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Anti-VEGF Therapy

Macugen (Pegaptanib Sodium) for Diabetic Retinopathy

Phase 1
Waitlist Available
Research Sponsored by Retina Institute of Hawaii
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
* Subjects of either gender aged 75 years or below diagnosed with tractional retinal detachment secondary to proliferative diabetic retinopathy.
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 5 years
Awards & highlights

Summary

Primary objective of this trial will be to evaluate the safety and efficacy of intravitreal injections of Macugen (pegaptanib sodium) when given at least 7-14 days prior to vitrectomy in subjects with tractional retinal detachment (with or withoutmacular involvement) secondary to proliferative diabetic retinopathy. Secondary objective is to evaluate regression of neovascularization and progression of macular traction utilizing OCT and fundus photographs.

Eligible Conditions
  • Diabetic Retinopathy

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 5 years
This trial's timeline: 3 weeks for screening, Varies for treatment, and up to 5 years for reporting.

Treatment Details

Trial Design

1Treatment groups
Experimental Treatment
Group I: Macugen (Pegaptanib Sodium)Experimental Treatment1 Intervention
Open-label, single-center trial. Subjects will recieve intravitreous injections of Macugen 7-14 days before Vitrectomy.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Pegaptanib
FDA approved

Find a Location

Who is running the clinical trial?

Retina Institute of HawaiiLead Sponsor
7 Previous Clinical Trials
760 Total Patients Enrolled
1 Trials studying Diabetic Retinopathy
500 Patients Enrolled for Diabetic Retinopathy
~0 spots leftby Sep 2025
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