This Phase 2/3, multicenter, randomized, double-blind, placebo-controlled trial will evaluate the Objective Response Rate (ORR) of IFx-Hu2.0 as an adjunctive therapy to pembrolizumab in adult participants (≥18 years) with advanced or metastatic Merkel Cell Carcinoma. A total of 118 participants will be randomized to receive either IFx-Hu2.0 or placebo via intralesional injection in a single lesion, followed by pembrolizumab.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
118
Therapeutic Classification: • Innate immune agonist Route of Administration: • Intralesional
Route of Administration: • Intralesional
Therapeutic Classification: • Immunotherapy (Immune checkpoint inhibitor) Route of administration: • Intravenous (IV) infusion
USC Norris Comprehensive Cancer Center
Los Angeles, California, United States
RECRUITINGStanford Health Care - Skin Cancer Program
Palo Alto, California, United States
RECRUITINGUniversity of California San Francisco - Helen Diller Family Comprehensive Cancer Center
San Francisco, California, United States
RECRUITINGDana-Farber Cancer Institute
Boston, Massachusetts, United States
RECRUITINGAtlantic Health System
Morristown, New Jersey, United States
RECRUITINGEast Carolina University
Greenville, North Carolina, United States
RECRUITINGVirginia Commonwealth University - Massey Cancer Center
Richmond, Virginia, United States
RECRUITINGFred Hutchinson Cancer Research Center
Seattle, Washington, United States
RECRUITINGObjective response rate (ORR)
ORR defined as the proportion of participants who achieve a complete response (CR) or partial response (PR) at 12 weeks and confirmed on a second response assessment at least 28 days after the initial response assessment, in the treatment arm based on BICR assessment according to RECIST v1.1. Confirmed response persisting at the time of response assessment, at approximately 24 weeks will constitute the data utilized for the endpoint analysis.
Time frame: 12 weeks post-treatment initiation and confirmed on a second response assessment at least 28 days after the initial response assessment
Progression free survival (PFS)
PFS is defined as the time (months) from the date of randomization to the date of the documented PD based on BICR assessment according to RECIST v1.1, or death, whichever occurs first. Participants without progression or death will be censored on the date of last disease assessment.
Time frame: Up to 5 years
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