A Long-term Follow-up Study in Participants Who Received CS-101

Recruiting N/A Interventional Study
Beta-Thalassemia
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
3 – 17
Sex
Any
Study type
Interventional
Purpose
Other
Participants needed
5 (estimated)
Sponsor
Children's Hospital of Fudan University · Other
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About This Trial

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)

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * 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 Exclusion Criteria: * There are n…
Contacts

Xiaowen Zhai, M.D.

+86-021-64931126

zhaixiaowendy@163.com

CONTACT

Zifeng Li, M.S.

+86-13920704768

zfli18@fudan.edu.cn

CONTACT