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Study of RP3 in Combination With Nivolumab and Other Therapy in Patients With Locoregionally Advanced or Recurrent SCCHN

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NCT05743270

Sponsored by Replimune, Inc. (industry) · REPL — their whole pipeline →. With Bristol-Myers Squibb.

Phase
Phase 2
Status
Withdrawn
Study type
Interventional
Design
Randomized · None · Treatment
Enrollment
0actual
Sites
34
Countries
Czechia, France, Germany +5

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Why the sponsor stopped it

Sponsor decision

As filed on the registry record, in the sponsor's own words.

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2024-01-30estimatedWhen the study began enrolling
Primary completion2026-03-01estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2026-06-01estimatedThe whole study's end, after follow-up
First posted2023-02-24actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2025-03-11actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Squamous Cell Carcinoma of Head and Neck
  • Locally Advanced Head and Neck Squamous Cell Carcinoma
  • Recurrent Head and Neck Squamous Cell Carcinoma

Interventions

  • Biological: RP3
  • Other: CCRT(concurrent chemoradiation therapy)
  • Other: carboplatin and paclitaxel
  • Biological: nivolumab

Primary outcomes

what the primary-completion date above is the date OF
LA Cohort: Progression-free Survival
measured From Day 1 to documented progression of disease (up to 3 years)
R/M Cohort: Objective Response Rate
measured From Day 1 to documented progression of disease (up to 3 years)

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