CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 304 enrolled
Drug / intervention
M7824 +1 moredrug
Likely dose
M7824 1200 milligramsfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03631706
NCT03631706Phase 3Completed

An Adaptive Phase III, Multicenter, Randomized, Open-Label, Controlled Study of M7824 (Bintrafusp Alfa) Versus Pembrolizumab as a First-line Treatment in Patients With PD-L1 Expressing Advanced Non-small Cell Lung Cancer

EMD Serono Research & Development Institute, Inc.·interventional·Posted Aug 15, 2018·Updated Apr 8, 2025

In Brief

A Phase 3 clinical trial evaluating M7824 and Pembrolizumab for Non-small Cell Lung Cancer. Completed, enrolled 304 participants across 119 sites in 18 countries.

Detailed Summary

The purpose of the study is to evaluate the efficacy and safety of bintrafusp alfa (M7824) compared with pembrolizumab in participants with advanced NSCLC with high PD-L1-tumor expression, with no epidermal growth factor receptor (EGFR) mutation or anaplastic lymphoma kinase (ALK) translocation. The Phase III adaptive design allows for the option to recruit up to 584 patients based on pre-specified rules.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesArgentina, Belgium, Brazil, Canada, China, France, Germany, Greece, Hong Kong, Italy, Japan, Netherlands, South Korea, Spain, Taiwan, Turkey (Türkiye), Ukraine, United States

Timeline

Phase 3CompletedFinished
20192020202120222023202420252026
First PostedAug 15, 2018
Enrollment StartOct 1, 2018
Primary CompletionJun 7, 2021
Study CompletionJun 25, 2024
TodayJul 2, 2026
Enrollment to primary: 2.7 yearsPosted 7.9 years ago

Interventions

M7824drug

Participants received intravenous infusion of M7824 at a dose of 1200 milligrams (mg) once every 2 weeks until confirmed progression of disease, death, unacceptable toxicity, or study withdrawal.

Pembrolizumabdrug

Pembrolizumab: Participants received intravenous infusion of Pembrolizumab at a dose of 200 milligrams (mg) once every 3 weeks until confirmed progression of disease, death, unacceptable toxicity, or study withdrawal.