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

Last updated: January 17, 2025
Sponsor: Staidson (Beijing) Biopharmaceuticals Co., Ltd
Overall Status: Completed

Phase

2

Condition

Hemophilia

Treatment

STSP-0601 for Injection

Clinical Study ID

NCT06289166
STSP-0601-04
  • Ages 18-70
  • All Genders

Study Summary

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 inhibitor.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  1. 18 ≤age≤70 years of age,male.

  2. Hemophilia A or B patients. (No less than 3 patients with hemophilia B)

  3. Peak historical inhibitor titer ≥ 5 BU and apositive inhibitor test when enrolled.

  4. Establish proper venous access.

  5. 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).

  6. Agree to use adequate contraception to avoid pregnancy. Agree not to donate sperm oreggs.

  7. Provide signed informed consent.

Exclusion

Exclusion Criteria:

  1. Have any coagulation disorder other than hemophilia.

  2. Plan to receive prophylactic treatment of coagulation factor during the trail.

  3. Patients plan to receive Emicizumab during the trial.

  4. Patients received anticoagulant or antifibrinolytic therapy 7 days before enrollmentor plan to receive these drugs during the trial.Patients received anticoagulationtherapy (such as coagulation factor replacement therapy, prothrombin complex,plasma, etc.) 7 days before enrollment.

  5. Have a history of arterial and/or venous thrombotic events.

  6. Platelet <100×109/L.

  7. Hemoglobin<90g/L.

  8. Severe liver or kidney disease.

  9. Severe bleeding event occurred within 4 weeks before enrollment.

  10. Accepted major operation or blood transfusion within 4 weeks before enrollment.

  11. Have a known allergy to STSP-0601.

  12. Pregnant, lactating, or blood pregnancy test positive female subjects

  13. Participate in other clinical research within 4 weeks before enrollment(except forparticipating in prothrombin complex, FVII, FVIIa, FVIII, FIX trails).

  14. Within 1 day prior to enrollment, FVII, FVIIa, tranexamic acid, and aminocaproicacid were used. Within 3 days prior to enrollment, prothrombin complex, FVIII, andFIX were used. Within 4 weeks prior to enrollment, treatment with amisulumab wasreceived.

  15. Patients not suitable for the trail according to the judgment of the investigators.

Study Design

Total Participants: 25
Treatment Group(s): 1
Primary Treatment: STSP-0601 for Injection
Phase: 2
Study Start date:
March 18, 2024
Estimated Completion Date:
October 17, 2024

Connect with a study center

  • Anhui Provincial Hospital

    Hefei, Anhui 230000
    China

    Site Not Available

  • The Second Affiliated Hospital of Chongqing Medical University

    Chongqing, Chongqing 400000
    China

    Site Not Available

  • Fujian Medical University Affiliated Union Medical College Hospital

    Fuzhou, Fujian 350005
    China

    Site Not Available

  • Lanzhou University First Hospital

    Lanzhou, Gansu 730000
    China

    Site Not Available

  • Southern Medical University Southern Hospital

    Guangzhou, Guangdong 510000
    China

    Site Not Available

  • Shenzhen Second People's Hospital

    Shenzhen, Guangdong 518000
    China

    Site Not Available

  • Guizhou Medical University Affiliated Hospital

    Guiyang, Guizhou 550000
    China

    Site Not Available

  • Harbin First Hospital Hematology Tumor Research Center

    Harbin, Heilongjiang 150000
    China

    Site Not Available

  • Henan Cancer Hospital

    Zhengzhou, Henan 450000
    China

    Site Not Available

  • Xiangya Hospital of Central South University

    Changsha, Hunan 410000
    China

    Site Not Available

  • Nanjing University School of Medicine Affiliated Gulou Hospital

    Nanjing, Jiangsu 210000
    China

    Site Not Available

  • The First Affiliated Hospital of Nanchang University

    Nanchang, Jiangxi 330038
    China

    Site Not Available

  • The first hospital of Jilin University

    Changchun, Jilin 130000
    China

    Site Not Available

  • Shengjing Hospital Affiliated to China Medical University

    Shenyang, Liaoning 110000
    China

    Site Not Available

  • Affiliated Hospital of Qingdao University

    Qingdao, Shandong 266000
    China

    Site Not Available

  • Ruijin Hospital Affiliated to Shanghai Jiao Tong University School of Medicine

    Shanghai, Shanghai 200000
    China

    Site Not Available

  • Xi'an Central Hospital

    Xi'an, Shanxi 710000
    China

    Site Not Available

  • West China Hospital of Sichuan University

    Chengdu, Sichuan 610000
    China

    Site Not Available

  • Hospital of Hematology, Chinese Academy of Medical Sciences

    Tianjin, Tianjin 300020
    China

    Site Not Available

  • The Second Affiliated Hospital of Kunming Medical University

    Kunming, Yunnan 650000
    China

    Site Not Available

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