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Lynparza Ovarian Cancer Clinical Experience Investigation (All Case Investigation)

Ovarian Cancer Clinical Trial

Official title:
Lynparza Tablets 100mg, 150mg Clinical Experience Investigation (All Case Investigation) in Patients With Platinum-sensitive Relapsed Ovarian Cancer

Clinical Trial Summary

[Objectives] Objectives include following to capture safety and efficacy of LYNPARZA in actual clinical use. 1. ADR development in actual clinical use 2. Factors which may affect safety and efficacy 3. ADRs not expected from "Precautions for Use"

Clinical Trial Description

The objective of the Clinical Experience Investigation (CEI) is to collect following data to characterise safety and efficacy of LYMPARZA Tablets 100mg and 150mg (LYMPARZA) in usual post-marketing use. 1. Development of adverse drug reactions (ADRs) 2. Factors which may affect safety and efficacy of LYMPARZA 3. Development of adverse drug reactions (ADRs) unexpected from "Precautions for Use" of the LYMPARZA JPI ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03505307
Study type Observational
Source AstraZeneca
Contact
Status Completed
Phase
Start date May 21, 2018
Completion date December 7, 2020
View Details
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