventions are excluded from patentability, such as gene sequences, methods of medical treatment or mere computer programs.

Under Swiss law, protection of an invention as a utility model is not available and the Federal Council (the Swiss government) recently abandoned its plan to introduce a utility model as part of the partial revision of the PatA that is currently underway.

Undisclosed inventions may qualify as trade secrets and are then protected by law against unlawful use and disclosure, which may qualify as an act of unfair competition (Article 6, Act against Unfair Competition) or a criminal act (Article 162, Penal Code). In addition, trade secrets can be protected through contractual means. The Directive (EU) 2016/943 on the protection of undisclosed know-how and business information (trade secrets) is not directly applicable in Switzerland, which is not an EU country, nor has any analogous law been adopted in Switzerland. Overall, the Swiss provisions on trade secret protection are less detailed than the legal framework in the European Union, but they provide effective protection that meets the requirements of Article 39, paragraph 2 of the Agreement on Trade-Related Aspects of Intellectual Property Rights (TRIPS).

A Swiss national patent is granted pursuant to the PatA upon application to the Swiss Federal Institute of Intellectual Property (Institut Fédéral de la Propriété Intellectuelle, or IPI). European patent applications with protection for Switzerland may be filed with the European Patent Office (EPO) pursuant to the EPC.

European patent applications have the same effect in Switzerland as national patent applications filed with the IPI (Article 110, PatA) and are recorded in the Swiss register once granted by the EPO.

IPI Procedure and “Unexamined” Patents

The IPI currently examines national patent applications only with respect to formal requirements and selected legal requirements, such as the technical nature of the invention, whether the invention is contrary to public policy or morality, the clarity and uniformity of the claims and added matter. In contrast to the examination procedure of European patents by the EPO, the IPI does not examine the material requirements of novelty and non-obviousness before granting the patent (Article 59, paragraph 4, PatA).

In the context of an ongoing partial revision of the PatA, the Federal Council proposed to introduce an optional full examination – which was unanimously accepted in parliament in 2024. The newly established compromise allows applicants seeking a fast-track patent to continue applying for a “partially examined” national patent, as before. In contrast, those desiring greater legal certainty at the time of application can now opt for a “fully examined” national patent comparable to a patent granted through the European Patent Office. As a result, inventors would have the choice between applying for an “unexamined” or a “fully examined” national patent with the IPI. It is worth noting that the request for full examination may also be filed by third parties, against whom the patent resulting from the application could potentially be held at a later date. In addition, in each case, a public state-of-the-art search report would be prepared, which is intended to give preliminary indications as to the novelty and inventive step of the claimed invention.

Application Procedure

Under the revised PatA, the application documents may also be filed in English, thereby allowing patent applicants to use documents that have been prepared in an international context in the Swiss grant procedure without the need to prepare translations. However, procedural decisions and orders will still be issued in an official language of Switzerland.

Currently, the average costs for the grant of a patent by the IPI amount to approximately EUR700 (without any fees for optional searches). To take a patent application through to the grant stage before the EPO, one may expect costs of around EUR5,000. These costs do not include the fees for the consultancy services of a patent attorney.

Swiss residents do not need to be represented by a patent attorney before the IPI, but applicants (natural or legal persons) who have neither residence nor a place of business in Switzerland are obliged to be represented by a local professional representative. Similar rules apply for residents of non-contracting states in front of the EPO.

Trade secret protection is granted by law, without any examination or registration by any authority, provided that the undisclosed invention meets the conditions for protection, such as confidentiality and an interest in such confidentiality.

Currently, patent examination by the IPI for granting a national patent may last between one and two years or even longer, depending on whether the IPI is asked to provide a report on the state of the art or arrange an international-type search (Article 59, paragraph 5, PatA). Patent-granting proceedings by the EPO usually take longer, as the examination of the novelty and obviousness requirements takes time. The European patent grant procedure generally takes about three to five years from the date the application is filed, but in certain cases it can last considerably longer depending on the complexity of the file.

Following the revision of the PatA, the duration of a patent examination is likely to become longer in Switzerland, as the preparation of a state-of-the-art search report by the IPI will be mandatory prior to each patent application and, in the case of a full examination, the IPI will also analyse novelty and inventive step.

For both Swiss national patents and European patents with protection for Switzerland, the term of protection is 20 years from the filing date of the patent application (Article 14, PatA).

Inventions that qualify as trade secrets are protected by law as long as the invention meets the conditions for protection – ie, as long as the invention remains confidential and the inventor has an interest in its confidentiality.

Obligations

In order to maintain both Swiss national patents and Swiss parts of European patents, once granted, the patent owner’s primary obligation is to timely pay the registration and annual renewal fees. The amount of the renewal fees is progressive based on the years of protection.

Rights

Both Swiss national patents and European patents with protection for Switzerland confer on their owners the right to prohibit others from commercially using the invention (Article 8, PatA). It is the responsibility of the patent owner to enforce their exclusivity rights. Possible civil legal actions include:

  • an action for permanent injunction or remedy of the unlawful situation (Article 72, PatA);
  • an action for monetary relief, including damages such as lost profits, accounts of the infringer’s profits and surrender of the unjust enrichment in the form of a reasonable licence fee (Article 73, PatA); and
  • an action for declaratory judgment on the existence or non-existence of a circumstance or right governed by the PatA (Article 74, PatA).

Besides the initiation of civil actions, the patent owner may file a complaint in order to start criminal proceedings against the infringer of their patent rights (Articles 81 et seq, PatA). The PatA also provides for custom measures (Articles 86a et seq, PatA). If the patent owner has clear indications that goods infringing their patent may imminently be imported into or exported out of Swiss customs territory, they may request the Customs Administration to refuse the release of the goods. The Customs Administration may withhold the goods for a maximum period of ten working days, so that the applicant may obtain preliminary measures.

Inventions that are only protected as trade secrets enjoy protection either under Swiss unfair competition law (Article 6, Act Against Unfair Competition), under criminal law (Article 162, Penal Code) or by contractual means. Unfair competition law provides for civil injunctions, remedies and monetary relief actions as well as for criminal sanctions.

Upon an application by the owner of a Swiss national patent or a European patent with protection for Switzerland, the IPI may grant a supplementary protection certificate (SPC) for the active ingredients or a combination of the active ingredients of medicinal products or plant protection products (Articles 140a et seq, PatA). An SPC can only be granted on the basis of a valid patent and a granted marketing authorisation for the medicinal product.

The period of protection for the SPC begins as soon as patent protection expires and is valid for a maximum period of five years. This term may be extended for a further six months if paediatric studies have been carried out and the results are reflected in the product information of the respective medicinal product (paediatric extension).

For situations where the patent owner is not eligible to apply for an ordinary SPC, which could be prolonged through a paediatric extension, the PatA also provides the possibility of a paediatric SPC that is directly linked to the patent and not to the ordinary SPC.

Third parties currently do not have any right to participate in the grant proceedings for a Swiss national patent or an SPC – eg, by filing third-party observations. However, any person can file an opposition against a Swiss national patent once it is granted by the IPI. Due to the limited scope of the examination by the IPI, national opposition proceedings following grant of Swiss national patents are unattractive. In fact, to date, it appears that the opposition proceedings have never been made use of. The grant of an SPC can be challenged by appeal if the appealing party can show a legal interest in the outcome of the proceedings.

In proceedings before the EPO, third parties can file observations concerning the patentability of the invention (third-party observations) in order to try to prevent a patent from being granted. However, third parties cannot take part in the grant proceedings as a formal party. Any person may, however, file an opposition against a European patent once it is granted by the EPO.

Against a refusal to grant patent protection or an SPC by the IPI, an appeal can be filed with the Swiss Federal Administrative Court and thereafter to the Swiss Federal Supreme Court. Once the partial revision of the PatA enters into force, the Federal Patent Court will be the new appeal instance against administrative grant decisions in patent matters.

A decision of the EPO refusing to grant a European patent may be appealed with the EPO’s Board of Appeal.

A patent registered in the Swiss patent register is cancelled (and the patent protection terminates with effect ex nunc) if the annual renewal fees are not paid on time.

Where the patent owner provides prima facie evidence of having been prevented, through no fault on their part, from observing a time limit, the IPI may grant, on request, the re-establishment of their rights (Article 47, PatA). Acceptance of the request has the effect of restoring the situation that would have resulted from carrying out the act in good time. However, due to the quite strict practice on the no-fault requirement, Article 47 of the PatA is often not applicable.

Alternatively, the patent owner may file a request for further processing with the IPI (Article 46a, PatA). The request must be made within two months after receiving notification of the missed time limit or within six months after the time limit has expired. Within this time, the action that has been omitted must be executed. If the request for further processing is approved, the situation that would have resulted from executing the act on time will be restored.

Once the patent has been granted (and the opposition period has expired), the patent owner may file a request with the IPI for a declaration of partial surrender of a Swiss national patent or the Swiss part of a European patent in order to:

  • surrender a patent claim;
  • limit an independent claim by combining one or more patent claims, which are dependent on it; or
  • limit an independent claim in some other way – in such cases, the limited claim must refer to the same invention and define an embodiment that is included in the specification of the published patent and in the version of the patent application that determined the date of filing.

The partial surrender may not be used to file new patent claims or to make up for something else that was overlooked in the granting procedure.

On the occasion of registration of a partial surrender, the patent owner may, within a three-month period, file an application for the establishment of one or more new patents to cover the dropped patent claims; such new patents are given the filing date of the original patent.

Under Swiss law, civil legal actions include:

  • actions for permanent injunction or remedy of the unlawful situation (which may also be requested as preliminary measures);
  • actions for monetary relief; and
  • declaratory judgment actions.

Moreover, the patent owner may also initiate criminal proceedings or apply for customs measures.

See 1.5 Rights and Obligations of Owners of Intellectual Property Rights for more detail.

Opposition Proceedings

Within nine months of publication, any third party, without the need to demonstrate a proven interest, may file an opposition against a Swiss national patent granted by the IPI or against a European patent granted by the EPO.

Swiss national patents

Grounds for opposition against a Swiss national patent are rather limited. The opposing party may claim that the patent contains inventions that are excluded from patentability because:

  • the invention relates to the human body or its elements;
  • the invention relates to naturally occurring sequences or partial sequences of genes; or
  • the invention’s exploitation is contrary to human dignity or disregards the integrity of living organisms, or is in any other way contrary to public policy or morality according to Article 2 of the PatA.

European patents

The EPC allows for more grounds for opposition. In addition to similar opposition grounds allowed under Swiss law, a third party may also claim that:

  • the invention is not new;
  • the invention does not involve an inventive step;
  • the invention is not susceptible to industrial application;
  • the invention is not disclosed clearly and completely enough for a person skilled in the art to carry it out; or
  • the patent’s subject-matter extends beyond the content of the application as filed.

PatA revision

After the PatA revision, besides the above-mentioned opposition grounds, the grounds of appeal in national opposition proceedings for fully examined patents will be expanded to include an examination for novelty and inventive step.

Another important change concerns the abolition of the opposition procedure itself. Instead, third parties will be provided with the opportunity to directly appeal grant decisions to the Federal Patent Court. Up until now, the Federal Administrative Court was the appeal instance for all federal administrative matters; eg, opposition decisions of the IPI.

In March 2024, the Swiss Parliament adopted the partial revision of the Patent Act. Following this, at the end of April 2025, the Federal Council submitted the fully revised Patent Ordinance for consultation. The Federal Council is expected to approve the revised Patent Ordinance in May 2026 and determine the date when the revised patent law will take effect – the anticipated effective date is currently 1 January 2027.

An additional major development, pursued within the framework of a separate revision process, relates to patents in the field of plant breeding. While plant varieties cannot be patented, certain breeding methods and specific traits can be. According to Swiss law, all protected varieties can be freely used for breeding. If a patented trait is present in a new variety, however, breeders must obtain permission, typically through a licence, before marketing it. Currently, it is challenging to identify whether or not a variety is subject to a patent, as patented traits are not labelled on seeds or easily found in patent searches. To address this issue, a clearinghouse solution has been proposed. Breeders would submit details of their intended varieties to the IPI, which would make this information accessible to patent holders. Patent holders have 90 days to notify the clearinghouse if their patents apply to the notified variety, and the breeder is informed with the relevant patent details. This would enable breeders to assess the patent’s impact and decide whether to proceed or switch to a non-patented variety. If the breeders choose a patented variety, they must negotiate a licensing agreement. This revision project is highly controversial for several legal and practical reasons. It is currently unclear if it will be proposed to parliament, and, if so, in what form.

Civil Proceedings

Third parties, with a proven interest, may also initiate civil proceedings in order to claim the invalidity or partial invalidity of a Swiss national patent or of the Swiss part of a European patent if the invention is excluded from patentability, is obvious, not novel or not disclosed in a way that a person skilled in the art could carry it out, or if matter was added after the filing date (Article 26 et seq, PatA).

In addition, when the patent has been filed by an applicant who was not entitled to that patent, the entitled person may apply for assignment of the patent application or, if the patent has already been granted, of the patent itself (Article 29, PatA).

Compulsory Licensing

Under Swiss law, third parties with a legitimate interest may, under certain conditions, also initiate actions for the grant of compulsory licences (Article 36 et seq, PatA), if:

  • a patented invention cannot be used without infringing a prior patent, provided that the invention represents an important technical advance of considerable economic significance in relation to the invention that is the subject matter of the prior patent;
  • a patent is not sufficiently exploited in Switzerland, and where such a failure to exploit cannot be justified;
  • the public interest so requires;
  • a licence to patents in the field of semiconductor technology is required to remedy a practice held to be anti-competitive; or
  • a licence to use a patented biotechnological invention is required for research purposes.

Requests for the granting of compulsory licences are rare and to date no compulsory licence appears to have ever been granted by a court in Switzerland.

The Swiss Federal Patent Court rules on civil actions concerning patents at first instance. Pursuant to Article 26 of the Patent Court Act (PCA), it has exclusive jurisdiction over civil patent litigation concerning patent validity as well as patent infringement, compulsory licence actions, requests for preliminary measures and enforcement of judgments made under its exclusive jurisdiction.

The Federal Patent Court also has jurisdiction in other civil actions that have a connection to patents, in particular those concerning contractual rights to patents (ownership and licensing) or their assignment. In such cases, the jurisdiction of the Federal Patent Court does not preclude the jurisdiction of the cantonal courts.

An appeal against the decision of the Federal Patent Court or of a cantonal court can only be lodged with the Federal Supreme Court directly as second instance. The decision of the Federal Supreme Court is final. The Federal Supreme Court can, however, remand the case back to the Federal Patent Court for new consideration of certain aspects. In such event, the Federal Patent Court’s second decision can again be appealed to the Federal Supreme Court.

The Federal Patent Court is a specialised court for patent matters. It comprises judges with legal training and judges with a technical qualification.

Besides the Federal Patent Court and cantonal courts, arbitral tribunals may also be competent to resolve disputes related to patents. According to Swiss case law, all aspects of intellectual property disputes are arbitrable, including contractual issues related to patents as well as disputes over the validity of patents. Although arbitral awards on the validity of patents are recognised and enforced in Switzerland, arbitration proceedings related to mere validity disputes are rather rare, because of the multi-jurisdictional nature of most arbitral proceedings and hence possible enforcement issues with respect to certain jurisdictions. However, contractual disputes in connection with patents, such as licensing disputes, are often submitted to arbitral tribunals.

There are no special prerequisites for filing a patent action in Switzerland. Civil actions relating to intellectual property rights can be filed with the competent court without any need to attempt conciliation in front of a conciliation authority.

The issuance of warning letters is also not required, although mostly recommended to consolidate the legitimate interest of the claimant and to support the attribution of the procedural costs to the defendant. Sometimes litigation costs can even be avoided following settlement discussions or voluntary undertakings triggered by warning letters.

If patent infringement proceedings are commenced by an entitled licensee (see 3.1 Necessary Parties to an Action for Infringement), it is not required that the licence is registered in the patent register.

Parties may decide, but do not have any obligation, to be represented by an attorney at law in intellectual property matters. If a party decides to be represented in front of a Swiss court, the representative must be a qualified attorney at law. In proceedings concerning the validity of a patent in front of the Federal Patent Court, the parties may also be represented by a qualified and admitted patent attorney (Article 29, PCA).

Measures for interim relief are available under Swiss law if the applicant can provide prima facie evidence that the following requirements are met:

  • the right to which they are entitled has been infringed or an infringement is imminent;
  • such infringement threatens to cause not easily reparable harm;
  • the requested relief is relatively urgent; and
  • the requested relief is proportionate to the harm caused by the alleged infringement (Article 261 et seq, Civil Procedure Code (CPC)).

Note that urgency is not a strict requirement for granting interim relief. However, interim relief will not be granted if the applicant has waited for a substantial period of time (according to current practice, for more than 14 months) before requesting measures for interim relief.

In cases of special urgency, and in particular where there is a risk that the enforcement of the measure will be frustrated, the court may order the interim measure immediately and without hearing the opposing party (ex parte interim measures) (Article 265, CPC). The ex parte interim measures must subsequently be confirmed in inter partes proceedings granting the opposing party its right to be heard.

In addition, all interim relief proceedings require confirmation in main proceedings. In an interim judgment, the Federal Patent Court will set a deadline for the commencement of main proceedings, whereby the injunction lapses if the applicant does not initiate main proceedings, in which case the applicant is liable for any damages caused to the defendant.

In interim relief proceedings the applicant can, in particular, request:

  • an injunction;
  • an order to remedy an unlawful situation;
  • an order to a registering authority or to a third party; or
  • performance in kind.

Any person who has reason to believe that an ex parte interim measure will be applied against them, may set out their position in advance by filing a protective letter (Article 270, CPC).

Protective letters must be filed with the Federal Patent Court and/or the cantonal courts that are likely to have jurisdiction for ordering the ex parte interim measures in the case at hand. The other party will be served with the protective letter only if they actually initiate the respective ex parte proceedings. The protective letter becomes ineffective six months after it was filed.

Statute of Limitation

Monetary claims in patent infringement proceedings are time-barred after three years from the date on which the injured party became aware of the loss or damage and the identity of the person liable for them, but in any event ten years after the date on which the loss or damage was caused. If the action for damages is derived from an offence for which criminal law envisages a longer limitation period, that longer period also applies to the civil claim.

Claims for injunctive and declaratory relief are, in principle, not time-barred, but rather remain available as long as there is a legitimate interest in obtaining such a relief.

Forfeiture

The enforcement of rights might be limited due to their forfeiture based on Article 2 of the Swiss Civil Code, which requires every person to act in good faith in the exercise of their rights. If a person waits too long before initiating enforcement proceedings, their rights may be forfeited if the court determines, taking into account all relevant circumstances, that the claimant acted against good faith. As an example, the right to apply for interim measures is considered forfeited 14 months after the patent owner actually learned, or should have learned, of the infringement unless there are special circumstances (see 2.7 Interim Injunctions). With regard to main proceedings, forfeiture is likely to occur after approximately eight years. Based on Swiss case law, urgent status will not be granted by the courts if the patent owner has waited so long.

Swiss procedural law does not provide any procedural mechanisms for far reaching US-style fishing expeditions in order to obtain all evidence from the opposing party that might be relevant. However, there exist certain mechanisms allowing a party to obtain specific evidence.

PatA

Under the PatA, a patent owner with a legitimate interest – ie, providing prima facie evidence that their patent has been infringed or an infringement is suspected – may request that the Federal Patent Court order as an interim measure:

  • the securing of evidence; and/or
  • a precise description to be made of the allegedly unlawful processes used and/or of the allegedly unlawful products manufactured, as well as the means used to manufacture them (Article 77, PatA).

The procedure for making the description is typically carried out by a technically trained judge and a clerk at the location where the alleged infringement took place. Upon the request of an opposing party, the court will take necessary measures to safeguard business and trade secrets and might exclude the applicant (but not its representatives) from taking part in the inspection. The court will draft a written report describing the product or process and before the applicant receives the report, the opposing party is given the opportunity to comment (Article 77, PatA).

Under Swiss law there is no limitation as to how the evidence obtained through a description can be used, which means that a Swiss description can also be used to support proceedings abroad.

Swiss Civil Procedure Code

The Swiss Civil Procedure Code also allows a more general right to ensure preliminary taking of evidence without any need to start civil litigation (Article 158, CPC). Similar evidence as during a pending litigation on the merits can be the subject of such a preliminary taking of evidence – ie, the party may request witness hearings, the production of specifically identified documents, the inspection of goods or places, or the drafting of a court-appointed expert’s report. The questioning of the parties, however, can only be part of the proceedings on the merits.

In general, the parties to the case, and third parties, have a duty to co-operate in the taking of evidence (Article 160, CPC). However, the court cannot enforce its order, if a party to the proceedings does not produce the required evidence. But the court will take such conduct into account when assessing the evidence and the facts of the dispute.

Under Swiss procedural law, the statement of claim must contain:

  • the prayers for relief;
  • a statement of the value in dispute;
  • the allegations of fact;
  • a notice of the evidence offered for each allegation of fact; and
  • the date and signature.

It is not required by law to state the legal arguments (since the court must know the law), but it is common practice to do so and some courts expressly expect the parties to briefly state on which grounds their actions are based.

In general, in main proceedings, each party is entitled to two submissions during which it may provide new facts and evidence, amend its prayers for relief and limit the patent claims at stake, either inter partes or through a limitation request at the IPI. After the second submission, new facts and new evidence are admissible only if presented immediately after they become known and (i) if they occurred after the second submission (proper nova), or (ii) if they existed before but could not have been submitted despite reasonable diligence (improper nova). At such stage, a limitation of the patent claims at stake will only be considered if it were triggered by new arguments or evidence brought forward in the rejoinder. In any case, new facts and new evidence are admitted only until the court begins its deliberations.

Under Swiss law, no class actions or other collective actions are permitted. However, joinder of parties in civil proceedings is admissible.

Restrictions on the assertion of patent rights may apply from the law against unfair competition and antitrust law, in particular with respect to restrictions against parallel imports which are not justified (Article 9a, PatA and Article 5, Swiss Cartel Act) and unlawful practices by market-dominant undertakings or undertakings with relative market power (Article 7, Swiss Cartel Act).

Furthermore, a patent owner might be restricted in the enforcement of their rights due to their forfeiture based on Article 2 of the Swiss Civil Code (acting in good faith), in particular if they were to wait too long before initiating enforcement proceedings (see 2.9 Special Limitation Provisions).

Civil Actions

A patent owner who has their rights infringed, or is threatened with an infringement, may initiate a civil action. The exclusive licensee, irrespective of the registration of the licence in the patent register, may also bring an infringement action independently, provided this is not expressly excluded by the licence agreement (Article 75, PatA). Non-exclusive licensees, however, may only join the infringement proceedings filed by the patent owner or the exclusive licensee in order to claim their own losses or damages.

An infringement action can be raised against any person:

  • who uses a patented invention unlawfully;
  • who refuses to notify the authority concerned of the origin and quantity of products in their possession which are unlawfully manufactured or placed on the market, and to name the recipients and disclose the extent of any distribution to commercial and industrial customers;
  • who removes the patent mark from products or their packaging without authorisation from the proprietor of the patent or the licensees; and
  • who abets any of the said offences, participates in them, or aids or facilitates the performance of any of these acts (Article 66, PatA).

If there are several infringers, the claimant is not obliged to initiate the infringement action against all potential infringers.

Criminal Proceedings

Criminal proceedings can be initiated against the same persons provided that they wilfully committed the patent infringement, on complaint by the patent owner or ex officio, if the infringer acts for commercial gain (Article 81, PatA).

Swiss law does not explicitly contain a doctrine distinguishing between direct and indirect patent infringement. Whoever commits an infringement act as described in Article 66 of the PatA may be held liable under Swiss civil and criminal law.

However, the PatA implicitly distinguishes between direct infringement (Article 66 littera a, b and c, PatA) and contributory infringement (Article 66 littera d, PatA), according to which any person who abets, participates in, aids or facilitates the performance of any (direct) infringement may also be held liable under civil and criminal law. According to case law of the Swiss Federal Supreme Court, a contributory infringement is accessory to a direct infringement, meaning that an unlawful principal act is required for a contributory infringement, whereby it is sufficient for a claim for injunctive relief against the contributory infringer that a direct infringement is imminent.

With regard to its application in an international context, the accessoriness has the effect that the contributory infringer acting in Switzerland but contributing to a direct infringement abroad cannot be held liable under Swiss law. On the other hand, if the direct infringement takes place in Switzerland, a contributory infringer contributing to that infringement may be liable irrespective of whether the contributory acts are performed in Switzerland or abroad.

Regarding the supply of (non-infringing) materials or parts to a customer who uses these parts or materials for the manufacture of goods infringing a patent, the Swiss Federal Supreme Court has clarified that the supplier is liable as contributory infringer if they knew or should have known that the means supplied were suitable for, and intended to be used by, the customer for use in the infringing goods.

The most important particularity of process patent infringement proceedings concerns the burden of proof. In general, the claimant carries the burden of proof in infringement proceedings. However, the burden of proof may be reversed if the patent in question is a process patent. If an invention concerns a process for the manufacture of a new product, every product of the same composition is presumed to have been made by the patented process until proof to the contrary has been provided (Article 67, paragraph 1, PatA). The same applies by analogy to a process for the manufacture of a known product if the patent owner provides prima facie evidence of an infringement of the patent (Article 67, paragraph 2, PatA).

Regarding the territorial scope of a process patent infringement, the general rules apply, meaning that a direct infringement must occur in Switzerland in order for Swiss law to apply. Accordingly, the Swiss Federal Supreme Court held in a case that if a device intended for carrying out a patented process is manufactured in Switzerland, but the process itself is only carried out abroad, the process patent is not infringed in Switzerland.

Literal Infringements

The patent claims determine the scope of protection of a patent (Article 51, paragraph 2, PatA). According to established practice, the patent claims must be interpreted from the viewpoint of a skilled person, starting with the claim language but also taking into account the description and the drawings. General technical knowledge is also accepted as a means of interpretation.

The Swiss Federal Supreme Court held that the prosecution history of a patent is, in general, not decisive for the interpretation of the patent claims. Waivers and limitations made by the patent applicant during prosecution are to be taken into account only to the extent that they are ultimately reflected in the patent claims and/or the description.

Equivalent Infringements

The PatA explicitly holds that an imitation is also deemed to constitute a use (Article 66 littera a, PatA) and, hence, not only literal infringements but also equivalent infringements are known under Swiss law. The Swiss Federal Supreme Court and the Federal Patent Court have elaborated in several decisions, taking into account other European courts’ practice, a standard test for the assessment of an equivalent infringement based on three main steps.

  • Equal effect – the modified feature must objectively fulfil the same technical function as the corresponding feature of the patent claim.
  • Accessibility – the modified feature must be obvious to the skilled person in light of the teaching of the patent; the Federal Patent Court has clarified that the starting point for the assessment of accessibility is not the general prior art, but the patent at issue, as this step should not be confused with the assessment of the inventive step.
  • Equality – the skilled person must consider the modified feature as an equivalent solution taking into account the claim language and the description.

If all three requirements are fulfilled, an equivalent patent infringement exists according to Swiss practice.

Within Swiss patent infringement proceedings, the defendant may attack the validity of the claimant’s patent or raise non-infringement arguments.

Validity Defences

The defendant may plead the invalidity of the patent as a defence in the form of an objection or as a formal counterclaim. If the defendant raises the invalidity as an objection and the court determines that the patent is in fact invalid, that decision has only a direct effect between the parties – ie, the infringement action is rejected but the patent is not revoked from the patent register. If the defendant decides to file a counterclaim, this has the same effect as a standalone invalidity action – ie, if the invalidity of the patent is confirmed by the court, the infringement action is rejected and the patent is also declared invalid and formally revoked.

Lawful-Use Defences

Alternatively, or additionally, defendants may also claim to have lawfully used the allegedly infringed patent. Defendants may argue the following.

  • That they have been granted a valid licence right.
  • That they can rely on a statutory exception as per Article 9 of the PatA, including the exceptions of:
    1. private use for non-commercial purposes;
    2. use for research or experimental purposes (in order to obtain knowledge about the subject-matter of the invention);
    3. use for teaching purposes;
    4. use for obtaining marketing authorisation for a medicinal product (Bolar-type exemption);
    5. use by a medicinal professional for an individual person (medical prescription exemption); or
    6. use for a direct individual preparation of a medicinal product in a pharmacy (pharmacists’ exemption).
  • That the patent owner’s rights were exhausted (Article 9a, paragraph 1, PatA); whereas in general EEA-wide exhaustion applies, but if the patent is of subordinate importance for the functional characteristics of the goods, global exhaustion applies, and if the price of the patented goods is fixed by the state (such as with medicinal products), national exhaustion applies.
  • That they have a prior-use right (ie, have commercially used the invention in good faith in Switzerland or have made special preparations for that purpose prior to the filing or priority date of the patent application (Article 35, PatA)); in this case, the defendant might have to pay the patent owner appropriate compensation (Article 48, PatA).
  • That the patent in question is a standard essential patent and defendants rely on a FRAND (fair, reasonable and non-discriminatory) licence; so far, no case law in this respect has been established in Switzerland since all FRAND cases in front of the Federal Patent Court have been settled.

As a general rule, the Federal Patent Court makes its decisions as a three- or five-member body (panel), of whom at least one member must possess technical training. One of the technically trained judges will issue a written opinion (the “Technical Opinion”) covering all technical aspects of the case and the parties are given the opportunity to comment. Such Technical Opinions do not bind the other judges, although in many instances they will be largely followed in the judgment.

Additional technical know-how, at the request of a party or ex officio, may be obtained by an opinion from one or more external experts appointed by the court ad hoc (Article 183, CPC). However, external expert opinions basically do not play a role in patent proceedings, since the Federal Patent Court has technically trained judges with expertise in all relevant fields of science.

The parties may submit written expert statements. However, these are considered as assertions of the parties only.

All arguments against the infringement of patent claims must be raised within the same proceedings. There is no separate procedure for construing patent claims.

Swiss law does not provide for a mechanism in which a third party that is not a party to the patent proceedings could file, on its own, any kind of amicus brief to the court.

There are several reasons for a revocation or cancellation of a patent.

Often, a patent registered in the Swiss patent register is cancelled because the renewal fees are not paid on time.

Swiss national patents or Swiss parts of European patents are also cancelled, and removed from the Swiss patent register, if an action for invalidity of the patent has been successful. The cancellation is done by the IPI upon the provision of full official copies of the final judgments. Any person with a proven interest may bring an invalidity action if the invention is excluded from patentability (eg, human body), is obvious, not novel, or not disclosed in a way that a person skilled in the art could carry it out, or if the application has been unduly amended (Article 26 et seq, PatA). The requirements for the interest to be demonstrated by the claimant are rather low. The only exception is an invalidity action based on the allegation that the patent owner has no right to the grant of the patent. This particular ground for invalidity can only be asserted by the person claiming to actually be entitled to the patent.

An action for the cancellation of a patent could also be brought by a person with a demonstrated interest if the granting of licences does not suffice to meet the demand of the domestic market after a period of two years from the granting of the first compulsory licence (Article 38, PatA). Such actions are very rare and to date no patent appears to have ever been cancelled based on such action in Switzerland.

Finally, based on the prohibition against double patenting, a Swiss patent is revoked in favour of a European patent for one and the same invention with effect in Switzerland and granted to the same inventor or to their successor in title with the same filing or priority date (Article 125, paragraph 1, PatA).

Partial cancellation is possible if the successful invalidity action relates to certain patent claims only (Article 27, PatA).

A patent owner may amend a patent by surrendering a patent claim, limiting an independent claim by combining one or more patent claims which are dependent on it, or limiting an independent claim in some other way (see 1.10 Post-Grant Proceedings Available to Owners of Intellectual Property Rights).

A patent may also be amended during invalidity or infringement proceedings. However, the patent owner is only able to rely on the amended patent up to a certain stage of the proceedings.

The Swiss Federal Supreme Court has clarified that if the patent owner amends the patent through the IPI during pending infringement proceedings, this has an ex tunc effect and thus the original patent that is the subject of the infringement proceedings no longer exists. If the introduction of new facts (ie, the amended patent) is no longer admissible at the stage of the proceedings in question, the infringement proceedings must be dismissed. This is generally the case if the patent is limited after the second pleading, at which stage new facts and new evidence are admissible only under very strict circumstances (see 2.11 Initial Pleading Standards). Hence, if the patent owner wants to proceed against the alleged infringer based on the amended version of the patent, they must commence new infringement proceedings.

Where an invalidity claim is raised as a defence within patent infringement proceedings, that invalidity claim is heard at the same time and within the same proceedings. The Swiss patent litigation system is not bifurcated.

In this context it is noteworthy that in December 2025, the Swiss Federal Patent Court revised its practice concerning nullity actions. Under the new approach, when a nullity claim is directed against a patent or other IP right that forms the basis of a pending infringement action, the proceedings are now handled on an accelerated track. The court dispenses with the traditional instruction hearing, enabling first instance resolution within a maximum of one year.

The new accelerated nullity proceedings must be viewed against the backdrop of the Unified Patent Court’s (UPC) emerging case law on long-arm jurisdiction, which has increased the strategic importance of swift and co-ordinated validity assessments across Europe.

Procedural Provisions

The Swiss Federal Patent Court has exclusive jurisdiction in certain civil patent litigations. However, the proceedings before the Federal Patent Court are primarily based on the ordinary Swiss Civil Procedure Code, which applies to all civil proceedings. The Patent Court Act only contains a few provisions relating to the proceedings (eg, composition of the panel, jurisdiction and legal representatives).

Typical Steps of Infringement Proceedings

Ordinary infringement proceedings are initiated by filing a written statement of claim, followed by a written statement of defence in which the defendant usually asserts invalidity of the patent either by way of a defence or by filing a counterclaim.

After the exchange of the first briefs, the parties are summoned to an instruction hearing in front of a delegation of the court, normally consisting of the court president, the leading technical judge and a court clerk. The instruction hearing consists of two parts. In a first part that is minuted, the court delegation can pose questions to the parties to seek specific clarifications or to get information with respect to parallel proceedings. The delegation will also mention if further substantiation is required. This part is normally quite short. The second, informal part of the instruction hearing is not minuted. The delegation of the court will present a confidential preliminary assessment of the case and the parties may then engage in court-mediated settlement negotiations.

If no settlement is found, the proceedings continue and the parties will exchange their second briefs (ie, reply, rejoinder and comments on new invalidity arguments and evidence in the rejoinder). Thereafter, the technical judge will issue their written expert opinion, on which the parties may comment in writing. As a final step, the parties are summoned to the main hearing. After the parties’ pleadings, the court can decide whether a court expert will be appointed, witnesses will be heard, or other evidence will be taken. In most cases the court closes the proceedings after the main hearing and renders its judgment in writing within four to six weeks.

Ordinary proceedings on the merits concerning infringement or the nullity of a patent generally take about 18 to 24 months.

Action by Stages

An infringement action is typically initiated as a so-called action by stages (Stufenklage). In the first stage, the Federal Patent Court renders a partial judgment on the validity of the patent (if contested), the infringement, injunctive relief and the disclosure of information for the calculation of monetary relief. In the second stage, the patent owner asserts the amount of its monetary relief claim based on the information received and the Federal Patent Court decides on the monetary relief.

The Federal Patent Court makes its decisions as a three-member (or occasionally a five-member) body (panel), of whom at least one member must possess technical training.

In the rare proceedings concerning patent matters that are ruled before civil cantonal courts (see 5.4 Other Court Proceedings), external technical experts may be appointed to submit an expert opinion ex officio or at the request of a party (Article 183, CPC). However, the final decision remains with the judges and also with regard to technical questions.

Settlements may be agreed at any stage of civil proceedings. They may be discussed with the mediation of the court or upon separate negotiations among the parties only. Swiss courts often actively support the parties in order to find a settlement.

In front of the Swiss Federal Patent Court, the parties are summoned to an instruction hearing after the exchange of the first briefs (see 5.1 Special Procedural Provisions for Intellectual Property Rights). During this hearing, the court will present a confidential preliminary assessment of the case, which should serve as a basis for settlement discussions. A considerable number of disputes are settled at this stage.

In respect of contractual rights related to patents, such as ownership and licence rights, legal actions may not only be filed with the Federal Patent Court but also with the cantonal courts (Article 26, paragraph 2, PCA). Where the invalidity or infringement of a patent is to be adjudicated in such proceedings as a preliminary question or on a defence basis, the cantonal court grants the parties a reasonable period of time for filing the validity or infringement action before the Federal Patent Court, which has exclusive jurisdiction over this subject matter (see 2.3 Courts With Jurisdiction). The cantonal court must then stay the proceedings until a final decision has been made by the Federal Patent Court. However, considering that actions before cantonal courts with regard to patents have become very rare since the establishment of the Federal Patent Court, the influence of cantonal proceedings on the others are, in practice, very limited.

If infringement proceedings before the Federal Patent Court relate to a European patent which is the subject of pending opposition or appeal proceedings before the EPO, the Federal Patent Court may stay its proceedings. In practice, however, this plays only a very limited role, since the Federal Patent Court emphasises that it only suspends its proceedings if a decision by the EPO can be expected in a short time. Instead, it is the Federal Patent Court’s standard practice to submit an acceleration request to the EPO.

Parallel infringement proceedings in front of other European courts do not have a direct influence on proceedings before the Federal Patent Court. The Federal Patent Court, however, is generally interested in judgments of other European courts when parallel parts of European patents are involved, although such judgments do not bind the Swiss courts in any way.

Anti-suit injunctions of foreign courts are generally considered as inadmissible under Swiss law.

Civil remedies for patent owners include injunctions or reparatory remedies, damages (including legal costs), declaratory judgments, delivery up or destruction of infringing goods, a recall order and publication of the judgment. See 1.5 Rights and Obligations of Owners of Intellectual Property Rights for further detail.

Permanent injunctions are the most common remedy sought in infringement proceedings and are generally granted if an infringement is affirmed. In order to enforce the injunction, the judgment provides for administrative fines (per day of violation) if the infringer does not comply with the injunction, and for criminal sanctions.

For past infringements, the patent owner may claim monetary remedies in the form of damages such as lost profits or, if the infringer acted in bad faith, account of the infringer’s profit. Alternatively, the patent owner can choose to ask for surrender of the unjust enrichment in the form of a reasonable royalty rate. Swiss law does not provide for punitive or exemplary damages or the like.

Since the patent owner usually does not have all the necessary information to prove the amount of damages or the profit to be surrendered, Swiss law grants the patent owner a claim for the necessary information and the infringer may be ordered to render account of the sales and gross turnover made from the infringing activities. Such a claim is usually asserted in a so-called “action by stages”. See 5.1 Special Procedural Provisions for Intellectual Property Rights.

The court is bound by the available civil remedies and the parties’ prayers for relief and has no discretion in ordering other remedies.

According to Swiss civil procedure law, the losing party must bear the court costs and has to reimburse the prevailing party for its legal costs and expenses, including the costs for assisting patent attorneys. The compensation for legal costs is calculated based on tariffs depending on the value of the dispute. Such compensation will often not cover all the fees actually incurred.

If the defendant has incurred damages as a consequence of the proceedings, they may claim compensation for such damages. Within proceedings for interim measures, the court may make the interim measure conditional on the payment of a security deposit by the applicant, if it is anticipated that the measures may cause damage to the opposing party. An applicant for interim relief is liable for any damages caused in the event such measures are later found to be unjustified. If the applicant proves, however, that they applied for the measures in good faith, the court may reduce the damages or entirely release the applicant from liability (Article 264, CPC).

The same types of remedies are available for infringements relating to Swiss national patents and Swiss parts of European patents. Essentially, the same types of remedies are available for civil proceedings involving inventions protected as trade secrets. See 1.5 Rights and Obligations of Owners of Intellectual Property Rights for further detail.

An appeal to the Swiss Federal Supreme Court does not have suspensive effect and, accordingly, injunctions granted at first instance are enforceable during the appeal proceedings. Upon request, the Federal Supreme Court may grant suspensive effect, but this is quite rare.

Appeals to the Swiss Federal Supreme Court against decisions of the Federal Patent Court or the civil cantonal courts as sole instance follow the same rules as appeals in civil matters.

The Swiss Federal Supreme Court’s discretion when reviewing final decisions of prior instances on the merits is limited to legal questions. In a recent judgment, the Swiss Federal Supreme Court decided that the construction of patent claims is a legal question. In addition, the assessment of invalidity grounds is also a legal question. In contrast, a review of the facts is only possible in a very limited manner by ascertaining an abuse of law by the prior instance in arbitrarily determining the facts (Article 97, Supreme Court Act (SCA)).

With regard to decisions on interim measures, the discretion of the Swiss Federal Supreme Court is narrower and limited to a review of a violation of constitutional rights (Article 98, SCA).

Prior to filing a patent lawsuit, there may be significant costs associated with the technical assessment of a patent’s validity (as the defendant’s usual defence will be to bring an invalidity action against the patent) and the assessment of the potential infringement of said patent by the allegedly violating goods of the counterparty. Additional costs may arise for the issuance of warning letters or the preparation and filing of protective briefs.

Court costs are calculated based on tariffs depending on the value of the dispute.

Upon filing an action, the claimant is requested to advance part of the court costs. As of January 2025, the revised Swiss Code of Civil Procedure (CPC) stipulates that the advance payment cannot exceed half of the anticipated court costs in all civil proceedings. In proceedings before the Federal Patent Court, this amount typically corresponds to the expected costs incurred up to and including the instruction hearing.

As a principle, the losing party must bear the court costs and has to reimburse the prevailing party for its legal costs. A proportionate allocation in relation to the outcome is also possible. Both court costs and the compensation for legal costs are calculated based on tariffs depending on the value of the dispute.

In Switzerland, alternative dispute resolution (ADR), or, more specifically, arbitration, is an important means of resolving intellectual property disputes, particularly in international cases where a single decision is advantageous.

ADR in Switzerland is attractive for patent disputes as Switzerland provides for arbitration experts in most fields of technology and has a liberal regime regarding the recognition and enforcement of arbitral awards.

According to Swiss case law, all aspects of intellectual property disputes are arbitrable, including contractual issues related to patents as well as disputes over the validity of patents. Whereas arbitration proceedings related to mere validity disputes are rather rare, contractual disputes are often the subject of arbitration proceedings (see 2.4 Specialised Bodies/Organisations for the Resolution of Disputes).

Under Swiss law, the assignment of intellectual property rights consists of the undertaking to assign the right and the actual disposition of the right. While the undertaking to assign the right is not required to fulfil specific formal requirements, the actual transfer of the patent or patent application rights must be made in writing (Article 33, paragraph 2bis, PatA).

In order to validly assign and transfer the patent or patent application rights, neither the approval of the IPI nor its recording in the Swiss patent register is required. However, if the assignment is not recorded, it is invalid against persons who have acquired, in good faith, rights to the patent from the registered patent owner.

For the recording of the assignment of the patent or patent application rights, the IPI requests the written consent of both the assignor and the assignee.

See 10.1 Requirements or Restrictions for Assignment of Intellectual Property Rights.

Under Swiss law, there are no specific formal requirements for licence agreements. Licence agreements can even be concluded orally and no approval of the IPI is required. However, where the patent application or the patent is owned by two or more persons, a licence grant requires the consent of all co-owners.

Licences may be recorded in the Swiss patent register, but this is not required for their validity between the contractual parties. However, if the licence is not recorded, it is invalid against persons who have acquired the patent in good faith (Article 34, paragraph 4, PatA).

For the recording of the licence rights, the IPI requests the written consent of the licensor.

See 10.3 Requirements or Restrictions to License an Intellectual Property Right.

Pestalozzi

Feldeggstrasse 4
8008 Zurich
Switzerland

Cours de Rive 13
1204 Geneva
Switzerland

+41 44 217 91 11

zrh@pestalozzilaw.com pestalozzilaw.com/en/
Author Business Card

Trends and Developments


Authors



MLL Legal is a leading Swiss patent law firm. The IP team members are among the leaders in the field and have extensive experience in Swiss, EU and German law. The firm is highly recommended for patent and other IP disputes and transactions in Switzerland. MLL Legal is regularly ranked by Chambers and Partners in Chambers Global, Europe, High Net Worth and FinTech, all as a Leading Firm. The firm is deeply involved in patent litigation in Switzerland and brings broad experience to these matters. In recent years, MLL Legal has notably represented patent holders in high‑profile patent disputes, including FASLODEX® (fulvestrant), ELIQUIS® (apixaban), NEXAVAR® (sorafenib tosylate), TECFIDERA® (dimethyl fumarate), ELVANSE® (lisdexamfetamine), and XARELTO® (rivaroxaban).

Recent Cases in Swiss Patent Litigation

According to the Swiss Federal Patent Court’s annual report for 2024, the number of cases filed with the Court decreased from 31 to 20 compared to the previous year. Notably, the number of ordinary proceedings dropped significantly, from 20 to 11, whereas the number of summary proceedings fell only slightly. The number of cases brought before the Swiss Federal Patent Court in 2025 is likely to be similarly low compared to that of 2024. It is assumed that the decline in the number of cases in Switzerland is linked, among other things, to the successful launch of the Unified Patent Court (UPC), and in recent months there has been an increase in applications to the UPC or European national courts for cross-border injunctions, which include Switzerland. Therefore, several important and interesting measures have been taken by the Swiss Federal Patent Court to address procedural issues, with the aim of making the Court even more attractive and speeding up proceedings. For example, the Swiss Federal Patent Court changed its previous practice and ruled that, in PI (preliminary injunction) proceedings, a patent can only be enforced in one version, without relying on any auxiliary requests (Court Order of 29 October 2024 of the PI proceedings S2024_008). This will simplify and accelerate the preliminary injunction proceedings in Switzerland.

Another important change in practice was just recently published in a press release at the end of 2025. The Swiss Court announced that, starting in 2026, the proceedings will be expedited, if an action for declaration of nullity is brought against a patent forming the basis for an infringement action. There will be no instructional hearing; instead, after the first exchange of briefs, the parties will receive an extended notice to substantiate their case. Without the consent of the other party, extensions of deadlines will only be granted with extreme reluctance. The aim is to complete the proceedings at first instance within less than one year. Appeal proceedings in Switzerland have always been relatively quick, with a duration of only about six months. Consequently, nullity proceedings under the accelerated regime can be completed in two instances, within one and a half years. This is undoubtedly a positive development, particularly in light of the rising number of cross-border proceedings that have been observed recently. Good preparation when starting or expecting patent litigation, which has always been crucial, will become even more important.

Although the number of cases was relatively small, those that the Federal Patent Court had to decide on in 2025, particularly in the pharmaceutical area, were of great economic significance. Noteworthy cases include those concerning Bayer’s patent for the once-daily administration of rivaroxaban (Xarelto®), Takeda’s patent for lisdexamfetamine (Elvanse®) and Biogen’s patent for dimethyl fumarate (Tecfidera®) at a dosage of 480 mg for the treatment of multiple sclerosis. As demonstrated by the proceedings in 2024 concerning “sorafenib tosylate” (Nexavar®) and “apixaban” (Eliquis®), the trend of successfully defending substance patents continued in 2025. In contrast, patentees with patents for second medical-use patents tend to find it more challenging to defend their patents before the Swiss Federal Patent Court – as well as elsewhere.

Below, the authors discuss selected judgments that they believe represent the highlights of Swiss patent litigation in 2025. For the sake of transparency, the authors acknowledge that MLL Legal was involved in most of these proceedings, representing the patentees.

Major but ultimately futile victory in PI appeal proceedings before the Federal Supreme Court (4A_418/2024, judgment of 20 December 2024; O2023_007, judgment of 17 January 2025)

A case that has gained significant attention internationally beyond the borders of Switzerland concerns Bayer’s blockbuster product XARELTO® containing the active ingredient rivaroxaban.

This is not only a case of utmost economic importance, but also a landmark case for patent litigation proceedings in Switzerland from a procedural point of view. In particular, the Federal Supreme Court clarified that in PI proceedings, following a possible rejection of the ex parte PI request, inter partes proceedings must follow in any case, in which the parties are given the opportunity to comment.

After the supplementary protection certificate (SPC) for rivaroxaban expired in Switzerland in June 2024, generic companies entered the market with their generic products, despite Bayer’s Swiss part of EP 1 845 961 B1 (EP 961) titled “Therapy of thromboembolic disorders with Rivaroxaban” with a maximum duration until January 2026. EP 961 specifically protected the once-daily administration of rivaroxaban for the treatment of thromboembolic diseases.

Following the launch of generics on the Swiss market, Bayer initiated PI proceedings before the Swiss Federal Patent Court. Since the validity of EP 961 had already been reviewed and confirmed by the EPO Board of Appeal, Bayer filed a PI application as an ex parte request. As it turned out later, the defendant had previously filed a protective letter with the Swiss Federal Patent Court. The judgment of the Federal Patent Court shows that the Court considered this protective letter and concluded that EP 961 was likely not valid due to alleged lack of inventive step. Bayer’s request for an ex parte PI was rejected, without the plaintiff being able to comment on the allegations made in the protective letter. Moreover, the Court ordered Bayer to pay not only the court costs, but also party compensation that had not even been requested. The Court justified this on the grounds that the protective letter had been filed (S2024_003, judgment dated 10 July 2024).

Bayer filed an appeal with the Federal Supreme Court, seeking to overturn the first instance decision and have the case remitted for further proceedings that would respect the parties’ right to be heard.

The Supreme Court examined whether or not the appeal was admissible, focusing on whether or not the lower court’s judgment caused irreparable harm of a legal nature – a threshold usually extremely difficult to pass. The Supreme Court found that, in this particular case, the first instance judgment was fundamentally flawed. The judges also found that introducing this fundamentally flawed judgment into related foreign proceedings would cause collateral damage that might constitute irreparable harm of a legal nature. This is why the appeal was deemed admissible. Substantively, the Supreme Court determined that the Patent Court had violated Bayer’s right to be heard by not conducting a two-stage procedure: after denying the ex parte request, the court should have given Bayer the opportunity to respond to the protective letter before issuing a final decision on the provisional measures. The Supreme Court also found that awarding party compensation to the defendant without a corresponding request violated the principle of party disposition.

As a result, the Supreme Court allowed the appeal, overturned the Patent Court’s decision, and remitted the case back for further proceedings that would respect the right to be heard and proper procedural conduct. The Court considered the appeal against the preliminary‑injunction decision of the Swiss Federal Patent Court to be admissible, something that had not occurred since the Swiss Federal Supreme Court changed its case law in 2011. However, the joy of the appellant did not last long as just a few days later the Federal Patent Court issued its judgment in the parallel nullity proceedings regarding the same patent EP 961 (O2023_007, judgment of 17 January 2025).

The core of the nullity proceedings centred on whether or not the claimed subject-matter of EP 961 – more specifically, the use of a rapid-release tablet of rivaroxaban administered once daily for at least five consecutive days – is inventive in light of the prior art. The court applied the problem–solution approach, identifying the closest prior art as a set of scientific abstracts and posters (notably the so-called “Harder Poster” and related studies) that were publicly available before the patent’s priority date. The court concluded that these documents disclosed that rivaroxaban, as a direct Factor Xa inhibitor, had a pharmacological profile suggesting suitability for once-daily dosing, and that such dosing regimens were already being considered and discussed in the scientific community. The court further found that the prior art provided a motivation for the skilled person to test once-daily administration of rivaroxaban in a rapid-release tablet form. According to the Court, the pharmacokinetic data, including half-life and plasma concentration profiles, as well as the pharmacodynamic effects, were sufficiently disclosed in the prior art to make the claimed regimen obvious.

The judgment further reviewed the status of the patent in other jurisdictions, noting that while some courts upheld the patent, others – including those in the UK and France – found it invalid. The Swiss court aligned itself with the latter view, concluding that the patent lacks inventive step and declared the patent invalid for Switzerland. Bayer filed an appeal with the Swiss Federal Supreme Court, which was dismissed (4A_91/2025, judgment of 23 May 2025).

Confirmation of the validity of the basic patent of the SPC for lisdexamfetamine (O2023_017, judgment of 12 June 2025) and finding of infringement of the SPC by a generic’s medicament (S2024_008, judgment of 12 June 2025)

These cases concern the SPC for lisdexamfetamine, the active ingredient in Elvanse®, used for treating ADHD.

Spirig HealthCare AG (Spirig) initiated the dispute by filing a nullity action against the Swiss part of European Patent EP 1 644 019 B2 (EP 019), which is the basic patent for the SPC for lisdexamfetamine. However, instead of waiting for the outcome of the nullity proceedings, Spirig launched its generic lisdexamfetamine on the Swiss market. This prompted the patentee and SPC holder, Takeda Pharmaceuticals U.S.A., Inc., to initiate PI proceedings based on its Swiss SPC 019. Both proceedings – the nullity proceedings and the PI proceedings – ran in parallel, resulting in judgments dated on the same day.

The nullity proceedings centred on the validity of the Swiss part of European Patent EP 1 644 019 B2 protecting Takeda’s lisdexamfetamine medicament. EP 019 had already undergone opposition proceedings at the EPO, resulting in it being upheld in a slightly amended form compared to the granted patent. In the Swiss proceedings, Spirig sought a declaration of nullity of EP 019, arguing lack of novelty and inventive step. In the nullity proceedings, Spirig explicitly attacked only the basic patent of the SPC for lisdexamfetamine, as the invalidation of a basic patent would also invalidate the associated SPC. Spirig did not invoke SPC-specific grounds of nullity to challenge the SPC itself.

The court analysed multiple prior art documents, including AU 54,168/65, a prior art document that was already subject to the EPO opposition proceedings, and assessed whether the claimed invention was novel and involved an inventive step. The court found that the subject-matter claimed in EP 019 was not directly and unambiguously disclosed in the prior art. Specifically, the claimed molecule, ie, L-lysine-d-amphetamine and salts thereof, was not anticipated by the cited references. Also, the court determined that the claimed invention was not obvious to a skilled person. The pharmacokinetic properties and reduced abuse potential of lisdexamfetamine were considered not obvious based on the prior art. In fact, the court considered that the patent demonstrated a sustained release of amphetamine with lower potential for abuse, which was supported by experimental data.

As a consequence, the court dismissed Spirig’s nullity action in its entirety. As Spirig did not file an appeal, this decision became final.

In the parallel PI proceedings Takeda claimed that Spirig’s generic lisdexamfetamine infringed its SPC 019 for lisdexamfetamine. In these proceedings, Spirig did not deny infringement, but argued that the SPC was allegedly invalid because it did not meet the requirements of the SPC provisions in the Swiss Patent Act. Spirig argued that lisdexamfetamine is allegedly not a new product, as D-amphetamine (the metabolite of lisdexamfetamine) had already been subject to a marketing authorisation in Switzerland in 1972. According to Spirig, the marketing authorisation for Elvanse® relied upon for the SPC did not constitute the first authorisation for the product. Takeda in turn countered, inter alia, that lisdexamfetamine is a distinct molecule and was authorised as a new active substance. The Court analysed whether the authorisation of Elvanse® was the first for the product under Swiss law and relevant ECJ case law. It concluded, inter alia, that lisdexamfetamine is a different molecule from D-amphetamine and was first authorised as a medicinal product in Switzerland as Elvanse®. Taking into account the simultaneous ruling in the nullity proceedings, in which the court confirmed the validity of the basic patent, for the purposes of preliminary measures, the court presumed that the SPC is valid and infringed.

The preliminary injunction prohibits Spirig from marketing its generic lisdexamfetamine in Switzerland, protecting Takeda’s market exclusivity for Elvanse® until ordinary proceedings are concluded. As an interesting side note, as far as proportionality is concerned, the court rejected Takeda’s requests for bans on storage and possession, finding them unnecessary to prevent irreparable harm. For the sake of completion, it is to be noted that Spirig filed an appeal against the decision in the PI proceedings. The Swiss Federal Supreme Court found the appeal inadmissible because Spirig was unable to demonstrate an irreparable harm of a legal nature. This case differed in particular from the appeal in the rivaroxaban PI proceedings S2024_003 discussed above because the PI decision in the first instance did not suffer from any fundamental procedural errors.

Difficult times for second medical-use claims (S2024_005, S2024_006, S2024_007, judgment of 8 July 2025)

The plaintiffs, Biogen MA Inc. and Biogen International GmbH, sought preliminary injunctions against three defendants to prohibit the manufacture, storage, sale, and distribution of specific dimethyl fumarate products in Switzerland, arguing infringement of the Swiss part of European Patent EP 2 653 873 (EP 873). The defendants opposed these requests, challenging both the validity and the alleged infringement of the patent.

On the merits, the court examined whether or not the patent’s subject matter was sufficiently disclosed and whether or not the claimed invention was novel and inventive. It found that the patent was sufficiently disclosed, as the application provided experimental evidence for the claimed medical effect of dimethyl fumarate at the specified dosage. The court also addressed arguments regarding the effectiveness of the compound for the treatment of PPMS (a specific subtype of multiple sclerosis), concluding that, while not proven, it was credible that dimethyl fumarate had at least a stabilising effect in PPMS at the claimed dosage.

Regarding novelty, the court determined that the relevant prior art, WO 2006/037342, did not directly and unambiguously disclose the specific combination of features claimed in the patent, particularly the use of dimethyl fumarate at a daily dose of 480 mg for treating multiple sclerosis. However, when assessing inventive step, the court applied the problem–solution approach and identified the closest prior art as a clinical study (Kappos I) that disclosed the use of dimethyl fumarate in RRMS (another subtype of multiple sclerosis) at various dosages. The only difference was the specific choice of a 480 mg daily dose. The court found that the selection of this dosage was obvious to the skilled person, motivated by the desire to minimise side effects while maintaining efficacy, and thus the claimed invention did not involve an inventive step.

The Swiss PI decision was not appealed and, meanwhile, the EPO Board of Appeal revoked EP 873 due to added matter.

Patent still in force due to withdrawal of nullity action at appeal stage (O2024_002, judgment of 12 August 2025 and judgment 437/2025, 4A_449/2025 of 3 November 2025)

The case was brought by Samsung Bioepis CH GmbH (Samsung) against Janssen Biotech, Inc. (Janssen), seeking a declaration of invalidity for the Swiss and Liechtenstein part of EP 3 883 606 (EP 606). EP 606 covers the use of ustekinumab (an anti-IL-12/IL-23p40 antibody) for treating moderately to severely active ulcerative colitis. The defendant and patentee, Janssen, requested the court to dismiss the action as inadmissible or, alternatively, to reject it on the merits.

Central to the dispute was whether the patent’s main claim and its various auxiliary requests were novel and inventive over the so-called “Ochsenkühn Poster” and the underlying clinical study, which had been publicly presented at a conference before the relevant priority date. With regard to the content of the poster presented at a conference, the court summoned Professor Ochsenkühn as a witness. In its ruling, the court stated that, as far as the content of the poster presented is concerned, Professor Ochsenkühn credibly explained that its content corresponds to the PDF of the “Ochsenkühn Poster” filed in the proceedings. Apparently, there were differences between the submitted PDF and the poster displayed. However, based on Professor Ochsenkühn’s testimony, the court found it sufficiently proven that the noticeable formatting differences between the poster presented at the conference and the poster submitted as a PDF were due to the fact that Professor Ochsenkühn initially provided the lawyers with a different version of the file, which differed marginally from the version actually presented. In its judgment, the court literally stated that it was credible that a medical professional would not have been able to recognise the significance of the exact match and the obsessive attention to detail with which the trial lawyers focused on the formatting differences.

Ultimately, the court held that the patent was not novel and/or did not involve an inventive step in all relevant claim versions and ordered the Swiss and Liechtenstein part of EP 3 883 606 to be revoked.

However, during the subsequent appeal proceedings 4A_437/2025 and 4A_449/2025, the plaintiff withdrew its nullity action. As a consequence, the first instance judgment was set aside and the proceedings were written off. As a result, the patent EP 606 remains in force in Switzerland and Liechtenstein.

Outlook for 2026

In the context of multinational patent litigation, the Swiss Federal Patent Court is an important court and a relevant factor that must be taken into account in the overall strategy of international patent litigation. Given the procedural changes aimed at streamlining and expediting proceedings before the Federal Patent Court, it is all the more important to be well prepared when entering into Swiss proceedings. In light of the various recent developments and the attractive and expeditious procedures, the authors expect the Swiss Federal Patent Court to continue to play an important role in high‑stakes patent litigation and to also remain an influential forum in cross‑border proceedings.

MLL Legal

Schiffbaustrasse 2
P.O. Box 8031
Zürich
Switzerland

+41 58 552 08 00

+41 58 552 08 01

zurich@mll-legal.com mll-legal.com
Author Business Card

Law and Practice

Authors



Pestalozzi is a Swiss business law firm that has focused on high-end work for domestic and international clients since 1911. The firm guides and supports its clients in their strategic business decisions, anticipates their future challenges and helps them solve their critical issues. With over 100 professionals in Zurich and Geneva, the firm is at home in Switzerland’s two main commercial hubs. While being locally embedded, Pestalozzi has also developed sought-after expertise in dealing with multi-jurisdictional transactions and disputes. The firm has a long tradition in providing intellectual property services. Its IP practice group provides results-oriented, effective and pragmatic solutions for the protection and commercialisation of intangible assets, including representing clients from all industry sectors in enforcing and defending their intellectual property rights.

Trends and Developments

Authors



MLL Legal is a leading Swiss patent law firm. The IP team members are among the leaders in the field and have extensive experience in Swiss, EU and German law. The firm is highly recommended for patent and other IP disputes and transactions in Switzerland. MLL Legal is regularly ranked by Chambers and Partners in Chambers Global, Europe, High Net Worth and FinTech, all as a Leading Firm. The firm is deeply involved in patent litigation in Switzerland and brings broad experience to these matters. In recent years, MLL Legal has notably represented patent holders in high‑profile patent disputes, including FASLODEX® (fulvestrant), ELIQUIS® (apixaban), NEXAVAR® (sorafenib tosylate), TECFIDERA® (dimethyl fumarate), ELVANSE® (lisdexamfetamine), and XARELTO® (rivaroxaban).

Compare law and practice by selecting locations and topic(s)

{{searchBoxHeader}}

Select Topic(s)

loading ...
{{topic.title}}

Please select at least one chapter and one topic to use the compare functionality.