AstraZeneca PLC SILIQ (BRODALUMAB) APPROVED BY US FDA (0888X)
16 February 2017 - 11:01PM
UK Regulatory
TIDMAZN
RNS Number : 0888X
AstraZeneca PLC
16 February 2017
16 February 2017, 12 noon GMT
SILIQ (BRODALUMAB) APPROVED BY THE US FDA
FOR ADULT PATIENTS WITH MODERATE-TO-SEVERE PLAQUE PSORIASIS
Approval triggers $130 million milestone payment to AstraZeneca
from
US Partner Valeant Pharmaceuticals
AstraZeneca's partner Valeant Pharmaceuticals today announced
that the US Food and Drug Administration (FDA) has approved Siliq
(brodalumab) injection for the treatment of adult patients with
moderate-to-severe plaque psoriasis who are candidates for systemic
therapy or phototherapy and have failed to respond or have lost
response to other systemic therapies.
Siliq is an IL-17 receptor monoclonal antibody for patients with
moderate-to-severe plaque psoriasis, a chronic, debilitating skin
disease that causes red patches of skin covered with silvery
scales.
Through a collaboration agreement, AstraZeneca granted Valeant,
an expert in dermatology, the exclusive license to develop and
commercialise Siliq globally, except in Japan and certain other
Asian countries where rights are held by Kyowa Hakko Kirin Co., Ltd
through an agreement with Amgen, and in Europe, where LEO Pharma
holds exclusive rights to develop and commercialise brodalumab
through an agreement entered in July 2016.
Sean Bohen, Executive Vice President, Global Medicines
Development and Chief Medical Officer at AstraZeneca, said: "We are
pleased that our commitment to Siliq, from its development in our
biologics pipeline through to our partnership with Valeant, has led
to a new treatment option for psoriasis patients, many of whom have
previously not been able to achieve full clearance of their
skin."
Financial considerations
Under the terms of the agreement, AstraZeneca will receive a
milestone payment of $130 million from Valeant at first regulatory
approval. This milestone will be recorded in the AstraZeneca
financial statements as Externalisation Revenue. Following the
approval, AstraZeneca and Valeant will share profits from the sale
of Siliq in the US market.
Marc Dunoyer, Chief Financial Officer, AstraZeneca said: "Our
agreement with Valeant supports our externalisation strategy, which
allows us to focus on our three main therapy areas while partnering
other assets for the benefit of patients, generating sustainable
revenue for the future."
- ENDS -
NOTES TO EDITORS
About Siliq
Siliq (brodalumab) is a novel human monoclonal antibody that
binds to the interleukin-17 (IL-17) receptor and inhibits
inflammatory signalling by blocking the binding of several types of
IL-17 to the receptor. By stopping IL-17 from activating the
receptor, brodalumab prevents the body from receiving signals that
may lead to inflammation. The IL-17 pathway plays a central role in
inducing and promoting inflammatory disease processes.
The FDA approval is based on data from the three AMAGINE Phase
III pivotal studies that demonstrated that Siliq has an effective
mechanism of action that delivers clinical benefit and could help a
significant number of moderate-to-severe plaque psoriasis patients
achieve total clearance of their skin disease. At the 210mg dose,
Siliq was shown to be efficacious in total skin clearance of
psoriasis with approximately twice as many patients on Siliq
achieving total skin clearance compared to ustekinumab at week 12
in two replicate comparator trials involving over 2,400
patients.
About Valeant
Valeant Pharmaceuticals International, Inc. (NYSE/TSX:VRX) is a
multinational specialty pharmaceutical company that develops,
manufactures and markets a broad range of pharmaceutical products
primarily in the areas of dermatology, gastrointestinal disorders,
eye health, neurology and branded generics. More information about
Valeant can be found at www.valeant.com.
About AstraZeneca
AstraZeneca is a global, science-led biopharmaceutical company
that focuses on the discovery, development and commercialisation of
prescription medicines, primarily for the treatment of diseases in
three main therapy areas - Oncology, Cardiovascular & Metabolic
Diseases and Respiratory. The Company also is selectively active in
the areas of autoimmunity, neuroscience and infection. AstraZeneca
operates in over 100 countries and its innovative medicines are
used by millions of patients worldwide. For more information,
please visit www.astrazeneca.com and follow us on Twitter
@AstraZeneca.
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This information is provided by RNS
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