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OpenTrials
Completed

NCT Number: NCT03575260

500mg Fulvestrant Versus Exemestane in MBC

500mg Fulvestrant versus Exemestane in MBC

Completed

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Observational

Primary location

Biyun Wang, MD

Shanghai, Shanghai Municipality, 200032, China

About this study

500mg Fulvestrant versus Exemestane in Metastatic Breast Cancer (MBC) resistant to adjuvant Non-steroidal Aromatase Inhibitors in clinical practice- a multicenter retrospective study

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Postmenopausal woman, age > 18 years old
  • Diagnosed with ER/PR+,HER2- Metastatic Breast Cancer
  • Adjuvant treatment of Non-steroidal Aromatase Inhibitors
  • First line of Metastatic Breast Cancer is 500mg Fulvestrant or Exemestane for at least one month, starting from 2014.01.01-2017.06.01
  • Available medical history

Exclusion criteria

  • Incomplete medical history

Treatment and study plan

Primary outcomes

  1. PFS

    Time frame: 6 weeks

    Progression free survival

Secondary outcomes

  1. Number of participants with treatment-related adverse events as assessed by CTCAE v4.0

    Time frame: 6 weeks

Sponsors and collaborators

Lead sponsor

Fudan University

Other

Registry information

Official study title

500mg Fulvestrant Versus Exemestane in Metastatic Breast Cancer (MBC) Resistant to Adjuvant Non-steroidal Aromatase Inhibitors in Clinical Practice- a Multicenter Retrospective Study

Important dates

Study start
2017
Primary completion
2019
Study completion
2019
First posted
Jul 2, 2018
Registry last updated
Jul 30, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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