CTRI/2015/07/005970已完成未知
A Multicentric Open Label, Balanced, Randomized, Two Treatment, Two-Period, Two-Sequence, Crossover, Steady State Bioequivalence Evaluation of Clozapine Extended Release Capsule 200 mg once daily (Test Drug, Intas Pharmaceuticals Limited, India) with Clozaril® 100 mg Tablets twice daily (Reference Drug, Novartis Pharmaceuticals Corporation, Usa) after multiple dose administration in Adult Schizophrenic Patients under Fasting conditions- Pilot Study - NA
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 入组人数
- 20
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Ba/be
入排标准
入选标准
- •1.Written informed consent for participation in the study by the patient and Patientâ??s Legally Acceptable Representative (LAR)
- •2.Patient has a documented clinical diagnosis of schizophrenia according to DSM IV-TR at least six months prior to screening
- •3.Patients have a diagnosis of treatment-resistant schizophrenia (Treatment resistance is the failure to respond to two or more antipsychotic medications given in therapeutic dose for more than six weeks or more)
- •4.Patients between 18 and 60 years of age (both inclusive)
- •5.Having a BMI between 18 and 30 (both inclusive),calculated as weight in kg/height in m2
- •6.Patients have been on a daily stable dose of 200 mg clozapine formulation for at least 3 month prior to screening visit
- •7.Not having any significant diseases or clinically significant abnormal findings except schizophrenia.
排除标准
- •1.Patient with known hypersensitivity/ intolerance to clozapine or any other component of the drug.
- •2.Significant orthostatic hypotension (i.e., a drop in systolic blood pressure of 30 mm Hg or more and/or a drop in diastolic blood pressure of 20 mm Hg or more on standing)
- •3.Concurrent use of antihypertensive medication or any medication that might pre-dispose to orthostatic hypotension.
- •4.Supine blood pressure less than 110/70 mm Hg or pulse rate less than 60 or more than 100 beat per minute at screening and Day 1.
- •5.A total white blood cell count below 4000/mL, or an absolute neutrophil count <2000/ mL performed at the screening and a day prior to randomization.
- •6.Pregnant or lactating females.
研究者
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