Special Drug Use Surveillance of Leuprorelin for Injection Kit 22.5 mg in "Premenopausal Breast Cancer"

NCT03209518 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 312

Last updated 2019-11-01

Study results available
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Summary

The purpose of this survey is to evaluate the safety in patients with premenopausal breast cancer receiving Leuprorelin in the routine clinical setting.

Conditions

  • Premenopausal Breast Cancer

Interventions

DRUG

Leuprorelin acetate

Leuplin PRO for Injection Kit 22.5 mg

Sponsors & Collaborators

Principal Investigators

  • Study Director · Takeda

Eligibility

Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-03-18
Primary Completion
2018-10-10
Completion
2018-10-10

Countries

  • Japan

Study Locations

More Related Trials

Entities

Companies

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 NCT03209518 on ClinicalTrials.gov