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Study of PAN-90806 Eye Drops, Suspension for Neovascular AMD

Phase 1
Completed
Conditions
Neovascular Age-related Macular Degeneration
Interventions
Drug: PAN-90806 Ophthalmic Suspension
Registration Number
NCT03479372
Lead Sponsor
PanOptica, Inc.
Brief Summary

Double-masked, uncontrolled, multi-center, study in which participants will be randomized to one of 3 doses of topical ocular PAN 90806 administered once daily for 12 weeks.

Detailed Description

Patients with newly diagnosed, active, pathologic CNV associated with neovascular AMD will be screened for inclusion into the study after providing written informed consent. Participants who are eligible for the study will be centrally randomized at Day 1 to one of three doses of PAN-90806 Eye Drops. Participants will be instructed to apply one drop of PAN-90806 to the ocular surface of the identified study eye once daily for twelve (12) weeks.

Participants will return for follow-up visits at Week 2, Week 4, Week 8, Week 12, 1 week after stopping PAN-90806 treatment and 1 month after stopping PAN-90806 treatment.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
51
Inclusion Criteria
  • Diagnosis in the study eye of active, pathologic, newly diagnosed and previously untreated, subfoveal choroidal neovascular (CNV) lesions secondary to neovascular AMD
  • Aged 50 years or older
  • Demonstrate the ability, or have a family member who is willing and able, to instill topical ocular drops in the study eye
Exclusion Criteria
  • Prior ocular or systemic treatment or surgery for neovascular AMD in the study eye
  • Prior use within the last 3 months or a high possibility of requiring treatment with anti-VEGF therapy in the fellow eye during the study
  • Significant retinal serous pigment epithelial detachment (PED), atrophy, or fibrosis/scar involving the fovea
  • History of or current clinical evidence in the study eye of aphakia, diabetic macular edema, any ocular inflammation or infections, pathological myopia, retinal detachment, advanced glaucoma, and/or significant media opacity, including cataract
  • History or evidence of the following surgeries in the study eye: penetrating keratoplasty or vitrectomy; corneal transplant; corneal or intraocular surgery within 3 months of Screening
  • Uncontrolled hypertension despite use of antihypertensive medications
  • Participation in any investigational drug or device study, systemic or ocular, within past 3 months
  • Women who are pregnant or nursing
  • Women of child-bearing potential who are not using a highly effective form of birth control
  • Known serious allergies or hypersensitivity to the fluorescein dye used in angiography or to the components of the PAN-90806 formulation

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
PAN-90806 Eye Drops, dose 2PAN-90806 Ophthalmic SuspensionPAN-90806 Ophthalmic Suspension taken once daily for 12 weeks
PAN-90806 Eye Drops, dose 3PAN-90806 Ophthalmic SuspensionPAN-90806 Ophthalmic Suspension taken once daily for 12 weeks
PAN-90806 Eye Drops, dose 1PAN-90806 Ophthalmic SuspensionPAN-90806 Ophthalmic Suspension taken once daily for 12 weeks
Primary Outcome Measures
NameTimeMethod
Number of participants with treatment-related adverse eventsup to 12 weeks
Secondary Outcome Measures
NameTimeMethod
Mean change from baseline in study eye ETDRS Visual Acuitythrough Week 12
Mean change from baseline in study eye retinal thicknessthrough Week 12
Number of patients needing additional treatment with ranibizumabthrough Week 12

Trial Locations

Locations (16)

Retinal Consultants of Nevada

🇺🇸

Las Vegas, Nevada, United States

Duke University

🇺🇸

Durham, North Carolina, United States

University of Debrecen

🇭🇺

Debrecen, Hungary

Bradford Royal Infirmary

🇬🇧

Bradford, United Kingdom

Moorefields Eye Hospital

🇬🇧

London, United Kingdom

Cumberland Valley Retina Consultants

🇺🇸

Hagerstown, Maryland, United States

Colorado Retina Associates

🇺🇸

Golden, Colorado, United States

Vision Research Center

🇺🇸

Albuquerque, New Mexico, United States

Retina Center of New Jersey

🇺🇸

Teaneck, New Jersey, United States

Axon Clinical

🇨🇿

Praha, Czechia

Fakultní nemocnice Královské Vinohrady

🇨🇿

Praha, Czechia

Semmelweis University

🇭🇺

Budapest, Hungary

P. Stradina Clinical University hospital

🇱🇻

Riga, Latvia

Barnet Hospital

🇬🇧

Barnet, Hertfordshire, United Kingdom

New Cross Hospital

🇬🇧

Wolverhampton, West Midlands, United Kingdom

Manchester Royal Eye Hospital

🇬🇧

Manchester, United Kingdom

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