NCT03247309

Phase 1 Study Evaluating Genetically Modified Autologous T Cells Expressing a T-cell Receptor Recognizing a Cancer/Germline Antigen in Patients With Recurrent and/or Refractory Solid Tumors (ACTengine® IMA201-101)

Study 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).

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Interventions

IMA201 ProductBIOLOGICAL
The cell dose will be based on viable CD3+CD8+ HLA-Dextramer+ cells per body surface area (BSA) as defined by the Mosteller formula.
IMADetect®DIAGNOSTIC_TEST
IMADetect® is developed as a companion diagnostic to aid in selecting patients with relapsed and/or refractory solid cancers who might be eligible for enrollment in clinical trials with investigational IMA201 therapy. IMADetect® is intended for investigational use only.

Study Locations

FacilityCityStateCountry
University of Pittsburgh Medical CenterPittsburghPennsylvaniaUnited States
University of Texas MD Anderson Cancer CenterHoustonTexasUnited States
Universitätsklinikum Bonn, Venusberg-Campus 1BonnNorth Rhine-WestphaliaGermany
Universitätsklinikum Carl Gustav Carus, Fetscherstr. 74DresdenSaxonyGermany
Universitätsklinikum Hamburg-EppendorfHamburgGermany

Official Trial Information

View on ClinicalTrials.gov

Data sourced from ClinicalTrials.gov. Last updated: April 14, 2026