Report Publication Announcement • Nov 6, 2020
Report Publication Announcement
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BERGENBIO HOSTING VIRTUAL R&D DAY TODAY
Bergen, Norway, 06 November 2020 - BerGenBio ASA (OSE:BGBIO), a clinical-stage
biopharmaceutical company developing novel, selective AXL kinase inhibitors for
severe unmet medical need, is pleased to announce that it is hosting a Virtual
R&D Day today.
The online event will begin at 13.00pm CET (04.00am PST/06.00am CST). Please
click here (bergenbio@consilium
-comms.com?subject=I%20would%20like%20to%20attend%20the%20BerGenBio%20Virtual%20E
vent) to register.
The event will feature experts from academic institutions across Europe and the
US, highlighting the role of AXL kinase as an essential mediator of the
biological mechanisms underlying life-threatening diseases, such as cancer,
fibrosis and infectious diseases, including COVID-19.
Each presentation will be followed by a Q&A session. Further details on the
presentations can be found in the agenda below.
Richard Godfrey, Chief Executive Officer of BerGenBio, commented: "BerGenBio has
always been committed to pursuing excellence and innovation in R&D. We remain a
world leader in understanding the role and function of AXL biology, and with our
collaborators we have demonstrated that AXL is a key driver of immune evasive
and drug-resistant metastatic cancer, as well as other aggressive diseases. We
are grateful to all our speakers, who during today's event will be providing
insights into the latest AXL research, including the clinical benefit seen from
bemcentinib."
Agenda
(times in CET)
13:00 Introduction - Richard Godfrey, Chief Executive Officer,
BerGenBio
Presentations from
independent AXL
experts, followed
by Q&A sessions led
by Jim Lorens,
Chief Scientific
Officer and Hani
Gabra, Chief
Medical Officer at
BerGenBio
13:10 AXL in AML/MDS - Professor Sonja Loges, Director,
Department of Personalised Oncology, University Hospital
Mannheim and Division of Personalised Medical Oncology,
German Cancer Research Center - DKFZ (Heidelberg,
Germany)
13:40 AXL in lung cancer - Dr Matthew Krebs, Clinical Senior
Lecturer in Experimental Cancer Medicine and Honorary
Consultant in Medical Oncology, The Christie NHS
Foundation Trust (Manchester, UK)
14:10 AXL and viruses/COVID-19 - Professor Wendy Maury,
Professor of Microbiology and Immunology, University of
Iowa (Iowa City, USA)
14:40 AXL in fibrosis/IPF - Professor Cory Hogaboam, Professor
of Medicine, Cedars-Sinai Medical Center (Los Angeles,
USA)
15:10 Bemcentinib clinical development plan - Hani Gabra, Chief
Medical Officer, BerGenBio
15:25 Concluding remarks - Richard Godfrey, Chief Executive
Officer, BerGenBio
For further
information, please
contact Consilium
Strategic
Communications at
bergenbio@consilium
-comms.com or
- END -
About AXL
AXL kinase is a cell membrane receptor and an essential mediator of the
biological mechanisms underlying life-threatening diseases. In cancer, AXL
suppresses the body's immune response to tumours and drives cancer treatment
failure across many indications. AXL expression defines a very poor prognosis
subgroup in most cancers. AXL inhibitors, therefore, have potential high value
at the centre of cancer combination therapy, addressing significant unmet
medical needs and multiple high-value market opportunities. Research has also
shown that AXL mediates other aggressive diseases.
About Bemcentinib
Bemcentinib (formerly known as BGB324), is a potentially first-in-class
selective AXL inhibitor in a broad phase II clinical development programme.
Ongoing clinical trials are investigating bemcentinib in multiple solid and
haematological tumours, in combination with current and emerging therapies
(including immunotherapies, targeted therapies and chemotherapy), and as a
single agent. Bemcentinib targets and binds to the intracellular catalytic
kinase domain of AXL receptor tyrosine kinase and inhibits its activity.
Increase in AXL function has been linked to key mechanisms of drug resistance
and immune escape by tumour cells, leading to aggressive metastatic cancers.
About BerGenBio ASA
BerGenBio is a clinical-stage biopharmaceutical company focused on developing
transformative drugs targeting AXL as a potential cornerstone of therapy for
aggressive diseases, including immune-evasive, therapy resistant cancers. The
company's proprietary lead candidate, bemcentinib, is a potentially first-in
-class selective AXL inhibitor in a broad phase II clinical development
programme focused on combination and single agent therapy in lung cancer,
leukaemia and COVID-19. A first-in-class functional blocking anti-AXL antibody,
tilvestamab, is undergoing phase I clinical testing. In parallel, BerGenBio is
developing a companion diagnostic test to identify patient populations most
likely to benefit from bemcentinib: this is expected to facilitate more
efficient registration trials supporting a precision medicine-based
commercialisation strategy.
BerGenBio is based in Bergen, Norway with a subsidiary in Oxford, UK. The
company is listed on the Oslo Stock Exchange (ticker: BGBIO). For more
information, visit www.bergenbio.com
Contacts
Richard Godfrey CEO, BerGenBio ASA
+47 917 86 304
Rune Skeie, CFO, BerGenBio ASA
+47 917 86 513
International Media Relations
Mary-Jane Elliott, Chris Welsh, Lucy Featherstone, Carina Jurs
Consilium Strategic Communications
+44 20 3709 5700
Media Relations in Norway
Jan Petter Stiff, Crux Advisers
+47 995 13 891
Forward looking statements
This announcement may contain forward-looking statements, which as such are not
historical facts, but are based upon various assumptions, many of which are
based, in turn, upon further assumptions. These assumptions are inherently
subject to significant known and unknown risks, uncertainties and other
important factors. Such risks, uncertainties, contingencies and other important
factors could cause actual events to differ materially from the expectations
expressed or implied in this announcement by such forward-looking statements.
This information is subject to the disclosure requirements pursuant to section 5
-12 of the Norwegian Securities Trading Act.
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