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Completed Phase 2 Interventional Results available

The XENERA™ 1 Study Tests Xentuzumab in Combination With Everolimus and Exemestane in Women With Hormone Receptor Positive and HER2-negative Breast Cancer That Has Spread

ClinicalTrials.gov ID: NCT03659136

Public ClinicalTrials.gov record NCT03659136. 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 4, 2026, 5:52 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

XENERA™1: A Multi-centre, Double-blind, Placebo-controlled, Randomised Phase II Trial to Compare Efficacy of Xentuzumab in Combination With Everolimus and Exemestane Versus Everolimus and Exemestane in Women With HR+ / HER2- Metastatic Breast Cancer and Non-visceral Disease

Study identification

NCT ID
NCT03659136
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Boehringer Ingelheim
Industry
Enrollment
103 participants

Conditions and interventions

Interventions

  • Everolimus Drug
  • Exemestane Drug
  • Placebo Drug
  • Xentuzumab 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
Nov 27, 2018
Primary completion
Aug 29, 2021
Completion
May 10, 2022
Last update posted
Feb 23, 2025

2018 – 2022

United States locations

U.S. sites
16
U.S. states
14
U.S. cities
16
Facility City State ZIP Site status
Ironwood Cancer and Research Centers Chandler Arizona 85224
Cancer Treatment Centers of America at Western Regional Medical Center Goodyear Arizona 85338
Beverly Hills Cancer Center Beverly Hills California 90211
University of California San Francisco San Francisco California 94158
Yale Cancer Center New Haven Connecticut 06510
Florida Cancer Specialists Fort Myers Florida 33901
University Cancer and Blood Center Athens Georgia 30607
Hematology Oncology of Indiana Indianapolis Indiana 46260
University of Minnesota Minneapolis Minnesota 55455
HCA MidAmerica Division, Inc. Kansas City Missouri 64132
Hematology Oncology Associates of Rockland Nyack New York 10960
Southwestern Regional Medical Center Tulsa Oklahoma 74133
Tennessee Oncology, PLLC Nashville Tennessee 37203
The Center for Cancer and Blood Disorders Fort Worth Texas 76104
Utah Cancer Specialists Cancer Center Salt Lake City Utah 84106
Northwest Medical Specialties, PLLC 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 38 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03659136, 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 Feb 23, 2025 · Synced May 4, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03659136 live on ClinicalTrials.gov.

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