RecruitingPHASE1, PHASE2NCT04938817

Safety and Efficacy Study of Investigational Agents as Monotherapy or in Combination With Pembrolizumab (MK-3475) for the Treatment of Extensive-Stage Small Cell Lung Cancer (ES-SCLC) in Need of Second-Line Therapy (MK-3475-B98/KEYNOTE-B98)

Studying Autosomal dominant multiple pterygium syndrome

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Key facts

Sponsor
Merck Sharp & Dohme LLC
Principal Investigator
Medical Director
Merck Sharp & Dohme LLC
Intervention
coformulation pembrolizumab/quavonlimab(biological)
Enrollment
110 target
Eligibility
18 years · All sexes
Timeline
20212029

Study locations (30)

Collaborators

Daiichi Sankyo

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 NCT04938817 on ClinicalTrials.gov

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