A Single Centre, Double-blind, Placebo Controlled Crossover Study in Elderly Male Subjects to Investigate the Plarmacodynamic Interaction of VA106483 Administered Concomitanctly With Alpha-blocker Therapy
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 发起方
- Vantia Ltd
- 入组人数
- 12
- 试验地点
- 1
- 主要终点
- Blood pressure, Heart rate
研究概览
简要总结
The main purpose of this study is to investigate whether the hypotensive effects of an alpha-blocker are increased when VA106483 is given at the same time.
详细描述
VA106483 is intended to be used as a treatment for patients suffering from nocturia (defined as waking to urinate at least once per night between periods of sleep). Nocturia is a condition that often worsens as sufferers get older. This may be due to an over-active bladder muscle, the bladder being able to hold less urine at night-time or over production of urine in the bladder at night. Some of the treatments available for nocturia have side-effects which make them unsuitable for elderly patients. These side-effects have not been seen in studies with VA106483, which makes it potentially suitable for treating elderly patients.
Nocturia is commonly associated with Benign Prostatic Hypertrophy (or BPH, a non-cancerous enlargement of the prostate gland, which often results in problems passing water). Of the patients who suffer from BPH, an estimated 40-85% experience the symptoms of waking at night to pass water.
Treatments which are commonly prescribed for BPH include alpha-blockers which work by improving urine flow by a muscle relaxant effect. Alpha-blockers are known to cause hypotension (lowering of blood pressure which can cause dizziness in some patients) . Since it is likely that subjects may be co-prescribed VA106483 and alpha-blockers, the purpose of this study is to determine that giving VA106483 does not increase the hypotensive effects of alpha-blockers
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
- 65 Years 至 —(Older Adult)
- 性别
- Male
- 接受健康志愿者
- 是
入选标准
- •Male aged 65 years of age and above
- •No clinically important abnormal physical, laboratory or vital sign findings in the opinion of the Investigator
- •Provision of written informed consent to participate
- •No recent alpha-blocker therapy
- •Not taking any concomitant medication known to be a cytochrome 3A4 inhibitor
- •Not taking any prescribed or over the counter medications unless agreed with the Investigator and Sponsor
- •No evidence of serious pathology or disease including poorly controlled endocrine disorders; active liver or biliary disease or severe kidney problems; syndrome of inappropriate antidiuretic hormone secretion
- •No history of orthostatic hypotension or syncope.
- •No known hypersensitivity to the IMP or alpha blocker, including severe lactose intolerance.
- •No history of drug or alcohol abuse
- •Negative for HIV, hepatitis B or C
排除标准
- 未提供
研究组 & 干预措施
VA106483
干预措施: VA106483 (Drug)
Sugar pill
干预措施: Placebo (Drug)
结局指标
主要结局
Blood pressure, Heart rate
时间窗: For 8 hours after dosing
次要结局
未报告次要终点
