Clinical Trials in the USA / NCT07443202
Enrolling by invitation
Phase 2
Study of Lotilaner Ophthalmic Gel in Patients With Ocular Rosacea (KORE)
NCT07443202 · tracked via the Priya Life Science USA tracker
Condition(s) studied
Ocular Rosacea
Investigational drug(s) / intervention(s)
lotilanerVehicle
lotilaner: lotilaner
Vehicle: Vehicle of lotilaner
Study summary
To evaluate lotilaner treatment in patients with ocular rosacea.
Eligibility
Inclusion Criteria:
* 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
Exclusion Criteria:
* 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
Primary outcome measure(s)
- Incidence of Treatment Emergent Adverse Events — Week 16
Number of patients with treatment related emergent adverse events (TEAEs)
Trial sites (2)
| Facility | City | Region | Status |
|---|---|---|---|
| Site | Houston | Texas | |
| Site | Lynchburg | Virginia |
More Tarsus Pharmaceuticals, Inc. trials in the USA
Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07443202 on ClinicalTrials.gov ↗ ← All trials in the USA