14
Participants
Start Date
September 13, 2006
Primary Completion Date
September 2, 2009
Study Completion Date
January 10, 2011
3,4-methylenedioxymethamphetamine (125 mg)
Participants will receive an initial dose of 125 mg MDMA orally and, if investigator and participant deem appropriate, 2.5 hours later they will receive 62.5 mg MDMA orally.
3,4-methyelendioxymethamphetamine (25 mg)
Participants will receive a 25 mg MDMA orally, and if investigator and participant agree, 2.5 hours later they will receive 12.5 mg MDMA orally.
Therapy
Non-directive therapy performed by a team of two co-therapists
Offices of Peter Oehen MD, Biberist
Lead Sponsor
Swiss Medical Society for Psycholytic Therapy
OTHER
Lykos Therapeutics
INDUSTRY