NCT02957435撤回1 期
Phase I, Open-label, Three Periods Study in Health Male and Female Subjects, Under Fasting Condition for Evaluation of Pharmacokinetics Profile of Single Dose of Eplerenone in Coated Tablets Formulation on Concentrations of 25mg, 50mg and 100mg, Produced by Biolab Sanus Farmacêutica Ltda
Biolab Sanus Farmaceutica1 个研究点 分布在 1 个国家开始时间: 2017年7月最近更新:
适应症
干预措施
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 撤回
- 发起方
- 试验地点
- 1
- 主要终点
- Area under the curve (ASCo-t)
研究概览
简要总结
The purpose of this study is to evaluate the pharmacokinetics profile of the formulation of eplerenone coated tablets in the concentration of 25mg, 50mg and 100mg (2 coated tablets of 50mg) in male and female healthy subjects under fasting condition.
详细描述
This is a phase I study of eplerenone coated tablets of 25mg, 50mg and 100mg (2 coated tablets of 50mg) in fasting administration. Sample size is 12 subjects, male and female, aged between 18 and 50 years old.
This is an open-label, unicenter study with three periods, three treatments and one sequence. Each subject will receive the following treatments at the following periods:
- Period 1: one coated tablet of eplerenone 25mg in fasting
- Period 2: one coated tablet of eplerenone 50mg in fasting
- Period 3: two coated tablets of eplerenone 50mg (100mg of eplerenone) in fasting Formulations will be administered in a single dose, orally in each period. Trial subjects will be admitted in three different periods of 24 hours each, when investigational product will be administered and blood samples will be collected at pre-determined periods of time for pharmacokinetics evaluation.
Primary objective is to evaluate the pharmacokinetics of formulations of eplerenone coated tablets of 25mg, 50mg and 100mg (two coated tablets of 50mg) in healthy subjects under fasting condition. As a secondary objective, it will be also evaluated the safe and tolerability of coated tablets of eplerenone.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Other
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 50 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Male or female subjects, with age between 18 and 50 years old;
- •Body mass index (BMI) between 18.5 and 30 kg/m2;
- •Good health conditions or without significant diseases, at investigator discretion, according to the protocol and evaluation performed such as: clinical history, vital signs, physical examination, electrocardiogram (ECG) and laboratory exams;
- •Ability to understand the nature and the objective of the trial, including risks and adverse effects.
排除标准
- •Know hypersensitivity to the investigational product (eplerenone) or chemically related compounds;
- •History or presence of chronic hepatic or gastrointestinal diseases, or other condition that may interfere with drug absorption, distribution, metabolism or excretion;
- •Be in use of maintenance therapy with any drugs that interferes with the investigational product, except oral contraceptives;
- •History of hepatic, kidney, lungs, gastrointestinal, epileptic, hematologic, psychiatric diseases, hypertension of any etiology, history of myocardial infarction, angina and/or heart failure or malignant neoplasias, in other words, any current disease, acute or chronic, in monitoring or treatment;
- •Electrocardiographic findings that at investigator discretion are not recommended for study participation;
- •History of any cardiac surgery, kidney surgery (exeresis or kidney anegesis), intestinal (partial or full ablation of esophagus, stomach, duodenum, jejunum, ileum, ascending colon, transverse colon, descending colon, sigmoid or rectum) and liver or pancreas surgery;
- •Laboratory exams results out of the range considered normal in accordance with the reference ranges stipulated by the clinical laboratory, unless that are considered as not clinically significant by the investigator);
- •Be a smoker;
- •Ingestion of food that contains xanthine including more than five cups of coffee or tea per day;
- •Vegan habits;
- •History of abusive use of drugs and/or alcohol or excessive alcohol consumption;
- •Have used regular medication in two weeks prior to start of treatment and the date of evaluation or have used any medication one week before, except contraceptives or in cases that, based on the half-life of the drug and/or active metabolites may be assumed the complete elimination;
- •Have been hospitalized for any reason up to 8 weeks prior to start of the first period of trial treatment;
- •Have received any treatment with any drug with known and well-established toxic potential to major organs inside of the 3 months prior to the study;
- •Have participated from any experimental trial or have ingested any investigational drug within 12 months prior to the trial start;
- •Be pregnant or in breastfeeding period or want to get pregnant during the study period;
- •Have donated or have lost 450 mL or more of blood within 3 months prior to the trial or donation of more than 1500 mL of blood within 12 months prior to the trial;
- •Have any condition, that prohibits the subject to participate in the trial, at the investigator's discretion;
- •Have difficulty to swallow medicines and/or approximately 200 mL of water at the morning;
- •Inability to keep awake or seated during one hour or necessary time at investigator discretion;
- •Present a positive pregnancy test;
- •Present breathalyzer test higher than zero;
- •Present a positive result for a preliminary test of drugs.
研究组 & 干预措施
eplerenone
Experimental
(Single arm) Sequence 1: one eplerenone coated tablet 25 mg in fasting (period 1), one eplerenone coated tablet 50 mg in fasting (period 2) and two eplerenone coated tablets 50 mg (100 mg of eplerenone) in fasting (period 3)
干预措施: eplerenone (Drug)
结局指标
主要结局
Area under the curve (ASCo-t)
时间窗: 24 hours
Maximum serum concentration (Cmax)
时间窗: 24 hours
次要结局
- Time to reach Cmax (Tmax)(24 hours)
- Half-life (t1/2)(24 hours)
- Causality of adverse events(30 days)
- Elimination constant rate (Kel)(24 hours)
- Area under the curve (0-inf)(24 hours)
- Number of adverse events(30 days)
- Intensity of adverse events(30 days)
研究者
研究点 (1)
Loading locations...
相似试验
撤回
1 期
Pharmacokinetics of Eplerenone TabletHealthy VolunteersNCT02607657Biolab Sanus Farmaceutica
已完成
1 期
A Study of Epetraborole Tablets in Subjects With Degrees of Renal FunctionRenal InsufficiencyNCT05283746AN2 Therapeutics, Inc40
已完成
1 期
Study in Pediatric Subjects Evaluating Pharmacokinetics and Safety of EXPARELPostoperative Pain ManagementNCT03485014Pacira Pharmaceuticals, Inc15
已完成
4 期
EXPAREL Infiltration in Subjects Undergoing Femoral Nerve Block With Bupivacaine HCl for Total Knee ArthroplastyPainNCT02255500Pacira Pharmaceuticals, Inc23
终止
1 期
Study in Adult Subjects Undergoing Posterolateral ThoracotomyPostoperative Pain ManagementNCT03428984Pacira Pharmaceuticals, Inc5