NCT01721707撤回3 期
Safety and Efficacy to Reduce the IOP of the Fixed Association of Latanoprost 0.005% (50 μg/mL)/ Brinzolamide 1% (10mg/mL) Drops, Compared to Latanoprost 0.005% (50 μg/mL) Drops, in Patients With Open Angle Glaucoma or Ocular Hypertension
适应症
干预措施
相关药物
试验速览
- 阶段
- 3 期
- 状态
- 撤回
- 试验地点
- 1
- 主要终点
- IOP
研究概览
简要总结
This study is a double-masked, randomized, parallel group study in patients with open angle glaucoma or ocular hypertension.
The aim of this study is to verify the efficacy of the fixed combination of Latanoprost 50 mcg / mL / brinzolamide 10mg/ml eye drops compared to Latanoprost 50μg/mL eye drops in reducing IOP
详细描述
The study is divided into two sequential phases. The Phase I trial is a Phase Screening / Eligibility, which includes a screening visit, followed by 2 Visits Eligibility (3 visits). The Phase II study is the treatment phase randomized, double-masked that includes visits during therapy at Week 2, Week 6 and Month 3
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Double (Participant, Investigator)
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients 18 years of age or older, of either gender and of any race / ethnicity, diagnosed with open angle glaucoma or ocular hypertension, which in the opinion of the investigator does not have enough control with monotherapy or already receiving multiple medications for lowering IOP .
- •Patients should be able to understand and sign an informed consent form that has been approved by an Institutional Review Board.
- •Measurements of mean IOP in at least 1 eye:
- •≥ 24 mmHg and ≤ 36 mmHg at timepoint 9am and
- •≥ 21 mmHg and ≤ 36 mmHg in the 11h timepoint in both Visits Eligibility 1 and after washout of any medication to reduce IOP.
- •The mean IOP should not be> 36 mmHg at any timepoint
排除标准
- •Fertile women (those not surgically sterile or postmenopausal for at least 1 year) are excluded from study participation if meet any of the following conditions:
- •currently pregnant or
- •have tested positive in urine pregnancy Screening Visit or
- •planning to become pregnant during the study period, or
- •are breastfeeding, or not using highly effective contraceptive precautions.
- •Patients with angle Schaffer Grade <2, as measured by gonioscopy (extreme narrow angle with complete or partial closure).
- •Patients with a ratio cup / disc greater than 0.80 (horizontal or vertical).
- •Patients presenting with loss of central visual field impairment. The loss of central visual field is defined as a serious sensitivity less than or equal to 10 dB in at least four points of two visual field test closest to the point of attachment.
- •Patients who can not safely discontinue use of all medications to ocular IOP reduction for a minimum of 5 days ± 1 day to 28 days ± 1 day prior to Visit E
- •Chronic inflammatory eye disease, recurrent or severe (ie, scleritis, uveitis, herpetic keratitis).
- •Ocular trauma in the past 6 months.
- •Eye infection or inflammation of the eye in the last 3 months.
- •Retinal disease as clinically significant or progressive retinal degeneration, diabetic retinopathy or retinal detachment.
- •Best score corrected visual acuity (BCVA) worse than 55 ETDRS letters (equivalent to approximately 20/80 Snellen).
- •Another ocular pathology (including severe dry eye) that may, in the opinion of the investigator, preventing the administration of an alpha-adrenergic agonist and/or an inhibitor of topical carbonic anhydrase (CAI).
- •Intraocular surgery within the last 6 months.
- •Laser eye surgery in the last 3 months.
- •Any abnormality that prevents a reliable applanation tonometry.
- •Any other condition including severe illness that would make the patient, in the opinion of the investigator, unsuitable for the study.
- •History of cardiovascular disease (eg, coronary heart disease, hypertension, Raynaud's phenomenon, orthostatic hypotension, thromboangiitis), cerebrovascular (eg, cerebral insufficiency), active liver or kidney, severe, unstable or uncontrolled that would prevent the safe administration of an alpha-adrenergic topic or CAI in the opinion of the investigator.
- •Related to previous or concomitant medications
- •Patients with recent use (within 4 weeks of Visit Eligibility 1) salicylate therapy with high dose (> 1 g daily).
- •Current or planned treatment with any psychotropic drug that increases the adrenergic response (eg, desipramine, amitriptyline).
- •Concomitant use of monoamine oxidase inhibitors.
- •Therapy with another investigational agent within 30 days prior to the Screening Visit.
- •Hypersensitivity to the drug alpha-adrenergic agonists, oral or topical CAIs, sulfonamide derivatives or any component of the study drugs in the opinion of the investigator.
- •Less than 30 days regimen with stable administration before the Screening Visit any medications or substances administered by any route and used chronically that may affect IOP, including among others, β-adrenergic blocking agents.
- •Use of ocular hypotensive medication any additional topical or systemic throughout the study.
- •Concomitant use of glucocorticoids administered by any route.
研究组 & 干预措施
Latanoprost+Brinzolamide combination
Experimental
Latanoprost 0.005%(50 mg/ml)+brinzolamide 1%(10mg/ml) eye drops
干预措施: Latanoprost+Brinzolamide combination (Drug)
Latanoprost
Active Comparator
Latanoprost 0.005% (50 mg / ml)
干预措施: Latanoprost (Drug)
结局指标
主要结局
IOP
时间窗: Month 3
Change in mean diurnal IOP compared to baseline (Month 3)
次要结局
- IOP measures(week 2, week 6, month 3)
- IOP changes(week 2, week 6, month 3)
研究者
研究点 (1)
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