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临床试验/NCT06599684
NCT06599684已完成2 期

Phase 2a Pilot, Open Label, Multicenter, Study of INV-102 Ophthalmic Solution in Subjects With Diabetic Macular Edema (DME) Associated With Non-proliferative Diabetic Retinopathy (NPDR)

Invirsa, Inc.1 个研究点 分布在 1 个国家目标入组 19 人开始时间: 2024年9月7日最近更新:
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
Invirsa, Inc.
入组人数
19
试验地点
1
主要终点
Change from baseline in the Early Treatment Diabetic Retinopathy (ETDRS) Diabetic Retinopathy Severity Scale (DRSS) score

研究概览

简要总结

Phase 2 study to assess the efficacy of topically administered eyedrops of INV-102 during a 12-week dosing period in subjects with non-center involved DME (NCIDME) associated with NPDR [Part 1] and during an 8-week dosing period in subjects with center-involved DME (CIDME) associated with NPDR [Part 2].

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

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

入选标准

  • Male or female subjects ≥ 18 years of age and < 76 years of age
  • Diagnosed with diabetes (Type 1 or 2) with hemoglobin A1c ≤ 12.0%
  • Study eye must have NCIDME (Part 1) or CIDME (Part 2)
  • Study eye must be moderate to severe NPDR

排除标准

  • Prior laser treatment for DR in the study eye within 12 months from Screening Visit

研究组 & 干预措施

Part 1: INV-102 0.7% in NCIDME

Experimental

INV-102 0.7% Ophthalmic Solution given three times daily (TID) for 2 weeks followed by twice daily (BID) for 10 weeks

干预措施: INV-102 (Drug)

Part 2: INV-102 0.7% in CIDME

Experimental

INV-102 0.7% Ophthalmic Solution given three times daily (TID) for 2 weeks followed by twice daily (BID) for 6 weeks

干预措施: INV-102 (Drug)

结局指标

主要结局

Change from baseline in the Early Treatment Diabetic Retinopathy (ETDRS) Diabetic Retinopathy Severity Scale (DRSS) score

时间窗: Day 84 (Part 1) and Day 56 (Part 2)

Graded by an independent central reading center using Wide-field Color Fundus Photography. The DRSS divides diabetic retinopathy into levels ranging from absence of retinopathy (score = 10) to advanced retinopathy (score = 85). The scale is used to describe overall retinopathy severity as well as the change in severity over time.

Change from baseline in central subfield thickness (Part 2 only)

时间窗: Day 56

Measured using spectral domain optical coherence tomography (SD-OCT) and determined by an independent central reading center.

次要结局

  • Change from baseline in macular volume(Day 84 (Part 1) and Day 56 (Part 2))
  • Change from baseline in subfield thickness(Day 84 (Part 1) and Day 56 (Part 2))
  • Change from baseline in the retinal thickness at the thickest point of the subfield thickness(Day 84 (Part 1) and Day 56 (Part 2))
  • Change in best corrected visual acuity (BCVA) (Part 2 only)(Day 56)

研究者

发起方
Invirsa, Inc.
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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