DOMPÉ
28.1.2013 12:31:52 CET | Business Wire | Pressemeddelelse
Hope for the future from Reparixin : the first drug developed to improve the efficacy of the procedure
- At present in Europe only the UK and Switzerland have NHS reimbursement for this procedure
- According to NICE the procedure is indicated for patients experiencing severe hypoglycaemic episodes that are unmanageable and occur without warning.
Pancreatic islet transplantation has shown short-term efficacy with some evidence of long-term efficacy , as well as a satisfactory safety profile, according to the Guidance issued by NICE (National Institute for Health and Clinical Excellence), the UK medicines regulator. The National Specialised Commissioning Team (NSCT) formerly National Commissioning Group (NCG) has approved reimbursement for this procedure as a treatment option for type 1 diabetes patients experiencing hypoglycemic episodes that occur without warning and cannot be managed with current treatments. Type 1 diabetes is a disease affecting some 20 million people worldwide . In Europe only the strict UK regulator and Swiss health authorities have approved NHS reimbursement for this procedure that in the future may get even more space as a treatment option in patients with type 1 diabetes thanks to Reparixin. Developed by Dompé , one of Italy’s leading biopharmaceutical companies, Reparixin has shown to improve transplantation efficiency.
“Over the last 15 years, transplantation of pancreatic islet cells from donors into patients with severe type 1 diabetes, has moved from a relatively rare experimental procedure, to a more commonplace successful clinical treatment” - said Paul Johnson , Director of the Oxford Islet Transplant Programme. “Current data show, for example, that every year 15-25 of these transplants are performed in the United Kingdom, about 20 in Italy, c. 10 in France and Germany. However, despite considerable success worldwide, in most countries islet transplantation remains funded through research grants. In the UK, this procedure is now fully funded by the National Health Service (NHS) and is free for any patient who meets the inclusion criteria. It is therefore, really important that islet transplantation can be offered as a fully reimbursed life-saving treatment for patients throughout Europe and other parts of the world.”
The new frontier of research for a cure for type 1 diabetes has been the focus of attention of experts from all over the world at the Symposium titled “Current issues in pancreas/islet transplantation” held as part of the AIDPIT/EPITA Winter Symposium in Innsbruck (Austria).
Reparixin is a potent selective inhibitor of interleukin-8, a chemokine that plays a key role in the inflammatory response involved in the reduced efficacy of pancreatic islet transplantation. Reparixin was developed to specifically inhibit inflammation, preserve implanted cells function and hence improve the efficiency of the procedure. A recently launched randomized double-blind multicenter Phase III clinical trial is underway in 8 centres of 5 countries in Europe and the United States enrolling some 50 patients, i.e., about half the total number of patients undergoing this innovative treatment procedure every year. The study is designed to assess the efficacy of Reparixin in improving the efficiency of pancreatic islet transplantation, protecting transplanted cells function and graft survival as well as increasing the number of patients achieving insulin independence.
“The pharmaceutical industry has taken up the challenge of doing research in ‘hot fields’ and is committed to investing in areas where small patient populations have tremendous treatment needs” - said Eugenio Aringhieri , CEO, Dompé Group. “For this virtuous process to continue it is paramount to have a regulatory environment that warrants proper assessment as well as clear, consistent access rules. This has long been advocated but is now an absolute priority as this is the only way to truly respond to the treatment needs of patients.”
The role of pancreatic islet transplantation has emerged clearly during the Symposium in which some of the world’s leading experts in the field have participated. While the benefits for patients and national healthcare systems are apparent, at present the use of this procedure is still limited due to both the small number of centres where it can be performed and various factors involved in the progressive decline in transplanted pancreatic islet function. The inflammatory response that patients develop in the days following cell infusion, which is done by a simple injection into the portal vein, reduces cell function by 50 percent in the first week, with obvious repercussions on the ultimate efficacy of the procedure.
“My efforts as a scientist have always been focused on developing treatment approaches for diabetes prevention and cure. In particular, I have contributed to the experimental and clinical progress of pancreatic islet transplantation, a procedure that I am certain can become a true alternative to organ transplantation” – said Prof. Camillo Ricordi , Director of the Diabetes Research Institute, Miami, one of the world’s top diabetes experts. “Results shown so far by Reparixin confirm that targeted anti-inflammatory treatment can give a crucial contribution not only to prevent transplant rejection, but also to the establishment of pancreatic islet transplantation as a fully-fledged procedure. We hope that its treatment potential be confirmed so that the results of this technique can be optimised but especially significantly improve patients’ quality of life and at the same time reduce the risk associated with protracted immunosuppression that today is necessary for these patients.”
Contact:
Alessandro Aquilio
Corporate Communications Responsible
Email: alessandro.aquilio@dompe.it
+39
02 58383 556
+39 334 6550628
Information om Business Wire
Følg pressemeddelelser fra Business Wire
Skriv dig op her, og modtag pressemeddelelser på e-mail. Indtast din e-mail, klik på abonner, og følg instruktionerne i den udsendte e-mail.
Flere pressemeddelelser fra Business Wire
Galderma Buys Back Shares Worth CHF 232 Million in the Context of Accelerated Bookbuild Offering11.3.2026 07:00:00 CET | Press release
Ad hoc announcement pursuant to Art. 53 LR Galderma (SIX: GALD), the pure-play dermatology category leader, today announced that it has agreed to repurchase 1.6 million shares at a price of CHF 143.75 per share for a total consideration of CHF 232 million in the context of the accelerated bookbuild offering (“ABO”) of Galderma shares by Sunshine SwissCo GmbH (“EQT”), Abu Dhabi Investment Authority (Private Equities Department) and Auba Investment Pte. Ltd. (all together the “Selling Shareholders”) launched yesterday evening. The repurchase was made at the same price per share determined by the bookbuilding offering. As a result of yesterday evening’s ABO, the Selling Shareholders have fully divested their remaining stake in Galderma. The repurchase, which is expected to settle on March 13 is being financed by Galderma’s existing liquidity on hand and will not affect the company’s ability to deliver on its strategic and financing priorities. The shares will be held in treasury for futur
Thales Launches SkyDefender: The Integral Air and Missile Defence Dome With Artificial Intelligence11.3.2026 07:00:00 CET | Press release
SkyDefender is a multi-layer, multi-domain Integrated Air and Missile Defence system providing full protection against all types of air threats, on land, at sea and in space. SkyDefender integrates a network of advanced sensors and effectors with a versatile command and control (C2) system. With its open and modular architecture, it is fully compatible with existing air defence systems. Combining Thales’ expertise in cybersecurity and advanced artificial intelligence through cortAIx, Thales AI accelerator, SkyDefender enables operational superiority and proactive defence against cyberattacks and evolving threats. Thales is capable of delivering this critical protection globally from today. As air and missile threats are evolving faster than ever, from slow-moving drones to hypersonic missiles, attacks are becoming increasingly complex, saturating and unpredictable. This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20260310398606/
Curatis and Neupharma Announce Exclusive Licensing Agreement to Develop and Market Corticorelin (C-PTBE-01) for the Treatment of Peritumoral Brain Edema in Japan11.3.2026 07:00:00 CET | Press release
Japan is one of the world's most important pharmaceutical markets after the US and Europe. Neupharma’s team has extensive experience in developing and successfully commercialising orphan drugs as well as speciality care medicines in Japan, including a blockbuster drug. The agreement with Neupharma includes upfront and milestone payments of up to CHF 83.5 million as well as royalties of up to 20% on sales. The population of available patients eligible for corticorelin treatment associated with peritumoral brain edema is estimated at 60,000 in Japan and 500,000 worldwide. Global market potential is forecasted to exceed USD 1 billion annually. Curatis Holding AG (SIX: CURN) and Neupharma Co., Ltd. (“Neupharma”), a Japanese pharmaceutical company specializing in oncology, immunology, pulmonology and cardiology disorders, today announce an exclusive license and development agreement for corticorelin (C-PTBE-01) in Japan. Under the terms of the agreement, Neupharma will receive exclusive rig
Galderma Completes Successful Placement of EUR 500 Million Eurobond11.3.2026 06:55:00 CET | Press release
Galderma Group AG (SWX:GALD): NOT FOR DISTRIBUTION IN THE UNITED STATES OR IN ANY OTHER JURISDICTION IN WHICH SUCH DISTRIBUTION WOULD BE RESTRICTED BY APPLICABLE LAW OR REGULATION. Galderma Group AG (SIX:GALD), the pure-play dermatology category leader, today announced the successful placement of a single-tranche EUR 500 million Eurobond. The bond has a 5-year maturity and carries a fixed-rate annual coupon of 3.375%. The Eurobond was placed on March 10, 2026, with settlement expected on March 17, 2026, and will be listed on the SIX Swiss Exchange. Citigroup, ING, J.P. Morgan and RBC Capital Markets jointly led the transaction. Net proceeds from the transaction will be used to fully repay Galderma’s existing bank term loan issued in connection with the company’s initial public offering in March 2024. The transaction represents the final step in Galderma’s refinancing process, having obtained two investment grade credit ratings. Galderma is currently rated ‘BBB’ (stable outlook) by Fitc
Estithmar Holding Net Profit Surges 122% to QAR 938 Million; Revenue Rises 54% to QAR 6.4 Billion for the Year Ended 31 December 202510.3.2026 22:52:00 CET | Press release
- Sustainable Growth Driven by International Expansion - Significant Increase Across Key Metrics Estithmar Holding Q.P.S.C. has announced its financial results for the year ended 31 December 2025. The group reported a 54% increase in revenue to QAR 6.4 billion, compared with QAR 4.2 billion in 2024. Gross profit rose to QAR 2.1 billion, up from QAR 1 billion in 2024, representing growth of 111%. EBITDA reached QAR 1.5 billion, an increase of 102% year-on-year. This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20260310410214/en/ Estithmar Holding Net Profit Surges 122% to QAR 938 Million; Revenue Rises 54% to QAR 6.4 Billion for the Year Ended 31 December 2025 (Photo: AETOSWire) Net profit climbed 122% compared with 2024, reaching QAR 938 million. Earnings per share increased by 145% to QAR 0.264. The growth in net profit was primarily driven by higher revenues, particularly from the specialized contracting and healthcare sectors.
I vores nyhedsrum kan du læse alle vores pressemeddelelser, tilgå materiale i form af billeder og dokumenter samt finde vores kontaktoplysninger.
Besøg vores nyhedsrum
