Ihr Broker

  • DAX 0,70
  • EUR/USD 0,50
  • GOLD 0,30

Nur Spreads

Keine Kommission

Jetzt registrieren

CFDs sind komplexe Instrumente und umfassen aufgrund der Hebelfinanzierung ein hohes Risiko, schnell Geld zu verlieren.

UCB Pharma

UCB enters into collaboration with Roche to develop antibody treatment for people living with Alzheimer's Disease

29.07.2020 - 09:07:29

UCB enters into collaboration with Roche to develop antibody treatment for people living with Alzheimer's Disease. Brussels - - UCB to provide to Roche and Genentech exclusive, world-wide license to UCB's UCB0107, an innovative anti-Tau antibody treatment - UCB will receive an initial upfront payment and, after positive completion of proof-of-concept in Alzheimer's Disease, is ...

Brussels - - UCB to provide to Roche and Genentech exclusive, world-wide license to UCB's UCB0107, an innovative anti-Tau antibody treatment

- UCB will receive an initial upfront payment and, after positive completion of proof-of-concept in Alzheimer's Disease, is eligible to receive further potential payments with a total potential consideration approaching US $2 billion upon receipt of certain regulatory approvals and satisfying certain milestones.

- UCB to fund and perform initial proof-of-concept study in Alzheimer's Disease. Upon completion and availability of results, Genentech has the right to proceed with clinical development or return full rights back to UCB.

UCB today announced an agreement to enter into a world-wide, exclusive license agreement with Roche and Genentech, a member of the Roche Group, for the global development and commercialization of UCB0107 in Alzheimer's Disease (AD). The transaction remains subject to obtaining antitrust clearance and other customary closing conditions.

Charl van Zyl, Executive Vice President UCB and Head of Neurology said: "We are excited that Roche and Genentech, with their deep and wide-ranging expertise, capacity and know-how in Alzheimer's Disease, will collaborate with UCB on UCB0107 with a shared ambition to offer people living with Alzheimer's Disease a new treatment option. Our science driven, patient centric development approach, and leading experience in neurological diseases provides a uniquely holistic view towards the unmet needs and the potential for an effective anti-Tau antibody in the treatment of neurodegenerative diseases like Alzheimer's Disease and progressive supranuclear palsy. In-line with our ongoing and longstanding commitment to the neurodegeneration community, this partnership represents an important step in the potential development of this exciting new medicine."

James Sabry, Global Head of Roche Pharma Partnering said: "In Alzheimer's Disease, we are continuing to explore new molecules that address the key pathways of this complex disease. We are pleased to embark on this journey together with UCB to help expand our efforts on tau. Our commitment remains strong on exploring multiple approaches with the hope that our research and development, including this collaboration with UCB, will lead to a disease-modifying medicine that could positively impact millions of people with Alzheimer's Disease."

UCB0107 is an investigational monoclonal antibody drug being developed by UCB as a potential treatment for patients with tauopathies such as progressive supranuclear palsy (PSP) and Alzheimer's Disease.

UCB will provide an exclusive, world-wide license to Roche and Genentech to develop and commercialize UCB0107 in AD. In return, UCB will receive an initial upfront payment of US $120 million. UCB will fund and perform a proof-of-concept study in AD and, upon availability of the results of that study, Genentech has the right to progress with the development or return full rights back to UCB. After Genentech's decision to proceed with further clinical development, UCB will be eligible to receive further potential cost reimbursement, development and sales milestone payments as well as royalties with a total potential consideration approaching US $2 billion upon receipt of certain regulatory approvals and satisfying certain clinical and sales milestones.

This license agreement does not impact UCB's 2020 financial outlook.

UCB continues to develop UCB0107 in progressive supranuclear palsy (PSP), with a confirmatory phase 3 study due to commence in Q2 2021.

About UCB0107

UCB0107 is a recombinant, humanized, full-length IgG4 monoclonal antibody, targeting a central Tau epitope, which is being developed to block/reduce the spread of Tau pathology.

Tau is a microtubule-associated protein expressed in the central nervous system, which supports the assembly and stabilization of neuronal microtubules.[1] In tauopathies, Tau becomes pathogenic, forming tangles, which cause cell damage and ultimately neuronal death.[1.2.3] It is hypothesised that the spread of Tau protein from neuron to neuron underpins disease progression in tauopathies[4] providing the rationale for antibody therapies.

About UCB

UCB, Brussels, Belgium ( http://www.ucb.com ) is a global biopharmaceutical company focused on the discovery and development of innovative medicines and solutions to transform the lives of people living with severe diseases of the immune system or of the central nervous system. With more than 7 500 people in approximately 40 countries, UCB generated revenue of EUR 4.9 billion in 2019. UCB is listed on Euronext Brussels (symbol: UCB). Follow us on Twitter: @UCB_news

UCB - Corporate UCB - Investor Relations Antje Witte, Investor Communications Laurent Relations, UCB T +32.2.559.94.14, Schots, Media Relations, antje.witte@ucb.com UCB T+32.2.559.92.64, Laurent.schots@ucb.com

Jim BaxterNeurology Isabelle Ghellynck,Investor Relations, Communications, UCBT+32.2.559.9588,isabelle.ghellynck@ucb.com UCBT+32.2.473.78.85.01 jim.baxter@ucb.com


- Forward looking statements UCB

This press release may contain forward-looking statements including, without lim itation, statements containing the words "believes", "anticipates", "expects", " intends", "plans", "seeks", "estimates", "may", "will", "continue" and similar e xpressions. These forward-looking statements are based on current plans, estimat es and beliefs of management. All statements, other than statements of historica l facts, are statements that could be deemed forward-looking statements, includi ng estimates of revenues, operating margins, capital expenditures, cash, other f inancial information, expected legal, arbitration, political, regulatory or clin ical results or practices and other such estimates and results. By their nature, such forward-looking statements are not guarantees of future performance and ar e subject to known and unknown risks, uncertainties and assumptions which might cause the actual results, financial condition, performance or achievements of UC B, or industry results, to differ materially from those that may be expressed or implied by such forward-looking statements contained in this press release. Imp ortant factors that could result in such differences include: the global spread and impact of COVID-19, changes in general economic, business and competitive co nditions, the inability to obtain necessary regulatory approvals or to obtain th em on acceptable terms or within expected timing, costs associated with research and development, changes in the prospects for products in the pipeline or under development by UCB, effects of future judicial decisions or governmental invest igations, safety, quality, data integrity or manufacturing issues; potential or actual data security and data privacy breaches, or disruptions of our informatio n technology systems, product liability claims, challenges to patent protection for products or product candidates, competition from other products including bi osimilars, changes in laws or regulations, exchange rate fluctuations, changes o r uncertainties in tax laws or the administration of such laws, and hiring and r etention of its employees. There is no guarantee that new product candidates wil l be discovered or identified in the pipeline, will progress to product approval or that new indications for existing products will be developed and approved. M ovement from concept to commercial product is uncertain; preclinical results do not guarantee safety and efficacy of product candidates in humans. So far, the c omplexity of the human body cannot be reproduced in computer models, cell cultur e systems or animal models. The length of the timing to complete clinical trials and to get regulatory approval for product marketing has varied in the past and UCB expects similar unpredictability going forward. Products or potential produ cts which are the subject of partnerships, joint ventures or licensing collabora tions may be subject to differences disputes between the partners or may prove t o be not as safe, effective or commercially successful as UCB may have believed at the start of such partnership. UCB' efforts to acquire other products or comp anies and to integrate the operations of such acquired companies may not be as s uccessful as UCB may have believed at the moment of acquisition. Also, UCB or ot hers could discover safety, side effects or manufacturing problems with its prod ucts and/or devices after they are marketed. The discovery of significant proble ms with a product similar to one of UCB's products that implicate an entire clas s of products may have a material adverse effect on sales of the entire class of affected products. Moreover, sales may be impacted by international and domesti c trends toward managed care and health care cost containment, including pricing pressure, political and public scrutiny, customer and prescriber patterns or pr actices, and the reimbursement policies imposed by third-party payers as well as legislation affecting biopharmaceutical pricing and reimbursement activities an d outcomes. Finally, a breakdown, cyberattack or information security breach cou ld compromise the confidentiality, integrity and availability of UCB's data and systems. Given these uncertainties, you should not place undue reliance on any of such fo rward-looking statements. There can be no guarantee that the investigational or approved products described in this press release will be submitted or approved for sale or for any additional indications or labelling in any market, or at any particular time, nor can there be any guarantee that such products will be or w ill continue to be commercially successful in the future. UCB is providing this information, including forward-looking statements, only as of the date of this press release and it does not reflect any potential impact from the evolving COVID-19 pandemic, unless indicated otherwise. UCB is followin g the worldwide developments diligently to assess the financial significance of this pandemic to UCB. UCB expressly disclaims any duty to update any information contained in this press release, either to confirm the actual results or to rep ort or reflect any change in its forward-looking statements with regard thereto or any change in events, conditions or circumstances on which any such statement is based, unless such statement is required pursuant to applicable laws and reg ulations. Additionally, information contained in this document shall not constitute an off er to sell or the solicitation of an offer to buy any securities, nor shall ther e be any offer, solicitation or sale of securities in any jurisdiction in which such offer, solicitation or sale would be unlawful prior to the registration or qualification under the securities laws of such jurisdiction. References: 1. Courade J-P et al. Acta Neuropathol. 2018;136(5):729-45. 2. Albert M et al. Brain. 2019; 142:1736-50. 3. Fontaine S et al. Cell Mol Life Sci. 2015;72(10):1863-79. 4. Ling H. J Mov Disord. 2016;9(1):3-13. Logo - https://mma.prnewswire.com/media/1140810/UCB_logo.jpg

Additional content: http://presseportal.de/pm/55232/4664478 UCB Pharma

@ presseportal.de