Evaluation of Pembrolizumab in Lymphopenic Metastatic Breast Cancer Patients Treated With Metronomic Cyclophosphamide

PHASE2CompletedINTERVENTIONAL
Enrollment

36

Participants

Timeline

Start Date

June 27, 2017

Primary Completion Date

September 26, 2018

Study Completion Date

September 18, 2019

Conditions
Metastatic Breast Cancer
Interventions
DRUG

Cyclophosphamide 50mg

One tablet per day. Cyclophosphamide will continue to be administered as long as patient experiences clinical benefit in the opinion of the investigator or symptomatic deterioration attributed to disease progression as determined by the investigator after an integrated assessment of radiographic data and clinical status or withdrawal of consent.

DRUG

Pembrolizumab 100 MG in 4 ML Injection

IV infusion every 3 weeks. Pembrolizumab will continue to be administered as long as patient experiences clinical benefit in the opinion of the investigator or symptomatic deterioration attributed to disease progression as determined by the investigator after an integrated assessment of radiographic data and clinical status or withdrawal of consent.

Trial Locations (5)

42270

Institut de cancérologie Lucien Neuwirth, Saint-Priest-en-Jarez

44805

ICO - René Gauducheau, Saint-Herblain

49055

ICO - Paul Papin, Angers

69003

Centre Léon Bérard, Lyon

69008

Hôpital Privé Jean Mermoz, Lyon

All Listed Sponsors
collaborator

Merck Sharp & Dohme LLC

INDUSTRY

lead

Centre Leon Berard

OTHER

NCT03139851 - Evaluation of Pembrolizumab in Lymphopenic Metastatic Breast Cancer Patients Treated With Metronomic Cyclophosphamide | Biotech Hunter | Biotech Hunter