Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
Carcinoma Non-small-cell Lung
Type
Interventional
Phase
Phase 3
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentMasking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)Masking Description: Sponsor, excluding supply chain management personnel and unblinded monitors of site pharmacies, will remain blinded.Primary Purpose: Treatment

Participation Requirements

Age
Between 18 years and 130 years
Gender
Both males and females

Description

Approximately 360 patients will be randomized in a 2:1 to receive treatment with durvalumab or placebo therapy. The primary objective of this study is to assess the efficacy of durvalumab treatment compared with placebo in terms of PFS

Approximately 360 patients will be randomized in a 2:1 to receive treatment with durvalumab or placebo therapy. The primary objective of this study is to assess the efficacy of durvalumab treatment compared with placebo in terms of PFS

Tracking Information

NCT #
NCT03706690
Collaborators
Not Provided
Investigators
Principal Investigator: Yilong Wu, MD Guangdong General Hospital, Guangdong Lung Cancer Institute