A multicenter, open label, multiple-dose, randomized, two-treatment, two-period, two-sequence, two-way crossover, steady-state bioequivalence study of Felbamate Tablets 600 mg of Getz Pharma Research Pvt. Ltd., India with that of FELBATOLÂ® (Felbamate) Tablets 600 mg of MEDA Pharmaceuticals Inc., Somerset, New Jersey, 08873-4120,USA.,in adult male and non-pregnant female epilepsy (partial seizures with and without generalization) patients already established (run-in) on Felbamate as an monotherapy/adjunctive therapy under fasting condition.

Getz Pharma Research Pvt Ltd0 个研究点目标入组 38 人开始时间: 待定最近更新: 2021年11月24日

试验速览

阶段: 未知
状态: 已完成
发起方: Getz Pharma Research Pvt Ltd
入组人数: 38

研究概览入排标准研究者记录与标识符相似试验

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

•i.Patients should be in the range of 18 - 45 years of age (both inclusive).
•ii.BMI should be in the range of 18.5 to 24.9 kg/m2.
•iii.Patients having refractory partial seizures with and without generalization not controlled on standard antiepileptic drugs at therapeutic levels.
•iv.Patients with normal findings as determined by baseline history, physical examination and vital signs (seated blood pressure, radial pulse rate, respiratory rate and axillary temperature).
•v.Patients with normal / not significant laboratory values as determined by hematological tests, biochemistry, urine analysis, ECG and chest X-ray(P/A view) in correlation with clinical findings.
•vi.Willingness to follow the protocol requirement as evidenced by voluntary written informed consent.
•vii.Agreeing to, not using or conforming to not having any medication (prescription and over the counter, herbal products), including vitamins and minerals for 15 days prior to study & during the course of the study except any one of Valproic acid, Gabapentin, Levetiracetam or Pregabalin for ongoing therapy of any of their illnesses.
•viii.No history or presence of significant alcoholism( > 3 units of alcohol per day) within one year prior to drug administration.
•ix.No history of smoking and of drug abuse.
•x.All female patients who are of child bearing potential or those within the first two years of the onset of menopausal syndrome using acceptable methods of birth control at least 30 days prior to onset of screening period and till 30 days post last dose of study drug in period-II. Acceptable birth control methods include Barrier methods such as diaphragm/condom with spermicide, foams, jellies, diaphragm, intrauterine device (IUD), or abstinence. Unacceptable methods include oral or implanted or is surgically sterile (bilateral tubal ligation, bilateral oophorectomy, or hysterectomy has been performed on the study patient)

排除标准

•The patients meeting with any one of the following criteria should be excluded:
•i.History of aplastic anemia or hepatic failure.
•ii.Requiring medication for any ailment having enzyme-modifying activity in previous one month other than Felbamate, Valproic acid, Gabapentin, Levetiracetam or Pregabalin prior to drug administration day and during the course of the study.
•iii.History of cardiovascular, renal, hepatic, ophthalmic, pulmonary, neurological (other than refractory epilepsy), metabolic hematological, gastrointestinal, endocrine or immunological illness.
•iv.At baseline (Prior to randomization):
•Two-fold increase in the highest, 2-day pre-study seizure frequency;
•Single generalized, tonic-clonic seizure if none occurred during pre-treatment screening and/or;
•Significant prolongation of generalized, tonic-clonic seizures and Status Epilepticus.
•v.Participation in any other clinical study within 90 days prior to onset of screening period.
•vi.History of or currently active malignancy or any other serious diseases.
•vii.Any contraindication to blood sampling.
•viii.Refusal to abstain from smoking or consumption of alcohol and tobacco products 72.00 hours before morning drug administration on days- 10 and 20 and until after the last blood sample collection in each study period.
•ix.Use of xanthine containing food or beverages (chocolates, tea, coffee or cola drinks), grapefruit juice or products containing grapefruit and alcohol or any alcoholic products, for 72.00 hours before morning drug administration on days- 10 and 20 and until after the last blood sample collection in each study period.
•x.Blood donation within 90 days prior to the commencement of the study.
•xi.Patients with positive HIV I/II, HBsAg or HCV tests.
•xii.Patients with positive HBsAg, positive anti-Hbc and positive anti HBs.
•xiii.Positive urine screen for drugs of abuse and breath alcohol test done during check-in process.
•xiv.For female patients: Positive serum pregnancy test for female patients during screening and enrolment/check-in process.
•xv.A history of allergic or adverse reactions to Felbamate, its formulation excipients or any comparable or similar product (carbamates).
•xvi.A history of severe hepatic impairment, drug induced leucopenia/neutropenia, congenital prolongation of the QT interval, cardiac arrhythmias, myocardial infarction or unstable heart disease
•xvii.Concurrent primary psychiatric or neurological diagnosis, including organic mental disorder, severe tardive dyskinesia, or idiopathic Parkinsonâ??s disease.
•xviii.Complete blood counts below accepted normal values.
•xix.Elevation in liver enzymes, above the normal limits. A history of or currently active granulocytopenia or myeloproliferative disorders (drug-induced or idiopathic).
•xx.A medical or surgical condition that might interfere with the absorption, metabolism, or excretion of Felbamate.
•xxi.Concurrent use of other drugs known to suppress bone marrow function or causes a significant risk of drug induced hepatitis.
•xxii.Expected changes in concomitant medications during the period of study.
•xxiii.A history of alcohol or drug dependence by Diagnostic and Statistical Manual of Mental Disorders IV (DSM-IV) criteria during the 6-month period immediately prior to study entry.

研究者

发起方

Getz Pharma Research Pvt Ltd

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