A Long-term Follow-up Study in Participants Who Received CS-101
Enrolling by invitation
Conditions studied: Beta-Thalassemia
In brief
This is a study to evaluate the long-term safety and efficacy of CS-101 in participants who received CS-101 in study CS -101-06 (NCT06024876),No investigational drug product will be administered in the study.
Key facts
- Study ID
- NCT06685536
- Run by
- CorrectSequence Therapeutics Co., Ltd
- People needed
- 5
- Starts
- 2025-01-18
- Expected to finish
- 2039-07-01
- Last updated by the study team
- 2026-02-10
Who can join
Age: 6 and older, up to 35. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Participants (or his or her legally appointed and authorized representative or guardian) must sign and date informed consent form (ICF) and, where applicable, an assent form
- Participants must have received CS-101 infusion in last study
You may not qualify if…
- There are no exclusion criteria
Where it is running
- The First Affiliated Hospital of Guangxi Medical University — Nanning, Guangxi, China
Full record on ClinicalTrials.gov
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