Summary

Eligibility
for people ages 13 years and up (full criteria)
Location
at UCSD
Dates
study started
study ends around

Description

Summary

The goal of this clinical trial is to learn if ARD-101 works to treat hyperphagia-related behavior in patients with Prader-Willi syndrome (PWS) when used in a long term setting. It will also teach us about the safety of ARD-101.

The main questions it aims to answer are:

What medical problems do participants have when taking ARD-101 in a long term setting

Does ARD-101 improve the total score of the HQCT-9 (hyperphagia questionnaire for clinical trials, 9 questions)?

Eligible participants will:

Have completed treatment on the AVK-101-301 study through Week 12/End of Treatment

Take ARD-101 every day for up to 12 months.

Visit the clinic at Months 1, 3, 6 and 12 during dosing and then have tele-visits at Week 2, Months 3 and 9, then 4 weeks after stopping the ARD-101.

Patients/Caregivers will keep a daily diary.

Official Title

A Phase 3, Multicenter, Open-Label Extension Study to Assess the Safety and Efficacy of ARD-101 in Patients With Prader-Willi Syndrome

Keywords

Hyperphagia, Prader-Willi Syndrome, Hyperphagia in Prader-Willi Syndrome, ARD-101, PWS, Prader-Willi, Prader Willi, Prader Willi Syndrome

Eligibility

You can join if…

Open to people ages 13 years and up

  • Patients who have completed treatment on Aardvark Therapeutics clinical study AVK-101-301

You CAN'T join if...

  • Any complications that makes participation unsafe in the Investigator's opinion

Locations

  • Rady Children's Hospital accepting new patients
    San Diego California 92123 United States
  • Stanford Children's Health Specialty Services not yet accepting patients
    Palo Alto California 94304 United States
  • Children's Hospital Colorado accepting new patients
    Denver Colorado 80045-7106 United States

Details

Status
accepting new patients
Start Date
Completion Date
(estimated)
Sponsor
Aardvark Therapeutics, Inc.
ID
NCT07197034
Phase
Phase 3 research study
Study Type
Interventional
Participants
Expecting 90 study participants
Last Updated