A Study to Evaluate the Efficacy and Safety of Autologous CRISPR-Cas12b Edited Hematopoietic Stem Cells in Transfusion-dependent β Thalassemia Patients

Status: Recruiting
Location: See location...
Intervention Type: Biological
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This is a single-arm, open, single-injection exploratory clinical study with two transfusion-dependent β thalassemia (β-TDT) participants planned to enroll.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 3
Maximum Age: 35
Healthy Volunteers: f
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• Age 3-35 years old (inclusive), male or female;

• The subject and/or his/her legally recognized representative/parent/guardian fully understands the study and all information related to the study and has signed the informed consent form;

• Clinical diagnosis of transfusion-dependent β-thalassemia (TDT) with a blood transfusion record within 2 years (inclusive) prior to screening showing a history of ≥ 10 units (U)/kg/year (or ≥ 100 mL/kg/year) or ≥ 8 times/year of suspended RBC transfusions in at least 1 consecutive 12-month period;

• Karnofsky score (for subjects aged ≥ 16 years) or Lansky score (for subjects aged \< 16 years) of ≥ 80;

• Subjects in stable disease state who are eligible for hematopoietic stem cell transplantation as per investigator's judgment;

• Access to diagnosis and treatment records issued by medical professional institutions within 2 years prior to screening, including the records of blood transfusions, hematology, serum chemistry, and other examinations;

• Willing and able to comply with study procedures, with good compliance, and willing to receive and complete the follow-up study with a duration of at least 2 years;

• Subjects of childbearing potential (including female subjects of childbearing potential and male subjects whose partners are of childbearing potential) must use effective contraception within 12 months of treatment.

Locations
Other Locations
China
Regenerative Medicine Center
RECRUITING
Tianjin
Contact Information
Primary
Jun Shi, PhD
shijun@ihcams.ac.cn
13752253515
Time Frame
Start Date: 2023-08-31
Estimated Completion Date: 2026-06-30
Participants
Target number of participants: 2
Treatments
Experimental: VGB-Ex01
Each subject will accept one dose of VGB-Ex01.
Sponsors
Collaborators: Shanghai Vitalgen BioPharma Co., Ltd.
Leads: Institute of Hematology & Blood Diseases Hospital, China

This content was sourced from clinicaltrials.gov

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