HomeTrialNCT05131100
🔬NCT05131100RECRUITING

Korean Regulatory Post Marketing Surveillance for Somavert

Study Summary

Non-interventional observational study, to identify safety and effectiveness of Somavert during the post-marketing period based on the Korean RMP as required by the regulations of Ministry of Food and Drug Safety (MFDS)

Conditions
Interventions / Drugs
View on ClinicalTrials.gov ↗
Study Details
Enrollment100 participants
Primary Completion
Lead SponsorPfizer
Data Retrieved2026-04-11 02:55:53.190576+00:00
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