CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 100 enrolled
Drug / intervention
CC-486 +2 moredrug
Likely dose
CC-486 300 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/NCT02546986
NCT02546986Phase 2Completed

A Phase 2 Multicenter, Randomized, Placebo Controlled, Double Blind Study to Assess the Safety and Efficacy of CC-486 (Oral Azacitidine) in Combination With Pembrolizumab (MK-3475) Versus Pembrolizumab Plus Placebo in Subjects With Previously Treated Locally Advanced or Metastatic Non-small Cell Lung Cancer

Celgene·interventional·Posted Sep 11, 2015·Updated Aug 8, 2025

In Brief

A Phase 2 clinical trial evaluating CC-486, Pembrolizumab, and 1 other intervention for Carcinoma, Non-Small-Cell Lung. Completed, enrolled 100 participants across 33 sites in 6 countries.

Detailed Summary

The purpose of this study is to determine whether the combination therapy of CC-486 (oral azacitidine) and pembrolizumab provides improved patient outcomes compared to pembrolizumab alone in patients with previously treated locally advanced or metastatic non-small cell lung cancer.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesFrance, Germany, Greece, Italy, Spain, United States
Collaborators--

Timeline

Phase 2CompletedFinished
20162017201820192020202120222023202420252026
First PostedSep 11, 2015
Enrollment StartOct 9, 2015
Primary CompletionApr 13, 2017
Study CompletionJul 7, 2025
TodayJul 2, 2026
Enrollment to primary: 1.5 yearsPosted 10.8 years ago

Interventions

CC-486drug

CC-486 will be administered orally at a dose of 300 mg daily on days 1-14 of each 21-day cycle.

Pembrolizumabdrug

Pembrolizumab will be administered as a 30-minute IV infusion on day 1 of each 21-day cycle.

Placebodrug

Placebo will be administered orally daily on days 1-14 of each 21-day cycle.