COX Nicox SA

Nicox Announces Intention to Conduct a Registered Offering on NASDAQ in the United States

Nicox Announces Intention to Conduct a Registered Offering on NASDAQ in the United States

SOPHIA ANTIPOLIS, France, Sept. 06, 2018 (GLOBE NEWSWIRE) -- Nicox SA (Euronext Paris: FR0013018124, COX), an international ophthalmic company, announced today that it has previously confidentially submitted a draft registration statement on Form F-1 to the U.S. Securities and Exchange Commission relating to the proposed offering of American Depository Shares (ADS) representing Nicox ordinary shares in the United States. The timing, number of ADS representing ordinary shares and price of the proposed offering have not yet been determined.

This press release does not constitute an offer to sell or the solicitation of an offer to buy securities, and shall not constitute an offer, solicitation or sale in any jurisdiction in which such offer, solicitation or sale would be unlawful prior to registration or qualification under the securities laws of that jurisdiction.

About Nicox

Nicox S.A. is an international ophthalmology company developing innovative solutions to help maintain vision and improve ocular health. By leveraging our proprietary expertise in nitric oxide (NO) donation and other technologies, we are developing an extensive portfolio of novel product candidates that target multiple ophthalmic conditions, including glaucoma. Our portfolio includes three programs in development based on our proprietary NO-donating research platform and on reformulated molecules that have previously been used in other indications and therapeutic areas as well as future generation stand-alone NO donors in the preclinical research stage and other exploratory novel NO-donating compounds targeting ophthalmic conditions including glaucoma and ocular hypertension. In addition, we have two ophthalmology assets that have been approved by the U.S. Food and Drug Administration (FDA); VYZULTA™ (latanoprostene bunod ophthalmic solution), 0.024%, exclusively licensed worldwide to Bausch + Lomb, a Bausch Health Companies Inc. company, and commercialized in the U.S. by partner since December 2017 as well as ZERVIATE™ (cetirizine ophthalmic solution), 0.24%, exclusively licensed in the U.S. to Eyevance Pharmaceuticals. 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 & CoHugo SolvetParis, France
Invest SecuritiesMartial DescouturesParis, France
Gilbert DupontJamina El-Bougrini 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.

Contacts

Nicox 
Gavin Spencer, 
Executive Vice President, Chief Business Officer  
T +33 (0)4 97 24 53 00 
  
  
Investors & mediaInvestors & media
United StatesEurope
LifeSci Advisors, LLC LifeSci Advisors, LLC
Monique KosseHans Herklots
T T
M  
  
 Media
 France
 NewCap
 Nicolas Merigeau
 T +33 (0)1 44 71 94 98
  
  
 Media
 Italy 
 Argon Healthcare International 
 Pietro Pierangeli
  
 Chiara Tettamanti
  
 T .8300



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 the 4th chapter of the ‘Document de référence, rapport financier annuel et rapport de gestion 2017’ filed with the French Autorité des Marchés Financiers (AMF) on March 19, 2018, 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

EN
06/09/2018

Underlying

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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...

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