Overview

Long-term Safety and Efficacy of ABT-126 in Subjects With Schizophrenia: An Extension Study for Subjects Completing Study M10-855 (NCT01655680)

Status:
Terminated
Trial end date:
2014-11-01
Target enrollment:
0
Participant gender:
All
Summary
This is a study of ABT-126 in the treatment of cognitive impairment associated with schizophrenia (CIAS), a long-term extension study to study M10-855 (NCT01655680).
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
AbbVie
Criteria
Inclusion Criteria:

- The subject was randomized into Study M10-855 and completed through Week 26 in that
study.

- The subject is receiving one or more antipsychotic medications.

Exclusion Criteria:

- Additional history collected during participation in Study M10-855 provides evidence
that, in the investigator's judgement, the subject does not have schizophrenia.

- The subject experienced an adverse event or abnormal finding during physical
examination, vital signs, laboratory profile, and/or electrocardiogram (ECG)
measurements in Study M10-855 that indicates the subject is likely to become medically
unstable during the current study.

- The subject is currently taking or is expected to be prescribed any excluded
medication without the approval of AbbVie medical monitor.

- The subject is currently enrolled in, or plans to participate in, another
interventional study during the course of this trial.