RecruitingPhase 4NCT05191706

Evaluate the Safety of DEXYCU for the Treatment of Inflammation Following Ocular Surgery for Childhood Cataract

A Phase 3/4, Prospective, Randomized, Active Treatment-Controlled, Parallel-Design, Multicenter Study to Evaluate the Safety of DEXYCU for the Treatment of Inflammation Following Ocular Surgery for Childhood Cataract


Sponsor

EyePoint Pharmaceuticals, Inc.

Enrollment

60 participants

Start Date

Jan 4, 2022

Study Type

INTERVENTIONAL

Conditions

Summary

A Phase 3/4, Prospective, Randomized, Active Treatment-Controlled, Parallel-Design, Multicenter Study to Evaluate the Safety of DEXYCUfor the Treatment of Inflammation Following Ocular Surgery for Childhood Cataract


Eligibility

Max Age: 3 Years

Inclusion Criteria2

  • Undergoing uncomplicated cataract surgery with or without a posterior chamber intraocular lens (IOL) implantation.
  • If a contact lens is used for correction of post-operative aphakia, it must be a silicone elastomer lens or a rigid gas permeable lens (no water content).

Exclusion Criteria6

  • Presence of clinically significant gastrointestinal, cardiovascular, hepatic, renal, hematological, endocrine, neurological, psychiatric, respiratory, or other medical condition that could increase the risk to the subject as determined by the investigator.
  • Has a post-traumatic cataract.
  • Presence of active or suspected viral, bacterial, or fungal disease in the study eye.
  • Ocular hypertension with an IOP in the study eye >25 mmHg at Screening with or without treatment with anti-glaucoma monotherapy.
  • Subjects who have received a periocular corticosteroid injection in the study eye in the 3 months prior to Screening.
  • Subjects who have received any intravitreal corticosteroid delivery vehicle (eg, Retisert®, Ozurdex®, Iluvien®) in the study eye at any time.

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Interventions

DRUGDexamethasone

single anterior chamber injection

DRUGPrednisolone Acetate Ophthalmic

topical administration four times a day for 28 days, followed by treatment taper


Locations(9)

EyePoint Investigational Site

Huntington Beach, California, United States

EyePoint Investigational Site

Palo Alto, California, United States

EyePoint Investigative Site

Boston, Massachusetts, United States

EyePoint Investigational Site

Jackson, Mississippi, United States

EyePoint Investigational Site

Omaha, Nebraska, United States

EyePoint Investigational Site

Buffalo, New York, United States

EyePoint Investigative Site

New York, New York, United States

EyePoint Investigational Site

Rochester, New York, United States

EyePoint Investigational Site

Charleston, South Carolina, United States

View Full Details on ClinicalTrials.gov

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NCT05191706


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