RecruitingPhase 2NCT06946797

A Study to Evaluate Two Dosing Regimens of Subcutaneous Nivolumab in Combination With Intravenous Ipilimumab and Chemotherapy in Participants With Previously Untreated Metastatic or Recurrent Non-Small Cell Lung Cancer (NSCLC)

Studying NON RARE IN EUROPE: Non-small cell lung cancer

Last synced from ClinicalTrials.gov

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Key facts

Sponsor
Bristol-Myers Squibb
Principal Investigator
Bristol-Myers Squibb
Bristol-Myers Squibb
Intervention
Nivolumab(drug)
Enrollment
76 enrolled
Eligibility
18 years · All sexes
Timeline
20252028

Study locations (30)

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT06946797 on ClinicalTrials.gov

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