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NCT07203053RecruitingPhase 2

A clinical study to investigate the efficacy of tarlatamab in people with extensive-stage small cell lung cancer (ES-SCLC) whose cancer has progressed during or after prior treatment and who have a limited health status.

ETOP 29-25 START-lung: A multicentre phase II trial of tarlatamab in patients with pretreated extensive-stage small cell lung cancer (ES-SCLC) and ECOG PS 2.

Source: EU CTIS (euclinicaltrials.eu) · Last updated 28 Oct 2026

Brief summary (registry, in English)

The primary objective of the trial is to assess the clinical efficacy of tarlatamab in terms of 12-month overall survival (OS) rate in patients with ES-SCLC and ECOG PS 2 who have previously received one line of platinum-etoposide doublet chemotherapy with an immune-checkpoint inhibitor and whose disease has progressed.

Status (registry)
Recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
40 (estimated)
First submitted
18 Dec 2025
Start date
21 May 2026
Lead sponsor
ETOP IBCSG Partners Foundation
Diseases
Lung cancer
NCT number
NCT07203053
EU CT number
2025-522288-13-00

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 40
  • 13 sites in 4 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of EU CTIS (euclinicaltrials.eu). It describes the study, not your situation.

Who cannot take part

Copied verbatim from EU CTIS (euclinicaltrials.eu) and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Prior history of immune-related recurrent pneumonitis (grade ≥2)) or severe immune-mediated adverse events

Other illness

  • Diagnosis or evidence of leptomeningeal disease or spinal cord compression
  • Evidence of interstitial lung disease or active, non-infectious pneumonitis
  • Active autoimmune disease
  • History of solid organ transplantation
  • Presence or history of an uncontrolled viral infection
  • History of other malignancy within the past 2 years

Other

  • Symptomatic CNS metastases

Who the study is looking for

  • Histologically or cytologically confirmed ES-SCLC
  • Previous treatment with only one line of platinum-etoposide doublet chemotherapy with immune-checkpoint inhibition for SCLC
  • Progressive disease on or after the first-line treatment for SCLC
  • ECOG Performance Status 2
  • Age ≥18 years
  • Adequate organ function
  • Negative pregnancy test for female participants of childbearing potential
  • Written Informed Consent signed before any trial-related intervention

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on EU CTIS (euclinicaltrials.eu)

Sites (13)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Hospital General Universitario Dr. Balmis
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AlicanteSpainRecruiting
Hospital Universitari Vall d'Hebron
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BarcelonaSpainRecruiting
Hospital de la Santa Creu i Sant Pau
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BarcelonaSpainRecruiting
ICO l'Hospitalet - Hospital Duran i Reynals
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BarcelonaSpainRecruiting
Hospital Universitario Puerta de Hierro de Majadahonda
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MajadahondaSpainRecruiting
Centre Hospitalier Universitaire D'Angers
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AngersFranceRecruiting
Institut Bergonie
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BordeauxFranceRecruiting
Centre Leon Berard
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LyonFranceRecruiting
Centre Hospitalier Regional De Marseille
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MarseilleFranceRecruiting
Henry Dunant Hospital Center
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AthensGreeceRecruiting
Istituto Romagnolo per lo Studio dei Tumori "Dino Amadori" - IRST S.r.l
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MeldolaItalyRecruiting
Azienda Ospedaliera di Perugia
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PerugiaItalyRecruiting
Irccs Istituto Nazionale Tumori Regina Elena
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RomeItalyRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.