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RecruitingNCT05131100

Korean Regulatory Post Marketing Surveillance for Somavert

Korean Post-marketing Surveillance for Somavert

Status
Recruiting
Phase
Study type
Observational
Enrollment
100 (estimated)
Sponsor
Pfizer · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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

TypeNameDescription
DRUGSomavertAs provided in real world practice

Timeline

Start date
2022-07-13
Primary completion
2026-09-15
Completion
2026-09-15
First posted
2021-11-23
Last updated
2025-07-04

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT05131100. Inclusion in this directory is not an endorsement.

Korean Regulatory Post Marketing Surveillance for Somavert (NCT05131100) · Clinical Trials Directory