drugset / Trial / NCT05153434

A Study of Oral ARD-101 in Patients With Prader-Willi Syndrome

NCT05153434

NaSingle-groupOpen-labelTreatment

Summary

A Phase 2, Single-Arm, Open-Label Study to Evaluate the Safety and Efficacy of ARD-101 in Patients with Prader-Willi Syndrome

Timeline

Start
2022-05-27
Primary completion
2024-09-24
Completion
2024-09-24

Drugs

EvaluationDrugModalityDoseRoute
Subject ARD-101 Small molecule 800 mg Oral

Indications