A Long Term Follow-up Study of TScan TCR-T Products

Recruiting Observational Study
AML ALL MDS
No Placebo Group Every participant receives an active treatment — no one gets a placebo. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
18 – 110
Sex
Any
Study type
Observational
Participants needed
1,000 (estimated)
Sponsor
TScan Therapeutics, Inc. · Industry
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About This Trial

The purpose of this Long-Term Follow-Up (LTFU) study is to monitor participants who have previously received TSC-100 or TSC-101 TCR-T therapies in the TSCAN-001 study. Participants will be monitored for 15 years from the date of TCR-T cell therapy administration to assess long-term safety and efficacy.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Participants who received a TCR-T cellular therapy in a clinical study sponsored by TScan Therapeutics. * Signed informed consent. Exclusion Criteria: * None
Contacts

Madhavi Desai

(857) 399-9832

medicalaffairs@tscan.com

CONTACT