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Comparison of PDT Combination With Ranibizumab vs. Ranibizumab Monotherapy in Persistent PCV With Initial Loading Dose

Phase 4
Conditions
Age-related Macular Degeneration
Interventions
Registration Number
NCT02864472
Lead Sponsor
Seoul National University Hospital
Brief Summary

The aim of this study is to compare the efficacy of early intervention of PDT combination compared with consecutive monthly treatment of intravitreal ranibizumab injections in PCV patients showing insufficient response with initial loading dose.

Detailed Description

PCV is generally recognized as a subtype of wet AMD characterized by the presence of aneurysmal orange-red polypoidal lesions with or without branching vascular network (BVN) in the choroidal vasculature as observed on indocyanine angiography (ICGA), representing 13% to 54.7% of newly diagnosed patients with neovascular AMD. Fifty percent of PCV had persistent leakage or recurrent bleeding with poor visual outcome, if left untreated.

And in the EVEREST study has shown that synergistic effects of anti-VEGF and vPDT combination: vPDT strongly regress polyp and anti-VEGF control to up-regulation of VEGF induced by vPDT compared to ranibizumab monotherapy in newly diagnosed PCV patients. Additionally, combination offers an opportunity for individualized treatment with potentially fewer treatments and less costs.

Therefore, the aim of this study is to compare the efficacy of early intervention of PDT combination compared with consecutive monthly treatment of intravitreal ranibizumab injections in PCV patients showing insufficient response with initial loading dose.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
40
Inclusion Criteria
  1. Age equal to or older than 50 years
  2. Insufficient responder to ranibizumab Tx
  3. ICGA-confirmed PCV
  4. BCVA letter score of 73 to 24 using Early Treatment of Diabetic Retinopathy Study charts
  5. Ability to provide written informed consent and comply with study assessments for the full duration of the study
Exclusion Criteria
  1. Prior treatment with other anti-VEGF treatments in the study eye.
  2. Prior treatment with other anti-VEGF treatments within 3 months prior to Visit 1 in the non-study eye.
  3. Prior treatment with verteporfin within 6 months prior to Visit 1 in the study eye.
  4. Prior treatment with verteporfin within 7 days prior to Visit 1 in the non-study eye.
  5. Previous subfoveal focal laser photocoagulation involving the foveal center in the study eye
  6. Previous submacular surgery in the study eye
  7. A history of angioid streaks, presumed ocular histoplasmosis syndrome, or pathologic myopia
  8. Experienced RPE tear, retinal detachment, macular hole, or uncontrolled glaucoma
  9. Previous participation in a clinical trial involving anti-angiogenic drugs
  10. Intraocular surgery: 2 months before Visit 1 in the study eye.
  11. Previous participation in any studies of investigational drugs
  12. Administration of periocular, intravitreal, or systemic corticosteroid in the previous 3 months.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
combination TxPDTcombination Tx(vPDT +ranibizumab) (M0) + ranibizumab PRN (M3-6)
combination Txranibizumab PRNcombination Tx(vPDT +ranibizumab) (M0) + ranibizumab PRN (M3-6)
mono Txranibizumab PRNRanibizumab (at 4 weeks interval) \*3 (M0-2) + ranibizumab PRN (M3-6)
mono TxRanibizumabRanibizumab (at 4 weeks interval) \*3 (M0-2) + ranibizumab PRN (M3-6)
Primary Outcome Measures
NameTimeMethod
Change in central retinal thicknessafter 6month

Change in central retinal thickness measured by OCT

Secondary Outcome Measures
NameTimeMethod
Change of ETDRS BCVAafter 6month

Change of ETDRS BCVA from baseline to 26 weeks and time course of it

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