COX Nicox SA

Nicox Announces Last Patients Complete Final Visit in NCX 470 Phase 3 Mont Blanc Glaucoma Trial

Nicox Announces Last Patients Complete Final Visit in NCX 470 Phase 3 Mont Blanc Glaucoma Trial

Press Release
Nicox Announces Last Patients Complete Final Visit in NCX 470 Phase 3 Mont Blanc Glaucoma Trial




  • The last patients completed their final (3-month) visit on September 16
  • 691 patients were enrolled in the Mont Blanc trial
  • Topline results of the Mont Blanc trial due in early November 2022
September 19, 2022– release at 7:30 am CET

Sophia Antipolis, France



Nicox SA (Euronext Paris: FR0013018124, COX), an international ophthalmology company, today announced that the last patients completed their final (3-month) visit in the Mont Blanc Phase 3 clinical trial of NCX 470 0.1% for the lowering of intraocular pressure (IOP) in patients with open-angle glaucoma or ocular hypertension. A total of 691 patients were enrolled in the trial. NCX 470, Nicox’s lead clinical product candidate, is a novel, potentially best-in-class, nitric oxide (NO)-donating prostaglandin analog eye drop.



We are pleased to have reached this milestone in the Mont Blanc Phase 3 clinical trial, and I would particularly like to thank our clinical sites and the Nicox development team for their incredible efforts in continuing to drive this trial to completion in the face of the COVID-19 pandemic situation.” said Doug Hubatsch, EVP, Chief Scientific Officer of Nicox.  “NCX 470 has the potential to be a best-in-class glaucoma treatment, and we look forward to sharing the topline results in early November.



Mont Blanc is a multi-regional, double-masked, 3-month, parallel group trial evaluating the efficacy and safety of NCX 470 ophthalmic solution 0.1% compared to latanoprost ophthalmic solution, 0.005%. Latanoprost is the most widely prescribed first-line therapy for open-angle glaucoma or ocular hypertension. The primary efficacy evaluation in Mont Blanc is based on time-matched IOP at 8 AM and 4 PM at Week 2, Week 6 and Month 3.



The second Phase 3 trial on NCX 470, Denali, is being jointly conducted and equally financed with our Chinese partner, Ocumension Therapeutics. Topline results is currently expected after 2024.
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 prostaglandin analog, for lowering intraocular pressure in patients with open-angle glaucoma or ocular hypertension. The company is also conducting research on NCX 1728, a nitric oxide-donating phosphodiesterase 5 inhibitor, in intraocular pressure lowering and retinal conditions. NCX 4251, a novel, patented, ophthalmic suspension fluticasone propionate nanocrystals for topical ocular application for dry eye disease, is being developed by Ocumension Therapeutics in China under an exclusive license agreement and is available for partnering elsewhere. Nicox generates revenue from VYZULTA® in glaucoma, licensed exclusively worldwide to Bausch + Lomb, and ZERVIATE® in allergic conjunctivitis, licensed in multiple geographies, including to Eyevance Pharmaceuticals, LLC (a wholly-owned subsidiary of Santen Pharmaceutical Co., Ltd.), in the U.S. and Ocumension Therapeutics in the Chinese and in the majority of Southeast Asian markets.



Nicox is headquartered in Sophia Antipolis, France, is listed on Euronext Paris (Compartment B: Mid Caps; Ticker symbol: COX) and is part of the CAC Healthcare, CAC Pharma & Bio and Next 150 indexes.



For more information on Nicox, its products or pipeline, please visit: .








Analyst coverage




Bryan, Garnier & Co         Dylan Van Haaften        Paris, France

Edison Investment Research        Pooya Hemami        London, UK

H.C. Wainwright & Co        Yi Chen        New York, U.S.

Kepler Cheuvreux        Arsene Guekam        Paris, France
 
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.




Nicox

Gavin Spencer

Executive Vice President, Chief Business Officer

& Head of Corporate Development

T +33 (0)4 97 24 53 00





Investors & Media

United States & Europe

LifeSci Advisors, LLC

Sandya von der Weid

T 8

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 the 3rd chapter of the ‘Document d’enregistrement universel, rapport financier annuel et rapport de gestion 2021’ filed with the French Autorité des Marchés Financiers (AMF) on April 29, 2022 which is available on Nicox’s website ()
Nicox S.A.

Drakkar 2

Bât D, 2405 route des Dolines

CS 10313, Sophia Antipolis

06560 Valbonne, France

T +33 (0)4 97 24 53 00

F +33 (0)4 97 24 53 99

 

Attachment



EN
19/09/2022

Underlying

To request access to management, click here to engage with our
partner Phoenix-IR's CorporateAccessNetwork.com

Reports on Nicox SA

 PRESS RELEASE

Nicox Highlights Positive NCX 470 Phase 3 Data Confirming Therapeutic ...

Nicox Highlights Positive NCX 470 Phase 3 Data Confirming Therapeutic Profile at the 2026 American Glaucoma Society Annual Meeting Press Release Nicox Highlights Positive NCX 470 Phase 3 Data Confirming Therapeutic Profile at the 2026 American Glaucoma Society Annual MeetingFebruary 24, 2026 – release at 7:30 am CET Sophia Antipolis, FranceNicox SA (Euronext Growth Paris: FR0013018124, ALCOX), an international ophthalmology company, today announced that positive data from the NCX 470 Phase 3 studies were highlighted in 2 podium presentations and a poster at the 2026 American Glaucoma Societ...

 PRESS RELEASE

Nicox présente des données de Phase 3 positives confirmant le profil t...

Nicox présente des données de Phase 3 positives confirmant le profil thérapeutique de NCX 470 lors du congrès annuel 2026 de l’American Glaucoma Society (AGS) Communiqué de presseNicox présente des données de Phase 3 positives confirmant le profil thérapeutique de NCX 470 lors du congrès annuel 2026 de l’American Glaucoma Society (AGS) 24 février 2026 – publication à 7H30Sophia Antipolis, FranceNicox SA (Euronext Growth Paris : FR0013018124, ALCOX, éligible PEA-PME), une société internationale spécialisée en ophtalmologie, annonce aujourd’hui que les données positives issues des études de p...

 PRESS RELEASE

Nicox Announces Positive Feedback from pre-NDA Meeting with U.S. FDA f...

Nicox Announces Positive Feedback from pre-NDA Meeting with U.S. FDA for NCX 470 Press Release Nicox Announces Positive Feedback from pre-NDA Meeting with U.S. FDA for NCX 470 U.S. NDA submission on track for summer 2026Nicox to receive milestone payment from Kowa upon submission of the NDANDA submission based on Phase 3 clinical data showing NCX 470 lowered intraocular pressure by up to 10mmHg in patients with open-angle glaucoma or ocular hypertension February 16, 2026 – release at 7:30 am CET Sophia Antipolis, FranceNicox SA (Euronext Growth Paris: FR0013018124, ALCOX), an international...

 PRESS RELEASE

Nicox annonce une réunion pré-NDA positive avec la FDA américaine pour...

Nicox annonce une réunion pré-NDA positive avec la FDA américaine pour NCX 470 Communiqué de presseNicox annonce une réunion pré-NDA positive avec la FDA américaine pour NCX 470  Le dépôt de la demande d’autorisation de mise sur le marché (NDA) aux Etats-Unis reste prévu pour l’été 2026Nicox percevra un paiement d’étape de Kowa lors du dépôt de la NDALa soumission de la NDA s’appuie sur les données cliniques de Phase 3 montrant que NCX 470 a réduit la pression intraoculaire jusqu’à 10 mmHg chez les patients atteints de glaucome à angle ouvert ou d’hypertension oculaire 16 février 2026 – pu...

 PRESS RELEASE

Nicox confirme son éligibilité au PEA-PME

Nicox confirme son éligibilité au PEA-PME Communiqué de presseNicox confirme son éligibilité au PEA-PME12 février 2026 – publication à 7H30Sophia Antipolis, FranceNicox SA (Euronext Growth Paris : FR0013018124, ALCOX, éligible PEA-PME), société internationale spécialisée en ophtalmologie, confirme son éligibilité au PEA-PME pour l’année à venir. Pour les besoins de cette confirmation, les critères d'éligibilité des titres de la société Nicox au PEA-PME, prévus par l'article L 221-32-2 du code monétaire et financier, ont été appréciés conformément aux modalités prévues par l'article D 221-11...

ResearchPool Subscriptions

Get the most out of your insights

Get in touch