Business Wire

DOMPÉ

12.12.2016 14:08:35 CET | Business Wire | Press release

Share
Neurotrophic Keratitis: EMA Validates the Marketing Authorisation Application for Cenegermin Eye Drops (Oxervate®) Submitted by Dompé

The biopharmaceutical company Dompé announced the acceptance of the registration application submitted to the European Medicines Agency (EMA) for Oxervate® eye drops, for the treatment of moderate and severe neurotrophic keratitis in adult patients.

Acceptance by EMA constitutes the initiation of the dossier's scientific review procedure, in order to obtain authorisation to market the medicinal product, which was designated an orphan drug for the treatment of neurotrophic keratitis by EMA's committee for Orphan Medicinal Products (COMP) in 2015. Cenegermin , the product's active substance, is the recombinant version of the human nerve growth factor (NGF), discovered by Nobel Prize winner Rita Levi Montalcini. It is a protein produced naturally by the human body and that is responsible for the development, maintenance and survival of nerve cells2 .

The investigational medicinal product has been studied in patients with moderate and severe neurotrophic keratitis. Neurotrophic keratitis is a rare degenerative eye disease affecting fewer than 5 in every 10,0003 people, which causes damage to the corneal epithelium and a loss of corneal sensitivity. In its more severe forms, it can cause corneal ulcers, melting and perforation, with consequences for the visual capacity of those suffering from it4 . A number of different clinical conditions such as viral infections of the cornea5 , eye injuries, chemical burns and lesions, corneal surgery6 , or even systemic conditions such as diabetes7 can cause the disease.

Considering the severity of the condition, the lack of valid treatment options for patients and the innovative nature of the product, at this first stage EMA decided to adopt an accelerated assessment of the dossier.

“We are proud to announce such an important breakthrough in our Research & Development pathway. If it is approved, this treatment option will bring benefits to the management of patients suffering from neurotrophic keratitis, by becoming the first biotech product to be developed by Dompé. An accomplishment testament to the passion and commitment of an extraordinary team who has believed in this project since the beginning”, explains Eugenio Aringhieri, Dompé's Chief Executive Officer . “Our daily commitment has always focussed on finding innovative answers to unmet health needs: we intend to continue providing all the information required by the regulatory authorities, in order to guarantee the availability of the medicinal product as soon as possible.”

“Being the first to have brought the nerve growth factor from discovery to a potential future therapy is a further confirmation of the research efforts conducted by us and by the pharmaceutical companies of our country. It is a major achievement that clearly demonstrates Italy’s strengths” , explains Sergio Dompé, Chairman of Dompé . “My thoughts and my thanks at this time go to the whole team of researchers, who have participated in the project at the international level according to their roles, ensuring a significant contribution to the development of this new drug, but especially to Professor Rita Levi Montalcini, whose ingenious intuition paved the way for this research. I am referring to the studies on the nerve growth factor that earned her the Nobel Prize.”

About Dompé

Dompé is one of the main biopharmaceutical companies in Italy focused on the development of innovative pharmaceutical solutions for diseases with high social impact and which are often incurable. Dompé has its headquarters in Milan and focuses its research efforts in areas with unmet therapeutic needs, such as diabetes, organ transplants, ophthalmology, and oncology. The industrial center in L'Aquila (Abruzzo) houses a biotechnology facility known worldwide for its excellence and develops primary care drugs intended for markets in about 40 countries worldwide. Dompé also has offices in Albania, France, Germany, the United Kingdom, Spain and the United States (New York).
For further information, please visit: www.dompe.com and www.dompetrials.com

Forward looking statements

This press release makes reference to certain information that may not coincide with expected future results. Dompé firmly believes in the soundness and reasonableness of the concepts expressed. However, some of the information is subject to a certain degree of indetermination in relation to its research and development activities and the necessary verifications to be performed by regulatory bodies. Therefore, as of today, Dompé cannot guarantee that the expected results will be consistent with the information provided above.

1 M. Sacchetti, and A. Lambiase, Diagnosis and management of neurotrophic keratitis. Clin Ophthalmol 8 (2014) 571-9.
2 R. Levi Montalcini, The nerve growth factor 35 years later , Science 1987
3 As above
4 As above
5 J. Gallar, T. M. Tervo, W. Neira, J. M. Holopainen, M. E. Lamberg, F. Minana, M. C. Acosta, and C. Belmonte, Selective changes in human corneal sensation associated with herpes simplex virus keratitis. Invest Ophthalmol Vis Sci 51 (2010) 4516-22; T. J. Liesegang, Corneal complications from herpes zoster ophthalmicus. Ophthalmology 92 (1985) 316-24
6 S. Bonini, P. Rama, D. Olzi, and A. Lambiase, Neurotrophic keratitis. Eye 17 (2003) 989-995.
7 R. A. Hyndiuk, E. L. Kazarian, R. O. Schultz, and S. Seideman, Neurotrophic corneal ulcers in diabetes mellitus. Arch Ophthalmol 95 (1977) 2193-6.

Contact:

Dompé
Laura Sprea
Corporate Communications Specialist
laura.sprea@dompe.com | +39 02 58383567 | +39 3355745188

About Business Wire

Business Wire
Business Wire
101 California Street, 20th Floor
CA 94111 San Francisco

http://businesswire.com

Subscribe to releases from Business Wire

Subscribe to all the latest releases from Business Wire by registering your e-mail address below. You can unsubscribe at any time.

Latest releases from Business Wire

Takeda Receives U.S. FDA Approval of MIMRYLO™ (rusfertide), Marking a Potential Shift in the Treatment Paradigm for Polycythemia Vera29.8.2026 00:40:00 CEST | Press release

MIMRYLO, a First-in-Class Medicine with a Unique Mechanism of Action, is Approved for the Treatment of Erythrocytosis in Adults with Polycythemia Vera (PV)MIMRYLO Has Been Shown to Maintain Hematocrit Control, the Primary Treatment Goal in PV, as Well as Reduce Phlebotomy Burden and Improve FatigueApproval Supported by Phase 3 VERIFY Results Showing 76.9% of Patients Achieved Clinical Response During Weeks 20-32 Takeda (TSE:4502/NYSE:TAK)announced U.S. Food and Drug Administration (FDA) approval of the New Drug Application (NDA)* for MIMRYLO™ (rusfertide) for the treatment of erythrocytosis in adults with polycythemia vera (PV), a blood cancer. This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20260824773270/en/ MIMRYLO Logo MIMRYLO is a first-in-class hepcidin mimetic designed to regulate iron distribution in the body and red blood cell overproduction to control hematocrit levels, which is the ratio of red blood cells to the tot

Rigaku and Tohoku University Establish a New Research Institute for X-Ray Metrology28.8.2026 16:00:00 CEST | Press release

Rigaku Corporation, a group company of Rigaku Holdings and a global solutions partner for X-ray analytical systems (Head Office: Akishima, Tokyo; President and CEO: Jun Kawakami; “Rigaku”), and Tohoku University (Sendai, Miyagi; President: Teiji Tominaga; “Tohoku University”) have established the Rigaku-Tohoku University Co-Creation Research Institute for X-ray Metrology: Beyond The Limits (the “Institute”) at Tohoku University on August 1, 2026. The Institute will advance X-ray metrology technology, develop new metrology methods, and foster the next generation of researchers through an initial three-year collaboration, with the possibility of extension based on its achievements. This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20260828688510/en/ Inside the Institute As semiconductors become smaller, more multilayered, and incorporate a wider range of materials, manufacturing processes are becoming increasingly complex. X-ray me

BLK: Portfolio Company of Enry’s Island S.p.A., Lists on Euronext Dublin28.8.2026 15:34:00 CEST | Press release

Enry’s Island S.p.A. (WBAG:EIOS), an international venture builder with headquarters in the Tremiti Islands and the Metaverse, announces that BLK Global PLC, one of the portfolio companies within its ecosystem, has successfully completed its admission to trading on Euronext Access Dublin. Trading in the company’s shares commenced on Friday, July 31, 2026, under ticker BLKX and ISIN GB00BPSKS130. BLK was one of the thousands of applications received by Enry’s Island which, following an assessment process based on the Enry’s Model, was selected for a one-year incubation and acceleration programme. The programme supported the company through its subsequent growth stages, ultimately leading to its current stock market listing. Alessandro Pacciana, Investor Relations Manager of Enry’s Island S.p.A., said: “BLK’s listing is the second stock market listing in two years among Enry’s Island’s portfolio companies, while Enry’s Island itself is the world’s first listed venture builder. We are pro

Zambon Announces European Commission Approval of Hopledo® for Adults with Parkinson's Disease and Moderate to Severe Motor Fluctuations28.8.2026 11:00:00 CEST | Press release

Hopledo® is a first-in-class, oral, modified-release formulation of levodopa/carbidopa (LD/CD) approved for the treatment of motor fluctuations of Parkinson’s disease Zambon expects to begin the phased introduction of Hopledo® across European markets starting October 2026 The approval is based on data from the Phase 3 RISE-PD trial where Hopledo® demonstrated a significant increase in Good ON time compared with immediate-release LD/CD with fewer daily doses and a comparable safety profile Zambon today announced that the European Commission (EC) has granted marketing authorization for Hopledo® (modified-release levodopa/carbidopa) for the treatment of adult patients with Parkinson’s disease and moderate to severe motor fluctuations who have not been sufficiently stabilized with oral levodopa/dopa decarboxylase (DDC) inhibitor-based treatment regimens. Zambon expects to begin the phased introduction of Hopledo® across European markets starting October 2026. The company is working closely

MTG-I2 Safely in Orbit, Unlocking Faster and Sharper Weather Monitoring Across Europe28.8.2026 10:16:00 CEST | Press release

The Meteosat Third Generation Imager 2 satellite (MTG-I2) has successfully passed its first critical post-launch milestones, completing the first full Meteosat Third Generation constellation in orbit. This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20260828243790/en/ Credit: Arianespace livestream The imager satellite MTG-I2 is safely in orbit and operating as expected following its successful launch yesterday at 22:11 CEST on board an Ariane 6 rocket from Europe’s Spaceport in French Guiana. Our teams have established communication with the spacecraft, which has also deployed its solar panels to ensure its autonomous production of energy. MTG-I2 is in perfect shape to start its Launch and Early Operations Phase that will bring it to a higher orbit, 36 000km above Earth over the following two weeks, where a longer period of calibration and validation of its instruments will begin. This summer’s extreme weather and wildfires hav

In our pressroom you can read all our latest releases, find our press contacts, images, documents and other relevant information about us.

Visit our pressroom
World GlobeA line styled icon from Orion Icon Library.HiddenA line styled icon from Orion Icon Library.Eye