drugset / Trial / NCT06312475

Efficacy and Safety of KN057 Prophylaxis in Patients With Haemophilia A or B With Inhibitors

NCT06312475 ↗

Phase 3 Active not recruiting 53 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 with inhibitors and is safe to use. Successfully screened participants will be randomly assigned to KN057 Prophylaxis (Arm 1) versus No Prophylaxis (Arm 2) at a ratio of 2:1. Participants in KN057 Prophylaxis will receive KN057 prophylaxis for 52 weeks upon enrollment. Participants in No Prophylaxis will first receive on-demand treatment for 26 weeks, then switch to KN057 prophylaxis for 26 weeks.The trial period is 59 weeks, including a 3-week screening period, a 26-week main trial, a 26-week extension period, and a 4-week follow-up period after the last administration.

Timeline

Start
2024-01-09
Primary completion
2025-10-15
Completion
2025-12-15

Drugs

EvaluationDrugModalityDoseRoute
Subject KN057 Unknown — Subcutaneous