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Completed Phase 3 Interventional Results available

Zoledronic Acid - Letrozole Adjuvant Synergy Trial (ZFAST) - Cancer Treatment Related Bone Loss in Postmenopausal Women With Estrogen Receptor Positive and/or Progesterone Receptor Positive Breast Cancer Receiving Adjuvant Hormonal Therapy

ClinicalTrials.gov ID: NCT00050011

Public ClinicalTrials.gov record NCT00050011. 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 28, 2026, 8:00 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

An Open-Label, Randomized, Multicenter Study to Evaluate the Use of Zoledronic Acid in the Prevention of Cancer Treatment-Related Bone Loss in Postmenopausal Women With Estrogen Receptor Positive and/or Progesterone Receptor Positive Breast Cancer Receiving Letrozole as Adjuvant Therapy

Brief summary

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

This protocol is designed to compare the effect on bone of Zoledronic Acid 4 mg every 6 months when given upfront versus delayed start (based on a post-baseline BMD T- Score below -2.0 SD at either the lumbar spine or total hip, or any clinical fracture unrelated to trauma, or an asymptomatic fracture discovered at the month 36 scheduled visit) in stage I-IIIb postmenopausal women with hormone receptor positive breast cancer who will receive Letrozole 2.5 mg daily as an adjuvant therapy.

Study identification

NCT ID
NCT00050011
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
602 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 85 Years
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
Sep 2002 (Type not available)
Primary completion
Jan 2009 (Actual)
Completion
Jan 2009 (Actual)
Last update posted
Mar 21, 2014

2002 – 2009

United States locations

U.S. sites
43
U.S. states
24
U.S. cities
42
Facility City State ZIP Site status
Highlands Oncology Group Springdale Arkansas 72764 —
East Valley Hematology & Oncology Burbank California 91505 —
Louisiana Oncology Associates Lafayette California 70506 —
Wilshire Oncology Medical Group LaVerne California 91750 —
Pacific Shores Medical Group Long Beach California 90813 —
Clinical Trials & Research Associates, Inc. Montebello California 90640 —
Redwood Regional Medical Group Santa Rosa California 95403 —
Cancer and Blood Institute of the Desert Rancho Mirage Colorado 92270 —
Eastern Connecticut Hematology/Oncology Associates Norwich Connecticut 06360 —
FL Community Cancer Center Brooksville Florida 34613 —
Robert R. Carroll, MD, PA Gainesville Florida 32605 —
Oncology Hematology Group of South Florida Miami Florida 33176 —
Pasco Pinellas Cancer Center New Port Richey Florida 34652 —
Ocala Oncology Center Ocala Florida 33479 —
Cancer Research Network, Inc. Plantation Florida 33324 —
Bay Area Oncology Tampa Florida 33607 —
Space Coast Medical Titusville Florida 32796 —
Elmhurst Memorial Hospital Elhurst Illinois 60126 —
Kentuckiana Cancer Institute Louisville Kentucky 40202 —
Frederick Memorial Hospital Regional Cancer Therapy Center Frederick Maryland 21701 —
New England Hematology/Oncology Associates Wellesley Massachusetts 02481 —
Cook Research Department at Spectrum Health Grand Rapids Michigan 49503 —
Metro Minnesota CCOP Saint Louis Park Minnesota 55416 —
Hematology-Oncology Centers of the Northern Rockies, PC Billings Montana 59101 —
Methodist Cancer Center Omaha Nebraska 68114 —
Hematology-Oncology Associates of Northern NJ Morristown New Jersey 07962 —
New Mexico Oncology Hematology, Ltd. Albuquerque New Mexico 87109 —
Hemoncare PC Brooklyn New York 11235 —
Odyssey Research Services Bismarck North Dakota 58501 —
Nashat Y. Gabrail MD Inc. Canton Ohio 44718 —
Oncology Partners Network Cincinnati Ohio 45238 —
Physician Associates, Inc. Cincinnati Ohio 45238 —
Dayton Clinical Oncology Program Dayton Ohio 45420 —
University of Pittsburgh Cancer Institute/Magee Womens Hospital Pittsburgh Pennsylvania 15213 —
Charleston Hematology Oncology Charleston South Carolina 29403 —
The Sarah Cannon Cancer Center Nashville Tennessee 37203 —
St. Joseph Regional Cancer Center Bryan Texas 77802 —
Cancer Specialists of South Texas Corpus Christi Texas 78412 —
Center for Oncology Research & Tx. PA Dallas Texas 75230 —
Northern Virginia Oncology Group Fairfax Virginia 22031 —
Virginia Physicians, Inc.- Oncology Richmond Virginia 23294 —
Swedish Cancer Institute Seattle Washington 98122 —
Rockwood Clinic, PS Spokane Washington 99220 —

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 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00050011, 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 21, 2014 · Synced Oct 28, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00050011 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →