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Clinical Trial Summary

IMC-F106C is an immune-mobilizing monoclonal T cell receptor against cancer (ImmTAC ®) designed for the treatment of cancers positive for the tumor-associated antigen PRAME. This is a first-in-human trial designed to evaluate the safety and efficacy of IMC-F106C in adult patients who have the appropriate HLA-A2 tissue marker and whose cancer is positive for PRAME.


Clinical Trial Description

The IMC-F106C-101 Phase 1/2 study will be evaluated in patients with metastatic/unresectable tumors which include select Advanced Solid Tumors and will be conducted in two phases. 1. Phase 1: To identify the Maximum Tolerated Dose (MTD) and/or Recommended Phase 2 dose (RP2D) of IMC-F106C as a single agent and administered in combination with chemotherapies, targeted therapies, and monoclonal antibodies. 2. Phase 2: To assess the efficacy of IMC-F106C in selected advanced solid tumors. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04262466
Study type Interventional
Source Immunocore Ltd
Contact Immunocore Medical Information
Phone 844-466-8661
Email medical.information@immunocore.com
Status Recruiting
Phase Phase 1/Phase 2
Start date February 25, 2020
Completion date June 2026

See also
  Status Clinical Trial Phase
Recruiting NCT06402201 - First in Human Study of CDR404 in HLA-A*02:01 Participants With MAGE-A4 Expressing Solid Tumors Phase 1
Terminated NCT03973333 - Safety and Efficacy of IMC-C103C as Monotherapy and in Combination With Atezolizumab Phase 1/Phase 2
Completed NCT02705482 - A Study to Evaluate MEDI0562 in Combination With Immune Therapeutic Agents in Adult Subjects With Advanced Solid Tumors Phase 1
Terminated NCT03515551 - Safety and Efficacy of IMCnyeso in Advanced NY-ESO-1 and/or LAGE-1A Positive Cancers Phase 1/Phase 2