Study of Lotilaner Ophthalmic Gel in Patients With Ocular Rosacea (KORE)
Enrolling by invitation · Phase 2
Conditions studied: Ocular Rosacea
In brief
To evaluate lotilaner treatment in patients with ocular rosacea.
Key facts
- Study ID
- NCT07443202
- Run by
- Tarsus Pharmaceuticals, Inc.
- People needed
- 155
- Starts
- 2025-12-05
- Expected to finish
- 2027-12-31
- Last updated by the study team
- 2026-03-02
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- 18 years of age or older at the time of consent.
- Has moderate to severe ocular rosacea
- Use of acceptable methods of contraception
- Are willing to sign the informed consent form and is deemed capable of complying with the requirements of the study protocol
You may not qualify if…
- Patient taking a topical or other therapy which may affect the patients rosacea
- Actively managed glaucoma or active ocular infection or ocular systemic disease
- Have hypersensitivity to lotilaner or any of the formulation components
- Are currently enrolled in an investigational drug or device study
- Are currently pregnant or lactating or planning to become pregnant during the study
Where it is running
- Site — Houston, Texas, United States
- Site — Lynchburg, Virginia, United States
Full record on ClinicalTrials.gov
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