Patient Guide: Study of Adjuvant Cemiplimab Versus Placebo After Surgery and Radiation Therapy in Patients With High Risk Cutaneous Squamous Cell Carcinoma

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 166 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT03969004
Status: ACTIVE_NOT_RECRUITING
Condition: Cutaneous Squamous Cell Carcinoma
Phase: PHASE3

Where You Can Participate

This study is available at 166 locations across the country.

Top locations include:
  • • Gilbert, Arizona
  • • Phoenix, Arizona
  • • Tucson, Arizona
  • • And 163 more locations

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Study of Adjuvant Cemiplimab Versus Placebo After Surgery and Radiation Therapy in Patients With High Risk Cutaneous Squamous Cell Carcinoma - Join Clinical Trial NCTNCT03969004

How to Join This Clinical Trial - NCTNCT03969004

Learn how to participate in this PHASE3 trial studying an investigational therapy for Cutaneous Squamous Cell Carcinoma. Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Cutaneous Squamous Cell Carcinoma
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT03969004 - 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 166 locations. Find a study site near you:

Clinical Research Site

Gilbert, Arizona 85234 - United States

Status: Contact for availability

Clinical Research Site

Phoenix, Arizona 85054 - United States

Status: Contact for availability

Clinical Research Site

Tucson, Arizona 85724-5024 - United States

Status: Contact for availability

Clinical Research Site

Los Angeles, California 90025 - United States

Status: Contact for availability

Clinical Research Site

Los Angeles, California 90033 - United States

Status: Contact for availability

Clinical Research Site

Palo Alto, California 94304 - United States

Status: Contact for availability

Clinical Research Site

San Francisco, California 94143-0981 - United States

Status: Contact for availability

Clinical Research Site

Washington D.C., District of Columbia 20037 - United States

Status: Contact for availability

Clinical Research Site

Gainesville, Florida 032608 - United States

Status: Contact for availability

Clinical Research Site

Miami, Florida 33136 - United States

Status: Contact for availability

And 156 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE3 clinical trial for Cutaneous Squamous Cell Carcinoma:

  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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