Patient Guide: A Study of Setanaxib Co-Administered With Pembrolizumab in Patients With Recurrent or Metastatic Squamous Cell Carcinoma of Head and Neck (SCCHN)

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 24 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT05323656
Status: ACTIVE_NOT_RECRUITING
Condition: Squamous Cell Carcinoma of Head and Neck
Phase: PHASE2

Where You Can Participate

This study is available at 24 locations across the country.

Top locations include:
  • • Miami Beach, Florida
  • • Creve Coeur, Missouri
  • • Florissant, Missouri
  • • And 21 more locations

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A Study of Setanaxib Co-Administered With Pembrolizumab in Patients With Recurrent or Metastatic Squamous Cell Carcinoma of Head and Neck (SCCHN) - Join Clinical Trial NCTNCT05323656

How to Join This Clinical Trial - NCTNCT05323656

Learn how to participate in this PHASE2 trial studying an investigational therapy for Squamous Cell Carcinoma of Head and Neck. Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Squamous Cell Carcinoma of Head and Neck. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
Squamous Cell Carcinoma of Head and Neck
Treatment Being Tested
Investigational treatment
Study Phase
PHASE2 - Safety and effectiveness study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT05323656 - ClinicalTrials.gov Identifier
Sponsored By
Study sponsor

What to Expect as a Participant

Participating in this clinical trial involves:

  • Initial screening to determine eligibility
  • Regular study visits and health assessments
  • Receiving the study treatment or placebo
  • Medical monitoring and follow-up care
  • Contributing to medical research that may help others
  • Potential access to new treatments before they're widely available

Clinical Trial Benefits and Compensation

Participants in this clinical research study may receive:

  • Close medical monitoring by healthcare professionals
  • Access to potential new treatments
  • Compensation for time and travel (varies by study)
  • No-cost study-related medical care
  • The opportunity to help advance medical knowledge

Where Is This Clinical Trial Located?

This study is enrolling participants at 24 locations. Find a study site near you:

Clinical Research Site

Miami Beach, Florida 33140 - United States

Status: Contact for availability

Clinical Research Site

Creve Coeur, Missouri 63141 - United States

Status: Contact for availability

Clinical Research Site

Florissant, Missouri 63031 - United States

Status: Contact for availability

Clinical Research Site

Saint Louis, Missouri 63110 - United States

Status: Contact for availability

Clinical Research Site

Saint Peters, Missouri 63376 - United States

Status: Contact for availability

Clinical Research Site

Vandœuvre-lès-Nancy, Grand Est 54519 - France

Status: Contact for availability

Clinical Research Site

Lille, Hauts-de-France 59000 - France

Status: Contact for availability

Clinical Research Site

Amiens Cedex 1, Picardie 80054 - France

Status: Contact for availability

Clinical Research Site

Bayonne, 64100 - France

Status: Contact for availability

Clinical Research Site

Bordeaux, 33000 - France

Status: Contact for availability

And 14 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE2 clinical trial for Squamous Cell Carcinoma of Head and Neck:

  1. Review the eligibility criteria with your healthcare provider
  2. Contact the study team for a pre-screening interview
  3. Schedule an in-person screening visit if eligible
  4. Review and sign the informed consent form
  5. Begin participation in the clinical trial

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