Long-term Safety Extension Study of OLZ/SAM in Pediatric Subjects

Inclusion Criteria:

• Subject has completed the treatment period in either the ALKS 3831-A311 or the ALKS 3831-A312 study within 10 days of enrolling into this extension study, or subjecthad terminated early from Study ALKS 3831-A312 due to the clinically significantweight gain criterion.

• Subject will benefit from continued therapy with OLZ/SAM per clinical judgment.

• Subject is able to be treated on an outpatient basis.

• Subject must not be a danger to self or others (per Investigator judgement) and hasfamily support available to be maintained as an outpatient.

• Subject's parent(s)/legal guardian(s) is considered reliable by the Investigator andhas agreed to provide support to the subject to ensure compliance with studytreatment, visits, and protocol procedures.

• Subject agrees to abide by the contraception requirements specified in the protocolfor the duration of the study.

Exclusion Criteria:

• Subject poses a current suicide risk as assessed by the Investigator or as confirmedby the baseline Columbia-Suicide Severity Rating Scale by a response of "Yes" toquestion numbers 4 or 5 with ideation or suicidal behavior since the last visit.

• Subject has any finding that in the view of the Investigator or Medical Monitorwould compromise the safety of the subject or affect their ability to fulfill theprotocol visit schedule or visit requirement.

• Subject is currently taking medications that are contraindicated with olanzapine useor exhibit drug-interaction potential with olanzapine

• Subject has a positive test for opioids.

• Subject has a positive urine pregnancy test, is currently pregnant or breastfeeding,or plans to become pregnant or begin breastfeeding at any point during the study andfor 90 days after any study drug administration.