RecruitingPhase 3NCT07005128

A Study Comparing Tarlatamab, Durvalumab, Carboplatin, and Etoposide Versus Durvalumab, Carboplatin, and Etoposide in First-line Extensive Stage Small-Cell Lung Cancer (ES-SCLC)

The main objective of the study is to compare the efficacy of tarlatamab in combination with durvalumab, carboplatin and etoposide to the combination of durvalumab, carboplatin and etoposide on prolonging overall survival (OS).

Checked against the public recordLast updated Jul 16, 2026 · Source: ClinicalTrials.gov

StatusRecruiting
PhasePhase 3
U.S. locations164
SponsorAmgen
01
Study overview

What this study is about

Purpose
Treatment
Study type
Interventional
Phase
Phase 3
Sponsor
Amgen
Interventions being studied
Drug: Tarlatamab; Drug: Durvalumab; Drug: Carboplatin; Drug: Etoposide
02
Explore related studies

How this study is categorized

These labels come from structured fields and exact terms in the public record.

03
Public criteria

Who may be able to participate

Inclusion Criteria: * Participant has provided informed consent before initiation of any study-specific activities/procedures. * Age ≥ 18 years or ≥ legal age within the country if it is older than 18 years. * Histologically or cytologically documented ES-SCLC (American Joint Committee on Cancer, 2017, Stage IV SCLC \[T any, N any, M1 a/b/c\]), or T3 to T4 due to multiple lung nodules that are too extensive or have tumor/nodal volume that is too large to be encompassed in a tolerable radiation plan. * Measurable disease as defined per RECIST 1.1. * Suitable to receive carboplatin, etoposide and durvalumab regimen as first-line treatment per investigator clinical assessment. * Minimum life expectancy ≥ 12 weeks. Exclusion Criteria: * Participants can have no history of other malignancy in the last 2 years. * Any symptomatic central nervous system (CNS) metastases, or leptomeningeal disease. * They will have no history of severe or life-threatening events to immune-mediated therapy. * History of arterial thrombosis (eg, stroke or transient ischemic attack) within 6 months prior to first dose of study treatment. * They will have no active autoimmune or inflammatory disorders. * Presence of active human immunodeficiency virus (HIV) or active Hepatitis (B/C) infection. * Evidence or interstitial lung disease (ILD) or active, non-infectious pneumonitis. * History of solid organ transplant. * They will not have had a myocardial infarction and/or symptomatic congestive heart failure (New York Heart Association \> class II) within 6 months prior to first dose of study treatment.

Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.

04
Study sites

U.S. locations

  • Cancer and Blood Specialists of ArizonaCasa Grande, Arizona
  • City of Hope Cancer Center PhoenixGoodyear, Arizona
  • Genesis Cancer CenterHot Springs, Arkansas
  • Saint Bernards Medical CenterJonesboro, Arkansas
  • Providence Saint Jude Medical CenterFullerton, California
  • Translational Research in Oncology US Inc, Trio Central PharmacyLos Angeles, California
  • University of California Los AngelesSanta Monica, California
  • Presbyterian Intercommunity Hospital Health Whitter HospitalWhittier, California
  • Colorado West Healthcare System dba Grand Valley OncologyGrand Junction, Colorado
  • Hartford HealthCare Cancer Institute at The Hospital of Central ConnecticutNew Britain, Connecticut
  • Yale New Haven HospitalNew Haven, Connecticut
  • Eastern Connecticut Hematology and Oncology AssociatesNorwich, Connecticut

Source and freshness
Processed from ClinicalTrials.gov. Last public update: Jul 16, 2026. Always confirm current availability with the study team.

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