drugset / Trial / NCT06569108

Efficacy and Safety of KN057 Prophylaxis in Patients With Haemophilia A or B Without Inhibitors

NCT06569108 ↗

Phase 3 Active not recruiting 125 enrolled Suzhou Alphamab Co., Ltd.
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to show that KN057 can prevent bleeds in patients with haemophilia A or B without inhibitors and is safe to use. Participants receiving on-demand treatment prior to screening will be randomly assigned to Experimental group or Control group at a ratio of 2:1 in Part A. Participants receiving prophylaxis prior to screening will be nonrandomly assigned to Prophylaxis group in Part B. Participants in Experimental group will receive KN057 prophylaxis for 52 weeks upon enrollment. Participants in Control group will first receive on-demand treatment for 26 weeks, then switch to KN057 prophylaxis for 26 weeks. Participants in Prophylaxis group will first receive prophylaxis with coagulation factor for 26 weeks, then switch to KN057 prophylaxis for 26 weeks.

Timeline

Start
2024-04-01
Primary completion
2026-10-15
Completion
2026-12-15

Drugs

EvaluationDrugModalityDoseRoute
Subject KN057 Unknown — Subcutaneous