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OpenTrials
Completed

NCT Number: NCT04106557

A Study of OV101 in Individuals With Angelman Syndrome (AS)

The purpose of this study is to assess the efficacy and safety of oral OV101 (gaboxadol) in pediatric subjects with Angelman syndrome.

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Key information

Age range

2 year–12 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Ovid Therapeutics Investigative Site, Brisbane, Queensland, Australia

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male or female and 2 to 12 years old (inclusive) at the time of informed consent
  • Confirmed molecular diagnosis of AS
  • Has a CGI-S-AS score of 3 or more at baseline.
  • Meets the following age-appropriate body weight criterion:
  • Subjects 2 to 3 years old must have a minimum body weight of 9 kg.
  • Subjects 4 years and older must be between 17 kg and 64 kg (inclusive).
  • Stable concomitant mediations for at least 4 weeks before study start

Exclusion criteria

  • Any condition that would limit study participation
  • Clinically significant lab or vital sign abnormalities at the time of screening
  • Poorly controlled seizures (weekly seizures of any frequency with a duration more than 3 minutes, weekly seizures occurring more than 3 times per week, each with a duration of less than 3 minutes, or as defined by investigator assessment)
  • Use of prescription medications for sleep, minocycline, or levodopa within the 4 weeks prior to Day 1 or during the study. Benzodiazepines chronically administered for seizure control are permitted.
  • Cannot comply with protocol study assessments during screening or caregiver unable to comply with study requirements.
  • Enrolled in any clinical trial or used any investigational agent within the 30 days before screening or concurrently with this study.

Treatment and study plan

Gaboxadol

Drug

OV101 versus placebo once daily at bedtime for 12 weeks

Placebo

Drug

Matching placebo capsules to OV101 capsules.

Primary outcomes

  1. Clinical Global Impressions- Improvement in Angelman Syndrome (CGI-I-AS) Rating at 12 Weeks

    Time frame: 12 weeks

    To evaluate the efficacy of OV101 versus placebo as assessed by the Clinical Global Impressions-Improvement-Angelman syndrome (CGI-I-AS) score at Week 12. CGIA-I-AS scores range from 1 (very much improved), to 4 (no change), to 7 (very much worse).

Sponsors and collaborators

Lead sponsor

Healx AI

Industry

Registry information

Official study title

A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Phase 3 Study to Evaluate the Efficacy and Safety of OV101 in Pediatric Individuals With Angelman Syndrome

Acronym: NEPTUNE

Important dates

Study start
2019
Primary completion
2020
Study completion
2020
First posted
Sep 27, 2019
Registry last updated
Jan 8, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.