drugset / Trial / NCT03247309

TCR-engineered T Cells in Solid Tumors (ACTengine IMA201-101)

NCT03247309 ↗

Phase 1 Completed 7 enrolled Immatics US, Inc.
NaSingle-groupOpen-labelTreatment

Summary

The study purpose is to establish the safety and tolerability of IMA201 in patients with solid tumors that express melanoma-associated antigen 4 and/or 8 (MAGEA4/8).

Timeline

Start
2018-12-19
Primary completion
2023-04-20
Completion
2023-09-18

Outcome

Results reported · no primary-endpoint met/missed verdict (typical of a dose-finding / safety study)

release “The combined data readout during early phases of dose escalation for the ACTengine ® programs, IMA201, IMA202 and IMA203, indicated first anti-tumor activity” immatics.com ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject IMA201 Unknown — Intravenous

Indications