Extension Study to Gather Data on Effect of Macugen on the Corneal Endothelium

NCT ID: NCT01573572

Last Updated: 2021-01-08

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE4
• Total Enrollment: 131 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2010-04-22
• Study Completion Date: 2019-11-14

Brief Summary

This study was conducted because the FDA requested clinical information on potential effects of intravitreal injections of Macugen (pegaptanib sodium injection) on the corneal endothelium from a 1-year (minimum) post-approval clinical study to support that there are no adverse effects on the corneal endothelium following intravitreal injections of Macugen.

Conditions

Age-Related Macular Degeneration; Retinal Vein Occlusion; Diabetic Macular Edema

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: OTHER
• Blinding Strategy: NONE

Study Groups

Intravitreal Injections of Macugen

Group Type: EXPERIMENTAL

pegaptanib sodium injection

Intervention Type: DRUG

0.3mg of Macugen in a single-use, prefilled glass syringe given every 6 weeks for 48 weeks

Interventions

pegaptanib sodium injection

0.3mg of Macugen in a single-use, prefilled glass syringe given every 6 weeks for 48 weeks

Intervention Type: DRUG

Other Intervention Names

Macugen

Eligibility Criteria

Inclusion Criteria

1. Subjects of either gender aged > or = to 50 years diagnosed with subfoveal neovascular Age-Related Macular Degeneration, Diabetic Macular Edema, or Retinal Vein Occlusion.

2. Best corrected visual acuity in the study eye between 85 and 20 ETDRS letters or between 20/20 and 20/400 using a Snellen chart.

3. Women must be using two forms of effective contraception, be post-menopausal for at least 12 months prior to study entry, or surgically sterile; if of child-bearing potential, a urine pregnancy test must be performed within 7 days prior to the first injection with a negative result. If the test is positive, a serum test must be done to confirm. The two forms of effective contraception must be implemented during the study and for at least 60 days following the last dose of test medication.

4. Provide written informed consent.

5. Ability to return for all study visits.

Exclusion Criteria

Subjects will not be eligible for the study if subjects cannot attend all study-required visits, or if any of the following criteria are present

1. Unilateral ocular blunt trauma within one year of enrollment and no greater than 5% difference in central endothelial cell density between the 2 eyes.

2. intraocular surgery (cataract surgery and surgery for glaucoma without tube shunt or mini-shunt) within one year of enrollment.

3. Anterior segment laser surgery (laser trabeculoplasty) performed within one year of enrollment.

4. Glaucoma tube-shunt surgery

5. Previous history of corneal transplant in the study or non-study eye

6. Presence of vitreous macular traction

7. Previous therapeutic radiation in the region of the study eye

8. Any treatment with an investigational agent in the past 30 days for any condition

9. Known serious allergies to the components of pegaptanib sodium formulation

Any of the following underlying diseases including:1. History or evidence of severe cardiac disease(e.g. NYHA Functional Class III or IV - see Appendix 2), clinical or medical history of unstable angina, acute coronary syndrome, myocardial infarction or revascularization within 6 months, ventricular tachyarrhythmias requiring ongoing treatment 7. History or evidence of clinically significant peripheral vascular disease, such as intermittent claudication or prior amputation 8. History or evidence of clinically significant impaired renal or hepatic function 8. Stroke (within 12 months of study entry) 9. Any major surgical procedure within one month of study entry 10. Significant media opacities, including cataract, which might interfere with visual acuity, assessment of toxicity. Subjects should not be entered if there is likelihood that they will require cataract or glaucoma surgery in either eye during the study treatment and follow-up period.

• Minimum Eligible Age: 50 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Bausch & Lomb Incorporated

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Mandeep Kaur, M.D.

Role: STUDY_DIRECTOR

Valeant Pharmaceuticals NA

Locations

Marietta Eye Clinic

Murrieta, California, United States

Wolfe Eye Clinic

Marshalltown, Iowa, United States

Associates in Ophthalmology

West Mifflin, Pennsylvania, United States

Valley Retina Institute

Harlingen, Texas, United States

Countries

United States

Provided Documents

Document Type: Study Protocol and Statistical Analysis Plan

View Document

Other Identifiers

EOP 1024

Identifier Type: -

Identifier Source: org_study_id