drugset / Trial / NCT03254004

Postoperative Pembrolizumab for the Patients Who Have Solid Predominant or Micropapillary Lung Adenocarcinoma With Pathologic Stage I and Primary Tumor Than 4 cm

NCT03254004 ↗

Phase 2 Unknown 70 enrolled Samsung Medical Center
NaSingle-groupOpen-labelTreatment

Summary

A single center, open-label, single arm study in patients who have solid or micropapillary adenocarcinoma with pathologic stage I and primary tumor no more than 4 cm. Pembrolizumab 200 mg every 3 weeks

Timeline

Start
2018-10-08
Primary completion
2021-03-30
Completion
2021-11-30

Outcome

Met primary endpoint

paper the 3-year disease-free survival (DFS) was 83·2%, meeting the survival endpoint of >80%. PMID 40524802 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Pembrolizumab Monoclonal antibody 200 mg —

Indications