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NCT05136677CompletedPhase 2

A Study to Evaluate Nivolumab in Combination With Ipilimumab Versus Pemetrexed With Cisplatin or Carboplatin for Unresectable Pleural Mesothelioma in Chinese Participants

A Phase II, Randomized, Open-label Trial of Nivolumab in Combination With Ipilimumab Versus Pemetrexed With Cisplatin or Carboplatin as First-line Therapy for Unresectable Pleural Mesothelioma in Chinese Participants

Source: ClinicalTrials.gov · Last updated 23 Jan 2026

Brief summary (registry, in English)

The purpose of this study is to assess the efficacy and safety of the combination of nivolumab and ipilimumab in Chinese participants with malignant pleural mesothelioma.

Status (registry)
Completed
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
102 (actual)
First submitted
18 Nov 2021
Start date
25 Jan 2022
Primary completion date
12 Nov 2025
Lead sponsor
Bristol-Myers Squibb
NCT number
NCT05136677

What you commit to

  • Study type: Interventional · Phase 2
  • Participants enrolled: 102
  • From 25 Jan 2022 to the primary completion date, 12 Nov 2025
  • 21 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Brain metastasis, except if surgically resected or treated with stereotaxic radiotherapy
  • Prior therapy for MPM (including chemotherapy, radical pleuropneumonectomy and non-palliative radiotherapy)
    • Other protocol-defined inclusion/exclusion criteria apply

Other

  • Primitive peritoneal, pericardial, testis or tunica vaginalis mesothelioma

Who the study is looking for

  • Histologically proven diagnosis of Malignant Pleural Mesothelioma (MPM) with determination of epithelioid vs non-epithelioid histology
  • Must have advanced unresectable disease that is not amenable to therapy with curative intent (surgery with or without chemotherapy)
  • Available tumor samples for centralized testing
  • Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 to 1
  • Measurable disease

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

Full criteria on ClinicalTrials.gov

Sites (21)

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

SiteCityCountrySite status
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BeijingChinaUnknown status
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ChangchunChinaUnknown status
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ChangshaChinaUnknown status
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ChengduChinaUnknown status
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HangzhouChinaUnknown status
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HangzhouChinaUnknown status
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HarbinChinaUnknown status
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JinanChinaUnknown status
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KunmingChinaUnknown status
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NingboChinaUnknown status
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NingboChinaUnknown status
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QingdaoChinaUnknown status
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ShanghaiChinaUnknown status
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ShenyangChinaUnknown status
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ShenyangChinaUnknown status
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TaiyuanChinaUnknown status
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TianjinChinaUnknown status
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TianjinChinaUnknown status
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WuhanChinaUnknown status
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YangzhouChinaUnknown status
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ZhengzhouChinaUnknown status

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