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Completed Phase 2 Interventional Results available

Study to Evaluate Exemestane With and Without Entinostat (SNDX-275) in Treatment of Postmenopausal Women With Advanced Breast Cancer

ClinicalTrials.gov ID: NCT00676663

Public ClinicalTrials.gov record NCT00676663. 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 Jun 25, 2026, 9:54 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 2, Randomized, Double-Blind, Multicenter Study of Exemestane With and Without SNDX-275 in Postmenopausal Women With Locally Recurrent or Metastatic Estrogen Receptor-Positive Breast Cancer, Progressing on Treatment With a Non-Steroidal Aromatase Inhibitor

Study identification

NCT ID
NCT00676663
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Syndax Pharmaceuticals
Industry
Enrollment
130 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
Female
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
Jun 12, 2008
Primary completion
Jan 28, 2011
Completion
Nov 25, 2012
Last update posted
May 10, 2022

2008 – 2012

United States locations

U.S. sites
24
U.S. states
15
U.S. cities
23
Facility City State ZIP Site status
California Cancer Care Greenbrae California
Moores UCSD Cancer Center La Jolla California
Scripps Health La Jolla California
University of Colorado Aurora Colorado
Rocky Mountain Cancer Center Denver Colorado
Florida Cancer Specialists Fort Myers Florida
Memorial Cancer Institute Hollywood Florida
University of Southern Florida -Moffitt Cancer Center Tampa Florida
Palm Beach Cancer Institute West Palm Beach Florida
Medical College of Georgia Augusta Georgia
Indiana University Indiana Cancer Pavilion Indianapolis Indiana
University of Maryland Greenebaum Cancer Center Baltimore Maryland
Kansas City Cancer Center Kansas City Missouri
Hematology-Oncology Associates of Northern New Jersey Morristown New Jersey
Carolinas Healthcare System Clinical Trials Charlotte North Carolina
Wake Forest University Baptist Medical Center Winston-Salem North Carolina
Oncology Hematology Care Cincinnati Ohio
Cancer Centers of the Carolinas Greenville South Carolina
Chattanooga Oncology Hematology Associates Chattanooga Tennessee
Sarah Cannon Cancer Center Nashville Tennessee
South Texas Cancer Center McAllen Texas
Virginia Cancer Institute Richmond Virginia
Columbia Basin Hematology & Oncology Kennewick Washington
Puget Sound Cancer Center 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.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 14 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00676663, 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 May 10, 2022 · Synced Jun 25, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00676663 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →