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Terminated Phase 1Phase 2 Interventional Results available

Study CB-839 in Combination With Nivolumab in Patients With Melanoma, Clear Cell Renal Cell Carcinoma (ccRCC) and Non-Small Cell Lung Cancer (NSCLC)

ClinicalTrials.gov ID: NCT02771626

Public ClinicalTrials.gov record NCT02771626. 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 24, 2026, 4:51 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 Phase 1/2 Study of the Safety, Pharmacokinetics, and Pharmacodynamics of the Glutaminase Inhibitor CB-839 in Combination With Nivolumab in Patients With Advanced/Metastatic Melanoma, Renal Cell Carcinoma and Non-Small Cell Lung Cancer

Brief summary

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

This study is an open-label Phase 1/2 evaluation of CB-839 in combination with nivolumab in participants with clear cell renal cell carcinoma, melanoma, and non-small cell lung cancer.

Study identification

NCT ID
NCT02771626
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
Calithera Biosciences, Inc
Industry
Enrollment
118 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
Aug 1, 2016 (Actual)
Primary completion
Apr 24, 2020 (Actual)
Completion
Apr 24, 2020 (Actual)
Last update posted
Mar 17, 2023

2016 – 2020

United States locations

U.S. sites
17
U.S. states
12
U.S. cities
13
Facility City State ZIP Site status
Honor Health Scottsdale Arizona 85016 —
Stanford University Palo Alto California 94304 —
University of Colorado Aurora Colorado 80045 —
University Cancer Blood Center Athens Georgia 30607 —
Beth Israel Deaconess Medical Center Boston Massachusetts 02114 —
Massachusetts General Hospital Boston Massachusetts 02114 —
Dana-Farber Cancer Institute Boston Massachusetts 02215 —
Karmanos Caner Center Detroit Michigan 48201 —
New York University New York New York 10016 —
Columbia University Medical Center New York New York 10032 —
Memorial Sloan Kettering Cancer Center New York New York 10655 —
University Hospitals Cleveland Cleveland Ohio 44106 —
University of Pennsylvania Philadelphia Pennsylvania 19104 —
Vanderbilt University Nashville Tennessee 37232 —
University of Texas MD Anderson Cancer Center Houston Texas 77030 —
Seattle Cancer Care Alliance/University of Washington Seattle Washington 98109 —
Northwest Medical Specialties Tacoma Washington 98405 —

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 NCT02771626, 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 Mar 17, 2023 · Synced Oct 24, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02771626 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →