HomeTrialNCT05599412
NCT05599412RECRUITING

Post Marketing Surveillance(PMS) Study of Lorviqua in Korea

Study Summary

The objective of this study is to monitor the usage of Lorviqua in real practice within label, including the adverse events associated with Lorviqua

Interventions / Drugs
View on ClinicalTrials.gov ↗
Study Details
Enrollment600 participants
Primary Completion
Lead SponsorPfizer
Data Retrieved2026-04-11 02:55:53.189845+00:00
What This Trial Means for Biotech Investors
Trial Phase Context
Status & Expected Data

Currently recruiting: the trial is enrolling patients. A data readout is not expected until after enrollment closes and the follow-up period is complete.

Enrolled: 600 participants
Sponsor Catalyst Profile

Pfizer Inc (PFE) is the sponsoring company for this trial. BiotechSign currently grades this company F (33/100) based on composite catalyst signals across its full pipeline. This trial is one data point in that overall catalyst picture.

Not financial advice. BiotechSign data is sourced from ClinicalTrials.gov, SEC EDGAR, and other public databases for research and informational purposes only. It does not constitute investment recommendations. Always do your own due diligence before making investment decisions.