An Open-label Study to Evaluate the Safety of KN057 Long-term Prophylaxis in Patients With Hemophilia A or Hemophilia B With or Without Inhibitors

Suzhou Alphamab Co., Ltd.1 site in 1 country70 target enrollmentStarted: March 13, 2026Last updated: April 22, 2026

ConditionsHemophilia A or B

InterventionsKN057

DrugsKN057

Overview

Phase: Phase 3
Status: Recruiting
Sponsor: Suzhou Alphamab Co., Ltd.
Enrollment: 70
Locations: 1
Primary Endpoint: Incidence of TEAE.

Overview Study Design Eligibility Criteria Arms & Interventions Outcomes Investigators Sites Records & Identifiers Similar Trials

Overview

Brief Summary

The purposes of this open-label, multicenter III clinical trial are to evaluate the safety and efficacy of long-term preventive treatment with KN057 in Haemophilia A or B patients with or without inhibitors, and to assess the pharmacokinetic characteristics of the new and old processes KN057.

The participants in Part PK will be randomly assigned to Old process Group or New process Group in a 1:1 ratio. The participants in Old process Group will receive old process KN057 prophylaxis for the first 26 weeks and new process KN057 prophylaxis for the following 26 weeks. The participants in New process Group will receive new process KN057 prophylaxis for both the first 26 weeks and the last 26 weeks.

The participants in Part non-PK will be non-randomized and treated with new process KN057 for 52 weeks prophylaxis after enrollment.

Priority screening and enrollment of participants who have participated in the KN057-A-301 or KN057-A-302 study.

Study Design

Study Type: Interventional
Allocation: Randomized
Intervention Model: Parallel
Primary Purpose: Treatment
Masking: None

Eligibility Criteria

Ages: 12 Years to 65 Years (Child, Adult, Older Adult)
Sex: Male
Accepts Healthy Volunteers: No

Inclusion Criteria

•Male, 12 to 65 years old at the time of signing informed consent, body weight ≥30 kg and BMI \<28 kg/m\^2 at screening.
•For participates with inhibitors: Tested positive for high-titer FVIII or FIX inhibitors (≥ 5 BU/mL) at screening; or tested positive for low-titer FVIII or FIX inhibitors (0.6 BU/mL or upper limit of normal \[ULN\] \< inhibitor titer \< 5 BU/mL) at screening, with ongoing treatment using bypassing agents (rFVIIa or PCC).
•For participates without inhibitors: Severe and moderately severe hemophilia A or hemophilia B (FVIII or FIX activity level ≤2%); FVIII or FIX inhibitor test is negative (\<0.6 BU/ml) or lower than the lower limit of laboratory normal values during the screening period; There is no history of FVIII or FIX inhibitors in the past, or there has been an inhibitor, but the inhibitor has turned negative for at least 5 years before screening and has not reappeared (no positive inhibitor was detected); Use coagulation factor replacement therapy for no less than 100 exposure days before screening.
•Participates with inhibitors agree to avoid using PCC for treatment when breakthrough bleeding occurred. Participates without inhibitors agree to be treated with standard half-life coagulation factors (FVIII or FIX) in the event of breakthrough bleeding.

Exclusion Criteria

•Have serious or poorly controlled chronic diseases or obvious systemic diseases.
•Have a history of thromboembolic disease, or currently have symptoms or signs related to thromboembolic disease or being treated with thrombolytic/antithrombotic therapy.
•Have high-risk factors for thrombosis: such as atrial fibrillation, atherosclerotic diseases of important arteries, ischemic disease of important organs, vascular occlusive disease, autoimmune diseases with a high risk of thrombosis, or indwelling central venous catheter.
•Known or suspected hypersensitivity to any constituent of the trial product or related products.
•Have undergone major surgery (as determined by the investigator) within 3 months before screening, or have elective surgery planned during the study.
•Used Emicizumab treatment within 6 months before screening.
•Have received any gene therapy for hemophilia in the past.
•Other factors that the investigator deems inappropriate for participating in this trial, such as the presence of concomitant diseases, treatment or examination abnormalities that affect the subject's safety during the trial or affect the interpretation of trial results.

Arms & Interventions

Part non-PK

Experimental

The participants in Part non-PK will be treated with new process KN057 for 52 weeks prophylaxis after enrollment.

Intervention: KN057 (Drug)

Part PK # Old process Group

Experimental

The participants in Old process Group will receive old process KN057 prophylaxis for the first 26 weeks and new process KN057 prophylaxis for the following 26 weeks.

Intervention: KN057 (Drug)

Part PK # New process Group

Experimental

The participants in New process Group will receive new process KN057 prophylaxis for both the first 26 weeks and the last 26 weeks.

Intervention: KN057 (Drug)