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Phase 3 N=438 Randomized Double-blind Treatment

OTX-15:003: A Phase 3 Study Evaluating the Safety and Efficacy of OTX-DP for the Treatment of Ocular Inflammation and Pain After Cataract Surgery

Post-Surgical Ocular Pain · Post-Surgical Ocular Inflammation

Enrolled (actual)
438
Serious AEs
1.1%
Results posted
Oct 2017
Primary outcome: Primary: Absence of Anterior Chamber Inflammation — 52.3; 31.1 percentage of total participants

Study Design & Population

Study type
Interventional
Phase
Phase 3
Interventions
Dexamethasone (Drug); Placebo Vehicle (Other)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Ocular Therapeutix, Inc.
Primary completion
May 2016

Outcome Measures

OutcomeResultp-value
PRIMARY
Absence of Anterior Chamber Inflammation
52.3; 31.1
PRIMARY
Absence of Ocular Pain
79.6; 61.3

Summary

The objective of the study was to evaluate the safety and efficacy of OTX-DP (dexamethasone insert) 0.4 mg for intracanalicular use when placed in the canaliculus of the eyelid for the treatment of post-surgical inflammation and pain in subjects who had undergone cataract extraction with intraocular lens implantation

Eligibility Criteria

Inclusion Criteria

  • Has a cataract and is expected to undergo clear corneal cataract surgery with phacoemulsification and implantation of posterior chamber lens
  • Has a potential post-operative pinhole corrected Snellen VA of at least 20/200 or better in both eyes

Exclusion Criteria

  • Any intraocular inflammation in the study eye present during the screening slit lamp examination
  • Score greater than "0" on the Ocular Pain Assessment in the study eye at Screening
  • Any intraocular inflammation in the study eye present during the screening slit lamp examination
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02736175). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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