BERGEN, Norway, Nov.
2, 2018 /PRNewswire/ -- BerGenBio ASA (OSE: BGBIO) announces
that the analysis of the first stage of its Phase II clinical trial
with bemcentinib, a first-in-class selective oral AXL inhibitor, in
combination with the anti-PD-1 therapy KEYTRUDA® (pembrolizumab) in
patients with previously treated, advanced non-small cell lung
cancer (NSCLC) has been selected as a Late-breaking Abstract at the
annual Society for Immunotherapy in Cancer (SITC) 2018 congress in
Washington D.C. (7-10 November
2018).
Late-breaking abstracts highlight novel and potentially
practice-changing studies, and their acceptance for presentation is
subject to favourable assessment by a panel of clinical and
scientific experts. In total, only 21 abstracts were accepted in
the late-breaking category at this year's SITC congress:
https://sitc.sitcancer.org/2018/abstracts/titles/late-breaking/
An update from BerGenBio's biomarker and companion diagnostic
programme will also be presented as a poster within the regular
abstract section. See details below.
|
Presentations at
SITC: Friday 9 November, 12:45 – 2:15 p.m. and 6:30 – 8
p.m. EST, Hall E
|
|
A Phase II
study of bemcentinib (BGB324), a first-in-class selective AXL
inhibitor, in combination with pembrolizumab in patients with
advanced NSCLC: Analysis of the first stage
- Category: 33rd Annual Meeting Late-Breaking
Abstracts
- Presentation number: P715
Predictive and
pharmacodynamic biomarkers associated with treatment with the oral
selective AXL Inhibitor bemcentinib in combination with
pembrolizumab in patients with advanced NSCLC and
Melanoma
- Category: Biomarkers and Immune
Monitoring
- Presentation number: P115
|
The full abstracts will be published on November 6th at 8 a.m.
Eastern time at https://www.sitcancer.org/2018/home.
About SITC
The Society for Immunotherapy of Cancer (SITC) is the world's
leading member-driven organisation specifically dedicated to
improving cancer patient outcomes by advancing the science and
application of cancer immunotherapy. Over 4,000 delegates are
expected to attend the SITC 33rd Annual Congress in Washington D.C. on Nov
7-10 2018. For more information please
see www.sitcancer.org
About the BGBC008 trial: A Phase II study of bemcentinib in
combination with pembrolizumab in patients with previously treated
advanced NSCLC
The BGBC008 trial is a phase II multi-centre open-label study
of bemcentinib in combination with KEYTRUDA
(pembrolizumab) in previously treated, immunotherapy naïve,
patients with advanced adenocarcinoma of the lung, the most common
form of non-small cell lung cancer (NSCLC). The objective of the
trial is to determine the anti-tumour activity of this novel drug
combination. Responses will be correlated with biomarker status
(including AXL kinase and PD-L1 expression).
For more information please access trial NCT03184571
at www.clinicaltrials.gov.
About AXL
AXL kinase is a cell membrane receptor and an essential mediator
of the biological mechanisms that drive aggressive and
life-threatening diseases. In cancer, AXL drives tumour survival,
treatment resistance and spread, as well as suppressing the
body's immune response to tumours. AXL expression has been
established as a negative prognostic factor in many cancers. AXL
inhibitors, therefore, have potential value at the centre of cancer
combination therapy, addressing significant unmet medical needs and
multiple high-value market opportunities.
About BerGenBio ASA
BerGenBio is a clinical-stage biopharmaceutical company focused
on developing transformative drugs targeting AXL as a
potential cornerstone of therapy for advanced and aggressive
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. 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.
In parallel, BerGenBio is developing a companion diagnostics
test to identify patient populations most likely to benefit
from bemcentinib: this is expected to facilitate more efficient
registration trials and support 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). www.bergenbio.com
Contacts
Richard Godfrey
CEO, BerGenBio ASA
+47-917-86-304
Rune Skeie, CFO, BerGenBio
ASA
rune.skeie@bergenbio.com
+47-917-86-513
International Media Relations
David Dible, Mark Swallow, Marine
Perrier, Citigate Dewe Rogerson
bergenbio@citigatedewerogerson.com
+44-207-638-9571
Media Relations in Norway
Jan Petter Stiff, Crux
Advisers
stiff@crux.no
+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.
This information was brought to you by Cision
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SOURCE BerGenBio ASA