A Study to Assess the Pharmacokinetics, Safety, and Tolerability of Paliperidone Palmitate in Patients With Schizophrenia

This is a multicenter, randomized (the study drug is assigned by chance), open-label (all
people know the identity of the intervention), parallel-group (each group of patients will
be initiated simultaneously) study in 4 panels (A, B, C and D). Each panel will comprise 2
single-dose treatment periods. In Period 1, all patients from the 4 panels will receive an
intramuscular (i.m.) injection with 1 mg paliperidone as an immediate release (IR) solution
to assess tolerability and allergic or hypersensitivity reactions potentially related to
paliperidone, and to establish the relative bioavailability (the extent to which a drug or
other substance becomes available to the body) of paliperidone palmitate versus paliperidone
IR. Patients in Panels A and C will receive an i.m. injection with 1 mg paliperidone IR
solution in the gluteal muscle, and patients in Panel B and D will receive an i.m. injection
with 1 mg paliperidone IR solution in the deltoid or gluteal muscle. Patients who tolerate
this injection and have completed all assessments on Day 5 of Period 1 will be enrolled in
Period 2. In Period 2, patients will receive a single dose of 3-month paliperidone palmitate
i.m. injection at the dosages defined for each panel. The study drug injection will be
followed by a 96-hour observation period in Period 1, and a 364-day or 544-day observation
period in Period 2. Successive study drug administrations will be separated by a washout
period (period when receiving no treatment) of at least 7 and no more than 21 days. The
total study length for all patients is from 53 weeks to a maximum of 58 weeks. Patients in
Panel B, if consented, and Panel D will participate in the extension period of approximately
26 weeks in order to obtain additional assessments to be able to characterize the
pharmacokinetics (PK) profile. Pharmacokinetics explores how the drug is absorbed in the
body, distributed within the body, and how it is removed from the body over time. Therefore,
for those who participate in the extension period, the total study duration will be
approximately 84 weeks.

Inclusion Criteria:

- Patients diagnosed with schizophrenia or schizoaffective disorder, for at least 1
year before screening

- Clinically stable with no hospitalizations for schizophrenia exacerbation or change
in current antipsychotic medications for 3 months prior to screening

- Stabilized on antipsychotic medications other than risperidone, paliperidone,
ziprasidone, clozapine, thioridazine, or any long acting injectable.

- For panel D only, no detectable plasma concentration of risperidone or paliperidone >
0.1ng/mL at screening. A quantifiable and stable level of paliperidone not exceeding
0.25 ng/mL is allowed if such paliperidone value is explained by (documented) use of
paliperidone palmitate (last dose administered > 12 months prior to baseline)

- Has a total PANSS score of 70 or less at both screening and Day-1 (Period 1)

- Woman is postmenopausal, surgically sterile, abstinent or, if sexually active,
practices an effective method of birth control during participation in the study or
for at least 6 months after the last dose of study drug, whichever is longer

- Woman has negative pregnancy test at screening and on Day -1 of Period 1

- Man agrees to use an adequate contraception method as deemed appropriate by the
investigator and agrees to not donate sperm during participation in the study or for
at least 6 months after the last dose of study drug, whichever is longer

- Body Mass Index (BMI) between 17 and 35 kg/m2 (inclusive). Body weight of at least 50
kg for patients enrolled in panel A, B and C. For patients enrolled in panel D only:
body weight of at least 47 kg

Exclusion Criteria:

- Attempted suicide within 12 months before screening or is at imminent risk of suicide
or violent behavior

- Has diagnosis of alcohol or substance dependence, with the exception of nicotine or
caffeine dependence, within 12 months prior to screening, or diagnosis of substance
abuse within 3 months prior to screening

- Has a positive drug screen test for barbiturates, cocaine, amphetamines or opiates,
or has a positive alcohol screen test unless positive toxicology screen is explained
by a prescribed allowed medication

- Is in his/her first episode of psychosis

- Has a history of or has a current clinically significant medical illness that the
investigator considers should exclude the patients or that could interfere with the
interpretation of the study results

- Has clinically significant abnormal values at screening or at baseline for
hematology, clinical chemistry or for urinalysis, as deemed appropriate by the
investigator

- Has a clinically relevant abnormality in the physical examination, vital signs or 12
lead electrocardiogram (ECG) at screening or at baseline as deemed appropriate by the
investigator

- Has a history or presence of circumstances that may increase the risk of the
occurrence of torsade de pointes and/or sudden death in association with the use of
drugs that prolong the QTc interval

- Concomitant use of medications that the investigator considers should exclude the
patients or that could interfere with the interpretation of the study results

- Any other condition or circumstance that the investigator considers should exclude
the patients or that could interfere with the interpretation of the study results