Using Aflibercept Injection to Treat Blood Vessel Growth Over the Cornea

Stopped early · Phase 1 · Has a placebo group

Conditions studied: Corneal Neovascularization

In brief

The cornea is the clear front part of the eye. Corneal neovascularization, the excessive growth of blood vessels into the cornea, is a sight-threatening condition. Corneal neovascularization is also a well recognized risk factor for corneal graft failure. The current standard of care to prevent graft rejection includes use of topical steroids and medicines that suppress the immune system. These medicines do not address corneal neovascularization. The purpose of the study is to establish the safety and potential efficacy of subconjunctival injections of aflibercept (EYLEA® , marketed by Regeneron) injection in inducing regression of blood vessels growing into the cornea and promoting graft survival. This study is being conducted by Dr. Balamurali Ambati at the Moran Eye Center.

Key facts

Study ID

NCT01868360

Run by

Balamurali Ambati

People needed

2

Starts

2013-06-01

Expected to finish

2015-10-01

Last updated by the study team

2015-10-07

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• A patient must meet the following criteria to be eligible for inclusion in the study:
• Candidates for corneal transplantation (only one eye per patient would be enrolled)
• Patients with corneal neovascularization in one or more quadrants crossing more than 1.0 mm over the limbus at time of enrollment in the study
• Willing and able to comply with clinic visits and study-related procedures
• Provide signed informed consent
• Age 18 or over

You may not qualify if…

• A patient who meets any of the following criteria will be excluded from the study:
• Patients receiving antiangiogenic anti-VEGF medication either systemically or intravitreally for other pathology or have received these drugs within 3 months of study enrollment
• Patients with active corneal infection requiring additional treatment modalities
• Patients receiving coumadin with INR >2.0, other anti-thrombotic agents (e.g., aspirin, Plavix) permitted at discretion of investigator
• History of cerebrovascular accident or myocardial infarction within 6 months prior to study enrollment
• Uncontrolled blood pressure- defined as SBP>160 mmHg or DBP >95mmHg while patient is sitting
• Pregnant or breast-feeding women
• Sexually active men* or women of childbearing potential** who are unwilling to practice adequate contraception during the study (adequate contraceptive measures include stable use of oral contraceptives or other prescription pharmaceutical contraceptives for 2 or more menstrual cycles prior to screening; intrauterine device [IUD]; bilateral tubal ligation; vasectomy; condom plus contraceptive sponge, foam, or jelly, or diaphragm plus contraceptive sponge, foam, or jelly) *Contraception is not required for men with documented vasectomy. **Postmenopausal women must be amenorrheic for at least 12 months in order not to be considered of child bearing potential. Pregnancy testing and contraception are not required for women with documented hysterectomy or tubal ligation.

Where it is running

• John A. Moran Eye Center — Salt Lake City, Utah, United States

Full record on ClinicalTrials.gov

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