drugset / Trial / NCT02635035

Shire SCT: Lisdexamfetamine Treatment for ADHD and SCT

NCT02635035

Phase 2 Completed 38 enrolled NYU Langone Health Shire · collab
RandomizedCrossoverDouble-blindTreatment

Summary

The primary purpose of this study is to test the efficacy of Lisdexamfetamine in Adults With Attention Deficit Hyperactivity Disorder (ADHD) and Sluggish Cognitive Tempo (SCT). This is a placebo controlled, cross-over clinical trial of oral Lisdexamfetamine Dimesylate 30-70mg/day in adults with attention-deficit hyper-activity disorder and Sluggish Cognitive Tempo (ACT). Patients will be assigned either LDX/Placebo for 10 weeks with a two week placebo washout period.

Timeline

Start
2015-11
Primary completion
2019-01-09
Completion
2019-01-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Lisdexamfetamine Other / unclassified 30 mg Oral
Subject Lisdexamfetamine Other / unclassified 50 mg Oral
Subject Lisdexamfetamine Other / unclassified 70 mg Oral