Select Advanced Solid Tumors Clinical Trial
Official title:
Phase 1/2 Study of IMC-F106C in Advance PRAME-Positive Cancers
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.
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. ;
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 |