Long-Term Safety Extension Trial of Asenapine in Schizophrenia Participants Who Completed Protocol P05688 (P05689)

PHASE3CompletedINTERVENTIONAL
Enrollment

105

Participants

Timeline

Start Date

December 31, 2012

Primary Completion Date

March 31, 2015

Study Completion Date

March 31, 2015

Conditions
Schizophrenia
Interventions
DRUG

Asenapine

2.5 mg or 5 mg fast dissolving active asenapine tablets administered sublingually, same number of tablets are taken in the morning and the evening

DRUG

Placebo Asenapine

2.5 mg or 5 mg fast dissolving placebo asenapine tablets administered sublingually, same number of tablets are taken in the morning and the evening

DRUG

Olanzapine

15 mg film-coated active olanzapine tablets administered orally QD. The time of the active olanzapine dose (either morning or evening) is not disclosed in order to preserve blinding.

DRUG

Placebo Olanzapine

15 mg film-coated placebo olanzapine tablets administered orally QD. The time of the active olanzapine dose (either morning or evening) is not disclosed in order to preserve blinding.

Trial Locations (1)

78754

Forest Investigative Site 2001, Austin

Sponsors
All Listed Sponsors
lead

Forest Laboratories

INDUSTRY