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Alexion Pharmaceuticals v Amgen Technology (Ireland) Unlimited Company (CoA, 19 June 2025)

Date19 June 2025
CourtCoA
DivisionLuxembourg (LU)
Type of actionGeneric application
Registry referenceApp_8339/2025 · ORD_11876/2025
PartiesAlexion Pharmaceuticals, Inc.

Official decision (PDF) · UPC registry entry

Dhenne Avocats represents claimants and defendants in European patent disputes before the Unified Patent Court, including the Paris divisions.

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Dhenne Avocats · 10 October 2026

Our analysis

Summary

By decision of 19 June 2025, the Court of Appeal rejects as not allowable Alexion Pharmaceuticals’ application for rehearing of its order of 20 December 2024, which had upheld the refusal of provisional measures against nine Amgen group companies based on EP 3 167 888 B1 (UPC_CoA_405/2024). The headnote sets out the general principles governing rehearing for a fundamental procedural defect (Art. 81(1)(b) UPCA and Rule 247(c)). The decision matters to any litigant tempted to reopen an appellate ruling: rehearing remains an extraordinary remedy, unavailable for mere disagreement with the Court’s reasoning. On the same day, by a separate decision, the Court rejects Alexion’s parallel application concerning the order made against Samsung Bioepis (UPC_CoA_402/2024).

Facts and procedure

Alexion had sought provisional measures against Amgen before the Hamburg Local Division. The application was refused because the validity of the patent could not be established with sufficient certainty, and the Court of Appeal upheld that refusal on 20 December 2024 (paragraphs 2 and 3). Alexion applied for rehearing, arguing that the Court had applied a completely new standard of claim interpretation without hearing it on the point and had relied on incorrect facts (paragraph 4). Amgen contended that the application was late and therefore inadmissible and, in any event, unfounded (paragraph 6), the Court does not rule on lateness.

The applicable law

Decisions of the Court of Appeal are final and rehearing is an extraordinary remedy, not an appeal (paragraphs 9 and 11). Only a defect so serious as to be intolerable for the legal system justifies rehearing, legal certainty generally prevailing. The applicant must also show that without the defect the same decision would not have been taken, applying the test in the CJEU’s Kamino judgment (paragraphs 12 and 13). The assessment of arguments, evidence and expert opinions is not open to rehearing, even if debatable (paragraphs 14 to 16). The right to be heard (Art. 76(2) UPCA) does not require the Court to disclose its preliminary view in advance, unless the outcome would be unforeseeable to a well-informed representative (paragraphs 23 and 24).

Question

Is the order of 20 December 2024 vitiated by a fundamental procedural defect within Art. 81(1)(b) UPCA and Rule 247(c), so as to justify rehearing?

Decision

The Court answers in the negative (paragraphs 7 and 26). Claim interpretation is a question of law that the Court of Appeal decides freely, without being bound by the parties’ arguments or expert opinions (paragraph 18), decisions of the EPO Boards of Appeal may be taken into account and parties are expected to know that case law and anticipate its application (paragraphs 19 to 21). The Court need not address every argument, and the requirement is lower in provisional measures proceedings (paragraph 22), where the right to be heard applies to a less stringent standard (paragraph 25). The preliminary introduction under Rule 112.4 may, but need not, contain a preliminary opinion (paragraph 24). Alexion’s complaints amount to disagreement with the Court’s reasoning, which is no ground for rehearing (paragraph 27). Alexion bears the costs of the rehearing proceedings (paragraph 29).

Key points for practice

Provisions applied

Agreement on a Unified Patent Court
Art. 76(2) and (3) and Art. 81(1)
Rules of Procedure
Rules 112.4, 207.8, 210.2, 245, 247 and 248
Case law cited
Kodak v Fujifilm, Court of Appeal, 17 April 2025, Insulet v EoFlow, Court of Appeal, 30 April 2025 (UPC_CoA_768/2024).

Related decisions

Prepared by Dhenne Avocats from the official decision, consulted on 10 October 2026. The database is updated every week, on Friday. Only the official text is authoritative.


Going further

Lexicon: UPC Court of Appeal, Supplementary protection certificate (SPC), Biosimilar medicinal product, Launch at risk.

Dhenne Avocats blog: UPC Appeals: What the Numbers Show, Pharmaceutical patents and the UPC: is the Court hostile to them?.

Publications by Matthieu Dhenne: The Launch Letter: How Generics and Biosimilars Should Write to Avoid UPC Urgency (Kluwer Patent Blog).

Source and translations

Official source
Unified Patent Court registry link recorded in the record
Original language
not recorded
Translation available
no translation recorded the firm’s French record is a summary, not a translation
Date checked
not recorded
Only the official text is authoritative. A machine translation is never presented as official, republishing a third-party document requires a verified basis in rights, and a link to the source is preferred.

Follow this case

Proceedings, related decisions, appeals, parties and patents as recorded in the registry and in the Dhenne Avocats corpus. Each link states its source.

Proceedings

No case number recorded in this record.

Parties

Exact name as it appears in the record, group affiliation only where sourced and dated.

Decisions in the same proceedings and documented appeals

No other decision in the corpus bears the same case number, and no appeal is documented in the corpus to date.

What the record states

Nature of the act
Generic application
Outcome (Dhenne Avocats summary)
La cour d’appel rejette la requête en révision d’Alexion : aucun vice fondamental de procédure n’est établi, le grief relevant d’un simple désaccord avec son interprétation des revendications.
Appeal
Decision of the Court of Appeal.
Instance
Court of Appeal decision.

Patents mentioned

Related decisions cited in the analyses

Scope: Dhenne Avocats corpus. Registry-based links are marked “official number”; links derived from the analyses are marked as such. An erroneous link can be withdrawn without deleting any record.

Patents and standards

PublicationRole in the disputeFamilyStandard and declarationPoolSources
EP 3 167 888
Treatment of paroxysmal nocturnal hemoglobinuria patients by an inhibitor of complement
recorded proprietor: Alexion Pharmaceuticals Inc
Mentioned in the analysis (role not qualified)
Also mentioned in 11 other decision(s): Samsung Bioepis NL v Alexion Pharmaceuticals (CoA, 18 February 2026) · Alexion Pharmaceuticals v Samsung Bioepis NL (CFI, 1 August 2025) · Alexion Pharmaceuticals v Samsung Bioepis (CFI, 1 August 2025) · Alexion Pharmaceuticals v Samsung Bioepis (CoA, 19 June 2025) · Alexion Pharmaceuticals v Samsung Bioepis NL (CoA, 20 December 2024) · Alexion Pharmaceuticals v Amgen Technology (Ireland) Unlimited Company · Alexion Pharmaceuticals v Amgen Technology (Ireland) (CoA, 8 August 20 · Alexion Pharmaceuticals v Amgen Technology (Ireland) Unlimited Company
not recordednot recordednot recordedEspacenet · European Patent Register
existence and title of the publication checked on 30 October 2026 (Google Patents, Espacenet and Register links are not checked automatically)
mentioned in: Dhenne Avocats analysis
The statuses “asserted in litigation”, “declared essential”, “listed by a pool” and “essentiality examined by a court” are distinct and may coexist. Validity, infringement and technical essentiality are different questions. Scope: patents cited in the decisions of the Dhenne Avocats corpus, with no essentiality score or prediction.

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