Start: November 2011
End: September 2013
The purpose of this study is to assess the safety and tolerability of the experimental drug RG1662 in individuals with Down syndrome.
Minimum Age: 18 Years
Maximum Age: 30 Years
++Males and nonpregnant, nonlactating females with a diagnosis of Down syndrome (confirmed by karyotype)++Parent or legal guardian/representative and caregiver willing to give written informed consent++Subject willing and consenting to participate
++Major depressive disorder not adequately controlled by a selective serotonin reuptake inhibitor or serotonin norepinephrine reuptake inhibitor++Clinical diagnosis of autistic spectrum disorder or attention deficit or hyperactivity disorder that makes study participation unlikely++Other primary psychiatric diagnosis++Evidence or clinical diagnosis of dementia++Personal history of cardiac abnormalities; patients that have previously undergone congenital heart surgery can be enrolled provided they have no residual complication requiring intervention (e.g., pacemaker)++Clinically significant obstructive pulmonary disease or asthma that is not adequately treated (oral steroids are not allowed)++Thyroid dysfunction that is not adequately controlled and stabilized on treatment for at least 8 weeks++Sustained elevated supine blood pressure exceeding 140/90 mmHg or notable resting tachycardia or blood pressure below 90/40 mmHg++Have taken any other investigational medications within past 3 months++Body mass index (BMI) of more than 40 kg/m2
Contact study personnel listed either under the general study contact or the location nearest you.
Who Is the General Study Contact?
For more information about this trial and its study sites, please call 1-888-662-6728 (U.S. only) or email firstname.lastname@example.org. Reference study ID number BP25543.
Contact NIA’s Alzheimer’s and related Dementias Education and Referral (ADEAR) Center at 800-438-4380 or email ADEAR.
Lead: Hoffmann-La Roche
Source: ClinicalTrials.gov ID: NCT01436955