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Terminated Phase 2 Interventional Results available

Ruxolitinib in Combination With Pemetrexed/Cisplatin in Non Small Cell Lung Cancer

ClinicalTrials.gov ID: NCT02119650

Public ClinicalTrials.gov record NCT02119650. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 17, 2026, 2:58 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Double-Blind Phase 2 Study of Ruxolitinib or Placebo in Combination With Pemetrexed/Cisplatin and Pemetrexed Maintenance for Initial Treatment of Subjects With Nonsquamous Non-Small Cell Lung Cancer That Is Stage IIIB, Stage IV, or Recurrent

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study was to determine if ruxolitinib, in combination with Pemetrexed/Cisplatin and Pemetrexed Maintenance, is safe and effective in the treatment of nonsquamous non-small cell lung cancer (NSCLC) that is Stage IIIB, Stage IV, or recurrent.

Study identification

NCT ID
NCT02119650
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Incyte Corporation
Industry
Enrollment
76 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Feb 11, 2014 (Actual)
Primary completion
Feb 11, 2016 (Actual)
Completion
Jun 21, 2016 (Actual)
Last update posted
Feb 13, 2018

2014 – 2016

United States locations

U.S. sites
30
U.S. states
21
U.S. cities
30
Facility City State ZIP Site status
Not listed Phoenix Arizona — —
Not listed Fayetteville Arkansas — —
Not listed Fresno California — —
Not listed La Jolla California — —
Not listed San Diego California — —
Not listed San Francisco California — —
Not listed Lone Tree Colorado — —
Not listed Norwich Connecticut — —
Not listed Southington Connecticut — —
Not listed Augusta Georgia — —
Not listed Joliet Illinois — —
Not listed Indianapolis Indiana — —
Not listed Lafayette Indiana — —
Not listed Kansas City Kansas — —
Not listed Detroit Michigan — —
Not listed St Louis Missouri — —
Not listed Reno Nevada — —
Not listed Lebanon New Hampshire — —
Not listed Mount Kisco New York — —
Not listed New York New York — —
Not listed Winston-Salem North Carolina — —
Not listed Canton Ohio — —
Not listed Portland Oregon — —
Not listed Chattanooga Tennessee — —
Not listed Knoxville Tennessee — —
Not listed Memphis Tennessee — —
Not listed Ogden Utah — —
Not listed Leesburg Virginia — —
Not listed Kennewick Washington — —
Not listed Seattle Washington — —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02119650, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 13, 2018 · Synced Oct 17, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02119650 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →