drugset / Trial / NCT01924078

Capecitabine Metronomic Chemotherapy Plus Aromatase Inhibitor for Postmenopausal Hormone Receptor Positive Breast Cancer

NCT01924078

Phase 2 Unknown 100 enrolled Fudan University
NaSingle-groupOpen-labelTreatment

Summary

The present study is to determine the adverse effects and clinical efficacy of AI combined with Capecitabine metronomic chemotherapy in postmenopausal breast cancer patients with Estrogen receptor and/or Progestrogen receptor positive.

Timeline

Start
2010-10
Primary completion
2015-03
Completion
2015-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Anastrozole Other / unclassified 1 mg Oral
Subject Capecitabine Small molecule 500 mg Oral
Subject Exemestane Small molecule 25 mg Oral
Subject Letrozole Other / unclassified 2.5 mg Oral

Indications