RecruitingPhase 3NCT07284381
A Clinical Study to Evaluate the Effect and Side Effect of a New Artificial Tear Formulation (ABBV-444) Compared to Refresh Optive Unit Dose in Adult Participants With Dry Eye Disease
Studying ADULT syndrome
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- AbbVie
- Principal Investigator
- ABBVIE INC.AbbVie
- Intervention
- ABBV-444(drug)
- Enrollment
- 250 target
- Eligibility
- 18 years · All sexes
- Timeline
- 2025 – 2026
Study locations (20)
- Trinity Research Group /ID# 279914, Dothan, Alabama, United States
- Arizona Eye Center - West Ray Road /ID# 267993, Chandler, Arizona, United States
- Canyon City Eyecare /ID# 267948, Azusa, California, United States
- Global Research Management /ID# 267980, Glendale, California, United States
- Lakeside Vision Center /ID# 268544, Irvine, California, United States
- Eye Research Foundation /ID# 267931, Newport Beach, California, United States
- Lee Shettle Eye and Hearing /ID# 268118, Largo, Florida, United States
- Clayton Eye Center /ID# 268097, Morrow, Georgia, United States
- Coastal Research Associates - Roswell /ID# 279915, Roswell, Georgia, United States
- Kannarr Eye Care /ID# 267979, Pittsburg, Kansas, United States
- Butchertown Clinical Trials /ID# 267887, Louisville, Kentucky, United States
- Moyes Eye Centers /ID# 267944, Kansas City, Missouri, United States
- Northern New Jersey Eye Institute /ID# 267974, South Orange, New Jersey, United States
- Rochester Ophthalmological Group - Rochester /ID# 268374, Rochester, New York, United States
- Core Inc /ID# 267946, Shelby, North Carolina, United States
- +5 more locations on ClinicalTrials.gov
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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