Efficacy and Safety of NFC-1 in Adolescents With Genetic Disorders Impacting mGluR and ADHD
Researchers compared NFC-1 and placebo to find out how the approaches affected ADHD symptoms in young people with ADHD.
Understand this study
What did researchers investigate?
Researchers compared NFC-1 and placebo to find out how the approaches affected ADHD symptoms in young people with ADHD.
Who was this study for?
Listed age limits: 12 years to 17 years.
- Listed locations
- Baltimore, United StatesSee all locations and recruitment
- Activities
- Medication described in the protocol · Placebo comparator
- Compensation
- Payment and expense reimbursement have not been verified.
Study information
- Recruitment status
- Completed
- Enrollment listed in the registry
- 101
- Sponsor
- Aevi Genomic Medicine, LLC, a Cerecor company
- Sponsor type
- Pharmaceutical company
- Study type
- Drug
- Intervention type
- Medication / drug
- Study phase
- Phase 2, Phase 3This study spans more than one phase, so it may combine goals such as safety, dosing, and early effectiveness.
- Locations
- United States
- Age range
- From 12 Years to 17 Years
- Official registry ID
- NCT02777931
- Official title
Show the full official title
A Multicenter, 6-week, Double-blind, Randomized, Placebo-controlled, Parallel-design Study to Assess the Efficacy and Safety of NFC-1 in Adolescents (Ages 12-17) With Genetic Disorders Impacting Metabotropic Glutamate Receptors and ADHD
Recruitment & locations
CompletedBaltimore
Questions about this study
What did researchers investigate?
Researchers compared NFC-1 and placebo to find out how the approaches affected ADHD symptoms in young people with ADHD.
Who is behind this study?
The study sponsor is Aevi Genomic Medicine, LLC, a Cerecor company, a pharmaceutical company.
Did this study involve medication?
Yes. The study involved medication, including NFC-1 and Placebo.
Who was this study for?
Listed age limits: 12 years to 17 years.
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