Ph II Study of Pembrolizumab & Eribulin in Patients With HR+/HER2- MBC Previously Treated With Anthracyclines & Taxanes

PHASE2CompletedINTERVENTIONAL
Enrollment

44

Participants

Timeline

Start Date

December 14, 2017

Primary Completion Date

October 31, 2018

Study Completion Date

December 23, 2020

Conditions
Breast Cancer
Interventions
DRUG

Pembrolizumab

MK3475 (pembrolizumab) will be supplied directly as a solution for infusion in a single-use vial. Each vial contains 100 mg of MK3475 (pembrolizumab) in 4 ml of solution.

DRUG

Eribulin

Eribulin will be supplied as a clear and colourless aqueous solution for injection provided in glass vials containing 2 ml. Each 2 ml vial contains eribulin mesylate equivalent to 0.88 mg eribulin.

Trial Locations (11)

Unknown

Corporació Sanitaria Sanitari Parc Taulí, Sabadell

Hospital de Navarra, Pamplona

Complejo Hospitalario Universitario A Coruña (CHUAC), A Coruña

Hospital Clínic de Barcelona, Barcelona

Instituto Oncológico Baselga - Hospital Quirónsalud Barcelona, Barcelona

Hospital Universitario Ramón y Cajal, Madrid

MD Anderson, Madrid

Hospital Clínico Universitario Virgen de la Arrixaca, Murcia

Hospital Universitario Virgen del Rocío, Seville

Hospital Arnau de Vilanova de Valencia, Valencia

Hospital Clínico de Valencia, Valencia

All Listed Sponsors
lead

MedSIR

OTHER

NCT03222856 - Ph II Study of Pembrolizumab & Eribulin in Patients With HR+/HER2- MBC Previously Treated With Anthracyclines & Taxanes | Biotech Hunter | Biotech Hunter