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A Study of the Response to AG-86893 in Patients With Pterygium Hyperemia

Phase 2
Completed
Conditions
Pterygium
Interventions
Drug: 0.1% AG-86893 Eye Drops
Drug: Vehicle Eye Drops
Drug: 0.3% AG-86893 Eye Drops
Registration Number
NCT03533244
Lead Sponsor
Allgenesis Biotherapeutics Inc.
Brief Summary

A pterygium is a wing-shaped, benign tissue growth which forms on the surface of the conjunctiva and grows towards the cornea. It can eventually lead to vision impairment. The precise cause of pterygium formation is unknown but new blood vessel growth and fibroblastic structures are characteristics of the disease. AG-86893 is an eye drop being developed to treat hyperemia (redness) and growth of the pterygium.

Hypothesis

1. AG-86893 dosed three times daily for 28 consecutive days has an acceptable safety profile as measured by the incidence and severity of adverse events (AEs) compared with vehicle

2. At least 1 concentration of AG-86893 is effective, as measured by the mean change from baseline in conjunctival hyperemia (redness), compared with vehicle

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
64
Inclusion Criteria
  • Good health with no clinically significant findings based on the medical history, electrocardiogram, vital signs, blood chemistry, hematology, and urinalysis findings, as determined by the investigator
  • Females of childbearing potential must have a negative pregnancy test at baseline and must be on established, adequate contraception and males must use condoms if their partner is of childbearing potential and their female partner should also use an additional effective means of contraception, or they must agree to abstain from sexual intercourse with a female partner for the duration of the study; contraception should be continued for 3 months after the last dose.
  • Presence of pterygium with associated conjunctival hyperemia (redness) of grade ≥2 as assessed by a central reading center.
Exclusion Criteria
  • History or presence of any ocular diseases other than pterygium or its sequelae (after-effects), including neoplasia (uncontrolled overgrowth)
  • Diagnosis of ocular hypertension or glaucoma requiring use of intraocular pressure-lowering medication
  • Use of contact lenses during the study in the study eye
  • History or evidence of ocular surgeries in the study eye at any time
  • History of liver dysfunction or current abnormal liver enzymes
  • Pregnancy, plans for pregnancy, or breastfeeding during the study

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
0.1% AG-86893 Eye Drops0.1% AG-86893 Eye DropsOne drop, three times daily to the study eye for 28 days
Vehicle Eye DropsVehicle Eye DropsOne drop, three times daily to the study eye for 28 days
0.3% AG-86893 Eye Drops0.3% AG-86893 Eye DropsOne drop, three times daily to the study eye for 28 days
Primary Outcome Measures
NameTimeMethod
Change From Baseline in Overall Conjunctival Hyperemia ScoreBaseline and Day 28

Assessed by digital ocular photography; each quadrant of the eye (superior, inferior, nasal, temporal) will be scored using a 5-point scale (0 = none, 1 = mild, 2 = moderate, 3 = severe, and 4 = very severe) and graded by a reading center. The overall conjunctival score is the average of the four quadrants. Assessments are made by subtracting the score at Baseline from the score on Day 28. An increase in value indicates worsening of hyperemia, while a decrease indicates improvement.

Secondary Outcome Measures
NameTimeMethod
Change From Baseline in Conjunctival Hyperemia Score in the Quadrant With the PterygiumBaseline and Day 28

Assessed by digital ocular photography; the quadrant with the pterygium will be scored using a 5-point scale (0 = none, 1 = mild, 2 = moderate, 3 = severe, and 4 = very severe) and graded by a reading center. Assessments are made by subtracting the score at Baseline from the score on Day 28. An increase in value indicates worsening of hyperemia, while a decrease indicates improvement.

Trial Locations

Locations (6)

Essendon Eye Clinic

🇦🇺

Essendon, Victoria, Australia

The Geelong Eye Centre

🇦🇺

Waurn Ponds, Victoria, Australia

H2Vision Centre

🇦🇺

Sippy Downs, Queensland, Australia

Bendigo Eye Clinic

🇦🇺

Bendigo, Victoria, Australia

Lions Eye Institute

🇦🇺

Nedlands, Western Australia, Australia

M.T. Coroneo Pty Ltd

🇦🇺

Randwick, New South Wales, Australia

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