A Long-term Follow-up Study in Participants Who Received CS-101
Recruiting now · Not applicable
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 -101-03 (NCT06065189)
Key facts
- Study ID
- NCT06479616
- Run by
- Children's Hospital of Fudan University
- People needed
- 5
- Starts
- 2024-06-18
- Expected to finish
- 2027-06-01
- Last updated by the study team
- 2025-09-10
Who can join
Age: 3 and older, up to 17. 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 IIT study
You may not qualify if…
- There are no exclusion criteria
Where it is running
- Children's Hospital of Fudan University — Shanghai, Shanghai Municipality, China (enrolling)
Full record on ClinicalTrials.gov
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