Patient Guide: Study of Durvalumab + Tremelimumab, Durvalumab, and Placebo in Limited Stage Small-Cell Lung Cancer in Patients Who Have Not Progressed Following Concurrent Chemoradiation Therapy

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 183 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT03703297
Status: ACTIVE_NOT_RECRUITING
Condition: Small Cell Lung Cancer
Phase: PHASE3

Where You Can Participate

This study is available at 183 locations across the country.

Top locations include:
  • • Tucson, Arizona
  • • Santa Rosa, California
  • • New Haven, Connecticut
  • • And 180 more locations

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Study of Durvalumab + Tremelimumab, Durvalumab, and Placebo in Limited Stage Small-Cell Lung Cancer in Patients Who Have Not Progressed Following Concurrent Chemoradiation Therapy - Join Clinical Trial NCTNCT03703297

How to Join This Clinical Trial - NCTNCT03703297

Learn how to participate in this PHASE3 trial studying an investigational therapy for Small Cell Lung Cancer. Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Small Cell Lung Cancer
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT03703297 - 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 183 locations. Find a study site near you:

Clinical Research Site

Tucson, Arizona 85715 - United States

Status: Contact for availability

Clinical Research Site

Santa Rosa, California 95403 - United States

Status: Contact for availability

Clinical Research Site

New Haven, Connecticut 06510 - United States

Status: Contact for availability

Clinical Research Site

Fort Myers, Florida 33901 - United States

Status: Contact for availability

Clinical Research Site

Orange City, Florida 32763 - United States

Status: Contact for availability

Clinical Research Site

Saint Petersburg, Florida 33705 - United States

Status: Contact for availability

Clinical Research Site

Marietta, Georgia 30060 - United States

Status: Contact for availability

Clinical Research Site

Hines, Illinois 60141 - United States

Status: Contact for availability

Clinical Research Site

Fort Wayne, Indiana 46804 - United States

Status: Contact for availability

Clinical Research Site

Muncie, Indiana 47303 - United States

Status: Contact for availability

And 173 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 Small Cell Lung Cancer:

  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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