Advanced Accelerator Applications Signs Exclusive License Agreement with Cancer Targeted Technology to Develop CTT1057, an F-...
February 12 2018 - 7:00AM
Advanced Accelerator Applications S.A.
(NASDAQ:AAAP) (AAA or the Company), a Novartis company and leader
in nuclear medicine theragnostics, today announced that it has
entered into an exclusive worldwide license agreement with Cancer
Targeted Technology, LLC (CTT) to develop and market an
investigational new drug product, F-18-labeled CTT1057. CTT1057 is
a ligand of Prostate-Specific Membrane Antigen (PSMA) for Positron
Emission Tomography (PET) imaging of prostate cancer.
CTT has developed a phosphoramidate-based
peptide, which specifically binds to PSMA. A Phase I study in 20
patients was conducted at the University of California, San
Francisco. AAA will work to further develop and commercialize this
diagnostic agent for prostate cancer. The terms of the agreement
include an upfront licensing fee, as well as certain milestone and
royalty payments.
Susanne Schaffert, Ph.D., Chairperson and
President of Advanced Accelerator Applications, stated, “This
agreement expands our position in the important prostate cancer
space. PSMA diagnostics represent an accurate staging and risk
assessment tool with the potential to change patient management
decisions. CTT1057 is highly complementary to our existing F-18 PET
portfolio and AAA is well suited to exploit this opportunity with
our proven manufacturing and development capabilities.”
“We are very excited to enter into this license
agreement with AAA,” commented Beatrice Langton-Webster, Ph.D.,
Chief Executive Officer of Cancer Targeted Technology. “We are very
encouraged by the results of our recently completed Phase I
clinical trial and believe that AAA has the right expertise and
team to rapidly develop this important new PSMA-directed diagnostic
for prostate cancer.”
Prostate cancer is the most frequent malignant
tumor in men worldwide, affecting nearly one in seven men during
their lifetime. After initial therapy, biochemical recurrence is
common and is usually expressed by an elevation in
prostate-specific antigen (PSA) levels. PET imaging with PSMA
ligands has been shown to improve the detection of metastatic
lesions, even at low serum PSA values in biochemically recurrent
prostate cancer.
Disclaimer
This press release contains forward-looking
statements within the meaning of the United States Private
Securities Litigation Reform Act of 1995. Forward-looking
statements can generally be identified by words such as
“potential,” “can,” “will,” “plan,” “expect,” “anticipate,” “look
forward,” “believe,” “committed,” “investigational,” “pipeline,”
“launch,” or similar terms, or by express or implied discussions
regarding potential marketing approvals, new indications or
labeling for CTT1057 or the other investigational or approved
products described in this press release, or regarding potential
future revenues from such products or the license agreement with
Cancer Targeted Technology. You should not place undue reliance on
these statements. Such forward-looking statements are based on our
current beliefs and expectations regarding future events, and are
subject to significant known and unknown risks and uncertainties.
Should one or more of these risks or uncertainties materialize, or
should underlying assumptions prove incorrect, actual results may
vary materially from those set forth in the forward-looking
statements. There can be no guarantee that CTT1057 or the other
investigational or approved products described in this press
release will be submitted or approved for sale or for any
additional indications or labeling in any market, or at any
particular time. Neither can there be any guarantee that the
license agreement with Cancer Targeted Technology will achieve any
or all of its intended goals and objectives, or be commercially
successful. Nor can there be any guarantee that CTT1057 or the
other investigational or approved products described in this press
release will be commercially successful in the future. In
particular, our expectations regarding such products, and the
license agreement with Cancer Targeted Technology, could be
affected by, among other things, the uncertainties inherent in
research and development, including clinical trial results and
additional analysis of existing clinical data; regulatory actions
or delays or government regulation generally; global trends toward
health care cost containment, including government, payor and
general public pricing and reimbursement pressures; our ability to
obtain or maintain proprietary intellectual property protection;
the particular prescribing preferences of physicians and patients;
general political and economic conditions; safety, quality or
manufacturing issues; potential or actual data security and data
privacy breaches, or disruptions of our information technology
systems, and other risks and factors referred to in Novartis AG’s
current Form 20-F on file with the US Securities and Exchange
Commission. Novartis is providing the information in this press
release as of this date and does not undertake any obligation to
update any forward-looking statements contained in this press
release as a result of new information, future events or
otherwise.
About Advanced Accelerator Applications
S.A.
Advanced Accelerator Applications (NASDAQ:AAAP),
a Novartis company, is an innovative radiopharmaceutical company
developing, producing and commercializing molecular nuclear
medicine theragnostics. AAA’s theragnostic platform is based on
radiolabeling a targeting molecule with either gallium Ga 68 for
diagnostic use, or lutetium Lu 177 for therapy. AAA’s first
theragnostic pairing for neuroendocrine tumors includes diagnostic
drugs NETSPOT® in the US and SomaKit TOC® in Europe; and
therapeutic Lutathera® (USAN: lutetium Lu 177 dotatate/INN:
lutetium (177Lu) oxodotreotide). Additional theragnostics in
development target gastrointestinal stromal tumors (GIST), and
prostate and breast cancer. AAA is also an established leader in
molecular nuclear diagnostic radiopharmaceuticals for PET and
SPECT, mainly used in clinical oncology, cardiology and neurology.
Headquartered in Saint-Genis-Pouilly, France, AAA currently has 20
production and R&D facilities, and more than 600 employees in
13 countries (France, Italy, the UK, Germany, Switzerland, Spain,
Poland, Portugal, The Netherlands, Belgium, Israel, the US and
Canada). AAA reported sales of €109.3 million in 2016 (+23% vs.
2015) and €106.4 million for the first 9 months of 2017 (+31% vs.
first 9 months of 2016). For more information, please visit:
www.adacap.com.
Contacts:
AAA Corporate Communications Rachel
LevineDirector of Communications rachel.levine@adacap.comTel: +
1-212-235-2395
AAA Investor Relations Jordan Silverstein Head
of Investor Relations jordan.silverstein@adacap.com Tel: +
1-212-235-2394
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