CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 492 enrolled
Drug / intervention
pembrolizumab +4 morebiological
Likely dose
Not stated in 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/NCT03515837
NCT03515837Phase 3Completed

A Randomized, Double-Blind, Phase 3 Study of Pemetrexed + Platinum Chemotherapy With or Without Pembrolizumab (MK-3475) in TKI-resistant EGFR-mutated Tumors in Metastatic Non-squamous Non-small Cell Lung Cancer (NSCLC) Participants (KEYNOTE-789)

Merck Sharp & Dohme LLC·interventional·Posted May 4, 2018·Updated Nov 22, 2024

In Brief

A Phase 3 clinical trial evaluating pembrolizumab, pemetrexed, and 3 other interventions for Non-small Cell Lung Cancer. Completed, enrolled 492 participants across 158 sites in 17 countries.

Detailed Summary

The purpose of this study is to evaluate the efficacy and safety of pemetrexed plus platinum chemotherapy (carboplatin or cisplatin) with or without pembrolizumab (MK-3475; KEYTRUDA®) in the treatment of adults with the following types of tyrosine kinase inhibitor (TKI)-resistant, epidermal growth factor receptor (EGFR)-mutated, metastatic non-squamous non-small cell lung cancer (NSCLC) tumors: 1) TKI-failures (including osimertinib \[TAGRISSO®\] failure) with T790M-negative mutation tumors, 2) T790M-positive mutation tumors with prior exposure to osimertinib, and 3) first-line osimertinib failure regardless of T790M mutation status. The primary study hypotheses are that the combination of pembrolizumab plus chemotherapy has superior efficacy compared to saline placebo plus chemotherapy in terms of: 1) Progression-free Survival (PFS) per Response Evaluation Criteria in Solid Tumors Version 1.1 (RECIST 1.1) based on blinded independent central review, and 2) Overall Survival (OS). This study will be considered to have met its success criteria if the combination of pembrolizumab plus chemotherapy is superior to saline placebo plus chemotherapy in terms of PFS or OS. Upon study completion, participants are discontinued and may be enrolled in a pembrolizumab extension study, if available.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesAustralia, Brazil, Canada, China, France, Germany, Hong Kong, Israel, Italy, Japan, Mexico, South Korea, Spain, Sweden, Taiwan, United Kingdom, United States
Collaborators--

Timeline

Phase 3CompletedFinished
20192020202120222023202420252026
First PostedMay 4, 2018
Enrollment StartJun 29, 2018
Primary CompletionJan 17, 2023
Study CompletionOct 2, 2023
TodayJul 2, 2026
Enrollment to primary: 4.5 yearsPosted 8.2 years ago

Interventions

pembrolizumabbiological

IV infusion

pemetrexeddrug

IV infusion

carboplatindrug

IV infusion

cisplatindrug

IV infusion

saline solutiondrug

IV infusion