Core Viewpoint - Tarsus Pharma has an FDA-approved treatment for Demodex blepharitis, with significant market potential and multiple late-stage assets in its pipeline, including formulations of its key molecule, lotilaner [3][4][11] Market Opportunity - An estimated 25 million Americans suffer from Demodex blepharitis, with Tarsus's XDEMVY being the first and only FDA-approved treatment, establishing it as the definitive standard of care [3][4] - The company sees a 1billionopportunityintheinitialaddressablesegment,withover7millionpatientsidentifiedintheU.S.[4]PipelineDevelopments−Tarsushasthreeproductcandidates:TP−03forMeibomianglanddisease(MGD),TP−04forrosacea,andTP−05forLymedisease,allinvariousstagesofclinicaltrials[5]−TP−05demonstrateda97977 million and a cash balance of 323million,withrevenuesreportedat40.8 million [7] - The company has seen a significant increase in SG&A expenses, which rose to 58.8million,primarilyduetocompensationandcostsrelatedtothecommerciallaunchofXDEMVY[7]IntellectualProperty−TarsuslicensedtheintellectualpropertyforlotilanerfromElancoAnimalHealth,withfavorabletermsthatallowforalow−costdevelopmentpathway[8][9]−Theassociatedpatentsforlotilanerarevaliduntilapproximately2032,providingalimitedtimeframeformarketexclusivity[9]InvestmentOutlook−Withamarketcapofaround1 billion and a target market also valued at $1 billion, Tarsus presents an attractive investment opportunity, bolstered by upcoming catalysts and strong data from its programs [11]