DOMPÉ
12.12.2016 14:08:35 CET | Business Wire | Press release
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.
View source version on businesswire.com: http://www.businesswire.com/news/home/20161212005584/en/
Contact:
Dompé
Laura Sprea
Corporate Communications Specialist
laura.sprea@dompe.com
| +39 02 58383567 | +39 3355745188
About Business Wire
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
Incyte Announces the European Commission Approval of Zynyz® (retifanlimab) for the First-Line Treatment of Advanced Squamous Cell Carcinoma of the Anal Canal (SCAC)6.3.2026 22:42:00 CET | Press release
- Zynyz® (retifanlimab) in combination with carboplatin and paclitaxel (platinum-based chemotherapy) is the first systemic treatment for adult patients with advanced SCAC in Europe- The EC approval is based on results of the POD1UM-303 study which showed that adult patients with advanced SCAC achieved significantly improved progression-free survival with Zynyz in combination with carboplatin and paclitaxel as a first-line treatment compared to chemotherapy alone.1 Incyte (Nasdaq:INCY) today announced that the European Commission (EC) has approved Zynyz® (retifanlimab) in combination with carboplatin and paclitaxel (platinum-based chemotherapy) for the first-line treatment of adult patients with metastatic or with inoperable locally recurrent squamous cell carcinoma of the anal canal (SCAC). “The EC approval of Zynyz marks an important step forward for patients with advanced SCAC, a rare cancer for which meaningful treatment advances have not occurred in several decades,” said Bill Meur
Dfns Launches Payouts6.3.2026 21:27:00 CET | Press release
Dfns today announced the launch of Payouts, a new API enabling institutions to convert stablecoins to fiat and route payouts across multiple bank accounts while keeping wallet-level governance and controls in place. This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20260305327930/en/ Convert stablecoins to fiat and settle payouts to bank accounts in 94 countries, today. Solving the problem of single-rail off-ramps Today, most fintechs and institutions still hard-wire a single payout provider into their stack, or rely on vertically integrated models that bundle routing, pricing, custody, and settlement together. That approach may be convenient early on, but it creates structural problems at scale: weak price discovery because there is no competitive pressure on margins, limited auditability because routing decisions are opaque, and operational fragility because a single provider degradation in any corridor requires architectural i
Klarna Group Plc Clarifies Mechanics of March 9 Lock-Up Expiration6.3.2026 20:23:00 CET | Press release
Klarna Group plc (NYSE: KLAR) today issues the following clarification to ensure investors and market participants have accurate information regarding the mechanics of its lock-up expiration on March 9, 2026, the processes required before pre-IPO shares can be traded on the NYSE, and the prior liquidity opportunities already available to shareholders. This release contains only factual descriptions of the Company's share structure and applicable processes. It does not constitute guidance or a projection of any kind regarding future trading volumes, share price, or the intentions of any shareholder and speaks only as of the date of this press release. 1. 335 million locked-up shares — but two different categories Of the 378 million total ordinary shares outstanding, approximately 335 million are subject to lock-up restrictions expiring March 9, 2026. However, these shares fall into two distinct categories governed by separate sets of regulations. A. 159 million shares (48% of locked-up
Lone Star Funds Announces Agreement to Acquire the Capsules & Health Ingredients Division of Lonza Group AG6.3.2026 18:30:00 CET | Press release
Lone Star Funds (“Lone Star”) today announced that an affiliate of Lone Star Fund XII, L.P. has entered into a definitive agreement to acquire the Capsules & Health Ingredients (“CHI”) division of Lonza Group AG. As part of the transaction, Lonza will retain a 40% equity position in the business. Headquartered in Basel, Switzerland, CHI operates globally across the Americas, Europe and Asia Pacific. The business comprises three segments: Hard Empty Capsules: leading global manufacturer of gelatin and plant-based capsules offering a broad range of innovative solutions for pharmaceutical and nutraceutical customers. Dosage Form Solutions: end-to-end development and manufacturing platform serving nutraceutical and pharmaceutical customers. Health Ingredients: provider of branded, science-backed nutrition ingredients serving joint health, energy and active lifestyle markets. Lone Star believes CHI is a high-quality, globally recognized platform with strong technical capabilities, different
Sutherland Launches FinAI Hub to Industrialize Agentic AI for Banking and Financial Services6.3.2026 14:00:00 CET | Press release
A domain-trained AI agent workforce enables production-scale AI across regulated financial institution operations Today, Sutherland announced the launch of Sutherland FinAI Hub, an enterprise Agentic AI platform built exclusively for Banking and Financial Services. As financial institutions accelerate AI adoption, many initiatives remain confined to pilots, unable to scale across legacy systems and core operations. Sutherland FinAI Hub is designed to help close that gap. FinAI Hub is an innovation ecosystem where Sutherland works with clients to design, prototype, and scale Agentic AI workflows across core operations. At launch, the platform brings together a large and expanding workforce of domain-trained AI agents purpose-built for financial institutions, supporting functions across retail banking, payments, cards, consumer and commercial lending, servicing, back office, risk and compliance functions. These modular agents can operate independently or be orchestrated across end-to-end
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
