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Placebo-Controlled Trial of IFx-Hu2.0 Followed By Pembrolizumab In Checkpoint Inhibitor Naïve Participants With Advanced Or Metastatic Merkel Cell Carcinoma
Sponsor: TuHURA Biosciences, Inc.
Summary
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.
Official title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled Trial Of IFx-Hu2.0 As An Adjunctive Therapy To Pembrolizumab In Checkpoint-Inhibitor Naïve Participants With Advanced Or Metastatic Merkel Cell Carcinoma
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
118
Start Date
2025-10
Completion Date
2032-12-30
Last Updated
2025-10-14
Healthy Volunteers
No
Interventions
IFx-Hu2.0
Therapeutic Classification: • Innate immune agonist Route of Administration: • Intralesional
Placebo
Route of Administration: • Intralesional
Pembrolizumab
Therapeutic Classification: • Immunotherapy (Immune checkpoint inhibitor) Route of administration: • Intravenous (IV) infusion
Locations (8)
USC Norris Comprehensive Cancer Center
Los Angeles, California, United States
Stanford Health Care - Skin Cancer Program
Palo Alto, California, United States
University of California San Francisco - Helen Diller Family Comprehensive Cancer Center
San Francisco, California, United States
Dana-Farber Cancer Institute
Boston, Massachusetts, United States
Atlantic Health System
Morristown, New Jersey, United States
East Carolina University
Greenville, North Carolina, United States
Virginia Commonwealth University - Massey Cancer Center
Richmond, Virginia, United States
Fred Hutchinson Cancer Research Center
Seattle, Washington, United States