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TARS US Equity

Tarsus Pharmaceuticals, Inc.Health Care · Biological Products, (No Diagnostic Substances) · CIK 1819790 · FY ends Dec 31
$71.03
+0.42 (+0.59%)
USD · as of 2026-08-18 · marketstack
12 registered studies · 2 active

Studies where TARS is the lead sponsor, as filed with ClinicalTrials.gov. Completion dates are the sponsor's own projected windows and are revised as a study runs. Active studies first, then completed and stopped — newest readout first within each.

12 interventional · 3 with posted results

Held by 13 tracked-famous managers (MILLENNIUM MANAGEMENT LLC, D. E. Shaw & Co., Inc., Squarepoint Ops LLC, Artisan Partners Limited Partnership, CITADEL ADVISORS LLC, +8 more) · FINRA short interest 6.6 days to cover (settled 2026-07-31) · insider 90d: 0 buys / 6 sells · government filings 180d: none disclosed

StudyPhaseStatusInterventionsConditionsEnrollmentPrimary completionReadout inUpdated
A Study to Evaluate Safety and Efficacy of TP-05 in Healthy Participants With Tick ExposureNCT07562087The Incidence of Treatment Emergent Adverse Events From BaselineRandomized · Double-masked · TreatmentPhase 2Active, not recruitingDrug: TP-05 (lotilaner) Low Dose, TP-05 (lotilaner) High Dose, PlaceboLyme Disease722Oct 2027≤ 438 d2026-07-09
Study of Lotilaner Ophthalmic Gel in Patients With Ocular Rosacea (KORE)NCT07443202Incidence of Treatment Emergent Adverse EventsRandomized · Quadruple-masked · TreatmentPhase 2Enrolling by invitationDrug: lotilaner, VehicleOcular Rosacea1552026-12-31in 134 d2026-03-02
Impact of XDEMVY® on Demodex Blepharitis in Soft Contact Lens WearersNCT06182358Reduction of collarettes at Day 43Randomized · Quadruple-masked · TreatmentPhase 4CompletedDrug: Lotilaner ophthalmic solution, 0.25%, Vehicle controlDemodex Blepharitis1452025-01-27actual2025-07-02
A Human Tick Kill Study to Investigate the Safety, Tolerability, and Whole Blood Concentration of TP-05NCT05387083The Incidence of treatment emergent adverse events from baselineRandomized · Quadruple-masked · OtherPhase 2CompletedDrug: Low Dose TP-05, High Dose TP-05, Placebo ComparatorHealthy Volunteer302024-06-26actual2024-09-19
Effect of an Exploratory Vehicle on Meibomian Gland Dysfunction in Patients With DemodexNCT06054217Treatment Emergent Adverse Events (TEAEs)Randomized · Double-masked · TreatmentPhase 2Unknown statusDrug: Vehicle of TP-03Meibomian Gland Dysfunction, Demodex Infestation of Eyelid, Blepharitis, Demodectic Blepharitis362024-06-152024-04-09
Study of TP-04 in Participants With Papulopustular RosaceaNCT05838170The incidence of treatment emergent adverse events from baselineRandomized · Quadruple-masked · TreatmentPhase 2CompletedDrug: Lotilaner Gel, 2.0% · Other: Vehicle control gelPapulopustular Rosacea372023-11-13actual2023-11-24
Study to Evaluate the Food Effect of TP-05 in Healthy ParticipantsNCT05720364Concentration of TP-05 in whole bloodRandomized · Open-label · TreatmentPhase 1CompletedDrug: TP-05 (lotilaner oral), fasted group, TP-05 (lotilaner oral), high-fat group, TP-05 (lotilaner oral), low-fat groupHealthy422023-05-30actual2023-06-28
Pilot Study Comparing the Safety and Efficacy of Two Dosing Regimens of TP-03 for the Treatment of MGDNCT05454956results2025-10-01Number of Participants With Treatment Emergent Adverse Events (TEAEs)Randomized · Quadruple-masked · TreatmentStudy Protocol · Statistical Analysis PlanPhase 2CompletedDrug: TP-03, TP-03 VehicleMeibomian Gland Dysfunction, Blepharitis, Demodex Infestation392023-05-18actual2025-10-01
Trial to Evaluate the Safety and Efficacy of TP-03 for the Treatment of Demodex BlepharitisNCT04784091results2023-12-21The Proportion of Participants Cured Based on Their Collarette Score of 0 for the Upper Eyelid.Randomized · Quadruple-masked · TreatmentStudy Protocol · Statistical Analysis PlanPhase 3CompletedDrug: TP-03, TP-03 VehicleBlepharitis4122022-05-09actual2023-12-21
A Pharmacokinetic Study of TP-05 in Healthy SubjectsNCT05138796Incidence of treatment emergent adverse events (TEAEs)Randomized · Triple-masked · Basic sciencePhase 1CompletedDrug: TP-05 (lotilaner oral capsules), PlaceboHealthy672022-03-25actual2022-08-03
A Six Week Pharmacokinetic Study of TP-03 in Healthy SubjectsNCT05138861To evaluate the concentration of lotilaner in blood multiple doses of TP-03, 0.25% in whole blood following topical ocular administration in healthy adult subjects for 42 days.Open-label · Basic sciencePhase 1CompletedDrug: TP-03 (Lotilaner Ophthalmic Solution), 0.25%Healthy242021-09-03actual2024-04-12
Safety and Efficacy of TP-03 for the Treatment of Demodex BlepharitisNCT04475432results2023-12-21Proportion of Participants Cured Based on a Collarette Score at Day 43.Randomized · Quadruple-masked · TreatmentStudy Protocol · Statistical Analysis PlanPhase 2/3CompletedDrug: TP-03, 0.25%, TP-03 VehicleBlepharitis4212021-05-04actual2023-12-21

Primary completion is the date the sponsor filed with the registry — their own projection, revised whenever they revise it, unless the row is marked actual.

Source: ClinicalTrials.gov, retrieved 2026-08-19