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临床试验/NCT02050828
NCT02050828已完成2 期

A Phase 2, Randomized, Active-Controlled, Double-Masked, Multi-Center Study to Assess the Safety and Efficacy of Daily Subcutaneous AKB-9778 Administered for 3 Months, as Monotherapy or Adjunctive to Ranibizumab, in Subjects With Diabetic Macular Edema

Aerpio Therapeutics0 个研究点目标入组 144 人开始时间: 2014年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
144
主要终点
Mean change from baseline in spectral domain optical coherence tomography (sdOCT)-measured central subfield thickness (CST)

研究概览

简要总结

The purpose of this study is to evaluate the safety and efficacy of AKB-9778 administered as daily subcutaneous injections with and without monthly intravitreal injections of ranibizumab for 3 months in patients with diabetic macular edema.

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

AKB-9778 15 mg BID monotherapy

Experimental

Subcutaneous AKB-9778 15 mg BID (total daily dose of 30 mg/day) plus monthly sham intravitreal injection for 3 months.

干预措施: AKB-9778 (Drug)

AKB-9778 15 mg BID monotherapy

Experimental

Subcutaneous AKB-9778 15 mg BID (total daily dose of 30 mg/day) plus monthly sham intravitreal injection for 3 months.

干预措施: Sham (Drug)

AKB-9778 15 mg BID + ranibizumab 0.3 mg

Experimental

Subcutaneous AKB-9778 15 mg BID (total daily dose of 30 mg/day) plus ranibizumab 0.3 mg monthly intravitreal injection for 3 months.

干预措施: AKB-9778 (Drug)

AKB-9778 15 mg BID + ranibizumab 0.3 mg

Experimental

Subcutaneous AKB-9778 15 mg BID (total daily dose of 30 mg/day) plus ranibizumab 0.3 mg monthly intravitreal injection for 3 months.

干预措施: ranibizumab (Drug)

ranibizumab 0.3 mg monotherapy

Active Comparator

Placebo subcutaneous injection (BID) plus ranibizumab 0.3 mg monthly intravitreal injection for 3 months.

干预措施: ranibizumab (Drug)

ranibizumab 0.3 mg monotherapy

Active Comparator

Placebo subcutaneous injection (BID) plus ranibizumab 0.3 mg monthly intravitreal injection for 3 months.

干预措施: Placebo (Drug)

结局指标

主要结局

Mean change from baseline in spectral domain optical coherence tomography (sdOCT)-measured central subfield thickness (CST)

时间窗: Month 3

次要结局

  • Mean change from baseline in Early Treatment Diabetic Retinopathy Study (ETDRS) Best Corrected Visual Acuity (BCVA)(Month 3)

研究者

发起方
Aerpio Therapeutics
申办方类型
Industry
责任方
Sponsor

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