A Long-Term, Open-Label, Study on Schizophrenia

The study includes 2 treatment periods. Study Period I will begin at patient randomization
(enrollment into Study HBBO) and continue through the first 2 years of treatment. Study
Period II will be only for patients randomized to treatment with LY2140023, and will begin
after the patient has completed the second year of treatment. Patients who qualify for
enrollment will be randomized in a 3:1 ratio (LY2140023 versus standard of care,
respectively) into 2 treatment groups: flexible, twice-daily dose of LY2140023 or
standard-of-care (olanzapine, risperidone, aripiprazole, or quetiapine). Those assigned to
LY2140023 will have the option to continue on LY2140023 after 2 years if deemed appropriate
by the investigator.

Inclusion Criteria:

- Must have met all entry criteria for, and have completed, an acute,
placebo-controlled clinical trial of LY2140023 (such as Study H8Y-MC-HBBM, or other
acute, placebo-controlled LY2140023 studies if allowed by the protocols for those
studies).

- Female patients of childbearing potential must agree to use a single, effective,
medically acceptable method of birth control.

- Patients must be considered reliable and have a level of understanding sufficient to
perform all tests and examinations required by the protocol.

- Patients must be able to understand the nature of the study and have given their own
informed consent.

Exclusion Criteria:

- Are currently enrolled in, or discontinued within the last 30 days from a clinical
trial involving an investigational product or nonapproved use of a drug or device
(other than LY2140023), or concurrently enrolled in any other type of medical
research judged not to be scientifically or medically compatible with this study.

- Patients for whom treatment with olanzapine, risperidone, aripiprazole, quetiapine,
or LY2140023, as specified in this protocol, is relatively or absolutely clinically
contraindicated.

- Patients who have received treatment with clozapine at doses greater than 200 mg
daily within 12 months prior to study enrollment, or who have received any clozapine
at all during the month before study enrollment.

- Patients who require concomitant treatment with any other medication with primary
central nervous system activity, other than those allowed in study protocol.

- Patients have risk of suicide.

- Patients diagnosed with substance dependence or substance abuse within the 6 months
prior to study enrollment.

- Patients diagnosed with substance-induced psychosis within 7 days of study enrollment
or at any time during the study.

- Female patients who are pregnant, nursing, lactating or who intend to become pregnant
within 30 days of completing the study.

- Have known glaucoma.

- Have a history of some types of seizures.

- Have seizure liability inconsistent with the exclusion criteria of the completed
acute feeder study.

- Patients who have had electroconvulsive therapy (ECT) within 3 months of study
enrollment or who will have ECT at any time during the study.

- Patients with known Human Immunodeficiency Virus positive (HIV+) status.

- Patients have a serious disease, such as recent stroke, heart, liver, kidney, lung or
blood diseases

- Patients with Parkinson's disease

- Are incapable of participating in the study or are unwilling to engage in a
meaningful way as study participants.