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Phase 2 N=69 Randomized Quadruple-blind Treatment

Safety and Efficacy of TOP1630 for Dry Eye Syndrome

Dry Eye Syndrome

Enrolled (actual)
69
Serious AEs
0.0%
Results posted
Feb 2024
Primary outcome: Primary: Visual Acuity — 0.05; -0.09; 0.017; 0.075 logMAR

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
TOP1630 Ophthalmic Solution (Drug); Placebo to TOP1630 Ophthalmic Solution (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
ORA, Inc.
Primary completion
Jun 2017

Outcome Measures

OutcomeResultp-value
PRIMARY
Visual Acuity
0.05; -0.09; 0.017; 0.075
PRIMARY
Slit-lamp Biomicroscopy
6; 2; 31; 30
PRIMARY
Drop Comfort Assessment
0.71; 1.38
PRIMARY
Intraocular Pressure
12.3; 15.5; 12.4; 12.8
PRIMARY
Corneal Sensitivity
59.8; 59.4
PRIMARY
Undilated Fundoscopy
31; 30
PRIMARY
Vital Signs - Pulse
64.3; 75.0; 68.8; 70.5
PRIMARY
Vital Signs - O2 Saturation
95.8; 97.0; 96.3; 95.7
PRIMARY
Vital Signs - Systolic Blood Pressure
128.0; 148.5; 120.9; 128.2
PRIMARY
Vital Signs - Diastolic Blood Pressure
72.7; 89.5; 71.2; 72.0
SECONDARY
Ocular Discomfort
3.5; 3.9 0.02 sig
SECONDARY
Dry Eye Symptoms
1.7; 2.8 0.0001 sig
SECONDARY
Dry Eye Signs
5.88; 6.60 0.03 sig
SECONDARY
Tear Film Break up Time
1.629; 1.480 0.39
SECONDARY
Schirmer's Test
6.2; 6.7 0.97
SECONDARY
Daily Symptom Assessment
2.33; 2.69 0.06

Summary

In subjects with Dry Eye Syndrome: The primary objective of this study is to compare the safety and tolerability of TOP1630 Ophthalmic Solution to placebo. The secondary objectives are to compare the efficacy of TOP1630 Ophthalmic Solution to placebo for the treatment of the signs and symptoms of dry eye syndrome.

Eligibility Criteria

Inclusion Criteria

  • Be at least 18 years of age;
  • Provide written informed consent;
  • Have a reported history of dry eye;
  • Have a history of use of eye drops for dry eye symptoms;

Additionally for Part 2

Symptoms of dry eye syndrome including:

  • Ocular discomfort
  • Conjunctival redness
  • Tear film break up time
  • Schirmer test score

Signs of dry eye syndrome including:

Conjunctival staining score

Exclusion Criteria

  • Have any clinically significant slit lamp findings at entry visit ;
  • Be diagnosed with an ongoing ocular infection;
  • Have any significant ocular lesion that could interfere with assessment of safety or efficacy or prevent study conduct in the opinion of the PI;
  • Have any planned ocular and/or lid surgeries over the study period;
  • Have an uncontrolled systemic disease;
  • Be a woman who is pregnant, nursing or planning a pregnancy;
  • Be a woman of childbearing potential who is not using an acceptable means of birth control;
  • Have a known allergy and/or sensitivity to the test article or its components;
  • Have a condition or be in a situation which the investigator feels may put the subject at significant risk, may confound the study results, or may interfere significantly with the subject's participation in the study;
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03088605). 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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