Participants who have completed the 3-week trial P05691 (NCT00764478) can be screened for eligibility for this 26-week extension study in which they will continue treatment. The primary purpose of this trial is to evaluate the long-term safety of asenapine.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
165
Forest Investigative Site 1000
Austin, Texas, United States
Number of participants experiencing clinical and laboratory adverse events (AEs)
Time frame: Baseline up to 212 days
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.