Nicox Announces First Commercial Sale of ZERVIATE in China by Partner Ocumension, Creating a New Recurrent Revenue Stream
December 04 2024 - 1:30AM
UK Regulatory
Nicox Announces First Commercial Sale of ZERVIATE in China by
Partner Ocumension, Creating a New Recurrent Revenue Stream
Press Release |
Nicox Announces First Commercial Sale of ZERVIATE in China by
Partner Ocumension, Creating a New Recurrent Revenue
Stream |
- First
commercialized product from the Nicox-Ocumension
collaboration
- Recent
acquisitions have enhanced OcuMension's leadership in the
ophthalmology field in the China market
- Product
made available quickly after approval thanks to a rapid
manufacturing campaign at Ocumension’s state-of-the-art
factory
- Major
milestone for this strong collaboration, which also includes our
lead asset, NCX 470, where recruitment was just completed in the
Denali Phase 3 trial
December 4, 2024 – release at 7:30 am CET
Sophia Antipolis, France
Nicox SA (Euronext Growth Paris: FR0013018124,
ALCOX), an international ophthalmology company, today announced the
first commercial sale of ZERVIATE® (cetirizine ophthalmic
solution), 0.24% in China by its exclusive Chinese partner
Ocumension Therapeutics. ZERVIATE is indicated for ocular itching
associated with allergic conjunctivitis and was approved in China
in September 2024.
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.
“The first commercial sale of ZERVIATE in China by our partner
Ocumension, marks the next significant milestone in this broad
collaboration initiated in 2018 and provides a new revenue stream
for Nicox. Ocumension has proven itself to be a strong development
partner through their work on ZERVIATE and on the recruitment of
Chinese patients in the NCX 470 Denali Phase 3 study. They have
also been building out commercial operations through organic and
external growth, including acquiring products and operations from a
leading player in China, ideally placing them to maximise the value
of ZERVIATE in the Chinese market. We look forward to continuing to
work with them as we advance NCX 470 towards commercialisation as
well.” said Gavin Spencer, Chief Executive Officer of
Nicox.
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% on
net sales of ZERVIATE by Ocumension.
|
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 also has a
preclinical research program on NCX 1728, a nitric oxide-donating
phosphodiesterase-5 inhibitor, with Glaukos. Nicox’s first
product, VYZULTA® in glaucoma, licensed exclusively worldwide to
Bausch + Lomb, is available commercially in the U.S. and over 15
other territories. Nicox generates revenue from 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 |
|
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” and in section 4 of the “Rapport semestriel
financier et d’activité 2024” which are 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 |
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