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临床试验/CTRI/2015/07/005970
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

Intas Pharmaceuticals Limited0 个研究点目标入组 20 人开始时间: 待定最近更新:

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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