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Korean Regulatory Post Marketing Surveillance for Somavert

Korean Regulatory Post Marketing Surveillance for Somavert

Recruiting
18 years and older
All
Phase N/A
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Overview

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)

Eligibility

Inclusion Criteria:

All patients who have been prescribed as per local label and investigators' judgement under the setting of routine practice in Korea who are eligible.

Exclusion Criteria:

Patients who are contraindicated for Somavert

Study details
    Acromegaly

NCT05131100

Pfizer

17 July 2025

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FAQs

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A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

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