A Double-blind, Randomised, Placebo-controlled, Cross-over Study to Investigate the Tolerability and Effect of Three Single-dose Regimens of BIA 9-1067 on the Levodopa Pharmacokinetics, Motor Response, and Erythrocyte Soluble Catechol-O-methyltransferase Activity in Parkinson's Disease Patients Concomitantly Treated With Levodopa/Dopa-decarboxylase Inhibitor

Bial - Portela C S.A.3 个研究点分布在 3 个国家目标入组 10 人开始时间: 2009年4月最近更新: 2015年1月12日

适应症

干预措施

试验速览

阶段: 2 期
状态: 已完成
发起方
入组人数: 10
试验地点: 3
主要终点: Cmax - Maximum Plasma Concentration Day 3

研究概览研究设计入排标准研究组 & 干预措施结局指标研究者研究点记录与标识符相似试验

研究概览

简要总结

The purpose of this study is to investigate the effect of BIA 9-1067 on the levodopa pharmacokinetics when administered in combination with immediate release levodopa/carbidopa or levodopa/benserazide in Parkinson's Disease (PD) patients.

详细描述

This was a three-centre, double-blind, randomised, placebo-controlled, crossover study with four consecutive single-dose treatment periods in PD patients treated with immediate release 100 mg/25 mg levodopa/carbidopa or 100 mg/25 mg levodopa/benserazide

研究设计

研究类型: Interventional
分配方式: Randomized
干预模型: Crossover
主要目的: Treatment
盲法: Triple (Participant, Investigator, Outcomes Assessor)

入排标准

年龄范围: 30 Years 至 75 Years（Adult, Older Adult）
性别: All
接受健康志愿者: 否

入选标准

•Male or female of non-childbearing potential (by reason of surgery or postmenopausal);
•Aged between 30 and 75 years, inclusive;
•A diagnosis of PD according to the UK PDS Brain Bank diagnostic criteria (bradykinesia and at least one of the following: muscular rigidity, rest tremor and postural instability);
•Predictable signs of end-of-dose deterioration despite "optimal" levodopa/carbidopa or levodopa/benserazide therapy;
•Been treated with a stable regimen of 3 to 8 doses of standard release 100 mg/25 mg levodopa/carbidopa or 100 mg/25 mg levodopa/benserazide per day within at least 1 week prior to randomisation;
•Modified Hoehn and Yahr stage of less than 5 in the off-state;
•Mean duration of OFF stage ≥ 1.5 h during waking hours (based on historical information);
•Concomitant anti-Parkinsonian medication (other than apomorphine, entacapone or tolcapone) in stable doses for at least 4 weeks prior to randomisation;
•Results of clinical laboratory tests acceptable by the investigator (not clinically significant for the well-being of the subject or for the purpose of the study);
•Able and willing to give written informed consent.

排除标准

•Non-idiopathic parkinsonism (atypical parkinsonism, symptomatic parkinsonism, Parkinson-plus syndrome);
•Treated with levodopa/carbidopa or levodopa/benserazide in a 10:1 ratio, or with levodopa/carbidopa in a controlled-release formulation;
•Treated with entacapone, tolcapone, neuroleptics, antidepressants (except serotonin-specific reuptake inhibitors or imipramines [desipramine, imipramine, clomipramine and amitriptyline]), monoamine oxidase inhibitors (except selegiline up to 10 mg/day in oral formulation or 1.25 mg/day in buccal absorption formulation or rasagiline up to 1 mg/day) or antiemetics (except domperidone) within 4 weeks prior to randomisation;
•Treated with apomorphine within 7 days prior to randomisation;
•Treated with any investigational product within 2 months prior to randomisation (or within 5 half-lives, whichever is longer);
•A psychiatric or any medical condition that might place him/her at increased risk or interfere with assessments;
•Known hypersensitivity to any of the ingredients of the investigational products;
•A history of abuse of alcohol, drugs or medications within the last 2 years;
•A clinically relevant ECG abnormality;
•A history or current evidence of heart disease, including but not limited to myocardial infarction, angina, congestive heart failure and cardiac arrhythmia;
•Unstable concomitant disease being treated with changing doses of medication;
•A history or current evidence of any relevant disease in the context of this study, i.e., with respect to the safety of the subject (e.g., hepatic or renal impairment) or related to the study conditions;
•A test positive for the human immunodeficiency viruses (HIV) 1 or 2 antibodies, or hepatitis B surface antigen (HBsAg), or hepatitis C antibody (HCVAb);
•Donated blood or received blood or blood products within the 6 months prior to randomisation;
•Pregnant, breast-feeding or of childbearing potential;
•Other condition or circumstance that, in the opinion of the investigator, may compromise the subject's ability to comply with the study protocol.

研究组 & 干预措施

Treatment Sequence A

Experimental

Treatment Sequence A Period 1 - 25 mg BIA 9-1067 Period 2 - 50 mg BIA 9-1067 Period 3 - 100 mg BIA 9-1067 Period 4 - Placebo