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Post Marketing Surveillance Study to Observe Safety and Efficacy of IBRANCE®

Breast Neoplasm Clinical Trial

Official title:
Post Marketing Surveillance Study to Observe Safety and Efficacy of IBRANCE®

Clinical Trial Summary

This non-interventional study is designated as a Post Marketing Surveillance Study and is a commitment to Ministry of Food and Drug Safety (MFDS). Before the approval of IBRANCE® in Korea, as a part of Risk Management Plan (RMP), which is required by MFDS, safety and efficacy information of new medication will be provided at minimum 1,000 participants administered in the setting of routine practice during the initial 9 years after the approval.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03445637
Study type Observational
Source Pfizer
Contact Pfizer CT.gov Call Center
Phone 1-800-718-1021
Email ClinicalTrials.gov_Inquiries@pfizer.com
Status Recruiting
Phase
Start date February 8, 2018
Completion date August 8, 2025
View Details
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