UPC Analytics
ENDE
Overview · Filed: Mar 19, 2024

UPC_CFI_124/2024

TREATMENT OF PAROXYSMAL NOCTURNAL HEMOGLOBINURIA PATIENTS BY AN INHIBITOR OF COMPLEMENT

Provisional measuresProvisional MeasuresHamburg LDProvisional measuresCase Closed
Plain-English summary

Alexion Pharmaceuticals applied for a preliminary injunction at the Hamburg Local Division against nine Amgen entities across multiple European countries regarding EP 3 167 888 B1 (eculizumab/paroxysmal nocturnal haemoglobinuria). Identical reasoning to UPC_CFI_123/2024: the court found infringement could be established but denied the measure because the TBA's consistent rejection of SEQ ID NO:4 correction attempts created insufficient certainty of patent validity; value of dispute was EUR 100,000,000.

Accepted arguments
What the court agreed with — by party.
  • Sufficient certainty of patent validity is required before granting provisional measures, assessed in light of likely EPO outcome

    RespondentLegal basis: Art. 62(4) UPCA; R. 211.2 RoP

    Note: Same legal reasoning as UPC_CFI_123/2024: the Hamburg court declined the PI because TBA history created serious doubt about EP 3 167 888 B1's validity.

Rejected arguments
What the court did not agree with — and why.
  • Preliminary injunction against Amgen entities based on EP 3 167 888 B1

    ClaimantLegal basis: Art. 62(4) UPCA; R. 211.2 RoP

    Reason: Although infringement could be established, the court lacked sufficient certainty of patent validity given the TBA's consistent rejection of all attempts to correct SEQ ID NO:4 and claim sets directed to eculizumab across the EP 888 patent family.

Claim construction notes

Identical to UPC_CFI_123/2024: the court construed EP 3 167 888 claims but found it could not be sufficiently certain of validity given the TBA's repeated holdings that SEQ ID NO:4 includes the signal peptide sequence and its refusal to allow correction.