Prospective, Randomized, Open Label, Phase II Study to Assess Efficacy and Safety of Macugen® (Pegaptanib 0.3 mg Intravitreal Injections) Plus Panretinal Photocoagulation and PRP (Monotherapy) in the Treatment With High Risk PDR.

This is an interventional treatment trial for High Risk Proliferative Diabetic Retinopathy focused on measuring High Risk Proliferative Diabetic Retinopathy, Diabetes Mellitus Type I, Type II, Pegaptanib, Panretinal Photocoagulation Read More

Inclusion Criteria:

• High-risk proliferative diabetic retinopathy (HR-PDR) eyes (as defined in section 2).
• BCVA at baseline > 20/320 (25 letters in the ETDRS Chart) in the study eye.
• Clear ocular media and adequate pupillary dilatation to permit good quality fundus photography.
• Intraocular pressure < 21 mmHg.
• Type I, or Type II diabetic subjects as defined by the WHO criteria of either gender, and aged ≥ 18 years.
• Women must be using effective contraception, be post-menopausal for at least 12 months prior to trial entry, or surgically sterile.
• Ability to provide written informed consent.
• Ability to return for all trial visits.

Exclusion Criteria:

• Eyes with prior scatter (panretinal).
• Focal/grid photocoagulation, within the previous 6 months.
• Fibrovascular proliferation with retinal traction.
• Other cause of retinal neovascularization (retinal vein occlusion, radiation retinopathy or others).
• Atrophy/scarring/fibrosis/ hard exudates involving the center of the macula.
• Subjects who have received YAG laser within the previous 6 months.
• Peripheral retinal cryoablation, or laser retinopexy (for retinal tears only),
• Significant media opacities, which might interfere with visual acuity, assessment of toxicity or fundus photography.
• Subjects should not be entered if there is likelihood that they will require cataract surgery within the following 1 year.
• Any intraocular surgery within 6 months before trial enrolment.
• Previous vitrectomy.
• HbA1C level >11% or recent signs of uncontrolled diabetes.
• Any of the following underlying systemic diseases:

• History or evidence of severe cardiac disease, e.g. NYHA Functional Class III or IV, clinical or medical history of unstable angina, acute coronary syndrome, myocardial infarction, or revascularization procedure within 6 months prior to baseline, or ventricular tachyarrhythmia requiring treatment.

  • History or evidence of clinically significant peripheral vascular disease such as intermittent claudication or prior amputation.
  • Clinically significant impaired renal function (serum creatinine >2.5 mg/dL or s/p renal transplant or receiving dialysis).
  • Clinically significant impaired hepatic function.
  • Stroke (within 12 months of trial entry).
  • Any major surgical procedure within one month before trial enrolment.
• Previous radiation to the head in the region of the study eye.
• Any prior treatment with an investigational agent for diabetic retinopathy or anti-VEGF therapy (including intravitreal, subconjunctival or subtenons corticosteroids) during the past 90 days for any other condition.
• Known serious allergies to fluorescein used in angiography, or to components of Macugen® formulation.
• Systolic BP > 170 (2 different readings) or diastolic BP > 100 (2 different readings).
• Acute ocular or periocular infection.
• Previous filtering surgery (e.g., trabeculectomy) or placement of a glaucoma drainage devise (e.g., tube-shunt surgery).
• Use of other investigational drugs at the time of enrollment.
• History of hypersensitivity to any of the study drugs or to drugs of similar chemical classes.
• History of malignancy of any organ system (other than localized basal cell carcinoma of the skin), treated or untreated, within the past 5 years, regardless of whether there is evidence of local recurrence or metastases.
• Pregnant or nursing (lactating) women, where pregnancy is defined as the state of a female after conception and until the termination of gestation, confirmed by a positive hCG laboratory test (> 5 mIU/mL).
• Women of child-bearing potential, defined as all women physiologically capable of becoming pregnant UNLESS they are: women whose career, lifestyle, or sexual orientation precludes intercourse with a male partner; women whose partners have been sterilized by vasectomy or other means using a highly effective method of birth control (i.e. one that results in a less than 1% per year failure rate when used consistently and correctly, such as implants, injectables, combined oral contraceptives, and some intrauterine devices - IUDs). Periodic abstinence (e.g. calendar, ovulation, symptothermal, post-ovulation methods) are not acceptable.