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Completed Phase 1Phase 2 Interventional Results available

Study to Evaluate the Efficacy and Safety of Eribulin Mesylate in Combination With Pembrolizumab in Participants With Metastatic Triple-Negative Breast Cancer (mTNBC)

ClinicalTrials.gov ID: NCT02513472

Public ClinicalTrials.gov record NCT02513472. 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 Sep 2, 2026, 5:28 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 Open-Label, Single-Arm Multicenter Phase 1b/2 Study to Evaluate the Efficacy and Safety of Eribulin Mesylate in Combination With Pembrolizumab in Subjects With Metastatic Triple-Negative Breast Cancer (mTNBC)

Brief summary

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

This is an open-label, single-arm, multicenter, Phase 1b/2 study of eribulin mesylate in combination with pembrolizumab in participants with mTNBC previously treated with 0 (stratum 1) or 1 to 2 (stratum 2) lines of systemic anticancer therapy (cytotoxic or targeted anticancer agents) in the metastatic setting.

Study identification

NCT ID
NCT02513472
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
Eisai Inc.
Industry
Enrollment
258 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
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
Aug 27, 2015
Primary completion
Jul 30, 2019
Completion
Apr 5, 2021
Last update posted
May 4, 2022

2015 – 2021

United States locations

U.S. sites
22
U.S. states
12
U.S. cities
19
Facility City State ZIP Site status
Facility #1 Duarte California 91010
Facility #1 Santa Barbara California 93105
Facility #1 Denver Colorado 80218
Facility #1 Miami Florida 33176
Facility #1 West Palm Beach Florida 33401
Facility #1 Boston Massachusetts 02115
Facility #2 Boston Massachusetts 02115
Facility #1 Minneapolis Minnesota 55407
Facility #1 St Louis Missouri 63110
Facility #1 Lebanon New Hampshire 03756
Facility #1 New York New York 10032
Facility #2 New York New York 10065
Facility #1 Chattanooga Tennessee 37404
Facility #1 Nashville Tennessee 37203
Facility #1 Austin Texas 78731
Facility #1 Fort Worth Texas 76104
Facility #1 San Antonio Texas 78217
Facility #2 San Antonio Texas 78229
Facility #1 Sherman Texas 75090
Facility #1 Salem Virginia 24153
Facility #1 Winchester Virginia 22601
Facility #1 Madison Wisconsin 53792

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 NCT02513472, 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 May 4, 2022 · Synced Sep 2, 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 protocol, eligibility criteria, and contact information for NCT02513472 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →