IFx-Hu2.0 As An Adjunctive Therapy To Pembrolizumab In Checkpoint Inhibitor Naïve Subjects With Advanced Or Metastatic Merkel Cell Carcinoma
Summary
This Phase 1, multicenter, open-label trial will assess the safety and feasibility of IFx-Hu2.0 as adjunctive therapy to pembrolizumab in adult patients (≥18 years) with non-cutaneous Merkel Cell Carcinoma. Nine subjects will receive IFx-Hu2.0 as a visceral lesion injection in a single lesion followed by pembrolizumab.
Arms & interventions
- DrugIFx-Hu2.0
Therapeutic Classification: • Innate immune agonist Route of Administration: • Intralesional
- DrugPembrolizumab
Therapeutic Classification: • Immunotherapy (Immune checkpointinhibitor) Route of administration: • Intravenous (IV) infusion
Outcome measures
Primary
Safety
Safety is defined as the absence of any grade 3-5, treatment-related Adverse Events (AEs) per Common Terminology Criteria for Adverse Events (CTCAE) v5.0 from first injection Day 1 to 28-day follow-up after the final dose of IFx-Hu2.0.
Time frame: 28 days from last dose of IFx-Hu2.0
Feasibility
Feasibility is defined as the ability to treat ≥50% of subjects (i.e. 5/9) in the per-protocol analysis.
Time frame: 28 days from last dose of IFx-Hu2.0
Eligibility criteria
Study locations (2)
H. Lee Moffitt Cancer Center and Research Institute
Tampa, Florida, 33612
University of Wisconsin Carbone Cancer Center
Madison, Wisconsin, 53792