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Clinical Trials in the EU / 2026-525827-25-00
Authorised, not yet recruiting Phase I/II

A multicenter, non-therapeutic, interventional, long-term follow-up clinical trial to evaluate the safety of autologous PRAME-directed TCR T cell therapy IMA203 or IMA203CD8 in patients with previously treated, advanced and/or metastatic solid tumors

2026-525827-25-00 · tracked via the Priya Life Science EU tracker
Sponsor
Immatics US Inc
Sponsor type
Pharmaceutical company
Therapeutic area
Neoplasms
Decision date
21/08/2026
Enrollment target
9
Sites
Germany

Condition studied

Solid tumors

Investigational medicinal product(s)

IMA203IMA203CD8

Every trial of Anzu-cel across our registers →

Eligibility

Age group
65+ years, 18-64 years
Sex
Female, Male

Primary endpoint

Number of patients with delayed adverse events as identified in the Clinical Trial Protocol

Official registry record

This page summarises publicly available CTIS data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View 2026-525827-25-00 on CTIS ↗ ← All trials in the EU