Galapagos regains rights to GLPG1690, announces end of alliance with Janssen
17 Marzo 2015 - 12:31AM
-
Fully owned and proprietary
clinical asset for pulmonary fibrosis
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GLPG1690 acts on autotaxin
target
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Novel mode of action,
originating from Galapagos target discovery engine
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Filing for Phase 2 clinical
trial in 2015
Mechelen,
Belgium; 17 March 2015 - Galapagos NV (Euronext: GLPG) announced
that Janssen Pharmaceutica NV and Galapagos have mutually agreed to
terminate the inflammation alliance and option agreements between
the companies. Galapagos views the molecules emerging from
the alliance as strong additions to its growing proprietary
pipeline. Among others, all rights to candidate drug
GLPG1690, a selective autotaxin inhibitor, return to
Galapagos. Galapagos has successfully completed a
First-in-Human Phase 1 trial for GLPG1690 and is preparing a Phase
2 clinical trial in idiopathic pulmonary fibrosis (IPF).
"We are pleased to regain the
rights to GLPG1690 to pursue the most suitable clinical application
of autotaxin inhibition. There is a large unmet medical need
in IPF, and our pre-clinical data with GLPG1690 supports its
potential as a competitive and novel approach in this disease
area," said Dr Piet Wigerinck, Chief Scientific Officer of
Galapagos. "The alliance with Janssen has been underway since
October 2007 and has generated three clinical molecules, two of
which are now proprietary Phase 2 assets of Galapagos: GLPG1205 and
GLPG1690. This program is a valuable component of our
development portfolio, and regaining the rights is a next step in
our transformation into a mature biotech company with a proprietary
product pipeline."
Galapagos identified autotaxin as
playing a key role in inflammation, using an inflammation assay in
its unique target discovery platform. Pharmacology and
translational studies published by other parties in the literature
since then suggest autotaxin may play a key role in metabolic
disease, arthritic pain, oncology, and lung disease.
GLPG1690 is a potent and selective
inhibitor of autotaxin. In a Phase 1 study in healthy human
volunteers, GLPG1690 demonstrated favorable safety and
tolerability, as well as a strong pharmacodynamic signal implying
target engagement. Galapagos is currently preparing a Phase 2
study in IPF, to be filed for approval before the end of 2015.
About
IPF
Idiopathic pulmonary fibrosis (IPF) is a chronic and ultimately
fatal disease characterized by a progressive decline in lung
function. Pulmonary fibrosis involves scarring of lung tissue
and is the cause of shortness of breath. Fibrosis is usually
associated with a poor prognosis. The term "idiopathic" is
used because the cause of pulmonary fibrosis is still unknown.
Estimated incidence of IPF is up to 16.3 per 100,000 persons
in the US and 7.4 per 100,000 persons in Europe, with approximately
30,000-35,000 new patients diagnosed with IPF worldwide each
year. The goals of treatment in IPF are essentially to reduce
the symptoms, slow down disease progression, reduce acute
exacerbations, and prolong survival. Approved treatments thus
far have improved the overall survival of IPF patients, but
unwanted side effects with these treatments are common, presenting
an unmet need for effective treatments with safer side effect
profiles.
About
Galapagos
Galapagos (Euronext: GLPG; OTC: GLPYY) is a clinical-stage
biotechnology company specialized in the discovery and development
of small molecule medicines with novel modes of action, with a
pipeline comprising three Phase 2 programs, two Phase 1 trials,
five pre-clinical studies, and 25 discovery small-molecule and
antibody programs in cystic fibrosis, inflammation, and other
indications. In the field of inflammation, AbbVie and
Galapagos signed a collaboration agreement for the development and
commercialization of filgotinib. Filgotinib is an
orally-available, selective inhibitor of JAK1 for the treatment of
rheumatoid arthritis and potentially other inflammatory diseases,
currently in Phase 2B studies in RA and in Phase 2 in Crohn's
disease. GLPG1205, a first-in-class inhibitor of GPR84, is
currently being tested in a Phase 2 proof-of-concept trial in
ulcerative colitis patients. GLPG1690, a first-in-class
inhibitor of autotaxin, has shown favorable safety in a Phase 1
trial and is expected to enter Phase 2 in idiopathic pulmonary
fibrosis. AbbVie and Galapagos also signed a collaboration
agreement in cystic fibrosis to develop and commercialize molecules
that address mutations in the CFTR gene. Potentiator GLPG1837
is currently in a Phase 1 trial, and corrector GLPG2222 is at the
pre-clinical candidate stage. The Galapagos Group, including
fee-for-service subsidiary Fidelta, has approximately 400
employees, operating from its Mechelen, Belgium headquarters and
facilities in The Netherlands, France, and Croatia. Further
information at: www.glpg.com
CONTACT
Galapagos NV
Elizabeth Goodwin, Head of Corporate Communications &
IR
Tel: +31 6 2291 6240
ir@glpg.com
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