Nicox Announces Approval of ZERVIATE in China
September 18 2024 - 12:30AM
UK Regulatory
Nicox Announces Approval of ZERVIATE in China
Press Release |
Nicox Announces Approval of ZERVIATE in China |
- Nicox’s
partner, Ocumension Therapeutics, has received approval for
ZERVIATE® for ocular
itching in China
-
ZERVIATE®
launch in China will add a further royalty revenue stream
for Nicox
September 18, 2024 – release at 7:30 am CET
Sophia Antipolis, France
Nicox SA (Euronext Growth Paris: FR0013018124,
ALCOX), an international ophthalmology company, today announced
that its exclusive Chinese partner, Ocumension Therapeutics, has
received approval of the New Drug Application (NDA) to
commercialize ZERVIATE® (cetirizine ophthalmic
solution), 0.24% in China for ocular itching associated with
allergic conjunctivitis.
“The approval of ZERVIATE for commercialization in China is an
excellent achievement by our partner, Ocumension Therapeutics. We
trust in their capabilities to support a quick launch and use their
strong commercial presence across China to maximize market
penetration. This new commercial launch will add another revenue
stream to Nicox as we will receive from 5% to 9% royalties and
commercial milestones on Ocumension’s net sales of ZERVIATE in
China. Ocumension forecasts peak sales in excess of $100 million
annually within 7 years.” said Emmet Purtill, VP
Business Development of Nicox.
ZERVIATE is the first and only eye drop formulation of the
antihistamine cetirizine, the active ingredient in
ZYRTEC®, and is currently commercialized in the U.S. for
ocular itching associated with allergic conjunctivitis by Nicox’s
exclusive U.S. partner, Harrow, Inc.
Ocumension emphasizes that ZERVIATE is suitable for the treatment
of allergic conjunctivitis in toddlers and preschoolers, which
significantly fills the medical gap in this field and benefits the
vast number of children in China. Ocumension plans to
manufacture ZERVIATE in their new state-of-the-art purpose-built
manufacturing facility located in Suzhou, China. ZERVIATE will be
promoted by Ocumension’s commercial team and its extensive network
of national and provincial distribution partners. The prescription
market for allergic conjunctivitis products in China is
expected1 to grow to almost $500 million by 2030.
ZERVIATE is exclusively licensed to Ocumension for development and
commercialization in the Chinese and the majority of the Southeast
Asian markets. Nicox may potentially receive sales milestones of up
to US$17.2 million together with royalties from 5% to 9% of net
sales of ZERVIATE by Ocumension. Since Nicox’s recent successful
financing, Ocumension is now its principal shareholder. |
About Nicox |
Nicox SA is an international ophthalmology company developing
innovative solutions to help maintain vision and improve ocular
health. Nicox’s lead program in clinical development is NCX 470
(bimatoprost grenod), a novel nitric oxide-donating bimatoprost eye
drop, for lowering intraocular pressure in patients with open-angle
glaucoma or ocular hypertension. Nicox generates revenue from
VYZULTA® in glaucoma, licensed exclusively worldwide to Bausch +
Lomb, and ZERVIATE® in allergic conjunctivitis, licensed in
multiple geographies, including to Harrow, Inc. in the U.S., and
Ocumension Therapeutics in the Chinese and in the majority of
Southeast Asian markets.
Nicox, headquartered in Sophia Antipolis, France, is listed on
Euronext Growth Paris (Ticker symbol: ALCOX) and is part of the CAC
Healthcare index.
For more information www.nicox.com |
Analyst coverage |
H.C. Wainwright & Co Yi Chen New York, U.S. |
|
The views expressed by analysts in their coverage of Nicox are
those of the author and do not reflect the views of Nicox.
Additionally, the information contained in their reports may not be
correct or current. Nicox disavows any obligation to correct or to
update the information contained in analyst reports. |
Contacts |
|
Nicox
Gavin Spencer
Chief Executive Officer
T +33 (0)4 97 24 53 00
communications@nicox.com |
Media / Investors
Sophie Baumont
Cohesion Bureau
+33 6 27 74 74 49 sophie.baumont@cohesionbureau.com |
Disclaimer |
The information contained in this document may be modified without
prior notice. This information includes forward-looking statements.
Such forward-looking statements are not guarantees of future
performance. These statements are based on current expectations or
beliefs of the management of Nicox S.A. and are subject to a number
of factors and uncertainties that could cause actual results to
differ materially from those described in the forward-looking
statements. Nicox S.A. and its affiliates, directors, officers,
employees, advisers or agents, do not undertake, nor do they have
any obligation, to provide updates or to revise any forward-looking
statements.
Risks factors which are likely to have a material effect on Nicox’s
business are presented in section 3 of the “Rapport Annuel
2023” which is available on Nicox’s website
(www.nicox.com).
Finally, this press release may be drafted in the French and
English languages. If both versions are interpreted differently,
the French language version shall prevail. |
Nicox S.A.
Sundesk Sophia Antipolis, Bâtiment C, Emerald Square, Rue Evariste
Galois, 06410 Biot, France
T +33 (0)4 97 24 53 00 |
1 Zhaoke Ophthalmology Limited IPO Prospectus, April
2021
- EN_OcumensionZerviateNDAChinaApproval_PR_FINAL
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