An Open Label Pilot Study of Adjunctive Asenapine for the Treatment of Posttraumatic Stress Disorder

PHASE4CompletedINTERVENTIONAL
Enrollment

18

Participants

Timeline

Start Date

June 30, 2012

Primary Completion Date

July 31, 2016

Study Completion Date

July 31, 2016

Conditions
Posttraumatic Stress Disorder
Interventions
DRUG

Adjunctive asenapine

participants who are not responding fully to antidepressant therapy for PTSD will receive adjunctive asenapine (flexible dosing beginning with 5 mg sublingual once per day, titrated up to 10 mg twice per day, as tolerated) for a total of 12 weeks.

Trial Locations (1)

35404

Tuscaloosa VA Medical Center, Tuscaloosa

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Merck Sharp & Dohme LLC

INDUSTRY

collaborator

Forest Laboratories

INDUSTRY

lead

Lori Davis, MD

OTHER