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Not Yet RecruitingNCT06298630

Long-term Follow-up Study of BRL-101 for TDT

Long-term Follow-up Study of BRL-101 in the Treatment of Transfusion-dependent β-thalassemia

Status
Not Yet Recruiting
Phase
Study type
Observational
Enrollment
45 (estimated)
Sponsor
Bioray Laboratories · Industry
Sex
All
Age
3 Years – 35 Years
Healthy volunteers
Not accepted

Summary

Observe long-term safety risk and long-term efficacy after intravenous infusion of BRL-101 in TDT subjects.

Detailed description

Observe long-term delayed safety risks such as emerging neoplasms, emerging haematological disorders, and long-term efficacy after intravenous infusion of BRL-101 in TDT subjects.

Conditions

Interventions

TypeNameDescription
OTHERAssessmentsSafety and efficacy assessments

Timeline

Start date
2024-12-08
Primary completion
2038-08-20
Completion
2038-10-15
First posted
2024-03-07
Last updated
2024-03-22

Locations

7 sites across 1 country: China

Source: ClinicalTrials.gov record NCT06298630. Inclusion in this directory is not an endorsement.