Study of Etoposide in Treating Patients With Recurrent or Metastatic Breast Cancer

NCT01492556 · Status: UNKNOWN · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2013-03-15

No results posted yet for this study

Summary

The purpose of this study is to determine whether Etoposide Monotherapy is effective and safe in the treatment of recurrent or metastatic breast cancer in Chinese female patients.

Conditions

Interventions

DRUG

Etoposide

Lastet (Etoposide Capsules, 25mg\*40 capsules/box), manufactured by Nippon Kayaku Co., Ltd.

Sponsors & Collaborators

  • Peking University Cancer Hospital & Institute

    collaborator OTHER
  • Peking Union Medical College Hospital

    collaborator OTHER
  • Beijing Chao Yang Hospital

    collaborator OTHER
  • China-Japan Friendship Hospital

    collaborator OTHER
  • Beijing Hospital of the Ministry of Health

    collaborator UNKNOWN
  • The First Affiliated Hospital of Dalian Medical University

    collaborator OTHER
  • The Second Affiliated Hospital of Harbin Medical University

    collaborator OTHER
  • Zhejiang Cancer Hospital

    collaborator OTHER
  • Henan Cancer Hospital

    collaborator OTHER_GOV
  • Guangxi Cancer Hospital

    collaborator UNKNOWN
  • Shanghai Putuo District Center Hospital

    collaborator OTHER
  • International Peace Maternity and Child Health Hospital

    collaborator OTHER
  • Xinjiang Medical University

    collaborator OTHER
  • Chinese Academy of Medical Sciences

    lead OTHER

Principal Investigators

  • Binghe Xu, M.D., Ph.D · Chinese Academy of Medical Sciences

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-12-31
Primary Completion
2014-06-30
Completion
2015-06-30

Countries

  • China

Study Locations

More Related Trials

Entities

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 NCT01492556 on ClinicalTrials.gov