Long-term Follow-up Study of BHC001 for TDT

NCT06314529 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 6

Last updated 2024-03-18

No results posted yet for this study

Summary

Observe long-term safety risk and long-term efficacy after intravenous infusion of BHC001 in TDT subjects.

Conditions

  • Thalassemia, Beta

Interventions

OTHER

Assessments

Safety and efficacy assessments

Sponsors & Collaborators

  • The 923rd Hospital of Joint Logistics Support Force of People's Liberation Army

    collaborator OTHER
  • Xiangya Hospital of Central South University

    collaborator OTHER
  • Bioray Laboratories

    lead INDUSTRY

Principal Investigators

  • Xiaochen Wang, PhD · Bioray Laboratories

Eligibility

Min Age
5 Years
Max Age
35 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-12-14
Primary Completion
2036-12-10
Completion
2037-05-10

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06314529 on ClinicalTrials.gov