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Clinical Trial Summary

This study will evaluate the safety and efficacy of Tesomet (tesofensine + metoprolol) in subjects with PWS.

Clinical Trial Description

For the double-blind portion of the study, dosing will be initiated in a subgroup of adults who are 18-65 years of age. Following independent Data Monitoring Board review of subgroup safety data, and review and confirmation to proceed by FDA, enrollment of subjects <18 years of age will commence. ;

Study Design

Related Conditions & MeSH terms

NCT number NCT05198362
Study type Interventional
Source Saniona
Status Withdrawn
Phase Phase 2
Start date December 28, 2021
Completion date December 9, 2022

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