The Efficacy and Safety of ZS802 in Chinese Hemophilia A Patients.

NCT ID: NCT05523128

Last Updated: 2025-02-21

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: NA
• Total Enrollment: 6 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2022-09-29
• Study Completion Date: 2025-10-31

Brief Summary

A non-randomized, open-label, dose-escalation study to evaluate the safety, tolerability, kinetics and efficacy of a single intravenous infusion of ZS802 in hemophilia A subjects with endogenous FVIII ≤2%.

Detailed Description

This study will seek to determine the safety, tolerability, kinetics and efficacy of a single IV infusion of ZS802.

Hemophilia A is a genetic bleeding disorder resulting in the lack of ability to produce blood-clotting factor VIII (FVIII). Individuals with hemophilia A suffer repeated bleeding events, which can cause chronic joint disease and sometimes leads to death due to the inability for blood to clot efficiently. The current treatment is intravenous infusion of FVIII protein products, either prophylactically or in response to bleeding. ZS802 is an adeno-associated viral (AAV) vector designed to drive expression of the human factor VIII (hFVIII) transgene and raise circulating levels of endogenous FVIII.

6 patients will be enrolled sequentially every 3 weeks or more between cohorts and administered with single infusion of ZS802. Dose escalation may occur based on the safety and FVIII activity on steady state. The dose levels are as follows: 1. 2.0×10^13vg/kg; 2. 6.0×10^13vg/kg. Subjects will provide informed consent and then undergo screening assessments up to 6-8weeks prior administration of ZS802. All subjects will undergo 52 weeks safety and efficacy observation.

Conditions

Hemophilia A

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

ZS802

Single intravenous (i.v.) infusion of ZS802 Intervention: Gene Therapy / Gene Transfer

Group Type: EXPERIMENTAL

ZS802

Intervention Type: GENETIC

A novel, bioengineered adeno-associated viral (AAV) vector carrying human factor VIII variant. The dose levels are as follows: 1. 2.0×10\^13vg/kg; 2. 6.0×10\^13vg/kg.

Interventions

ZS802

A novel, bioengineered adeno-associated viral (AAV) vector carrying human factor VIII variant. The dose levels are as follows: 1. 2.0×10\^13vg/kg; 2. 6.0×10\^13vg/kg.

Intervention Type: GENETIC

Eligibility Criteria

Inclusion Criteria

1. Male ≥18 years and ≤65years of age;

2. Confirmed diagnosis of hemophilia A, and endogenous FVIII ≤2%:

1. <1% (<1 IU/dL) endogenous FVIII activity levels as historically documented by a certified laboratory or screening data results; OR

2. 1%-2% (1-2 IU/dL) endogenous FVIII activity levels and >10 bleeding events per year (in the last 52 weeks prior to screening); OR

3. 1%-2% (1-2 IU/dL) endogenous FVIII activity levels and on prophylaxis;

3. Have had ≥150 prior exposure days (EDs) to any recombinant and/or plasma-derived FVIII protein products.

4. Agree to use reliable barrier contraception and prohibition of sperm donation until 52 weeks after the administration of ZS802.

5. 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 no measurable FVIII inhibitor as assessed by laboratory; or documented no prior history of FVIII 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 active hepatitis B infection (HBsAg positive or HBV-DNA positive) or active hepatitis C infection (HCVAb positive), or are currently receiving hepatitis B or hepatitis C antiviral therapy;

6. Have history of chronic infection or other chronic disease that the Investigator considers to constitute an unacceptable risk;

7. Diabetes mellitus that is poorly controlled after drug treatment;

8. Uncontrolled hypertension or hypotension;

5. laboratory values:

1. Hemoglobin<110g/L;

2. Platelets<100×10^9/L;

3. AST, ALT, 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 >1:5.

7. Those who have received clinical trials of gene therapy before screening, or have used FVIII 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 donated or 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.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: MALE
• Accepts Healthy Volunteers: No

Sponsors

Institute of Hematology & Blood Diseases Hospital, China

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Lei Zhang, MD

Role: PRINCIPAL_INVESTIGATOR

Institute of Hematology & Blood Diseases Hospital, China

Locations

Institute of Hematology & Blood Diseases Hospital

Tianjin, , China

Site Status: RECRUITING

Countries

China

Central Contacts

Lei Zhang, MD

Role: CONTACT

zhanglei1@ihcams.ac.cn

+86 022-23909240

Facility Contacts

Lei Zhang, MD

Role: primary

zhanglei1@ihcams.ac.cn

+86 022-23909240

Other Identifiers

IIT2022031

Identifier Type: -

Identifier Source: org_study_id