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ACTIVE NOT RECRUITING
NCT06735742

A Study to Learn About the Safety of TALZENNA for the Treatment of Breast Cancer

Sponsor: Pfizer

View on ClinicalTrials.gov

Summary

The purpose of this study is to learn about the safety of TALZENNA for the patients with breast cancer that cannot be removed by surgery and has come back. These participants also have a past treatment with medicines that try to stop the growth of cancer cells. This study is seeking for participants who: * have breast cancer that cannot be removed by surgery and has come back * have not used this medicine before. All patients in this study will receive TALZENNA according to the prescriptions. Patients will be followed up to 52 weeks (12 months) from the day of start of treatment start (Day 1). However, in cases where treatment has been completed or stopped less than 52 weeks (12 months) after the start of giving study medicine, the participants will be checked until completion (discontinuation) of treatment.

Official title: TALZENNA Capsules Special Investigation - Investigation on BRCA Mutation-Positive and HER2-Negative Unresectable or Recurrent Breast Cancer With a History of Cancer Chemotherapy -

Key Details

Gender

All

Age Range

0 Years - Any

Study Type

OBSERVATIONAL

Enrollment

3

Start Date

2025-04-12

Completion Date

2029-03-30

Last Updated

2025-11-17

Healthy Volunteers

No

Conditions

Locations (1)

Pfizer Japan

Tokyo, Japan