Treatment of Corneal Neovascularization With Topical Pazopanib

Completed · Phase 1/Phase 2

Conditions studied: Corneal Neovascularization

In brief

The purpose of this study is to determine the safety and efficacy of a drug \[Pazopanib (Votrient)\] as a treatment for corneal neovascularization. The cornea is the clear, central portion of the eye and neovascularization means blood vessel growth. The cornea is typically avascular, or without blood vessels. Corneal neovascularization in the cornea and can put vision at risk. Numerous diseases of the cornea such as inflammation, ischemia (restriction of blood supply), infection, degeneration (or deterioration), trauma, or corneal stem cell deficiency can lead to corneal neovascularization. This major ocular complication can lead to corneal scarring, edema (swelling), lipid deposits, and inflammation that may significantly alter your vision. In addition, it worsens the outcome of potential future treatments, such as a corneal transplant. A corneal transplant is a treatment that many patients with severe corneal disease may ultimately need.

Key facts

Study ID

NCT01257750

Run by

Reza Dana, MD

People needed

20

Starts

2010-11-01

Expected to finish

2012-01-01

Last updated by the study team

2018-01-18

Who can join

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

You may qualify if…

• Ability to provide written informed consent
• Ability to comply with study assessments and study requirements (for example, able to open the eye drop foil-wrap packaging and eye drop vials, willing to adhere to the daily dosing schedule) for the full duration of study
• Age > 18 years
• Patients with superficial or deep corneal neovascularization that extends farther than 1 mm from the limbus
• Patients are in stable overall health
• Alanine aminotransferase (ALT), aspartate aminotransferase (AST), alkaline phosphatase and bilirubin ≤ 1.5x upper limit of normal (ULN) or isolated bilirubin >1.5x ULN is acceptable if bilirubin is fractionated and direct bilirubin <35%
• Single QTcF < 450 msec; or QTcF < 480 msec in subjects with Bundle Branch Block
• A female is eligible to enter and participate in this study if she is of Non-childbearing potential (i.e., physiologically incapable of becoming pregnant),

You may not qualify if…

• Current or chronic history of liver disease, or known hepatic or biliary abnormalities (with the exception of Gilbert's syndrome or asymptomatic gallstones)
• History of any clotting disorder, including predisposition to hypercoagulation or any previous thromboembolic event
• Major surgery within 1 month of screening
• Has received treatment with anti-VEGF agents (topical, intraocular or systemic) within 60 days of study entry. This includes both approved and investigational treatments.
• Has received investigational therapy within 60 days prior to study entry
• Concurrent enrollment in another clinical investigational medicinal product or device study
• Concurrent use of anti-VEGF agents
• Corneal or ocular surface infection within 30 days prior to study entry
• Full thickness or lamellar keratoplasty within 90 days prior to study entry
• Other ocular surgeries within 60 days prior to study entry
• Ocular or periocular malignancy
• Soft Contact lens (excluding bandage contact lens) use within 2 weeks prior to study entry
• Persistent epithelial defect (>1mm and ≥14 days duration) within 2 weeks prior to study entry
• Intravitreal or periocular steroids within 4 weeks prior to study entry
• Change in dose/frequency of topical steroids and/or nonsteroidal anti-inflammatory drugs (NSAIDs) within 2 weeks prior to study entry
• Poorly controlled Hypertension: systolic blood pressure (BP) > 150 or diastolic BP > 90
• Medical history of uncontrolled diabetes mellitus, with hemoglobin A1c (HbA1c) >7%
• Women 45 years of age or younger that are of child bearing potential as defined by:
• No history of a hysterectomy
• No history of a bilateral oophorectomy (ovariectomy)
• No history of a bilateral tubal ligation
• Not post-menopausal
• Subjects using hormone replacement therapy (HRT) that have experienced total cessation of menses for ≤ 1 year, OR, in questionable cases, have a follicle stimulating hormone (FSH) value <40 mIU/mL and an estradiol value > 40pg/mL (>140 pmol/L) OR have documented evidence OR have had documented evidence of menopause based on FSH and estradiol concentrations prior to initiation of HRT. Signs of current infection, including fever and current treatment with antibiotics
• Participation in another simultaneous medical investigation or trial STUDY

Where it is running

• Massachusetts Eye and Ear Infirmary — Boston, Massachusetts, United States

Full record on ClinicalTrials.gov

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