Cancer Type: Cutaneous
Study Type: Treatment
Phase: Phase I
Principal Investigator: Brohl, Andrew
Phase 1 Trial of Intralesional Immunotherapy with IFx-Hu2.0 Vaccine in Patients with Advanced Merkel Cell Carcinoma or Cutaneous Squamous Cell Carcinoma
This is primarily a safety study that is designed to evaluate IFx-Hu2.0 monotherapy and provide foundational evidence to potentially support further studies investigating IFx-Hu2.0 + anti-PD-1 combination therapy for patients with advanced MCC or cSCC.
Primary Objective The primary objective is to assess the safety of vaccinating patients with advanced MCC or cSCC with intralesional IFx-Hu2.0. Secondary Objective Secondary objectives are to assess the feasibility of IFx-Hu2.0 administration and evaluate any preliminary efficacy in patients with advanced MCC or cSCC.
If you are interested in learning more about clinical trials, our clinical trial navigators can discuss your options and recommend opportunities that may be suitable for you. Call 813-745-6100 or 1-800-679-0775 (toll-free) or submit a clinical trials inquiry form.
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