63
Participants
Start Date
October 30, 2017
Primary Completion Date
May 31, 2022
Study Completion Date
May 31, 2022
Galantamine
The study will be performed using the 8mg, 16mg and 24mg doses of galantamine hydrobromide-ER. The dosing regimen will be an initial 4 weeks of drug run-up at the lowest 8mg q.d. dose, followed by 16mg q.d. for the following 4 weeks, and the dose will be increased for the last 4 weeks to 24mg. Participants will be instructed to take one 8mg 16mg or 24mg pill (galantamine-ER or placebo) every morning, preferably with food.
Placebo
Matched placebo will be made in-house using lactulose filler in gel capsules. Participants will be instructed to take one pills every morning for 12 weeks.
Center for Interdisciplinary Research on Nicotine Addiction, University of Pennsylvania, Philadelphia
National Institute on Drug Abuse (NIDA)
NIH
University of Pennsylvania
OTHER