Evaluating ZS801 for treating Hemophilia B in Chinese patients

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study is a non-randomized, open-label evaluation of the safety, kinetics, and efficacy of a single intravenous infusion of ZS801 in male patients with Hemophilia B and low endogenous FIX levels. Participants will undergo screening assessments for up to 6 weeks before receiving the treatment, followed by a 52-week observation period to monitor safety and efficacy outcomes. The study aims to determine the appropriate dosing and potential benefits of ZS801 in managing bleeding events associated with Hemophilia B.

Why it matters

Who can join: the full rules

Inclusion Criteria:

1. Male ≥18 years and ≤65years of age;
2. Confirmed diagnosis of hemophilia B, and endogenous FIX ≤2%:
3. Have had ≥100 prior exposure days (EDs) to any recombinant and/or plasma-derived FIX protein products;
4. The subject had at least 3 or more bleeding events and/or chronic hemophilia arthritis in one or more joints in the previous 1 year requiring treatment with FIX agents;
5. Agree to use reliable barrier contraception and prohibition of sperm donation until 52 weeks after the administration of ZS801.
6. Subjects voluntarily participate and are fully informed, fully understand the research and can comply with the requirements of the research protocol, are willing to complete the research as planned, and voluntarily cooperate with the provision of biological samples for testing.

Exclusion Criteria:

1. Hypersensitivity to any component of the study drug (including immunosuppressants) or a condition that can not use;
2. Inability to tolerate immunosuppressants or steroid drugs;
3. Have FIX inhibitor as assessed by laboratory; or documented history of FIX inhibitor;
4. Who have a history or are currently suffering from any of the following serious clinical diseases:

   1. History of malignancy or current presence of any malignancy;
   2. Have active autoimmune disease;
   3. Severe heart disease, including angina pectoris, myocardial infarction, heart failure, clinically significant congenital heart disease, heart valve disease, arrhythmia and atrioventricular block, etc.;
   4. Have underlying liver disease or history of liver disease (such as portal hypertension, ascites, splenomegaly, esophageal varices, hepatic encephalopathy or hepatic fibrosis);
   5. Have HBsAg positive or HCV-Ab positive, or are currently receiving hepatitis B or hepatitis C antiviral therapy;
   6. Diabetes mellitus that is poorly controlled after drug treatment;
   7. Uncontrolled hypertension or hypotension;
5. laboratory values:

   1. Hemoglobin\<110g/L;
   2. Platelets\<100×10\^9/L;
   3. aspartate aminotransferase, Alanine transaminase, alkaline phosphatase\>2×ULN;
   4. Total bilirubin\>1.5×ULN;
   5. Creatinine\>ULN;
   6. Albumin\<LLN;
   7. HIV antibody positive or Treponema pallidum antibody positive.
6. Have AAV5 capsid neutralizing antibody titers \>1:640;
7. Those who have received clinical trials of gene therapy before screening, or have used FIX clinical trial drugs within 1 month, or participated in other drug/device clinical trials within 3 months, or plan to participate in other clinical trials during this study;
8. Those who have planned surgery within 52 weeks after the infusion;
9. Those who lost more than 400 mL of blood within 3 months before screening;
10. Those with epilepsy, history of mental illness (such as schizophrenia, depression, mania or anxiety) or obvious mental disorder, incapacitated or incapacitated by other reasons;
11. Patients with a history of drug abuse or alcoholism;
12. Investigators believe that subjects have poor compliance or are expected to be less likely to complete follow-up;
13. There are clinically significant diseases or other reasons that the researcher and/or collaborators consider unsuitable to participate in this researcher.

Where it's running

• Institute of Hematology & Blood Diseases Hospital
  Tianjin, Tianjin Municipality, China Recruiting

Study contacts

• Principal investigator: Lei Zhang, MD — Institute of Hematology & Blood Diseases Hospital, China
• Study coordinator: Lei Zhang, MD
• Email: zhanglei1@ihcams.ac.cn
• Phone: +86 022-23909240

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

• SR604: a new treatment tested in adults with Hemophilia A/B or congenital Factor VII deficiency

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• Single-dose CSL222 gene therapy for adolescent males (12–17) with severe or moderately severe hemophilia B.

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• ATHNdataset registry for people with bleeding and clotting disorders

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• Is synovial proliferation in haemophilia joints active or inactive?

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• Observational study of blood clotting and bleeding disorders in Chinese patients

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• Comparing ANB-002 to standard treatment for hemophilia B

  This study is testing a new treatment called ANB-002 to see if it works as well as the standard treatment for adults with hemophilia B who have low FIX activity and no FIX inhibitors.

  Recruiting at 11 sites Phase 3 Biocad · Chelyabinsk and 13 other locations · NCT06700096

How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.