drugset / Trial / NCT06568302

The Long-term Safety and Efficacy of SerpinPC in Subjects with Hemophilia Who Completed a Sponsored SerpinPC Clinical Trial

NCT06568302 ↗

Phase 3 Terminated 15 enrolled ApcinteX Ltd Centessa Pharmaceuticals plc · collab
NaSequentialOpen-labelTreatment

Summary

The purpose of the study is to evaluate the efficacy, safety, tolerability and pharmacokinetic (PK) profile of prophylactic SerpinPC in participants with hemophilia

Timeline

Start
2024-07-11
Primary completion
2025-01-29
Completion
2025-01-29

Outcome

Outcome not reported

Stopped (Business): “Study terminated due to business and strategic decision.”

Drugs

EvaluationDrugModalityDoseRoute
Subject SerpinPC Unknown 1.2 mg/kg Subcutaneous