MedPath

Clinical Study of Diazoxide Choline Controlled-Release Tablet (DCCR) in Patients With Prader-Willi Syndrome

Phase 1
Completed
Conditions
Prader-Willi Syndrome
Interventions
Drug: Placebo
Registration Number
NCT02034071
Lead Sponsor
Essentialis, Inc.
Brief Summary

• This is a single-center, open-label, single-arm study with a double-blind, placebo-controlled, randomized withdrawal extension. Patients are initiated on a DCCR dose of about 1.5 mg/kg (maximum starting dose of 145 mg) and are titrated every 14 days to about 2.4 mg/kg, 3.3 mg/kg, 4.2 mg/kg, and 5.1 mg/kg (maximum dose of 507.5 mg). These DCCR doses are equivalent to diazoxide doses of 1.03, 1.66, 2.28, 2.9, and 3.52 mg/kg. The administered dose will be as close to the mg/kg dosing as can be achieved by the available dose strengths of DCCR. Patients will be up-titrated at each visit at the discretion of the investigator. All patients will be continued in the double-blind, placebo-controlled, randomized withdrawal extension. Any patient who showed an increase in resting energy expenditure and/or a reduction in hyperphagia from Baseline through Day 55 or Day 69 will be designated a responder, whereas all others will be designated non-responders. Responders will be randomized in a 1:1 ratio either to continue on active treatment at the dose they were treated with on Day 69 or to the placebo equivalent of that dose for an additional 4 weeks. Non-responders will continue open label treatment during the extension.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
13
Inclusion Criteria
  • Children. adolescents and young adults with genetically confirmed Prader-Willi syndrome
  • Ages at ≥ 10 years and ≤ 22 years
  • Generally healthy as documented by the medical history, physical examination, vital sign assessments, 12-lead electrocardiogram (ECG), and clinical laboratory assessments
  • BMI exceeds the 95th percentile of the age specific BMI value on the CDC BMI charts
  • Fasting glucose ≤ 126 mg/dL
  • HbA1c ≤ 6.5 %
Exclusion Criteria
  • Administration of investigational drugs within 1 month prior to Screening Visit
  • Anticipated requirement for use of prohibited medications
  • History of allergic reaction or significant intolerance to: diazoxide, thiazides or sulfonamides
  • Anticipate transitions in their care from family home to group home or other similar potentially disruptive changes
  • Congestive heart failure or known compromised cardiac reserve
  • Any other clinically significant endocrine, cardiovascular, pulmonary, neurological, psychiatric, hepatic, gastrointestinal, hematological, renal, or dermatological disease interfering with the assessments of the investigational drug, according to the Investigator

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
DCCR Open Label - DCCR Double BlindDCCRPatients are initiated on a DCCR dose of about 1.5 mg/kg (maximum starting dose of 145 mg) and are titrated every 14 days through 4 dose levels of DCCR. Patients will be up-titrated at each visit at the discretion of the investigator. Randomized to continue DCCR, at the same dose as they received on Day 69, in the Double-Blind, Placebo-Controlled, Randomized Withdrawal Extension
DCCR Open Label - Placebo Double BlindPlaceboPatients are initiated on a DCCR dose of about 1.5 mg/kg (maximum starting dose of 145 mg) and are titrated every 14 days through 4 dose levels of DCCR. Patients will be up-titrated at each visit at the discretion of the investigator. Randomized to receive placebo equivalent to the DCCR dose received on Day 69 in the Double-Blind, Placebo-Controlled, Randomized Withdrawal Extension
DCCR Open Label - Placebo Double BlindDCCRPatients are initiated on a DCCR dose of about 1.5 mg/kg (maximum starting dose of 145 mg) and are titrated every 14 days through 4 dose levels of DCCR. Patients will be up-titrated at each visit at the discretion of the investigator. Randomized to receive placebo equivalent to the DCCR dose received on Day 69 in the Double-Blind, Placebo-Controlled, Randomized Withdrawal Extension
Primary Outcome Measures
NameTimeMethod
Hyperphagia using hyperphagia questionnaireChange from Day 69 through Day 97
Resting energy expenditureChange from Day 69 through Day 97
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

University of California, Irvine

🇺🇸

Orange, California, United States

© Copyright 2025. All Rights Reserved by MedPath