Phase I/II Clinical Study to Evaluate the Safety, Tolerability, and Efficacy of GC310 Injection in Patients With Wilson's Disease (WD)

NCT ID: NCT07173933

Last Updated: 2025-09-15

Basic Information

• Recruitment Status: NOT_YET_RECRUITING
• Clinical Phase: PHASE1/PHASE2
• Total Enrollment: 15 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2025-10-31
• Study Completion Date: 2027-10-31

Brief Summary

The goal of this clinical trial is to learn if GC310 (AAV5-ATP7B) gene therapy can treat Wilson's Disease (WD) in patients over the age of 18 years old. The main questions it aims to answer are:

Is GC310 safe and tolerable to WD patients? What is the recommended phase II dose (RP2D)? What is the change from baseline in 24-hour urinary copper concentration after 52 weeks of administration?

Participants will be administrated GC310 intravenously and be followed up for 52 weeks to observe drug safety, tolerability and efficacy .

Conditions

Wilson Disease

Study Design

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

Study Groups

Cohort 1

Single intravenous administration of GC310 at a dose of 3.0E+13 d.vg/kg

Group Type: EXPERIMENTAL

GC310

Intervention Type: GENETIC

GC310 is an adeno-associated virus 5 (AAV5) vector delivering a functional copy of the truncated human ATP7B gene

Cohort 2

Single intravenous administration of GC301 at a dose of 6.0E+13 d.vg/kg

Group Type: EXPERIMENTAL

GC310

Intervention Type: GENETIC

GC310 is an adeno-associated virus 5 (AAV5) vector delivering a functional copy of the truncated human ATP7B gene

Interventions

GC310

GC310 is an adeno-associated virus 5 (AAV5) vector delivering a functional copy of the truncated human ATP7B gene

Intervention Type: GENETIC

Eligibility Criteria

Inclusion Criteria

• Aged ≥ 18 years, sex unrestricted;
• Definitive diagnosis of Wilson disease (WD) based on:

(i) or (ii) + (iii) and (iv), or (i) or (ii) + (v); (i) Neurological and/or psychiatric symptoms; (ii) Unexplained liver injury; (iii) Reduced serum ceruloplasmin and/or elevated 24-hour urinary copper; (iv) Positive corneal Kayser-Fleischer (K-F) ring; (v) Biallelic pathogenic ATP7B variants confirmed by segregation analysis and variant pathogenicity assessment;

• Serum ceruloplasmin concentration < ½ × lower limit of normal (LLN);
• Willing and able to comply with all study procedures, and has provided written informed consent.

Exclusion Criteria

Subjects meeting ANY of the following criteria will be excluded:

1. Screening serum anti-AAV5 neutralizing antibody titre > 1:100.

2. Clinically significant laboratory abnormality at screening or baseline:

1. ALT or AST ≥ 5 × ULN, direct bilirubin > 1 × ULN, or albumin < 1 × LLN;

2. Blood ammonia > 1 × ULN.

3. Renal impairment (any degree).

4. Current hepatic decompensation or history of hepatic decompensation.

5. Liver stiffness measurement (LSM) ≥ 15 kPa by transient elastography at screening.

6. History of acute liver failure from any cause.

7. Evidence of advanced liver disease defined by either:

1. MELD score ≥ 12, or

2. Child-Pugh score ≥ 7.

8. Severe neuro-psychiatric manifestations that, in the investigator's opinion, could compromise subject safety or interfere with study participation.

9. Positive for HIV antibody, hepatitis C antibody, Treponema pallidum antibody, or hepatitis B surface antigen.

10. Contraindications to glucocorticoid therapy judged by the investigator (e.g., uncontrolled hypertension, systemic fungal infection, glaucoma, osteoporosis, active tuberculosis).

11. Concurrent conditions that may interfere with study conduct or assessment, including significant gastrointestinal, cardiovascular, cerebrovascular, renal, endocrine, haematological, immunological, neurological or psychiatric disorders other than Wilson disease.

12. Pregnant or lactating women.

13. Women of child-bearing potential or fertile men who plan to conceive within 1 year after dosing or are unwilling to use highly effective contraception.

14. Body-mass index ≥ 24 kg/m².

15. History of severe hypersensitivity to foods or drugs, including recombinant proteins.

16. Vaccination within 2 weeks prior to planned dosing.

17. Prior exposure to any gene-therapy product.

18. Participation in any other clinical trial (WD-related or not) within 3 months before screening.

19. Any other condition or circumstance that, in the opinion of the investigator, renders the subject unsuitable for the study (e.g., poor compliance).

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

GeneCradle Inc

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Peking Union Medical College

Beijing, , China

Countries

China

Central Contacts

GeneCradle, Inc China

Role: CONTACT

ind@bj-genecradle.com

86-13501380583

Facility Contacts

Juan Ding

Role: primary

dingjuan8008@163.com

18810530992

Other Identifiers

JLJY-GC310-WD-001

Identifier Type: -

Identifier Source: org_study_id