Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 1 Interventional

An Investigational Drug (CAL) Versus Zoledronic Acid (Zometa®) in Patients With Breast Cancer

ClinicalTrials.gov ID: NCT00051779

Public ClinicalTrials.gov record NCT00051779. 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 20, 2026, 6:17 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 24-Week Blinded Study Conducted at Multiple Centers, Evaluating the Safety and Effectiveness of Various Doses of the Investigational Drug (CAL) Versus Zoledronic Acid (Zometa®) When Randomly Assigned to Patients With Breast Cancer That Has Metastasized to Bone

Brief summary

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

This study is intended to evaluate the safety, tolerability, and possible effectiveness of an investigational humanized monoclonal antibody (CAL) to the parathyroid hormone-related protein (PTHrP) when compared to zoledronic acid in patients with breast cancer metastatic to bone. The study will also evaluate the possible effects of both study drugs on performance status, markers of bone metabolism, and skeletal events related to bone metastasis including elevated blood calcium levels, bone pain, metastatic lesions, complications and interventions. The levels of CAL in the blood will also be evaluated.

Study identification

NCT ID
NCT00051779
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
Chugai Pharma USA
Industry
Enrollment
Not listed

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
Not listed
Primary completion
Not listed
Completion
Not listed
Last update posted
Jun 24, 2005

United States locations

U.S. sites
38
U.S. states
23
U.S. cities
35
Facility City State ZIP Site status
University of Arkansas for Medical Sciences Little Rock Arkansas 72205 —
Highlands Oncology Group Springdale Arkansas 72764 —
Bay Area Cancer Research Group Concord California 94520 —
California Cancer Care, Inc. Greenbrae California 94904 —
Institute of Cancer Therapies Los Angeles California — —
San Diego Cancer Research Institute Vista California 92083 —
Anschutz Cancer Pavilion at the University of Colorado Cancer Center Aurora Colorado 80010-0510 —
Yale University New Haven Connecticut 06520-8028 —
Holy Cross Hospital Fort Lauderdale Florida 33308 —
Rush Cancer Institute Chicago Illinois 60612-3824 —
University of Kentucky Medical Center Lexington Kentucky 40536-0098 —
Louisiana State University New Orleans Louisiana 70112-2278 —
Frederick Memorial Hospital Frederick Maryland 21701 —
Dana-Farber/Harvard Cancer Center Boston Massachusetts 02115 —
Josephine Ford Cancer Center Detroit Michigan 48202 —
Spectrum Health Grand Rapids Michigan 49503 —
Southfield Oncology Institute, Inc. Southfield Michigan 48076 —
St. Louis Center for Clinical Research St Louis Missouri 63128 —
Nevada Cancer Center Las Vegas Nevada 89109 —
Dartmouth Hitchcock Medical Center Lebanon New Hampshire 03756 —
New Mexico Cancer Care Associates Santa Fe New Mexico 87505 —
HemOnCare, P.C. Brooklyn New York 11235 —
Memorial Sloan Kettering Cancer Center New York New York 10021 —
SUNY Upstate Medical University Syracuse New York 12310 —
Montefiore Medical Center The Bronx New York 10467-2490 —
Duke University Medical Center Durham North Carolina 27710 —
Ireland Cancer Center Cleveland Ohio 44106 —
University Hospitals of Cleveland Cleveland Ohio 44106 —
Hematology Oncology Consultants, Inc. Columbus Ohio 43235 —
Penn State Hershey Medical Center Hershey Pennsylvania 17033 —
Palmetto Health Columbia South Carolina 29203 —
Boston Baskin Cancer Group Memphis Tennessee 38104 —
The Boston Baskin Cancer Group Memphis Tennessee 38104 —
The West Clinic Memphis Tennessee 38120 —
Cancer Specialists of South Texas, PA Corpus Christi Texas 78412 —
Center for Oncology Research & Treatment Dallas Texas 75230 —
Baylor College of Medicine Houston Texas 77030 —
Medical College of Wisconsin-FMLH East Neoplastic Diseases and Related Disorders Milwaukee Wisconsin 53226 —

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 NCT00051779, 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 24, 2005 · Synced Oct 20, 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 public registry record, listed eligibility criteria, and available contact information for NCT00051779 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →