CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 453 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/NCT03066778
NCT03066778Phase 3Completed

A Phase 3 Randomized, Double-Blind, Placebo-controlled Trial of Pembrolizumab (MK-3475/SCH900475) in Combination With Etoposide/Platinum (Cisplatin or Carboplatin) for the First-line Treatment of Subjects With Extensive Stage Small Cell Lung Cancer (KEYNOTE-604)

Merck Sharp & Dohme LLC·interventional·Posted Feb 28, 2017·Updated Oct 3, 2022

In Brief

A Phase 3 clinical trial evaluating Pembrolizumab, Normal saline solution, and 3 other interventions for Small Cell Lung Cancer (SCLC). Completed, enrolled 453 participants across 148 sites in 19 countries.

Detailed Summary

The purpose of this study is to assess the safety and efficacy of pembrolizumab plus standard of care (SOC) chemotherapy (etoposide/platinum \[EP\]) in participants with newly diagnosed extensive stage small cell lung cancer (ES-SCLC) who have not previously received systemic therapy for this malignancy. The primary study hypotheses are that pembrolizumab+EP prolongs Progression-free Survival (PFS) per Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1 by blinded independent central review (BICR) and Overall Survival (OS) compared with placebo+EP in adult participants with ES-SCLC. In this study, RECIST 1.1 has been modified to follow a maximum of 10 target lesions and a maximum of 5 target lesions per organ. With protocol Amendment 07 (03-Oct-2018), the outcome measure of "Change from Baseline at Weeks 12 and 24 in European Organization for Research and Treatment of Cancer (EORTC) Quality of Life Questionnaire Core 30 (QLQ-C30) Global Health Status/Quality of Life Scale" was replaced with a single time point analysis at Week 18.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesAustralia, Canada, Chile, France, Germany, Hungary, Ireland, Israel, Japan, New Zealand, Poland, Russia, South Korea, Spain, Switzerland, Taiwan, Turkey (Türkiye), United Kingdom, United States
Collaborators--

Timeline

Phase 3CompletedFinished
2017201820192020202120222023202420252026
First PostedFeb 28, 2017
Enrollment StartMay 2, 2017
Primary CompletionDec 2, 2019
Study CompletionSep 21, 2021
TodayJul 2, 2026
Enrollment to primary: 2.6 yearsPosted 9.3 years ago

Interventions

Pembrolizumabbiological

IV infusion on Day 1 of each cycle prior to chemotherapy

Normal saline solutiondrug

IV infusion on Day 1 of each cycle prior to chemotherapy

Carboplatindrug

IV infusion on Day 1 of each cycle

Cisplatindrug

IV infusion on Day 1 of each cycle

Etoposidedrug

IV infusion on Days 1, 2 and 3 of each cycle