Evaluating NCX 470 vs. Latanoprost in Subjects With Open-Angle Glaucoma or Ocular Hypertension (Denali)

In by alicia.green

Evaluating NCX 470 vs. Latanoprost in Subjects With Open-Angle Glaucoma or Ocular Hypertension (Denali)

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A Phase 3, Randomized, Multi-Regional, Double-Masked, Parallel-Group Trial Evaluating the Safety and Efficacy of NCX 470 0.1% vs. Latanoprost 0.005% in Subjects With Open-Angle Glaucoma or Ocular Hypertension (Denali)

clinicaltrials.gov

Eligibility

Inclusion Criteria
  1. Diagnosis of open-angle glaucoma or ocular hypertension in both eyes
  2. Qualifying IOP at 3 time points through the day at 2 visits following washout of IOP-lowering medication, if applicable
  3. Qualifying best-corrected visual acuity in each eye
  4. Ability to provide informed consent and follow study instructions
Exclusion Criteria
  1. Narrow anterior chamber angles or disqualifying corneal thickness in either eye
  2. Clinically significant ocular disease in either eye
  3. Previous complicated surgery or certain types of glaucoma surgery in either eye
  4. Incisional ocular surgery or severe trauma in either eye within the past 6 months
  5. Uncontrolled systemic disease
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