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Taking people in ChinaPhase 1/2

Testing BMS-986525 alone or with pumitamig in small cell lung cancer

Tests BMS-986525, alone or with pumitamig, in adults with small cell lung cancer.

Plain-language title generated from the registry record
Registry title: A Study to Assess the Safety and Tolerability of BMS-986525 Alone and in Combination Therapy in Participants With Relapsed/Refractory Small Cell Lung Cancer

Key facts

Where
Beijing and Shanghai, ChinaSee the 2 sites
Phase
Phase 1/2

AI summary: who the study is looking for

From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is looking for adults whose small cell lung cancer came back or stopped responding to treatment, after at least 1 platinum-based chemotherapy.

Age
18 years or older
Sex
All sexes can join.
Disease stage
Small cell lung cancer that has come back or has not responded to treatment (relapsed/refractory), confirmed by tissue or cell tests.
Earlier treatment
Must have had at least 1 platinum-based chemotherapy. Where the usual first treatment includes an anti-PD-(L)1 therapy, the cancer must have progressed on it, or the person cannot have it or has no access to it.

Main reasons for not taking part

  • Untreated cancer spread to the brain or spinal cord (CNS metastases)
  • Active, known or suspected autoimmune disease
  • Earlier organ or tissue allograft (donor transplant)
  • Other exclusion criteria set by the study protocol may apply

Read by machine on 12 November 2026.

Where in China

  • Beijing, Beijing MunicipalityHospital not named in the registryContact: Site 0029Not yet recruiting
  • Shanghai East HospitalShanghai, ChinaContact: Caicun Zhou, Site 0028Taking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Trial details

Who runs it
Bristol-Myers Squibb
Trial code
NCT07325136EU 2025-524090-16-00
Record updated
14 September 2026
Original description
The purpose of this study is to assess the safety and tolerability of BMS-986525 alone and in combination with Pumitamig in participants with Relapsed/Refractory Small Cell Lung CancerRead full original descriptionShow less

A Phase 1/2 Study of BMS-986525 as Monotherapy and in Combination Therapy in Participants With Relapsed/Refractory Small Cell Lung Cancer

The purpose of this study is to assess the safety and tolerability of BMS-986525 alone and in combination with Pumitamig in participants with Relapsed/Refractory Small Cell Lung Cancer

Inclusion: Participants must have histologically or cytologically documented relapsed/refractory small cell lung cancer (R/R-SCLC); Participants must have received at least 1 platinum-based chemotherapy regimen as per locally approved drug labels and institutional guidelines; In countries where standard of care first line systemic treatment includes platinum containing chemotherapy in combination with anti-PD-(L)1 therapy, it is required that participants have progressed on, are ineligible for or not have access to an anti-PD- (L)1 therapy.

Exclusion: Participants must not have had a prior organ or tissue allograft; Participants must not have an active, known or suspected autoimmune disease; Participants must not have any untreated CNS metastases; Other protocol-defined Inclusion/Exclusion criteria apply.

ClinicalTrials.gov NCT07325136 · EU CTIS 2025-524090-16-00