Tarsus Provides 2025 Update: Accelerating the Launch of XDEMVY® and Establishing Ocular Rosacea as the Next Category-Creating Opportunity in Eye Care
13 Januar 2025 - 2:30PM
Tarsus Pharmaceuticals, Inc. (NASDAQ: TARS) today provided an
update on the Company’s key priorities for 2025, including plans to
advance TP-04 for the potential treatment of Ocular Rosacea,
another category-creating opportunity in eye care.
“2024 was a groundbreaking year for Tarsus as we established
XDEMVY as one of the most successful eye care launches to date.
With consistent quarter-over-quarter revenue growth, rapid
physician adoption, broad payer coverage to date, and continued
acceleration in the number of bottles delivered to patients in the
fourth quarter of 2024, our path to eye care leadership is clear,”
said Bobak Azamian, M.D., Ph.D., Chief Executive Officer and
Chairman of Tarsus. “I expect 2025 to be even more transformational
as we turn up the dial on key strategic launch initiatives, plan to
generate more new evidence highlighting the impact of XDEMVY and
our pipeline candidates, and pursue Ocular Rosacea as the next
potentially revolutionary opportunity in eye care.”
XDEMVY (lotilaner ophthalmic solution, 0.25%) – Driving
One of the Fastest Growing Categories in Eye Care
- During the first nine months of 2024, the Company delivered
more than 104,000 bottles of XDEMVY to patients and generated more
than $113 million in XDEMVY net product sales.
- By the end of Q3 2024, more than 13,000 Eye Care Professionals
(ECPs) were prescribing XDEMVY with over 70% writing for multiple
patients.
- Broad commercial and Medicare reimbursement now extends to more
than 80% of lives covered and a gross-to-net discount percentage in
the low 40s as of the end of Q3 2024.
- The deployment of approximately 50 new sales representatives
and leaders in Q3 2024 started to deliver meaningful impact in Q4
2024.
- The Company initiated a trial run of its first
direct-to-consumer advertising campaign on network TV in January
2025, including spots during the Golden Globes and National
Football League (NFL) playoffs.
- Groundbreaking data from the Ersa and Rhea clinical trials for
the treatment of Demodex blepharitis (DB) in patients
with Meibomian Gland Disease (MGD) further underscore the utility
of XDEMVY broadly across DB patient types.
Ocular Rosacea – Pursuing The Next Potentially
Transformative Category in Eye Care
- Ocular Rosacea (OR) is a highly prevalent, undertreated eye
disease with no FDA-approved therapy. It affects ~15-18 million
Americans, and more than half of all cases are caused by an
infestation of Demodex mites. This inflammatory condition affects
the eyes and surrounding tissue and is often accompanied by the
presence of prominent blood vessels, and redness across the eyes
and eyelids.
- TP-04 is an investigational topical sterile ophthalmic gel
formulation of lotilaner designed for application across the eyelid
and surrounding tissue that represents a potentially
category-creating therapy in an area of high unmet need.
- Previous clinical trials of lotilaner in DB, MGD, and
papulopustular rosacea demonstrated statistically significant
improvements in key objective endpoint measures of disease.
- Patent exclusivity expected to extend through 2038.
- Based on FDA feedback, the Company has established a clear
regulatory path forward for TP-04 and plans to initiate a Phase 2
study in the second half of 2025. Results are anticipated in
2026.
Additional Potential Growth Drivers in 2025 and
Beyond
- On-track for potential European regulatory approval of a
preservative-free formulation of XDEMVY in 2027.
- In Japan, the Company expects to share results from an ongoing
DB prevalence study in 2025 and meet with Japanese regulatory
authorities to help determine a regulatory path forward.
- The Chinese regulatory agency, National Medical Products
Administration, accepted the New Drug Application (NDA) submitted
by Tarsus’s partner, Grand Pharmaceutical Group Ltd., for
TP-03 for DB. A decision is anticipated in 2027.
- The Company remains on-track to provide an update on TP-05 for
the potential prevention of Lyme Disease by the FY 2024 earnings
call.
Conference Call and WebcastTarsus will host a
conference call and webcast on Tuesday, January 14, 2025, at 8:00
a.m. P.T. / 11:00 a.m. E.T. A live webcast will be available on the
events section of the Tarsus website. A recorded version of the
call will be available on the website shortly after the completion
of the call and will be archived there for at least 90 days.
About XDEMVY® XDEMVY
(lotilaner ophthalmic solution, 0.25%), formerly known as TP-03, is
a novel prescription eye drop designed to treat Demodex blepharitis
by targeting and eradicating the root cause of the disease –
Demodex mite infestation. XDEMVY was evaluated in two pivotal
trials collectively involving more than 800 patients. Both trials
met the primary endpoint and all secondary endpoints, with
statistical significance and no serious treatment-related adverse
events. Most patients found the XDEMVY eye drop to be neutral to
very comfortable. The most common ocular adverse reactions observed
in the studies were instillation site stinging and burning which
was reported in 10% of patients. Other ocular adverse reactions
reported by less than 2% of patients were chalazion/hordeolum
(stye) and punctate keratitis.
XDEMVY Indication and Important Safety
Information
INDICATIONS AND USAGEXDEMVY is indicated for
the treatment of Demodex blepharitis.
Most common side effects: The most common side
effect in clinical trials was stinging and burning in 10% of
patients. Other side effects in less than 2% of patients were
chalazion/hordeolum and punctate keratitis.
For additional information, please see full prescribing
information available at: https://xdemvy.com/.
About TP-04TP-04 is an investigational aqueous
gel formulation of lotilaner, a well-characterized anti-parasitic
agent that paralyzes and kills mites by selectively inhibiting
parasite-specific GABA-Cl channels. Tarsus is studying TP-04 for
the potential treatment of Ocular Rosacea (OR).
About TP-05TP-05 is an investigational oral
systemic formulation of lotilaner, a well-characterized
anti-parasitic agent that selectively inhibits parasite-specific
GABA-Cl channels. TP-05 is believed to be the only non-vaccine,
drug-based, preventative therapeutic in development designed to
kill ticks to potentially prevent Lyme disease transmission.
About Tarsus Pharmaceuticals,
Inc.Tarsus Pharmaceuticals, Inc. applies proven science
and new technology to revolutionize treatment for patients,
starting with eye care. Tarsus is advancing its pipeline to address
several diseases with high unmet need across a range of therapeutic
categories, including eye care and infectious disease prevention.
XDEMVY (lotilaner ophthalmic solution, 0.25%) is FDA approved in
the United States for the treatment of Demodex blepharitis. Tarsus
is also developing TP-04 for the potential treatment of Ocular
Rosacea and TP-05 as an oral tablet for the potential prevention of
Lyme disease.
Forward-Looking
StatementsStatements in this press release about future
expectations, plans and prospects, as well as any other statements
regarding matters that are not historical facts, may constitute
“forward-looking statements.” These include statements regarding
the potential commercial success and growth of XDEMVY in Demodex
blepharitis, including market size, acceptance, demand,
prescription fill rate and adoption rate for XDEMVY; our ability to
successfully implement our sales force expansion and new
direct-to-consumer campaign including network TV; our ability to
achieve distribution and patient access for XDEMVY; our ability to
continue to drive a successful launch of XDEMVY and become an eye
care leader; our ability to continue to educate the market
about Demodex blepharitis; anticipated regulatory and
development milestones including potential regulatory pathways for
approval of XDEMVY in Europe, China, and Japan; the market size and
opportunity for our pipeline products including TP-04 for the
potential treatment of Ocular Rosacea; the timing of initiation and
results of our clinical studies including additional studies on the
impact of XDEMVY, a Japan DB prevalence study, TP-04, and TP-05;
the potential regulatory pathways and timing of discussions with
regulators including the FDA; the impact of our new sales force
representatives on our XDEMVY sales; our ability to continue
investing in our business, and the quotations of Tarsus’
management. The words, without limitation, “believe,”
“contemplate,” “continue,” “could,” “estimate,” “expect,” “intend,”
“may,” “might,” “plan,” “potential,” “predict,” “project,”
“should,” “target,” “will,” or “would,” or the negative of these
terms or other similar expressions are intended to identify
forward-looking statements, although not all forward-looking
statements contain these or similar identifying words. Further,
there are other risks and uncertainties that could cause actual
results to differ from those set forth in the forward-looking
statements and they are detailed from time to time in the reports
Tarsus files with the Securities and Exchange Commission, including
Tarsus’ Form 10-K for the year ended December 31, 2023 filed on
February 27, 2024 and the most recent Form 10-Q quarterly filing
filed with the SEC filed on November 13, 2024, which Tarsus
incorporates by reference into this press release, copies of which
are posted on its website and are available from Tarsus without
charge. However, new risk factors and uncertainties may emerge from
time to time, and it is not possible to predict all risk factors
and uncertainties. Accordingly, readers are cautioned not to place
undue reliance on these forward-looking statements. Any
forward-looking statements contained in this press release are
based on the current expectations of Tarsus’ management team and
speak only as of the date hereof, and Tarsus specifically disclaims
any obligation to update any forward-looking statement, whether as
a result of new information, future events or otherwise.
Media
Contact: |
|
Adrienne Kemp |
|
Sr. Director, Corporate
Communications |
|
(949) 922-0801 |
|
akemp@tarsusrx.com |
|
|
|
Investor
Contact: |
|
David Nakasone |
|
Head of Investor
Relations |
|
(949) 620-3223 |
|
DNakasone@tarsusrx.com |
|
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