A Post Marketing Surveillance on Piqray in Korea

NCT05293470 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 900

Last updated 2025-07-09

No results posted yet for this study

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

Conditions

Interventions

OTHER

Piqray

There is no treatment allocation. Patients administered Piqray by prescription will be enrolled.

Sponsors & Collaborators

Principal Investigators

  • Novartis Pharmaceuticals · Novartis Pharmaceuticals

Eligibility

Min Age
18 Years
Max Age
100 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-06-29
Primary Completion
2027-05-12
Completion
2027-05-12

Countries

  • South Korea

Study Locations

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Entities

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 NCT05293470 on ClinicalTrials.gov