A Study to Compare the Pharmacokinetics, Efficacy, Safety, and Immunogenicity of Pembrolizumab (SB27, EU Sourced Keytruda, and US Sourced Keytruda) in Subjects With Stage II-IIIA NSCLC Following Complete Resection and Adjuvant Platinum-based Chemotherapy

Key facts

Sponsor

Samsung Bioepis Co., Ltd.

Intervention

SB27(drug)

Enrollment

163 enrolled

Eligibility

18 years · All sexes

Timeline

2024 – 2026

Study locations (24)

• SB Investigative Site, Gdansk, Poland
• SB Investigative Site, Otwock, Poland
• SB Investigative Site, Ansan, South Korea
• SB Investigative Site, Busan, South Korea
• SB Investigative Site, Daegu, South Korea
• SB Investigative Site, Hwasun, South Korea
• SB Investigative Site, Incheon, South Korea
• SB Investigative Site, Jinju, South Korea
• SB Investigative Site, Seongnam, South Korea
• SB Investigative Site 3, Seoul, South Korea
• SB Investigative Site 4, Seoul, South Korea
• SB Investigative Site 5, Seoul, South Korea
• SB Investigative Site 6, Seoul, South Korea
• SB Investigative Site 1, Suwon, South Korea
• SB Investigative Site 2, Suwon, South Korea
• +9 more locations on ClinicalTrials.gov

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.

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