Biopharma Transcript

TScan Therapeutics, Inc. TCRX

Nasdaq · Phase 3 · oncology · cell therapy · EDGAR · Updated Oct 24, 2026

TScan Therapeutics, Inc. (Nasdaq: TCRX) is an oncology drug developer. Its lead program, TSC-101, is in Phase 3 for AML and MDS patients undergoing allogeneic HCT (prevention of relapse; HLA-A*02:01).

Upcoming catalysts

No catalyst is dated to the next 30 days or to an FDA action date.

Pipeline

ProgramIndicationModalityStage
TSC-101 (ALLOHA-2, Phase 3 registrational; first patient dosed July 2026)AML/MDS post-allogeneic HCTcell therapyPhase 3
TSC-101 (ALLOHA Phase 1, ongoing Cohort C)Heme malignancies post-allogeneic HCTcell therapyPhase 1
TSC-102-A01 / TSC-102-A03Heme malignancies post-HCT (HLA A*01:01 and A*03:01; CD45 epitopes)cell therapyPre-clinical
Multiplex TCR-T / in vivo engineered TCR-T (PLEXI-T Phase 1 enrollment paused)Solid tumorscell therapyPre-clinical
Autoimmune target discovery (with Amgen on Crohn's disease)Ankylosing spondylitis, ulcerative colitis, scleroderma, Crohn'scell therapyPre-clinical

Recent results and decisions

  1. Aug 12, 2026
    started First patient dosed in July 2026 in the Phase 3 ALLOHA-2 pivotal trial of TSC-101.In July, the Company announced that it has dosed the first patient in the ongoing Phase 3 Filing
  2. Aug 12, 2026
    positive Cohort C: 79% (11/14) achieved complete donor chimerism within about three weeks of first TSC-101 infusion; about 90% manufacturing success (17/19).79% of patients (11/14) achieved complete donor chimerism within ~three weeks of receiving their first infusion of TSC-101 Filing

For subscribers

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