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Trial record 2 of 7 for:    Ovid | Recruiting, Not yet recruiting Studies | United States

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

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details. Identifier: NCT04106557
Recruitment Status : Recruiting
First Posted : September 27, 2019
Last Update Posted : October 1, 2019
Information provided by (Responsible Party):
Ovid Therapeutics Inc.

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

Condition or disease Intervention/treatment Phase
Primary Disease or Condition Being Studied: Angelman Syndrome (AS) Drug: Gaboxadol Drug: Placebo Phase 3

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 65 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single (Participant)
Masking Description: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose: Treatment
Official 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
Actual Study Start Date : September 9, 2019
Estimated Primary Completion Date : July 2020
Estimated Study Completion Date : August 2020

Resource links provided by the National Library of Medicine

Arm Intervention/treatment
Experimental: OV101 once daily (weight-based dosing) Other Name:Gaboxadol
OV101 (gaboxadol), oral, provided once daily at bedtime for 12 week duration
Drug: Gaboxadol
OV101 versus placebo once daily at bedtime for 12 weeks

Placebo Comparator: Placebo once daily
Matching placebo,oral, provided once daily at bedtime for 12 week duration
Drug: Placebo
Matching placebo capsules to OV101 capsules.

Primary Outcome Measures :
  1. Clinical Global Impressions- Improvement in Angelman Syndrome (CGI-I-AS) [ Time Frame: 12 weeks ]
    Clinical Global Impressions-Improvement-Angelman Syndrome (CGI-I-AS) - Scale of 1-7 reflects a spectrum where 1 is most improved, 4 is no change, and 7 is most worsened.

Information from the National Library of Medicine

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Ages Eligible for Study:   2 Years to 12 Years   (Child)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

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:

    1. Subjects 2 to 3 years old must have a minimum body weight of 9 kg.
    2. 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.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT04106557

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Contact: Ovid - Neptune US Clinical Research Referral Network Media, PA 1-855-235-3138

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United States, Arizona
Ovid Therapeutics Investigative Site Recruiting
Phoenix, Arizona, United States, 85006
Contact: Ovid - Neptune US Clinical Research Referral Network    855-235-3138   
United States, Pennsylvania
Ovid Therapeutics Investigative Site Recruiting
Media, Pennsylvania, United States, 19063
Contact: Ovid - Neptune US Clinical Research Referral Network    855-235-3138   
Sponsors and Collaborators
Ovid Therapeutics Inc.

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Responsible Party: Ovid Therapeutics Inc. Identifier: NCT04106557     History of Changes
Other Study ID Numbers: OV101-19-001
First Posted: September 27, 2019    Key Record Dates
Last Update Posted: October 1, 2019
Last Verified: September 2019

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Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No
Additional relevant MeSH terms:
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Angelman Syndrome
Pathologic Processes
Movement Disorders
Central Nervous System Diseases
Nervous System Diseases
Abnormalities, Multiple
Congenital Abnormalities
Chromosome Disorders
Genetic Diseases, Inborn
Sensory System Agents
Peripheral Nervous System Agents
Physiological Effects of Drugs
GABA Agonists
GABA Agents
Neurotransmitter Agents
Molecular Mechanisms of Pharmacological Action