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Phase II Pilot Study Assessing Efficacy of a Cisplatin - Metronomic Cyclophosphamide Treatment in Patients With Metastatic Triple Negative Breast Cancer Resistant to Anthracyclines and Taxanes

NCT01910870 · Status: TERMINATED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 4

Last updated 2018-05-18

No results posted yet for this study

Summary

To evaluate response rate of cisplatin - metronomic cyclophosphamide treatment.

Conditions

Interventions

DRUG

Cisplatin

25 mg/m² I.V. (day 1 to day 3) Total dose : 75 mg/m² every 3 weeks

DRUG

Metronomic Cyclophosphamide

150 mg per os from day 1 to day 14 (total dose = 2100 mg) every 3 weeks

Sponsors & Collaborators

  • Centre Jean Perrin

    lead OTHER

Principal Investigators

  • Marie-Ange MOURET-REYNIER, MD · Centre Jean Perrin

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-07-31
Primary Completion
2016-09-30
Completion
2016-09-30

Countries

  • France

Study Locations

More Related Trials

Entities

Drugs
Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01910870 on ClinicalTrials.gov