ClinicalTrials.gov record
Completed Phase 2 Interventional Results available

Study of MEDI-573 Plus Standard Endocrine Therapy for Women With Hormone-sensitive Metastatic Breast Cancer

ClinicalTrials.gov ID: NCT01446159

Public ClinicalTrials.gov record NCT01446159. 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 May 19, 2026, 6:22 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 1b/2 Randomized Study of MEDI-573 in Combination With an Aromatase Inhibitor (AI) Versus AI Alone in Women With Metastatic Breast Cancer (MBC)

Study identification

NCT ID
NCT01446159
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
MedImmune LLC
Industry
Enrollment
188 participants

Conditions and interventions

Interventions

  • Aromatase Inhibitor Drug
  • MEDI-573 Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 99 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
Jun 12, 2011
Primary completion
Jun 27, 2019
Completion
Jun 27, 2019
Last update posted
Jun 1, 2020

2011 – 2019

United States locations

U.S. sites
34
U.S. states
15
U.S. cities
31
Facility City State ZIP Site status
Research Site Scottsdale Arizona 85259
Research Site Bakersfield California 93309
Research Site Pleasant Hill California 94523
Research Site Stamford Connecticut 06904
Research Site Fort Myers Florida 33901
Research Site Orlando Florida 32804
Research Site Port Saint Lucie Florida 34952-7596
Research Site St. Petersburg Florida 33705
Research Site Athens Georgia 30607
Research Site Augusta Georgia 30901
Research Site Lawrenceville Georgia 30046
Research Site Scarborough Maine 04074
Research Site Baltimore Maryland 21224
Research Site Baltimore Maryland 21231
Research Site Bethesda Maryland 20817
Research Site Frederick Maryland 21701
Research Site Rockville Maryland 20850
Research Site Ann Arbor Michigan 48106-0995
Research Site Lansing Michigan 48910
Research Site Rochester Minnesota 55904
Research Site Albuquerque New Mexico 87131
Research Site Lake Success New York 11041
Research Site Lake Success New York 11042
Research Site Canton Ohio 44718
Research Site Cincinnati Ohio 45267
Research Site Cleveland Ohio 44106
Research Site Cleveland Ohio 44195
Research Site Middletown Ohio 45042
Research Site Toledo Ohio 43608
Research Site Memphis Tennessee 38120
Research Site Nashville Tennessee 37205
Research Site Houston Texas 77030
Research Site Lubbock Texas 79410
Research Site Richmond Virginia 23230

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 37 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01446159, 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, 2020 · Synced May 19, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01446159 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →