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Clinical trialNCT01797120CompletedPhase 2Interventional

Study of Fulvestrant +/- Everolimus in Post-Menopausal, Hormone-Receptor + Metastatic Breast Ca Resistant to AI

SponsorPrECOG, LLC.Enrollment131Metastatic Breast Cancer
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

Post-menopausal women with hormone-receptor positive (HR+) metastatic breast cancer resistant to aromatase inhibitor (AI) therapy will be randomized to receive Fulvestrant (Faslodex) with Everolimus or Fulvestrant (Faslodex) with a placebo (no active ingredients). Fulvestrant has demonstrated activity when used as first, second, or third line endocrine therapy, making it an attractive therapy for combination with other agents. In addition, it is commonly reserved for use following disease progression on AI therapy. Everolimus is an orally administered drug that blocks a signaling pathway called "mTOR". "mTOR" acts as a regulator for many processes in the body, including cell growth. Blocking this pathway may have an effect on cell growth. The combination of a novel class of agents (mTOR inhibitors) and an established standard treatment for metastatic HR+ breast cancer may potentially increase the clinical benefit by targeting multiple different biological pathways.

Investigators

The overall officials registered on this study. Names that resolve to a FindMyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

25 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

United States
  • Marin Cancer Care

    Greenbrae, California, United States

  • Stanford University

    Stanford, California, United States

  • Swedishamerican Regional Cancer Center

    Rockford, Illinois, United States

  • Mcfarland Clinic, Pc

    Ames, Iowa, United States

  • Johns Hopkins University

    Baltimore, Maryland, United States

  • St. Joseph Mercy Hospital (mi Cancer Consortium)

    Ann Arbor, Michigan, United States

  • Metro Mn

    Saint Louis Park, Minnesota, United States

  • Missouri Valley Cancer Consortium

    Omaha, Nebraska, United States

  • Beth Israel

    New York, New York, United States

  • Montefiore Medical Center

    The Bronx, New York, United States

  • Ohio State University Medical Center

    Columbus, Ohio, United States

  • Toledo Cop

    Toledo, Ohio, United States

  • Hematology & Oncology Associates of Northeastern Pa, Pc

    Dunmore, Pennsylvania, United States

  • Penn State University

    Hershey, Pennsylvania, United States

  • Fox Chase Cancer Center

    Philadelphia, Pennsylvania, United States

  • Thomas Jefferson University

    Philadelphia, Pennsylvania, United States

  • University of Pittsburgh- Magee Women'S Hospital

    Pittsburgh, Pennsylvania, United States

  • Reading Hospital- Mcglinn Family Regional Cancer Center

    West Reading, Pennsylvania, United States

  • Main Line Heath System

    Wynnewood, Pennsylvania, United States

  • University of Texas Southwestern

    Dallas, Texas, United States

  • Charleston Area Medical Center (camc)

    Charleston, West Virginia, United States

  • St. Vincent Hospital

    Green Bay, Wisconsin, United States

  • Gundersen Health System

    La Crosse, Wisconsin, United States

  • Prohealth Care Inc. (waukesha)

    Waukesha, Wisconsin, United States

  • Aurora Cancer Care

    Wauwatosa, Wisconsin, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

The drug and biological interventions registered on this study, normalized to their RxNorm ingredient where possible.

Linked drugs open the directory filtered to KOLs working with them.clinicaltrials.gov ↗

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
31 May 2013
Primary completion
22 Mar 2017
Completion
12 Sept 2017
Last update posted
30 May 2018
Registered enrollment
131
Registry id
NCT01797120

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; FindMyKOL does not interpret them.