Phase
Condition
Sjogren's Syndrome
Dry Eye Disease
Eyelid Inflammation
Treatment
N/AClinical Study ID
Ages 18-99 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Subject-reported history of dry eye disease in both eyes for at least 6 months;
- History of use of artificial tear eye drops for dry eye symptoms;
- Total score of ≥40 on SANDE;
- TFBUT;
- Corneal fluorescein staining;
- Lissamine green conjunctival staining;
- Schirmer's test score.
Exclusion
Exclusion Criteria:
- Have participated in a previous tavilermide (MIM-D3) study;
- Have clinically significant slit lamp findings at Visit 1;
- Have a history of lacrimal duct obstruction within 12 months of Visit 1;
- 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 birthcontrol;
- Have a condition or be in a situation which the investigator feels may put the subjectat significant risk, may confound the study results, or may interfere significantlywith the subject's participation in the study;
- Be currently enrolled in an investigational drug or device study or have used aninvestigational drug or device within 45 days prior to Visit 1.
Study Design
Connect with a study center
Tavilermide Investigational Site
Phoenix, Arizona 85032
United StatesSite Not Available
Tavilermide Investigational Site
Los Angeles, California 90013
United StatesSite Not Available
Tavilermide Investigational Site
Newport Beach, California 92663
United StatesSite Not Available
Tavilermide Investigational Site
Fort Collins, Colorado 80528
United StatesSite Not Available
Tavilermide Investigational Site
Littleton, Colorado 80120
United StatesSite Not Available
Tavilermide Investigational Site
Boynton Beach, Florida 33437
United StatesSite Not Available
Tavilermide Investigational Site
Bradenton, Florida 34209
United StatesSite Not Available
Tavilermide Investigational Site
Coral Springs, Florida 33067
United StatesSite Not Available
Tavilermide Investigational Site
Ocala, Florida 34474
United StatesSite Not Available
Tavilermide Investigational Site
Indianapolis, Indiana 46290
United StatesSite Not Available
Tavilermide Investigational Site
Sioux City, Iowa 51104
United StatesSite Not Available
Tavilermide Investigational Site
Lexington, Kentucky 40509
United StatesSite Not Available
Tavilermide Investigational Site
Louisville, Kentucky 40206
United StatesSite Not Available
Tavilermide Investigational Site
Saint Louis, Missouri 63131
United StatesSite Not Available
Tavilermide Investigational Site
Shelby, North Carolina 28150
United StatesSite Not Available
Tavilermide Investigational Site
Fargo, North Dakota 58103
United StatesSite Not Available
Tavilermide Investigational Site
Cincinnati, Ohio 45236
United StatesSite Not Available
Tavilermide Investigational Site
Mason, Ohio 45040
United StatesSite Not Available
Tavilermide Investigational Site
Rapid City, South Dakota 57701
United StatesSite Not Available
Tavilermide Investigational Site
Maryville, Tennessee 37803
United StatesSite Not Available
Tavilermide Investigational Site
Nashville, Tennessee 37205
United StatesSite Not Available
Tavilermide Investigational Site
San Antonio, Texas 78248
United StatesSite Not Available
Tavilermide Investigational Site
Kenosha, Wisconsin 53142
United StatesSite Not Available
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