UCB (EBR:UCB) UCB Media Room: Cancer Research UK Collaboration

Directive transparence : information réglementée Communiqué sur comptes, résultats, chiffres d’affaires

09/03/2023 07:11
https://mb.cision.com/Public/18595/3729972/8531f186e443fa51_800x800ar.png ** Cancer Research UK Signs Multi-Project Collaboration With UCB To Advance= Oncology Antibody Candidates ------------------------------------------------------------ Brussels (Belgium), and London (UK) 9 March 2023 - Cancer Research UK, the = world=E2=80=99s largest charitable funder of cancer research, and UCB (EURO= NEXT BRUSSELS: UCB), a global biopharmaceutical company, today announced a = clinical development collaboration to advance two of UCB=E2=80=99s investig= ational oncology antibody candidates through clinical trials. The collaboration focuses on the development of two investigational antibod= y candidates, UCB6114 and UCB4594 by bringing together the oncology-focused= translational research and clinical development capabilities of Cancer Res= earch UK, and UCB=E2=80=99s renowned antibody discovery expertise. If succe= ssful in clinical trials the investigational candidates may have the potent= ial to offer cancer patients access to new targeted treatment options. UCB6= 114 is a potential first-in-class antibody targeting gremlin-1, a glycoprot= ein secreted by the tumour stroma^1*. UCB4594 is an antibody targeting the = immune checkpoint, human leukocyte antigen G, also known as HLA-G.=C2=A0 Under the terms of the collaboration, Cancer Research UK=E2=80=99s Centre f= or Drug Development will appoint the chief clinical and scientific investig= ators, and will lead the design, preparation, sponsorship and delivery of P= hase 1/2 clinical trials for both UCB antibody candidates. =C2=A0UCB will c= ontinue to manufacture both investigational antibody candidates, complete t= he ongoing UCB6114 clinical study (ONC001) and perform other supporting act= ivities. UCB will retain exclusive rights to further develop and commercial= ise both assets and will receive a licence to the results of the clinical t= rials from Cancer Research UK in return for undisclosed success-based miles= tone and royalty payments. Dr Nigel Blackburn, Director Cancer Research UK=E2=80=99s Centre for Drug D= evelopment, said:=C2=A0 =E2=80=9CAs funders of much of the world-class cancer research and innovati= on happening in the UK, we are able to offer our unparalleled access to som= e of the best oncology expertise and clinical development capabilities to o= ur commercial partners.=E2=80=9D =E2=80=9CWe are delighted to be collaborating with UCB to progress not one,= but two novel oncology antibodies and here at the Centre for Drug Developm= ent we are looking forward to progressing these programmes through early cl= inical development.=E2=80=9D Dhaval Patel, chief scientific officer of UCB, said: =E2=80=9CUCB=E2=80=99s strong research productivity together with our antib= ody expertise and desire to better understand and target the drivers of dis= ease, has resulted in two novel and potentially disruptive candidates in on= cology.=E2=80=9D =C2=A0 =E2=80=9CAs these candidates move forward, we are happy to enter this colla= boration with Cancer Research UK where they will bring world leading oncolo= gy expertise and access to a large network of clinical oncologists who can = enable the clinical trials.=E2=80=9D Financial details of the partnership were not disclosed. Notes to editor: * The tumour stroma is composed of extracellular matrix and specialized con= nective tissue cells, including fibroblasts and mesenchymal stromal cells^2= . References 1. Sarker D, Banerji U, Blagden SP, et al. A multi-modular phase I/II study= of UCB6114, a first-in-class, fully human IgG4P anti-Gremlin-1 monoclonal = antibody, as monotherapy and in combination with mFOLFOX6 or trifluridine/t= ipiracil, for patients with advanced gastrointestinal (GI) tumors. J Clin O= ncol. 2022;40(4):Suppl.TPS221. 2. Valkenburg KC, de Groot AE, Pienta KJ. Targeting the tumour stroma to im= prove cancer therapy. Nat Rev Clin Oncol. 2018;15:366-381. For media enquiries contact=C2=A0 Ellie Bennett in the Cancer Research UK press office on 020 3469 5370 or, o= ut of hours, on 07884 466 868. Antje Witte Investor Relations (UCB) on +32.2.559.94.14 or email antje.witt= e@ucb.com=C2=A0 Laurent Schots, Corporate Communications (UCB) on +32.2.559.92.64 or email = laurent.schots@ucb.com Scott Fleming, R&D Communications (UCB) on +447702777378 or email scott.fle= ming@ucb.com About UCB UCB, Brussels, Belgium (www.ucb.com) is a global biopharmaceutical company = focused on the discovery and development of innovative medicines and soluti= ons to transform the lives of people living with severe diseases of the imm= une system or of the central nervous system. With approximately 8 700 peopl= e in approximately 40 countries, the company generated revenue of =E2=82=AC= 5.5 billion in 2022. UCB is listed on Euronext Brussels (symbol: UCB).=C2= =A0 About Cancer Research UK=E2=80=99s Centre for Drug Development =C2=A0 Cancer Research UK has an impressive record of developing novel treatments = for cancer. The Cancer Research UK Centre for Drug Development has been pio= neering the development of new cancer treatments for 25 years, taking over = 140 potential new anti-cancer agents into clinical trials in patients. It c= urrently has a portfolio of 21 new anti-cancer agents in preclinical develo= pment, Phase I or early Phase II clinical trials. Six of these new agents h= ave made it to market including temozolomide for brain cancer, abiraterone = for prostate cancer and rucaparib for ovarian cancer. Two other drugs are i= n late development Phase III trials.=C2=A0 Forward looking statements - UCB This press release may contain forward-looking statements including, withou= t limitation, statements containing the words =E2=80=9Cbelieves=E2=80=9D, = =E2=80=9Canticipates=E2=80=9D, =E2=80=9Cexpects=E2=80=9D, =E2=80=9Cintends= =E2=80=9D, =E2=80=9Cplans=E2=80=9D, =E2=80=9Cseeks=E2=80=9D, =E2=80=9Cestim= ates=E2=80=9D, =E2=80=9Cmay=E2=80=9D, =E2=80=9Cwill=E2=80=9D, =E2=80=9Ccont= inue=E2=80=9D and similar expressions. These forward-looking statements are= based on current plans, estimates and beliefs of management. All statement= s, other than statements of historical facts, are statements that could be = deemed forward-looking statements, including estimates of revenues, operati= ng margins, capital expenditures, cash, other financial information, expect= ed legal, arbitration, political, regulatory or clinical results or practic= es and other such estimates and results. By their nature, such forward-look= ing statements are not guarantees of future performance and are subject to = known and unknown risks, uncertainties and assumptions which might cause th= e actual results, financial condition, performance or achievements of UCB, = or industry results, to differ materially from those that may be expressed = or implied by such forward-looking statements contained in this press relea= se. Important factors that could result in such differences include: the gl= obal spread and impact of COVID-19, changes in general economic, business a= nd competitive conditions, the inability to obtain necessary regulatory app= rovals or to obtain them on acceptable terms or within expected timing, cos= ts associated with research and development, changes in the prospects for p= roducts in the pipeline or under development by UCB, effects of future judi= cial decisions or governmental investigations, safety, quality, data integr= ity or manufacturing issues; potential or actual data security and data pri= vacy breaches, or disruptions of our information technology systems, produc= t liability claims, challenges to patent protection for products or product= candidates, competition from other products including biosimilars, changes= in laws or regulations, exchange rate fluctuations, changes or uncertainti= es in tax laws or the administration of such laws, and hiring and retention= of its employees. There is no guarantee that new product candidates will b= e discovered or identified in the pipeline, will progress to product approv= al or that new indications for existing products will be developed and appr= oved. Movement from concept to commercial product is uncertain; preclinical= results do not guarantee safety and efficacy of product candidates in huma= ns. So far, the complexity of the human body cannot be reproduced in comput= er models, cell culture systems or animal models. The length of the timing = to complete clinical trials and to get regulatory approval for product mark= eting has varied in the past and UCB expects similar unpredictability going= forward. Products or potential products, which are the subject of partners= hips, joint ventures or licensing collaborations may be subject to differen= ces disputes between the partners or may prove to be not as safe, effective= or commercially successful as UCB may have believed at the start of such p= artnership. UCB=E2=80=99s efforts to acquire other products or companies an= d to integrate the operations of such acquired companies may not be as succ= essful as UCB may have believed at the moment of acquisition. Also, UCB or = others could discover safety, side effects or manufacturing problems with i= ts products and/or devices after they are marketed. The discovery of signif= icant problems with a product similar to one of UCB=E2=80=99s products that= implicate an entire class of products may have a material adverse effect o= n sales of the entire class of affected products. Moreover, sales may be im= pacted by international and domestic trends toward managed care and health = care cost containment, including pricing pressure, political and public scr= utiny, customer and prescriber patterns or practices, and the reimbursement= policies imposed by third-party payers as well as legislation affecting bi= opharmaceutical pricing and reimbursement activities and outcomes. Finally,= a breakdown, cyberattack or information security breach could compromise t= he confidentiality, integrity and availability of UCB=E2=80=99s data and sy= stems.=C2=A0 Given these uncertainties, you should not place undue reliance on any of su= ch forward-looking statements. There can be no guarantee that the investiga= tional or approved products described in this press release will be submitt= ed or approved for sale or for any additional indications or labelling in a= ny market, or at any particular time, nor can there be any guarantee that s= uch products will be or will continue to be commercially successful in the = future. UCB is providing this information, including forward-looking statements, on= ly as of the date of this press release and it does not reflect any potenti= al impact from the evolving COVID-19 pandemic, unless indicated otherwise. = UCB is following the worldwide developments diligently to assess the financ= ial significance of this pandemic to UCB. UCB expressly disclaims any duty = to update any information contained in this press release, either to confir= m the actual results or to report or reflect any change in its forward-look= ing statements with regard thereto or any change in events, conditions or c= ircumstances on which any such statement is based, unless such statement is= required pursuant to applicable laws and regulations.=C2=A0 Additionally, information contained in this document shall not constitute a= n offer to sell or the solicitation of an offer to buy any securities, nor = shall there be any offer, solicitation or sale of securities in any jurisdi= ction in which such offer, solicitation or sale would be unlawful prior to = the registration or qualification under the securities laws of such jurisdi= ction. =C2=A0 GenericFile UCB PR CRUK March 9 ENG (https://mb.cision.com/Public/18595/3729972/940ceae= fd44d1d0f.pdf) ______________________ If you would rather not receive future communications from UCB SA, please g= o to https://eu.vocuspr.com/OptOut.aspx?2973226x20421x130790x1x6868579x2400= 0x6&Email=3Dregnews%40symexglobal.com. 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