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.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
9
Therapeutic Classification: • Innate immune agonist Route of Administration: • Intralesional
Therapeutic Classification: • Immunotherapy (Immune checkpointinhibitor) Route of administration: • Intravenous (IV) infusion
H. Lee Moffitt Cancer Center and Research Institute
Tampa, Florida, United States
RECRUITINGUniversity of Wisconsin Carbone Cancer Center
Madison, Wisconsin, United States
RECRUITINGSafety
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
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