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NCT04702880CompletedPhase 2

A Study of BMS-986012 in Combination with Carboplatin, Etoposide, andNivolumab as First-line Therapy in Extensive-stage Small Cell Lung Cancer

A Randomized, Open Label Phase II Clinical Trial of BMS-986012 in Combination with Carboplatin, Etoposide and Nivolumab as First-line Therapy in Extensive-Stage Small Cell Lung Cancer

Source: EU CTIS (euclinicaltrials.eu) · Last updated 19 Nov 2025

Brief summary (registry, in English)

To assess the safety and tolerability for participants randomized to BMS-986012 in combination with carboplatin, etoposide, and nivolumab for 4 cycles (induction) followed by BMS-986012 and nivolumab maintenance (Arm A) vs those randomized to carboplatin, etoposide, and nivolumab for 4 cycles (induction) followed by nivolumab maintenance (Arm B). To compare the PFS as assessed by BICR of participants treated in the combination induction and maintenance therapies of Arms A and B described above.

Status (registry)
Completed
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
135 (actual)
First submitted
29 Apr 2024
Start date
1 Jun 2021
Lead sponsor
Bristol Myers Squibb International Corporation
Diseases
Lung cancer
NCT number
NCT04702880
EU CT number
2024-510700-36-00
EudraCT number
2020-001863-10

What you commit to

  • Study type: Interventional · Phase 2
  • Participants enrolled: 135
  • 17 sites in 7 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.

Other illness

  • Paraneoplastic autoimmune syndrome requiring systemic treatment
  • History of idiopathic pulmonary fibrosis, drug-induced pneumonitis, idiopathic pneumonitis, organizing pneumonia, or evidence of active pneumonitis on screening chest CT scan
  • Significant uncontrolled cardiovascular disease
  • Active, known or suspected autoimmune disease or inflammatory disorder

Other

  • Women who are pregnant or breastfeeding
  • Grade ≥ 2 peripheral sensory neuropathy at study entry

Who the study is looking for

  • Eastern Cooperative Oncology Group performance status (ECOG PS) 0 or 1
  • At least 1 measurable lesion by computed tomography (CT) or magnetic resonance imaging (MRI) per Response Evaluation Criteria in Solid Tumors version 1.1 (Response Evaluation Criteria in Solid Tumors (RECIST) v1.1) criteria
  • Adequate hematologic and end organ function
  • Must agree to follow specific methods of contraception, if applicable

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

Full criteria on EU CTIS (euclinicaltrials.eu)

Sites (17)

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

SiteCityCountrySite status
Grand Hopital de Charleroi
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CharleroiBelgiumCompleted
Universitair Ziekenhuis Gent
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GentBelgiumCompleted
Centre Hospitalier Universitaire de Liège
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LiègeBelgiumCompleted
Hospital Universitari Vall d'Hebron
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BarcelonaSpainCompleted
Hospital Universitario 12 de Octubre
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MadridSpainCompleted
Hospital Universitario Puerta de Hierro de Majadahonda
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MajadahondaSpainCompleted
Thoracic General Hospital of Athens "I Sotiria"
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AthensGreeceCompleted
Metropolitan Hospital
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PireasGreeceCompleted
Ospedale P. Pederzoli Casa di Cura Privata S.p.A.
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Peschiera del GardaItalyCompleted
Humanitas Research Hospital
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RozzanoItalyCompleted
Amsterdam UMC Stichting
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AmsterdamNetherlandsCompleted
Rijnstate Ziekenhuis Stichting
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ArnhemNetherlandsCompleted
Universitair Medisch Centrum Groningen
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GroningenNetherlandsCompleted
Uniwersyteckie Centrum Kliniczne
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GdanskPolandCompleted
Instytut Centrum Zdrowia Matki Polki
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LodzPolandCompleted
Institute Of Oncology Prof. Dr. Ion Chiricuta Cluj-Napoca
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Cluj-NapocaRomaniaCompleted
Centrul De Oncologie SF Nectarie S.R.L.
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CraiovaRomaniaCompleted

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