Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 2 Interventional Results available

CB-839 With Everolimus vs. Placebo With Everolimus in Participants With Renal Cell Carcinoma (RCC)

ClinicalTrials.gov ID: NCT03163667

Public ClinicalTrials.gov record NCT03163667. 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 Sep 1, 2026, 1:43 PM 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, Placebo-Controlled Phase 2 Study Comparing CB-839 in Combination With Everolimus (CBE) vs. Placebo With Everolimus (PboE) in Patients With Advanced or Metastatic Renal Cell Carcinoma (RCC)

Brief summary

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

The primary objective of this study is to compare the progression-free survival (PFS) of participants treated with telaglenastat and everolimus versus placebo and everolimus for advanced or metastatic clear cell renal cell carcinoma (ccRCC) previously treated with the following: * At least 2 lines of therapy, including at least 1 vascular endothelial growth factor tyrosine kinase inhibitor (VEGF TKI) * Radiographic progression of metastatic RCC must have occurred (per investigator assessment) on or after the most recent systemic therapy and within 6 months prior to cycle 1 day 1

Study identification

NCT ID
NCT03163667
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Calithera Biosciences, Inc
Industry
Enrollment
69 participants

Conditions and interventions

Interventions

Drug

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
Sep 5, 2017
Primary completion
Apr 25, 2019
Completion
May 31, 2020
Last update posted
Sep 14, 2022

2017 – 2020

United States locations

U.S. sites
38
U.S. states
25
U.S. cities
37
Facility City State ZIP Site status
The University of Arizona Cancer Center Tucson Arizona 85724
Highlands Oncology Group Rogers Arkansas 72758
Los Angeles Hematology Oncology Medical Group Los Angeles California 90017
UCLA Department of Medicine - Hematology/Oncology Los Angeles California 90095
Stanford Cancer Center Stanford California 94305
Florida Cancer Specialists- South Fort Myers Florida 33901
Florida Cancer Specialists- North St. Petersburg Florida 33705
University Cancer & Blood Center, LLC Athens Georgia 30607
Northwest Georgia Oncology Centers, P.C. Marietta Georgia 30060
St. Luke's Mountain States Tumor Institute Boise Idaho 83712
Northwestern University Chicago Illinois 60611
Parkview Research Center Fort Wayne Indiana 46845
University of Iowa Hospitals and Clinics Iowa City Iowa 52242
Norton Cancer Institute, Norton Healthcare Pavilion Louisville Kentucky 40202
Ochsner Clinical Foundation New Orleans Louisiana 70121
Anne Arundel Medical Center Oncology and Hematology Annapolis Maryland 21401
University of Maryland, Greenebaum Comprehensive Cancer Center Baltimore Maryland 21201
Metro-Minnesota Community Oncology Research Consortium Saint Louis Park Minnesota 55416
Mercy Clinic Oncology & Hematology Joplin Missouri 64804
SCRI HCA Midwest Kansas City Missouri 64132
Washington University School of Medicine St Louis Missouri 63110
St. Vincent Frontier Cancer Center Billings Montana 59102
Comprehensive Cancer Centers of Nevada Las Vegas Nevada 89148
North Shore Hematology Oncology Associates PC DBA NY Cancer and Blood Specialists East Setauket New York 11733
NYU Winthrop Hospital - Cancer Clinical Trials Oncology/Hematology Mineola New York 11501
Memorial Sloan Kettering Cancer Center New York New York 10065
SUNY Upstate Medical University Syracuse New York 13210
Montefiore Medical Center The Bronx New York 10461
University of Cincinnati Medical Center Cincinnati Ohio 45219
Ann B. Barshinger Cancer Institute / Lancaster General Hospital Lancaster Pennsylvania 17604
Monongahela Valley Hospital Monongahela Pennsylvania 15063
Charleston Hematology Oncology Associates,PA Charleston South Carolina 29414
UT/Erlanger Oncology & Hematology Chattanooga Tennessee 37403
Sarah Cannon Research Institute - Tennessee Oncology Nashville Tennessee 37203
The University of Texas MD Anderson Cancer Center Houston Texas 77030
Utah Cancer Specialists Salt Lake City Utah 84106
Wenatchee Valley Hospital and Clinics Wenatchee Washington 98801
University of Wisconsin Carbone Cancer Center Madison Wisconsin 53705

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 NCT03163667, 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 Sep 14, 2022 · Synced Sep 1, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03163667 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →