TScan Therapeutics (TCRX) announced completion of enrollment into Cohort C of the ALLOHA study. Patients in Cohort C are being treated using the new commercial-ready manufacturing process. The Company also announced that the U.S. Food and Drug Administration, FDA, has cleared its investigational new drug, IND, applications for TSC-102-A01 and TSC-102-A03 for patients with HLA types A 01:01 and A 03:01, respectively.
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