drugset / Trial / NCT06947928

Placebo-Controlled Trial of IFx-Hu2.0 Followed By Pembrolizumab In Checkpoint Inhibitor Naïve Participants With Advanced Or Metastatic Merkel Cell Carcinoma

NCT06947928

Phase 2/3 Recruiting 118 enrolled TuHURA Biosciences, Inc.
RandomizedParallel-groupQuadruple-blindTreatment

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.

Timeline

Start
2025-12-11
Primary completion
2027-03-31
Completion
2032-12-30

Drugs

EvaluationDrugModalityDoseRoute
Subject IFx-Hu2.0 Vaccine 0.1 mg Other
Background Pembrolizumab Monoclonal antibody 200 mg Intravenous