2026-05-07 - LD The Hague - GlaxoSmithKline v. Moderna - UPC_CFI_616/2025

Aktenzeichen:
UPC_CFI_616/2025
Datum:
Spruchkörper:
Court of First Instance - The Hague (NL) Local Division
Art:
Order
Parteien:
GlaxoSmithKline Biologicals SA v. Moderna Netherlands B.V. Et al

Kernaussage: The Hague Local Division (judge-rapporteur) issues a consolidated procedural order in GSK's mRNA-vaccine patent litigation against Moderna (15 group defendants) covering two cases (UPC_CFI_616/2025 and UPC_CFI_1439/2025) and addressing three points ahead of the Interim Conferenc…

2026-05-07 - LD The Hague - GlaxoSmithKline v. Moderna - UPC_CFI_616/2025
Eine Entscheidung, mehrere Aktenzeichen

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🏛️Court of First Instance - The Hague (NL) Local Division• Order
📅2026-05-07
🔢UPC_CFI_616/2025
Parteien & Vertreter
Kläger / Berufungsführer
GlaxoSmithKline Biologicals SA
Tjibbe DOUMA
Beklagter / Berufungsbeklagter
Moderna Netherlands B.V.
Moderna Biotech Spain, S.L.
Moderna Biotech UK Limited
Moderna Biotech Distributor UK Ltd
Moderna Switzerland GmbH
Moderna Poland SP. Z.O.O.
Moderna, Inc.
ModernaTX, Inc.
Moderna Belgium S.R.L.
Moderna France SASU
Moderna Germany GmbH
Moderna Italy S.R.L.
Moderna Portugal Unipessoal LDA
Moderna Sweden AB
Moderna Norway A/S
Thomas WOLTER
Gertjan KUIPERS
⚖️Infringement Action
🌐English

notable
The Hague Local Division (judge-rapporteur) issues a consolidated procedural order in GSK's mRNA-vaccine patent litigation against Moderna (15 group defendants) covering two cases (UPC_CFI_616/2025 and UPC_CFI_1439/2025) and addressing three points ahead of the Interim Conference scheduled for 11 June 2026. First, GSK's R. 176 RoP application for the Court to hear five party experts (two GSK, three Moderna) in person on the day before the oral hearing is dismissed: the UPC procedural framework does not provide for a general examination of all party experts on the entirety of their written statements, and GSK failed to identify specific facts that each expert would be expected to confirm. If specific disputed facts later require clarification, experts can be questioned on those facts at the (one-day) oral hearing — the (at least online) presence of party experts at the oral hearing is therefore advisable. Second, Moderna's third R. 9.3 RoP application for a one-week extension of the rejoinder to the application to amend is dismissed: the UPC's front-loaded system and 12–14-month first-instance target reserve extensions for justified exceptional circumstances; the volume of auxiliary requests was already accommodated by the one-week extension granted on 1 March 2026 and is not, on its own, an exceptional circumstance, particularly where the opposing party (GSK) met its own deadlines without extension requests. Third, parties may suggest further IC topics within one week; the IC will, at minimum, address case-value setting and focusing the counterclaim for the oral hearing (validity attacks and number of ARs).

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