Phase 1/2 Study of IMC-R117C in Selected Advanced Cancers

Recruiting Phase 1 Phase 2 Interventional Study
Cancer HLA-A*02:01-positive
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 1/2
Study type
Interventional
Purpose
Treatment
Participants needed
600 (estimated)
Sponsor
Immunocore Ltd · Industry
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About This Trial

This phase 1/2 first-in-human study is designed to test the safety and efficacy of IMC-R117C (PIWIL1 × CD3 ImmTAC® Bispecific Protein) as a single agent and in combination with other therapies in HLA-A\*02:01-positive participants with selected advanced PIWIL1-Positive cancers.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Eastern Cooperative Oncology Group (ECOG) performance status score of 0 or 1 * HLA-A\*02:01-positive * Histologically confirmed advanced colorectal, esophageal, gastric, or ovarian carcinoma * Archived or fresh tumor tissue sample that must be confirmed as adequate * Evaluable…
Contacts

Immunocore Medical Information

844-466-8661

medical.information@immunocore.com

CONTACT

Immunocore Medical Information EU

+00 800-744-51111

medinfo.eu@immunocore.com

CONTACT