13
Participants
Start Date
July 31, 2008
Primary Completion Date
January 31, 2010
Study Completion Date
January 31, 2010
Lobeline sulfate
Each laboratory day, participants will receive one capsule containing either methylphenidate HCl (15 or 30 mg) or placebo, and one sublingual tablet containing either lobeline (7.5, 15, or 30 mg) or placebo.
Methylphenidate HCl
Each laboratory day, participants will receive one capsule containing either methylphenidate HCl (15 or 30 mg) or placebo, and one sublingual tablet containing either lobeline (7.5, 15, or 30 mg) or placebo.
Placebo
Each laboratory day, participants will receive one capsule containing either methylphenidate HCl (15 or 30 mg) or placebo, and one sublingual tablet containing either lobeline (7.5, 15, or 30 mg) or placebo.
General Clinical Research Center, University of Kentucky, Lexington
Lead Sponsor
National Institute of Mental Health (NIMH)
NIH
Yaupon Therapeutics
INDUSTRY