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Completed Phase 1Phase 2 Interventional Results available

Vorinostat and Trastuzumab in Treating Patients With Metastatic or Locally Recurrent Breast Cancer

ClinicalTrials.gov ID: NCT00258349

Public ClinicalTrials.gov record NCT00258349. 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 Jul 22, 2026, 10:14 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 Phase I/II Study of Suberoylanilide Hydroxamic Acid (SAHA) in Combination With Trastuzumab (Herceptin) in Patients With Advanced Metastatic and/or Local Chest Wall Recurrent Her-2 Amplified Breast Cancer

Study identification

NCT ID
NCT00258349
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
National Cancer Institute (NCI)
NIH
Enrollment
16 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
Jul 31, 2006
Primary completion
Jul 31, 2010
Completion
Aug 31, 2010
Last update posted
Jun 1, 2014

2006 – 2010

United States locations

U.S. sites
25
U.S. states
6
U.S. cities
14
Facility City State ZIP Site status
University of Alabama at Birmingham Birmingham Alabama 35294
Mercy Capitol Des Moines Iowa 50307
Iowa Methodist Medical Center Des Moines Iowa 50309
Iowa Oncology Research Association CCOP Des Moines Iowa 50309
Medical Oncology and Hematology Associates-Des Moines Des Moines Iowa 50309
Medical Oncology and Hematology Associates Des Moines Iowa 50314
Mercy Medical Center - Des Moines Des Moines Iowa 50314
Iowa Lutheran Hospital Des Moines Iowa 50316
Siouxland Hematology Oncology Associates Sioux City Iowa 51101
Mercy Medical Center-Sioux City Sioux City Iowa 51104
Saint Luke's Regional Medical Center Sioux City Iowa 51104
Johns Hopkins University Baltimore Maryland 21287-8936
Eastern Cooperative Oncology Group Boston Massachusetts 02215
Hutchinson Area Health Care Hutchinson Minnesota 55350
Meeker County Memorial Hospital Litchfield Minnesota 55355
Saint John's Hospital - Healtheast Maplewood Minnesota 55109
Virginia Piper Cancer Institute Minneapolis Minnesota 55407
Hennepin County Medical Center Minneapolis Minnesota 55415
Regions Hospital Saint Paul Minnesota 55101
Saint Joseph's Hospital - Healtheast Saint Paul Minnesota 55102
Saint Francis Regional Medical Center Shakopee Minnesota 55379
Woodwinds Health Campus Woodbury Minnesota 55125
Saint Vincent's Hospital and Medical Center of New York New York New York 10011
Albert Einstein College of Medicine The Bronx New York 10461
Montefiore Medical Center The Bronx New York 10467-2490

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 NCT00258349, 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 Jun 1, 2014 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00258349 live on ClinicalTrials.gov.

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