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Completed Phase 2 Interventional Results available

QUILT-2.015: A Study of AMG 479 With Exemestane or Fulvestrant in Postmenopausal Women With Hormone Receptor Positive Locally Advanced or Metastatic Breast Cancer

ClinicalTrials.gov ID: NCT00626106

Public ClinicalTrials.gov record NCT00626106. 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 23, 2026, 12:09 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 International, Randomized, Double-blind, Placebo-controlled, Phase 2 Study of AMG 479 With Exemestane or Fulvestrant in Postmenopausal Women With Hormone Receptor Positive Locally Advanced or Metastatic Breast Cancer

Study identification

NCT ID
NCT00626106
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
NantCell, Inc.
Industry
Enrollment
156 participants

Conditions and interventions

Interventions

  • AMG 479 Drug
  • Placebo Drug

Drug

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
Mar 26, 2008
Primary completion
May 4, 2010
Completion
Sep 22, 2011
Last update posted
Sep 18, 2024

2008 – 2011

United States locations

U.S. sites
25
U.S. states
13
U.S. cities
25
Facility City State ZIP Site status
Research Site Chandler Arizona 85224
Research Site Anaheim California 92801
Research Site Beverly Hills California 90211
Research Site Concord California 94520
Research Site Duarte California 91010
Research Site Montebello California 90640
Research Site San Francisco California 94115
Research Site Sylmar California 91342
Research Site Stamford Connecticut 06902
Research Site Boca Raton Florida 33428
Research Site Boynton Beach Florida 33435
Research Site Coral Springs Florida 33065
Research Site Gainesville Florida 32605
Research Site Lake Worth Florida 33467
Research Site Atlanta Georgia 30309
Research Site Marietta Georgia 30060
Research Site Chicago Illinois 60637
Research Site Lebanon New Hampshire 03756
Research Site Denville New Jersey 07834
Research Site High Point North Carolina 27262
Research Site Hershey Pennsylvania 17033
Research Site Pittsburgh Pennsylvania 15213
Research Site Memphis Tennessee 38120
Research Site American Fork Utah 84003
Research Site Tacoma Washington 98405

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 35 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00626106, 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 Sep 18, 2024 · Synced Jul 23, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00626106 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →