Patient Guide: Study Comparing Tarlatamab and Durvalumab Versus Durvalumab Alone in First-Line Extensive-Stage Small-Cell Lung Cancer (ES-SCLC) Following Platinum, Etoposide and Durvalumab

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 219 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06211036
Status: 🟢 Enrolling Now
Condition: Extensive-Stage Small-Cell Lung Cancer, Small-Cell Lung Cancer
Phase: PHASE3

Where You Can Participate

This study is available at 219 locations across the country.

Top locations include:
  • • Mobile, Alabama
  • • Los Angeles, California
  • • New Haven, Connecticut
  • • And 216 more locations

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Study Comparing Tarlatamab and Durvalumab Versus Durvalumab Alone in First-Line Extensive-Stage Small-Cell Lung Cancer (ES-SCLC) Following Platinum, Etoposide and Durvalumab - Join Clinical Trial NCTNCT06211036

How to Join This Clinical Trial - NCTNCT06211036

Learn how to participate in this PHASE3 trial studying an investigational therapy for Extensive-Stage Small-Cell Lung Cancer, Small-Cell Lung Cancer. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Extensive-Stage Small-Cell Lung Cancer, 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
Extensive-Stage Small-Cell Lung Cancer, Small-Cell Lung Cancer
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT06211036 - 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 219 locations. Find a study site near you:

Clinical Research Site

Mobile, Alabama 36607 - United States

Status: TERMINATED

Clinical Research Site

Los Angeles, California 90033 - United States

Status: TERMINATED

Clinical Research Site

New Haven, Connecticut 06510 - United States

Status: RECRUITING

Clinical Research Site

Athens, Georgia 30607 - United States

Status: RECRUITING

Clinical Research Site

Atlanta, Georgia 30322 - United States

Status: RECRUITING

Clinical Research Site

Gainesville, Georgia 30501 - United States

Status: TERMINATED

Clinical Research Site

Chicago, Illinois 60612 - United States

Status: RECRUITING

Clinical Research Site

Indianapolis, Indiana 46237 - United States

Status: RECRUITING

Clinical Research Site

Baton Rouge, Louisiana 70808 - United States

Status: TERMINATED

Clinical Research Site

Boston, Massachusetts 02215 - United States

Status: RECRUITING

And 209 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 Extensive-Stage Small-Cell Lung Cancer, 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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