A Study of RO5186582 in Down Syndrome Among Children 6 to 11 Years of Age
Status: | Terminated |
---|---|
Conditions: | Other Indications |
Therapuetic Areas: | Other |
Healthy: | No |
Age Range: | 6 - 11 |
Updated: | 4/1/2017 |
Start Date: | October 28, 2015 |
End Date: | August 3, 2016 |
A Randomized, Double-Blind, Placebo-Controlled, Parallel Group 26-Week Dose-Investigating Study to Explore the Pharmacokinetics, Pharmacodynamic Effects, Efficacy, Safety and Tolerability of RO5186582 in Children With Down Syndrome Aged 6-11 Years
This study will evaluate the safety, tolerability, efficacy, and pharmacokinetic and
pharmacodynamic activity of 3 different dosages of RO5186582 compared with placebo. A total
of approximately 46 participants will be enrolled, in order to have at least 32 evaluable,
and will be randomly assigned to 1 of 4 treatments in a 1:1:1:1 ratio, with 9 children per
treatment arm. The target ratio between 6-8 years and 9-11 years age groups is approximately
1:1 in each treatment arm, with a minimum of 3 children per age group in each treatment arm.
pharmacodynamic activity of 3 different dosages of RO5186582 compared with placebo. A total
of approximately 46 participants will be enrolled, in order to have at least 32 evaluable,
and will be randomly assigned to 1 of 4 treatments in a 1:1:1:1 ratio, with 9 children per
treatment arm. The target ratio between 6-8 years and 9-11 years age groups is approximately
1:1 in each treatment arm, with a minimum of 3 children per age group in each treatment arm.
Inclusion Criteria:
- Diagnosis of Down syndrome, except for mosaic Down syndrome
- Available parent or caregiver to attend clinic visits and provide information about
the participant's behavior and symptoms
Exclusion Criteria:
- Any primary psychiatric comorbid disorder
- History of infantile spasms, West syndrome, Lennox-Gastaut syndrome, early infantile
epileptic encephalopathy, treatment-refractory epilepsy with cognitive/developmental
regression, severe head trauma, or central nervous system (CNS) infection
- Seizure event of any type within 12 months prior to Screening or relevant changes in
anti-epileptic drugs 6 weeks prior to enrollment
- Significant sleep disruption
- Significant gastrointestinal, renal, hepatic, endocrine, or cardiovascular disease
- New-onset or ongoing hematologic/oncologic disorder
- Severe lactose intolerance
- Participation in another clinical study within 1 month or 6 half-lives prior to first
dose, or any extent of participation in Study BP29589 (NCT02451657)
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1211 Medical Center Dr
Nashville, Tennessee 37232
Nashville, Tennessee 37232
(615) 322-5000
Vanderbilt Univ Med Ctr Vanderbilt University Medical Center (VUMC) is a comprehensive healthcare facility dedicated...
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Rush University Medical Center Rush University Medical Center encompasses a 664-bed hospital serving adults and...
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2165 North Decatur Road
Decatur, Georgia 30033
Decatur, Georgia 30033
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600 Highland Ave
Madison, Wisconsin 53792
Madison, Wisconsin 53792
(608) 263-6400
University of Wisconsin Hospital and Clinics UW Health strives to meet the health needs of...
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