Status:
COMPLETED
A Safety and Pharmacokinetic Study of ER OROS Paliperidone in Pediatric Patients With Schizophrenia, Schizoaffective Disorder, or Schizophreniform Disorder
Lead Sponsor:
Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
Conditions:
Schizophrenia
Schizoaffective Disorder
Eligibility:
All Genders
10-17 years
Phase:
PHASE1
Brief Summary
The purposes of this study are to characterize the pharmacokinetics of paliperidone after single- and multiple-dose administration of paliperidone ER in children and adolescent patients (\>= 10 to \<=...
Detailed Description
The current study is designed as a multicenter, open-label, multiple-dose study in children and adolescent patients \>= 10 to \<= 17 years of age with schizophrenia, schizoaffective disorder, or schiz...
Eligibility Criteria
Inclusion
- Patients' height and weight must be within the 5th to 95th Physical Growth National Center for Health Statistics percentiles for age and sex
- Patients must have a diagnosis of schizophrenia of any subtype (295.10
- 20
- 30
- 60
- 90), schizoaffective disorder (295.70), or schizophreniform disorder (295.40), according to the DSM-IV-TR
- Patients must be healthy (other than the DSM-IV-TR classification), on the basis of the screening medical history, physical examination, 12-lead ECG, and clinical laboratory tests (hematology, serum chemistry, and urinalysis). Patients with laboratory results outside the normal reference range can be included only if the investigator, upon consultation with the sponsor, judges the deviations as not clinically significant
- QT values must be within normal limits and patients must have a CGI-S score of less than or equal to 3
- Female patients must be premenarchal, surgically sterile, abstinent, or, if sexually active, be practicing an effective method of birth control (e.g., prescription oral contraceptives, contraceptive injections, intrauterine device, double-barrier method, contraceptive patch, male partner sterilization) for at least 1 month before study entry and throughout the study, have a negative serum beta-human chorionic gonadotropin pregnancy test at screening, and a negative urine pregnancy test on Day 1
- Patients must sign an informed assent document indicating that they understand the purpose of and procedures required for the study and are willing to participate in the study, with Parent(s) or the legal guardian(s) of each patient signing an informed consent document indicating that they understand the purpose of and the procedures required for the study and give permission for their child's participation in the study and a responsible person must be available to accompany the patient to the investigational site at each visit
- Patients must agree to be hospitalized at any time during the study, and their parent(s) or legal guardian(s) must consent, if it is deemed clinically necessary by the investigator.
Exclusion
- Patients with an active DSM-IV-TR axis I diagnosis other than schizophrenia, schizoaffective disorder, or schizophreniform disorder
- Patients with a history of DSM-IV-TR diagnosis of substance dependence within 6 months before screening (nicotine and caffeine dependence are not exclusionary) or patients who are involuntarily committed to psychiatric hospitalization
- Patients with a significant risk of suicidal or violent ideation or behavior, as judged by the clinical investigator
- Female patients who are pregnant, who plan to become pregnant during the study, or who are breast-feeding
- Patients with any medical condition that can potentially alter the absorption, metabolism, or excretion of the study drug (e.g., Crohn's disease, severe gastrointestinal narrowing \[pathologic or iatrogenic\], liver disease, or renal disease)
- Patients with a history of any malignancy, with the exception of basal cell carcinoma, in the past 5 years
- Patients with a history of a positive result for any serology test (e.g., human immunodeficiency virus, hepatitis), with a history of neuroleptic malignant syndrome
Key Trial Info
Start Date :
January 1 2006
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
August 1 2006
Estimated Enrollment :
25 Patients enrolled
Trial Details
Trial ID
NCT00796081
Start Date
January 1 2006
End Date
August 1 2006
Last Update
June 8 2011
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