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RECRUITING
NCT05131100

Korean Regulatory Post Marketing Surveillance for Somavert

Sponsor: Pfizer

View on ClinicalTrials.gov

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)

Official title: Korean Post-marketing Surveillance for Somavert

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

100

Start Date

2022-07-13

Completion Date

2026-09-15

Last Updated

2025-07-04

Healthy Volunteers

No

Conditions

Interventions

DRUG

Somavert

As provided in real world practice

Locations (1)

Pfizer

Seoul, South Korea