Assessments
OtherSafety and efficacy assessments
NCT Number: NCT06298630
Observe long-term safety risk and long-term efficacy after intravenous infusion of BRL-101 in TDT subjects.
Interested in participating?
Request Info3 year–35 year
All sexes
Observational
Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, China
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Safety and efficacy assessments
Time frame: Up to 15 years post-drug product infusion
Such as new lymphoma, leukemia, MDS, etc.
Time frame: Within 2 years to 5years after BRL-101 Infusion
Frequency, grade, and relationship to BRL-101 of SAEs following BRL-101 reinfusion.
Contact information is provided by the study sponsor or research team.
Bioray Laboratories
Industry
Long-term Follow-up Study of BRL-101 in the Treatment of Transfusion-dependent β-thalassemia
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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