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Safety and Efficacy of IMC-F106C as a Single Agent and in Combination With Checkpoint Inhibitors

Safety and Efficacy of IMC-F106C as a Single Agent and in Combination With Checkpoint Inhibitors

Recruiting
18 years and older
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Phase 1/2
  • Simplified description (AI rewritten)
  • Technical description (Original)

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 (Arm A) and administered in combination with Checkpoint Inhibitors (Arm B).
  2. Phase 2: To assess the preliminary anti-tumor activity of IMC-F106C in up to 4 indications, as a single agent administration.
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Study details
    Select Advanced Solid Tumors

NCT04262466

Immunocore Ltd

19 February 2024

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