Skip to main content
OpenTrials
Completed

NCT Number: NCT05027230

A Safety and Efficacy Study of STSP-0601 in Adult Patients With Hemophilia A or B With Inhibitor

This study will assess the safety and efficacy of multiple-dose of STSP-0601 for the treatment of bleeding episodes in hemophilia A or B patients with inhibitors.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–65 year

Sex eligibility

Male

Study type

Interventional

Phase

Phase 1 / Phase 2

Primary location

Hospital of Hematology, Chinese Academy of Medical Sciences

Tianjin, Tianjin Municipality, 300020, China

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 18 years old ≤age≤65 years of age,male.
  • Hemophilia A or B patients with inhibitors.
  • Received hemostatic treatment with investigational drug, or to undergo minor surgical or other invasive procedures (Only for phase 2. Minor surgical procedures: procedures without general anesthesia and the wounds are easy to observe).
  • Peak historical inhibitor titer ≥ 5 BU and a positive inhibitor test when enrolled.
  • Establish proper venous access.
  • Agree to use adequate contraception to avoid pregnancy.
  • Provide signed informed consent.

Exclusion criteria

  • Have any coagulation disorder other than hemophilia A or B.
  • Treat with prophylactic treatment of coagulation factor.
  • Treat with anticoagulant within 7d of the time of study drug administration.
  • Have a history of arterial and/or venous thromboembolic events.
  • Have platelet <100,000/mL,hemoglobin<90g/L.
  • Severe liver or kidney disease.
  • Bleeding in the central nervous system or throat before screening.
  • Accept major operation or blood transfusion within 1 month of the time of screening.
  • HIV positive with current CD4+ count of less than 200/μl.
  • Have a known allergy to Blood product.
  • Participate in other clinical research within 1 month of the time of study drug administration.
  • Treat with coagulant within 7d of the time of study drug administration.

Treatment and study plan

STSP-0601 for Injection

Drug

A multiple-dose design to evaluate the safety,tolerability and efficacy of two doses of STSP-0601 for injection in patients with inhibitory hemophilia

Primary outcomes

  1. Incidence of adverse events

    Time frame: From day 0 to up to day 8

  2. Proportion of successfully treated bleeding episodes

    Time frame: 24 hours after administration of study drug

Secondary outcomes

  1. Proportion of bleeding episodes with clinical relief of signs and symptoms

    Time frame: 4 hours、8 hours、24 hours after first administration of study drug

Sponsors and collaborators

Lead sponsor

Staidson (Beijing) Biopharmaceuticals Co., Ltd

Industry

Registry information

Official study title

A Phase Ib/II,Multi-center, Open, Multiple-dose Design to Evaluate the Safety,Tolerability and Efficacy of STSP-0601 for Injection in Patients With Inhibitory Hemophilia

Important dates

Study start
2021
Primary completion
2023
Study completion
2023
First posted
Aug 30, 2021
Registry last updated
Sep 19, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.