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Study identifier: NCT05131100 Synced from ClinicalTrials.gov · August 02, 2026
● Completed

Korean Regulatory Post Marketing Surveillance for Somavert

Condition: Acromegaly  ·  Sponsor: Pfizer

PhaseN/A
Planned participants11
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

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)

This description comes directly from the study's public registry record.

Talk to the study team

No contact information is available for this study as per the public registry record.

Always discuss trial participation with your own doctor first.

Locations (1)

PfizerSeoul, South Korea—

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This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT05131100