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Terminated Phase 1 Interventional Results available

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

ClinicalTrials.gov ID: NCT06056310

Public ClinicalTrials.gov record NCT06056310. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 22, 2026, 10:31 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Single Arm, Open Label, Phase 1b Study of Xevinapant in Combination With Weekly Cisplatin and Intensity-modulated Radiotherapy to Assess Safety and Tolerability in Participants With LA SCCHN, Suitable for Definitive Chemoradiotherapy (HyperlynX)

Study identification

NCT ID
NCT06056310
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 1
Lead sponsor
EMD Serono Research & Development Institute, Inc.
Industry
Enrollment
18 participants

Conditions and interventions

Interventions

  • Xevinapant Drug
  • Cisplatin Drug
  • intensity-modulated radiation therapy (IMRT) Radiation

Drug · Radiation

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jan 17, 2024
Primary completion
Aug 19, 2024
Completion
Aug 19, 2024
Last update posted
Sep 28, 2025

2024

United States locations

U.S. sites
5
U.S. states
5
U.S. cities
5
Facility City State ZIP Site status
Mount Sinai Comprehensive Cancer Center Miami Beach Florida 33140
Karmanos Cancer Institute - PARENT Detroit Michigan 48201
Montefiore Medical Center PRIME The Bronx New York 10467
Cleveland Clinic Cleveland Ohio 44195
Avera McKennan Hospital and University Health Center Sioux Falls South Dakota 57105

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 18 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06056310, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 28, 2025 · Synced Jul 22, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06056310 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →