OSLO, NORWAY--(Marketwire - Feb 13, 2013) -
Intended for US Media only
Algeta ASA (OSE: ALGETA) announces that Bayer
has received notification that the New Drug Application (NDA) for
the
investigational compound Radium Ra 223 Dichloride (radium-223) has been
accepted
for filing and granted priority review by the US Food and Drug
Administration
(FDA). The application is currently under review for the
treatment of
castration-resistant prostate cancer (CRPC) patients with bone metastases.
Andrew Kay, Algeta's President & CEO, said: "With the granting of
priority
review for the NDA for Radium Ra 223 dichloride (radium-223) in the US,
there is
recognition that Radium Ra 223 dichloride (radium-223) has the
potential to
offer a treatment option for CRPC patients with bone metastases where
little or
no therapy exists. While we await the final decision from the regulators
later
this year, and together with Bayer, we continue with our
commercialization
planning and look forward to a potential approval, and to making this
compound
available to patients."
The FDA grants priority review to medicines that provide a treatment
where
little or no adequate therapy exists. Under the Prescription Drug User
Fee Act
(PDUFA), the FDA aims to complete its review within six months of the
60-day
filing receipt of the NDA submission (eight months total), rather
than the
standard 12-month review cycle.
In September 2009, Algeta signed an agreement with Bayer Pharma AG
(Berlin,
Germany) for the development and commercialization of radium-223.
Under the
terms of the agreement, Bayer will develop, apply for global health
authority
approvals, and commercialize radium-223 globally. Algeta will co-promote
radium-223 with Bayer in the US, and is eligible for milestones as well as
royalties on
Bayer's sales outside the US.
###
About Radium Ra 223 Dichloride
Radium Ra 223 Dichloride (radium-223), formerly referred to as
radium-223
chloride, is an investigational alpha particle-emitting
pharmaceutical in
development for CRPC patients with bone metastases.
Radium-223 is an investigational agent and is not approved by the
European
Medicines Agency (EMA), the US Food and Drug Administration (FDA) or
other
health authorities. Bayer submitted a Marketing Authorization Application
to the
EMA and a New Drug Application to the FDA for radium-223 in December
2012 for
the treatment of CRPC patients with bone metastases.
In January 2013, the US Nuclear Regulatory Commission (NRC) issued a
licensing
decision on the medical use of radium-223. The decision states that US
medical
sites can procure and administer radium-223 under 10 CFR Part 35,
Subpart E,
which includes 10 CFR § 35.300.
About CRPC and Bone Metastases
Prostate cancer is the most common cancer among men in the United States
(other
than skin cancer)[1].Approximately 16% of prostate cancer cases are
considered
regional or distant, which means that the cancer has spread beyond the
prostate
to nearby or distant areas of the body (metastasis)[2].
A majority of men with CRPC have radiological evidence of bone
metastases[3].
Bone metastases secondary to prostate cancer typically target the lumbar
spine,
vertebrae and pelvis[4].In fact, bone metastases are the main cause of
morbidity
and death in patients with CRPC[5].
About Algeta
Algeta is a company focused on developing novel targeted therapies for
patients
with cancer based on its alpha-pharmaceutical platform. The
Company is
headquartered in Oslo, Norway, and has a US subsidiary, Algeta US, LLC,
based in
Cambridge, MA performing commercial marketing operations in the US.
Algeta is
listed on the Oslo Stock Exchange (Ticker: ALGETA). For more information
please
visit www.algeta.com.
Forward-looking Statements
This news release contains certain forward-looking statements that are
based on
uncertainty, as they relate to events and depend on circumstances that
will
occur in the future and which, by their nature, may have an impact on
results of
operations and the financial condition of Algeta. Such
forward-looking statements reflect our current views and are based on the
information currently
available to Algeta. Algeta cannot give any assurance as to whether such
forward
looking statements will prove to be correct. These forward looking
statements
include statements regarding the potential timeline of FDA approval of
radium-223 and our anticipated co-promotion of
radium-223 in the US. There are a
number of factors that could cause actual results and developments to
differ
materially from those expressed or implied by these forward-looking
statements.
These factors include, among other things, risks or uncertainties
associated
with the ability to identify and hire a sufficient number of qualified
employees
for the US field force, growth management, general economic and
business
conditions and the pricing environment, the impact of competition, the
ability
to successfully commercialize radium-223, the risk that costs associated
with
the co-promotion of radium-223 may be greater than anticipated,
manufacturing
capacity, the risk of non-approval of patents not yet granted,
risks in
obtaining regulatory approvals for radium-223 and the other risks
and
uncertainties described in our annual report.
[1] American Cancer Society. Prostate Cancer: Detailed Guide. October 26,
2012.
Available at:
http://www.cancer.org/acs/groups/cid/documents/webcontent/003134-pdf.pdf.
Accessed May 17, 2012
[2] National Cancer Institute, Surveillance Epidemiology and End Results
(SEER).
SEER Stat Facts: Prostate; Survival & Stage, 2002-2008
[3] Sartor, O. "Radiopharmaceutical and chemotherapy combinations in
metastatic
castrate-resistant prostate cancer: a new beginning."
JCO. 2009;15:2417-2418
[4] Bone and Cancer Foundation. Questions & Answers about Prostate Cancer
Bone
Metastases and Treatment-Related Osteoporosis. Available at:
http://www.boneandcancerfoundation.org/pdfs/prostate-cancer-qa.pdf.
Accessed May
17, 2012
[5] Lange PH, Vasella RL. "Mechanisms, hypotheses and questions regarding
prostate cancer metastatic to bone." Cancer & Metastasis
Reviews.1999;17:331-336
Press release:
http://hugin.info/134655/R/1677597/547152.pdf
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Source: Algeta ASA via Thomson Reuters ONE
[HUG#1677597]