Results from Mont Blanc Phase 3 Trial of Nicox’s NCX 470 in Glaucoma Published in the American Journal of Ophthalmology
20 March 2024 - 5:30PM
Results from Mont Blanc Phase 3 Trial of Nicox’s NCX 470 in
Glaucoma Published in the American Journal of Ophthalmology
Press Release
Results from Mont Blanc Phase 3 Trial of Nicox’s
NCX 470 in Glaucoma Published in the American Journal of
Ophthalmology
- First
publication of the data from the Mont Blanc Phase 3 trial in a
peer-reviewed journal
- Authors
conclude: "NCX 470 could become an important first-line therapy for
IOP reduction in glaucoma."
- Topline
results from second Phase 3 trial of NCX 470, Denali, expected in
H2 2025
March 20, 2024 – release at 7:30 am CETSophia Antipolis,
France
Nicox SA (Euronext Growth
Paris: FR0013018124, ALCOX), an international ophthalmology
company, today announced that the results from the Mont Blanc
pivotal Phase 3 trial comparing NCX 470 to latanoprost in the
lowering of intraocular pressure (IOP) in patients with open-angle
glaucoma or ocular hypertension have been published in the
peer-reviewed journal American Journal of Ophthalmology. The
principal author of the publication is Dr. Robert Fechtner,
Professor and Chair of the Department of Ophthalmology at SUNY
Upstate Medical University, Syracuse, NY and Chairman of Nicox’s
U.S. Glaucoma Clinical Advisory Board.
“We are pleased to see the publication of these
data in such a recognized and respected journal,” said Doug
Hubatsch, Chief Scientific Officer of Nicox. “The data
from the Mont Blanc Phase 3 trial demonstrated the potential of NCX
470 and we look forward to seeing confirmation of this clinical
profile in the upcoming results from the ongoing Denali Phase 3
trial, expected in H2 2025. I’d also like to thank all the Mont
Blanc study sites for their excellent work on this trial.”
The publication entitled “A Randomized,
Controlled Comparison of NCX 470, a Nitric Oxide-Donating
Bimatoprost, and Latanoprost in Subjects with Open-Angle Glaucoma
or Ocular Hypertension: The MONT BLANC Study” was published online
in the American Journal of Ophthalmology on March 16, 2024 and is
available by clicking here.
The Mont Blanc publication concludes that “The
NO-donating prostaglandin analogue NCX 470 0.1% was well-tolerated
and lowered IOP more than latanoprost in subjects with open-angle
glaucoma or ocular hypertension at all 6 time points. With a dual
mechanism of action that enhances both uveoscleral and trabecular
outflow, NCX 470 could become an important first-line therapy for
IOP reduction in glaucoma.”
About NCX 470
NCX 470, Nicox’s lead clinical asset, is a novel
nitric oxide-donating bimatoprost eye drop. The Denali Phase 3
clinical trial evaluating NCX 470 for the lowering of IOP in
patients with open-angle glaucoma or ocular hypertension, being
conducted in the U.S. and China, is on track to generate topline
results in H2 2025. 80% of the target number of
patients have been randomized in the trial and completion of
recruitment of U.S. patients is expected in Q4 2024. Supportive
development data required for the preparation of the U.S. New Drug
Application (NDA) is expected to be available on or before the
completion of the Denali trial. The database from the trial will
not be locked until after the last patient has completed their
final trial visit in China, which drives the timing of the Denali
results.
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, 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
Bryan, Garnier & Co
Eric
Yoo Paris,
FranceH.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
NicoxGavin SpencerChief Executive Officer T +33
(0)4 97 24 53 00communications@nicox.com |
Media / InvestorsSophie BaumontCohesion Bureau+33
6 27 74 74 49sophie.baumont@cohesionbureau.com |
Forward-Looking Statements
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 2.7 of
the “Rapport Annuel 2022” and in section 4 of the “Rapport
semestriel financier et d’activité 2023” which are available on
Nicox’s website (www.nicox.com).
Nicox S.A.Sundesk Sophia Antipolis, Bâtiment C,
Emerald Square, Rue Evariste Galois, 06410 Biot, FranceT +33 (0)4
97 24 53 00
- EN_NCX470MontBlancPublicationAJO PR_20240320_F
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