Status:
COMPLETED
To Compare the Safety and Efficacy of Perrigo's Product to an FDA Approved Product for the Treatment of Glaucoma or Ocular Hypertension in Both Eyes
Lead Sponsor:
Padagis LLC
Conditions:
Glaucoma, Open-Angle
Ocular Hypertension
Eligibility:
All Genders
18+ years
Phase:
PHASE3
Brief Summary
To compare the safety and efficacy of Perrigo's product to an FDA approved product in the treatment of Primary Open Angle Glaucoma or Ocular Hypertension in Both Eyes.
Eligibility Criteria
Inclusion
- Male or nonpregnant females aged at least 18 years with chronic open angle glaucoma or ocular hypertension in both eyes
- Subject requires treatment of both eyes and is able to discontinue use of all ocular hypotensive medication(s) or switch ocular hypotensive medications and undergo appropriate washout period.
- Adequate wash-out period prior to baseline of any ocular hypotensive medication.
- Baseline (Day 0/hour 0) pressure ≥ 22 mm Hg and ≤ 34 mm Hg in each eye and any asymmetry of pressure between the eyes no greater than 5 mm Hg.
- Baseline best corrected visual acuity equivalent to 20/200 or better in each eye
Exclusion
- Females who are pregnant, breast feeding, or planning a pregnancy.
- Females of childbearing potential who do not agree to utilize an adequate form of contraception
- Current, or past history of, severe hepatic or renal impairment
- Current, or history within two months prior to baseline of, significant ocular disease, e.g., corneal edema, uveitis, ocular infection, or ocular trauma in either eye
- Current corneal abnormalities that would prevent accurate readings with the Goldmann applanation tonometer
- Functionally significant visual field loss
- Contraindication to brinzolamide or sulfonamide therapy or known hypersensitivity to any component of brinzolamide or sulfonamide therapy
- Use at any time prior to baseline of an intraocular corticosteroid implant
- Use within one week prior to baseline of contact lens
- Use within two weeks prior to baseline of: 1) topical ophthalmic corticosteroid, or 2) topical corticosteroid
- Use within one month prior to baseline of: 1) systemic corticosteroid or 2) high-dose salicylate therapy
- Use within six months prior to baseline of intravitreal or subtenon injection of ophthalmic corticosteroid
- Having undergone within six months prior to baseline any other intraocular surgery (e.g., cataract surgery)
- Having undergone within twelve months prior to baseline refractive surgery, filtering surgery, or laser surgery for pressure reduction
Key Trial Info
Start Date :
June 24 2019
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
April 30 2020
Estimated Enrollment :
495 Patients enrolled
Trial Details
Trial ID
NCT04024072
Start Date
June 24 2019
End Date
April 30 2020
Last Update
March 6 2023
Active Locations (1)
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1
James D. Branch Ophthalmology
Winston-Salem, North Carolina, United States, 27101