drugset / Trial / NCT00434213

Characterization of Dermal Reactions in Pediatric Patients With ADHD Using DAYTRANA

NCT00434213 ↗

Phase 4 Completed 309 enrolled Noven Therapeutics
NaSingle-groupOpen-labelTreatment

Summary

This is a study designed to characterize the dermal response of DAYTRANA. Subjects will visit the study site over a period of approximately 14 weeks.

Timeline

Start
2007-01
Primary completion
2007-08
Completion
2008-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Methylphenidate Small molecule 10 mg Topical
Subject Methylphenidate Small molecule 15 mg Topical
Subject Methylphenidate Small molecule 20 mg Topical
Subject Methylphenidate Small molecule 30 mg Topical