Safety and Efficacy of STSP-0601 in Adult Patients with Hemophilia a or B with Inhibitor

Prior treatment

• Patients received anticoagulant or antifibrinolytic therapy 7 days before enrollment or plan to receive these drugs during the trial.Patients received anticoagulation therapy (such as coagulation factor replacement therapy, prothrombin complex, plasma, etc.) 7 days before enrollment.
• Severe bleeding event occurred within 4 weeks before enrollment.
• Accepted major operation or blood transfusion within 4 weeks before enrollment.
• Participate in other clinical research within 4 weeks before enrollment(except for participating in prothrombin complex, FVII, FVIIa, FVIII, FIX trails).
• Within 1 day prior to enrollment, FVII, FVIIa, tranexamic acid, and aminocaproic acid were used. Within 3 days prior to enrollment, prothrombin complex, FVIII, and FIX were used. Within 4 weeks prior to enrollment, treatment with amisulumab was received.

Other illness

• Have any coagulation disorder other than hemophilia.
• Have a history of arterial and/or venous thrombotic events.
• Severe liver or kidney disease.
• Have a known allergy to STSP-0601.

Lab values

• Platelet \<100×109/L.
• Hemoglobin\<90g/L.

Other

• Plan to receive prophylactic treatment of coagulation factor during the trail.
• Patients plan to receive Emicizumab during the trial.
• Pregnant, lactating, or blood pregnancy test positive female subjects
• Patients not suitable for the trail according to the judgment of the investigators.

• 18 ≤age≤70 years of age,male.
• Hemophilia A or B patients. (No less than 3 patients with hemophilia B)
• Peak historical inhibitor titer ≥ 5 BU and apositive inhibitor test when enrolled.
• Establish proper venous access.
• There were at least 3 bleeding events that requiring treatment occurred in the past 6 months before screening (Only applicable to the on-demand treatment stage).
• Agree to use adequate contraception to avoid pregnancy. Agree not to donate sperm or eggs.
• Provide signed informed consent.