Tarsus Targets Initial Small Segment Of Blepharitis Population With Xdemvy Approval

The company plans to focus on 7 million of the 25 million potentially addressable Demodex blepharitis patients at first, but even that could yield blockbuster sales over the next decade.

Tarsus announced the approval of Xdemvy for blepharitis caused by Demodex mites • Source: Shutterstock

Tarsus Pharmaceuticals Inc. has a shot at reaching blockbuster sales with the US Food and Drug Administration approval of Xdemvy (lotilaner) for Demodex blepharitis, given the high prevalence of the condition – an eyelid disease that results from mite infestation – and the efficacy the drug demonstrated in pivotal trials.

Tarsus said 25 July that it plans to make the drug, formerly known as TP-03, available by prescription by the...

Read the full article – start your free trial today!

Join thousands of industry professionals who rely on Scrip for daily insights

  • Start your 7-day free trial
  • Explore trusted news, analysis, and insights
  • Access comprehensive global coverage
  • Enjoy instant access – no credit card required

More from New Products

Pipeline Watch: ASCO Dominates Phase III Readouts

Pipeline Watch is a weekly snapshot of selected late-stage clinical trial events and approvals announced by pharmaceutical and biotech companies at medical and industry conferences, in financial and company presentations, and in company releases and statements.

Santen Sees Potential In Myopia Market After Ryjunea Approval

 
• By 

The low-dose atropine eye drop slowed the progression of pediatric myopia by 30%.

Atai/Beckley Merger Comes At A Transformative Time For Psychedelics

 
• By 

All eyes are on the upcoming readout of BPL-003 for treatment-resistant depression.

Stock Watch: How GSK’s Nucala Info Drip Helped Share Price

 
• By 

The information flow in the months before the approval of GSK’s Nucala in COPD provides an interesting case study, and brings to mind the cautionary tale of Alnylam’s Onpattro.

More from Scrip

Genmab Looks To Keep Ahead Of Lilly In Folate ADCs

 

The firm has its ‘foot on the gas’ to accelerate development of its FRα-targeting antibody-drug conjugate, Rina-S, but rival Lilly is also moving rapidly into Phase III.

Stock Watch: On Q1 Vaccine Sales And Measles Outbreaks

 
• By 

A recent study suggested that measles could become endemic in the US due to low vaccination rates. However, first-quarter vaccine sales offered a more nuanced picture.

Merck & Co.’s RSV Antibody Approved In US In Time To Compete With Blockbuster Beyfortus

 
• By 

The US FDA approved Merck’s Enflonsia (clesrovimab) to prevent RSV in newborns and infants on the same day Sanofi assured that it would ship Beyfortus in time for the 2025-2026 RSV season.