CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 1,274 enrolled / 1,274 target
Drug / intervention
pembrolizumab +3 morebiological
Likely dose
200 mgfrom 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/NCT02220894
NCT02220894Phase 3CompletedMonitor (9.1/mo)Completion was 93mo ago

A Randomized, Open Label, Phase III Study of Overall Survival Comparing Pembrolizumab (MK-3475) Versus Platinum Based Chemotherapy in Treatment Naïve Subjects With PD-L1 Positive Advanced or Metastatic Non-Small Cell Lung Cancer (Keynote 042)

Merck Sharp & Dohme LLC·interventional·Posted Aug 20, 2014·Updated Jun 25, 2026

In Brief

A Phase 3 clinical trial evaluating pembrolizumab, carboplatin, and 2 other interventions for Non-small Cell Lung Cancer. Completed, enrolled 1,274 participants.

Signals

Enrolling slower than its timeline implies

Detailed Summary

In this study, participants with programmed cell death ligand 1 (PD-L1)-positive non-small cell lung cancer (NSCLC) will be randomized to receive single agent pembrolizumab for up to 35 treatments or standard of care (SOC) platinum-based chemotherapy (carboplatin + paclitaxel or carboplatin + pemetrexed for 4 to 6 21-day cycles). Participants in the platinum-based chemotherapy arms with non-squamous tumor histologies may receive pemetrexed maintenance therapy after the 4 to 6 cycles of chemotherapy. The primary study hypothesis is that pembrolizumab prolongs overall survival (OS) compared to SOC chemotherapy.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
Countries--
Collaborators--

Timeline

Phase 3CompletedFinished
201520162017201820192020202120222023202420252026
First PostedAug 20, 2014
Enrollment StartOct 30, 2014
Primary CompletionSep 4, 2018
Study CompletionSep 12, 2022
TodayJul 2, 2026
Enrollment to primary: 3.8 yearsPosted 11.9 years ago

Arms & Interventions

Pembrolizumabexperimental

Participants receive pembrolizumab 200 mg intravenous (IV) on Day 1 of every 21-day cycle (every 3 weeks, or Q3W) for up to 35 treatments.

Biological: pembrolizumab
SOC Treatmentactive_comparator

Participants receive carboplatin target dose Area Under Curve (AUC) 5 (maximum dose 750 mg) or AUC 6 (maximum dose 900 mg) + paclitaxel 200 mg/m\^2 IV on Day 1 of every 21-day cycle (Q3W) for a maximum of 6 cycles OR carboplatin target dose AUC 5 (maximum dose 750 mg) or AUC 6 (maximum dose 900 mg) + pemetrexed 500 mg/m\^2 IV on Day 1 Q3W for a maximum of 6 cycles; participants with non-squamous histologies may go on to receive optional treatment with pemetrexed 500 mg/m\^2 IV on Day 1 Q3W.

Drug: carboplatinDrug: paclitaxelDrug: pemetrexed

Interventions

pembrolizumabbiological

carboplatindrug

paclitaxeldrug

pemetrexeddrug