Phase 1b Safety Study of Xevinapant, Weekly Cisplatin, and RT in Participants With Unresected LA SCCHN (HyperlynX)

Stopped early · Phase 1

Conditions studied: Head and Neck Cancer

In brief

The purpose of this study is to evaluate the tolerability and safety of Xevinapant when added to weekly cisplatin-based concurrent chemoradiotherapy (CRT) in the treatment of participants with unresectable locally advanced squamous cell carcinoma of the head and neck, suitable for definitive chemoradiotherapy.

Key facts

Study ID
NCT06056310
Run by
EMD Serono Research & Development Institute, Inc.
People needed
18
Starts
2024-01-18
Expected to finish
2024-08-20
Last updated by the study team
2025-09-29

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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