Study Evaluating the Safety and Efficacy of AR-15512 (COMET-2)
Primary Purpose
Dry Eye Disease
Status
Completed
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
AR 15512 Ophthalmic Solution
Vehicle
Sponsored by
About this trial
This is an interventional treatment trial for Dry Eye Disease
Eligibility Criteria
Inclusion Criteria:
- Male or female, 30 years of age or older at the Screening visit
- Signs of DED at the Screening and Baseline visits assessed by corneal staining and Schirmer test
- Symptoms of DED at both Screening and Baseline visits assessed by SANDE questionnaire and ODS-VAS
- Corrected visual acuity (+0.70 LogMAR) or better in both eyes at both the Screening and Baseline visits
Exclusion Criteria:
- History or presence of any ocular disorder or condition (other than DED) in either eye that would, in the opinion of the investigator, likely interfere with the interpretation of the study results or subject safety
- Regular use of lid hygiene within 14 days prior to the Screening visit or any planned use during the study
- Use of artificial tears within 2 hours prior to the Screening visit or anticipated use during the study
- Use of any topical ocular anti-inflammatory medication within 30 days prior to the Screening visit or anticipated use during the study (e.g., ocular cyclosporine [Restasis®, Cequa™], lifitegrast [Xiidra®], or any other prescription ophthalmic solution for DED, topical ocular corticosteroid- or non-steroidal-anti-inflammatory agents
- Use of Tyrvaya™ (varenicline solution, nasal spray 0.03mg) within 30 days prior to the Screening visit or anticipated use during the study
- Use of medications for the treatment of severe DED and/or Meibomian gland disease such as oral tetracyclines, oral tetracycline derivatives and oral retinoids within 30 days prior to the Screening visit or anticipated use during the study
- Initiation, discontinuation, or change in dose of a systemic medication known to cause ocular drying (e.g. antihistamines or tricyclic antidepressants) less than 14 days prior to the Screening visit or a change in dosage is anticipated during the study.
- Initiation, discontinuation, or change in dose of a systemic corticosteroid less than 60 days prior to the Screening visit or a change in dosage is anticipated during the study.
- Initiation, discontinuation, or change in dose of a systemic immunomodulator (e.g., hydroxychloroquine, methotrexate, cyclosporine) less than 60 days prior to the Screening visit or a change in dosage is anticipated during the study
- History or presence of significant systemic disease (i.e.: cardiovascular, pulmonary, hepatic, renal, hematologic, immunologic)
Sites / Locations
- Global Research Management, Inc
- Premiere Practice Management, LLC
- Vision Institute
- The Eye Care Group
- Segal Drug Trials, Inc.
- Michael Washburn Center for Ophthalmic Research, LLC
- Butchertown Clinical Trials
- Central Maine Eye Care
- Moyes Eye Center
- Center for Sight
- Core, Inc.
- Bergstrom Eye Research
- Verum Research
- Erie Retina Surgery
- Advancing Vision Research
- Total Eye Care, PA
- Advancing Vision Research
- Austin Clinical Research
- Valley Retina Institute, PA
- Valley Retina Institute, PA
- Eye Clinics of South Texas
- R and R Eye Research, LLC
- Alpine Research Organization Inc.
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
AR 15512 Ophthalmic Solution (0.003%)
Vehicle
Arm Description
0.003% AR 15512 to be administered BID for 90 days. Both eyes will be treated.
AR-15512 vehicle to be administered BID for 90 days. Both eyes will be treated.
Outcomes
Primary Outcome Measures
Unanesthetized Schirmer test
Proportion of subjects ≥ 10 mm increase in unanesthetized Schirmer score.
Schirmer strips placed, without anesthesia, in both eyes measure the amount of tear wetting over a 5-minute period, in whole millimeters to a maximum score of 35 mm. An ≥ 10 mm score over time indicates a better outcome.
Secondary Outcome Measures
SANDE (Symptom Assessment iN Dry Eye) Questionnaire Score
Change from Baseline in SANDE score.
The SANDE questionnaire consists of two visual analogue scales (VAS), each ranging from 0mm to 100mm to indicate the frequency (from "Rarely" to "All the Time") and severity (from "Very Mild" to "Very Severe") of dry eye symptoms. A higher score indicates greater frequency or severity. Each subject marks both VAS to indicate their level of frequency and severity. The SANDE score is calculated by multiplying the frequency score by the severity score and obtaining the square root. A reduced SANDE score over time indicates a better outcome.
SANDE (Symptom Assessment iN Dry Eye) Questionnaire Score
Change from Baseline in SANDE score.
The SANDE questionnaire consists of two visual analogue scales (VAS), each ranging from 0mm to 100mm to indicate the frequency (from "Rarely" to "All the Time") and severity (from "Very Mild" to "Very Severe") of dry eye symptoms. A higher score indicates greater frequency or severity. Each subject marks both VAS to indicate their level of frequency and severity. The SANDE score is calculated by multiplying the frequency score by the severity score and obtaining the square root. A reduced SANDE score over time indicates a better outcome.
Unanesthetized Schirmer score
Change from Baseline
Schirmer strips placed, without anesthesia, in both eyes measure the amount of tear wetting over a 5-minute period, in whole millimeters to a maximum score of 35 mm. An increased score over time indicates a better outcome.
Ocular Discomfort Score (ODS) - VAS
Change from Baseline
Subjects mark a visual analogue scale (VAS) between 0mm to 100mm to indicate (from "no symptom" to "maximal symptom") their ocular discomfort. A reduced score over time indicates a better outcome.
Eye Dryness Score (EDS) - VAS
Change from Baseline
Subjects mark a visual analogue scale (VAS) between 0mm to 100mm to indicate (from "no symptom" to "maximal symptom") their eye dryness. A reduced score over time indicates a better outcome.
Unanesthetized Schirmer score
Proportion of subjects with ≥ 10 mm increase in score
Schirmer strips placed, without anesthesia, in both eyes measure the amount of tear wetting over a 5-minute period, in whole millimeters to a maximum score of 35 mm. An ≥ 10 mm score over time indicates a better outcome.
Quality of Life VAS
Change from Baseline
Subjects mark a visual analogue scale (VAS) between 0mm to 100mm to indicate (from "strongly disagree" to "strongly agree") their agreement with the statement "Over the past 3 days my dry eye has interfered with my daily activities and reduced my quality of life". A reduced score over time indicates a better outcome.
Ocular Pain - VAS
Change from Baseline Subjects mark a visual analogue scale (VAS) between 0mm to 100mm to indicate (from "no symptom" to "maximal symptom") their ocular discomfort. A reduced score over time indicates a better outcome.
Conjunctival Redness
Change from Baseline
Investigators or designated sub-Investigators grade redness of the eye on a scale from 0 to 4 (from 0 "normal" to 4 "severe"). A reduced score over time indicates a better outcome.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT05285644
Brief Title
Study Evaluating the Safety and Efficacy of AR-15512
Acronym
COMET-2
Official Title
A Phase 3 Study Evaluating the Safety and Efficacy of AR-15512, a Cold Thermoreceptor Modulator, for the Treatment of Dry Eye Disease (COMET-2)
Study Type
Interventional
2. Study Status
Record Verification Date
August 2023
Overall Recruitment Status
Completed
Study Start Date
May 9, 2022 (Actual)
Primary Completion Date
July 21, 2023 (Actual)
Study Completion Date
July 21, 2023 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Aerie Pharmaceuticals
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
This will be a Phase 3, multicenter, vehicle-controlled, double-masked, randomized study conducted at approximately 20 sites in the United States. All subjects enrolled will have dry eye disease (DED). The study will consist of Screening (Day -14) and Baseline (Day 1) visits as well as visits at Day 7, Day 14, Day 28, and Day 90 (Study Exit).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dry Eye Disease
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Model Description
Qualified subjects will be enrolled in the study and randomized in a 1:1 ratio within each site to receive 0.003% AR 15512 or AR-15512 vehicle to be administered twice daily (BID) as 1 drop in each eye for 90 days.
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
During the randomized treatment period, the investigator and site staff performing eligibility / efficacy and safety assessments and the subjects will be masked.
Allocation
Randomized
Enrollment
465 (Actual)
8. Arms, Groups, and Interventions
Arm Title
AR 15512 Ophthalmic Solution (0.003%)
Arm Type
Experimental
Arm Description
0.003% AR 15512 to be administered BID for 90 days. Both eyes will be treated.
Arm Title
Vehicle
Arm Type
Placebo Comparator
Arm Description
AR-15512 vehicle to be administered BID for 90 days. Both eyes will be treated.
Intervention Type
Drug
Intervention Name(s)
AR 15512 Ophthalmic Solution
Intervention Description
Topical ocular administration of one drop in both eyes BID for 90 days.
Intervention Type
Drug
Intervention Name(s)
Vehicle
Intervention Description
Topical ocular administration of one drop in both eyes BID for 90 days.
Primary Outcome Measure Information:
Title
Unanesthetized Schirmer test
Description
Proportion of subjects ≥ 10 mm increase in unanesthetized Schirmer score.
Schirmer strips placed, without anesthesia, in both eyes measure the amount of tear wetting over a 5-minute period, in whole millimeters to a maximum score of 35 mm. An ≥ 10 mm score over time indicates a better outcome.
Time Frame
Day 14
Secondary Outcome Measure Information:
Title
SANDE (Symptom Assessment iN Dry Eye) Questionnaire Score
Description
Change from Baseline in SANDE score.
The SANDE questionnaire consists of two visual analogue scales (VAS), each ranging from 0mm to 100mm to indicate the frequency (from "Rarely" to "All the Time") and severity (from "Very Mild" to "Very Severe") of dry eye symptoms. A higher score indicates greater frequency or severity. Each subject marks both VAS to indicate their level of frequency and severity. The SANDE score is calculated by multiplying the frequency score by the severity score and obtaining the square root. A reduced SANDE score over time indicates a better outcome.
Time Frame
Day 28
Title
SANDE (Symptom Assessment iN Dry Eye) Questionnaire Score
Description
Change from Baseline in SANDE score.
The SANDE questionnaire consists of two visual analogue scales (VAS), each ranging from 0mm to 100mm to indicate the frequency (from "Rarely" to "All the Time") and severity (from "Very Mild" to "Very Severe") of dry eye symptoms. A higher score indicates greater frequency or severity. Each subject marks both VAS to indicate their level of frequency and severity. The SANDE score is calculated by multiplying the frequency score by the severity score and obtaining the square root. A reduced SANDE score over time indicates a better outcome.
Time Frame
Day 7, 14 & 90
Title
Unanesthetized Schirmer score
Description
Change from Baseline
Schirmer strips placed, without anesthesia, in both eyes measure the amount of tear wetting over a 5-minute period, in whole millimeters to a maximum score of 35 mm. An increased score over time indicates a better outcome.
Time Frame
Day 7, 14, 28 & 90
Title
Ocular Discomfort Score (ODS) - VAS
Description
Change from Baseline
Subjects mark a visual analogue scale (VAS) between 0mm to 100mm to indicate (from "no symptom" to "maximal symptom") their ocular discomfort. A reduced score over time indicates a better outcome.
Time Frame
Day 28 & 90
Title
Eye Dryness Score (EDS) - VAS
Description
Change from Baseline
Subjects mark a visual analogue scale (VAS) between 0mm to 100mm to indicate (from "no symptom" to "maximal symptom") their eye dryness. A reduced score over time indicates a better outcome.
Time Frame
Day 28 & 90
Title
Unanesthetized Schirmer score
Description
Proportion of subjects with ≥ 10 mm increase in score
Schirmer strips placed, without anesthesia, in both eyes measure the amount of tear wetting over a 5-minute period, in whole millimeters to a maximum score of 35 mm. An ≥ 10 mm score over time indicates a better outcome.
Time Frame
Day 7, 28 & 90
Title
Quality of Life VAS
Description
Change from Baseline
Subjects mark a visual analogue scale (VAS) between 0mm to 100mm to indicate (from "strongly disagree" to "strongly agree") their agreement with the statement "Over the past 3 days my dry eye has interfered with my daily activities and reduced my quality of life". A reduced score over time indicates a better outcome.
Time Frame
Day 7, 14, 28 & 90
Title
Ocular Pain - VAS
Description
Change from Baseline Subjects mark a visual analogue scale (VAS) between 0mm to 100mm to indicate (from "no symptom" to "maximal symptom") their ocular discomfort. A reduced score over time indicates a better outcome.
Time Frame
Day 90
Title
Conjunctival Redness
Description
Change from Baseline
Investigators or designated sub-Investigators grade redness of the eye on a scale from 0 to 4 (from 0 "normal" to 4 "severe"). A reduced score over time indicates a better outcome.
Time Frame
Day 90
10. Eligibility
Sex
All
Minimum Age & Unit of Time
30 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Male or female, 30 years of age or older at the Screening visit
Signs of DED at the Screening and Baseline visits assessed by corneal staining and Schirmer test
Symptoms of DED at both Screening and Baseline visits assessed by SANDE questionnaire and ODS-VAS
Corrected visual acuity (+0.70 LogMAR) or better in both eyes at both the Screening and Baseline visits
Exclusion Criteria:
History or presence of any ocular disorder or condition (other than DED) in either eye that would, in the opinion of the investigator, likely interfere with the interpretation of the study results or subject safety
Regular use of lid hygiene within 14 days prior to the Screening visit or any planned use during the study
Use of artificial tears within 2 hours prior to the Screening visit or anticipated use during the study
Use of any topical ocular anti-inflammatory medication within 30 days prior to the Screening visit or anticipated use during the study (e.g., ocular cyclosporine [Restasis®, Cequa™], lifitegrast [Xiidra®], or any other prescription ophthalmic solution for DED, topical ocular corticosteroid- or non-steroidal-anti-inflammatory agents
Use of Tyrvaya™ (varenicline solution, nasal spray 0.03mg) within 30 days prior to the Screening visit or anticipated use during the study
Use of medications for the treatment of severe DED and/or Meibomian gland disease such as oral tetracyclines, oral tetracycline derivatives and oral retinoids within 30 days prior to the Screening visit or anticipated use during the study
Initiation, discontinuation, or change in dose of a systemic medication known to cause ocular drying (e.g. antihistamines or tricyclic antidepressants) less than 14 days prior to the Screening visit or a change in dosage is anticipated during the study.
Initiation, discontinuation, or change in dose of a systemic corticosteroid less than 60 days prior to the Screening visit or a change in dosage is anticipated during the study.
Initiation, discontinuation, or change in dose of a systemic immunomodulator (e.g., hydroxychloroquine, methotrexate, cyclosporine) less than 60 days prior to the Screening visit or a change in dosage is anticipated during the study
History or presence of significant systemic disease (i.e.: cardiovascular, pulmonary, hepatic, renal, hematologic, immunologic)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michelle Senchyna, PhD
Organizational Affiliation
Aerie Pharmaceuticals
Official's Role
Study Director
Facility Information:
Facility Name
Global Research Management, Inc
City
Glendale
State/Province
California
ZIP/Postal Code
90027
Country
United States
Facility Name
Premiere Practice Management, LLC
City
Torrance
State/Province
California
ZIP/Postal Code
90505
Country
United States
Facility Name
Vision Institute
City
Colorado Springs
State/Province
Colorado
ZIP/Postal Code
80907
Country
United States
Facility Name
The Eye Care Group
City
Waterbury
State/Province
Connecticut
ZIP/Postal Code
06708
Country
United States
Facility Name
Segal Drug Trials, Inc.
City
Delray Beach
State/Province
Florida
ZIP/Postal Code
33484
Country
United States
Facility Name
Michael Washburn Center for Ophthalmic Research, LLC
City
Indianapolis
State/Province
Indiana
ZIP/Postal Code
46240
Country
United States
Facility Name
Butchertown Clinical Trials
City
Louisville
State/Province
Kentucky
ZIP/Postal Code
40206
Country
United States
Facility Name
Central Maine Eye Care
City
Lewiston
State/Province
Maine
ZIP/Postal Code
04240
Country
United States
Facility Name
Moyes Eye Center
City
Kansas City
State/Province
Missouri
ZIP/Postal Code
64154
Country
United States
Facility Name
Center for Sight
City
Henderson
State/Province
Nevada
ZIP/Postal Code
89052
Country
United States
Facility Name
Core, Inc.
City
Shelby
State/Province
North Carolina
ZIP/Postal Code
28150
Country
United States
Facility Name
Bergstrom Eye Research
City
Fargo
State/Province
North Dakota
ZIP/Postal Code
58103
Country
United States
Facility Name
Verum Research
City
Eugene
State/Province
Oregon
ZIP/Postal Code
97401
Country
United States
Facility Name
Erie Retina Surgery
City
Erie
State/Province
Pennsylvania
ZIP/Postal Code
16507
Country
United States
Facility Name
Advancing Vision Research
City
Goodlettsville
State/Province
Tennessee
ZIP/Postal Code
37072
Country
United States
Facility Name
Total Eye Care, PA
City
Memphis
State/Province
Tennessee
ZIP/Postal Code
38119
Country
United States
Facility Name
Advancing Vision Research
City
Smyrna
State/Province
Tennessee
ZIP/Postal Code
37167
Country
United States
Facility Name
Austin Clinical Research
City
Austin
State/Province
Texas
ZIP/Postal Code
78750
Country
United States
Facility Name
Valley Retina Institute, PA
City
Harlingen
State/Province
Texas
ZIP/Postal Code
78550
Country
United States
Facility Name
Valley Retina Institute, PA
City
McAllen
State/Province
Texas
ZIP/Postal Code
78503
Country
United States
Facility Name
Eye Clinics of South Texas
City
San Antonio
State/Province
Texas
ZIP/Postal Code
78209
Country
United States
Facility Name
R and R Eye Research, LLC
City
San Antonio
State/Province
Texas
ZIP/Postal Code
78229
Country
United States
Facility Name
Alpine Research Organization Inc.
City
Clinton
State/Province
Utah
ZIP/Postal Code
84015
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
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Study Evaluating the Safety and Efficacy of AR-15512
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