A Post Marketing Surveillance on Piqray in Korea

Status Recruiting

Clinical Trial Summary

This is a prospective, multicenter, open-label, non-comparative, non-interventional, observational study to assess te safety and effectiveness of Piqray in the real-world setting

Clinical Trial Description

The observation duration will be up to 24 weeks after enrollment, which is sufficient to provide adequate information about the safety and effectiveness of Piqray. If the subject does not return for a follow-up visit or stops taking Piqray for any reason, all data collected until the date of the last contact of the subject will be used. Patients will be followed up (safety follow up) for 30 days afetr either 24 weeks-treatment or early withdrawal. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05293470
Study type	Observational
Source	Novartis
Contact	Novartis Pharmaceuticals
Phone	+41613241111
Email	novartis.email@novartis.com
Status	Recruiting
Phase
Start date	June 29, 2022
Completion date	May 12, 2027

View Details

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