Sandoz Initiates Two More Phase III Biosimilar Trials, Reinforcing Long-Term Global Leadership Commitment
Phase III clinical study for filgrastim
biosimilar (Neupogen®)[1] is expected to support expansion to
the US market
Phase III study for Sandoz pegfilgrastim
(Neulasta®) represents next major step in Sandoz's global
biosimilar development program
Latest milestones further reinforce Sandoz's
commitment to continued global biosimilar leadership, with a total
of 8-10 molecules at various stages of development
Holzkirchen, January 19, 2012 - Sandoz announced today that it has initiated two milestone Phase III clinical trials - one for biosimilar filgrastim (Amgen's Neupogen®) in the US market, the other for its global pegfilgrastim development program (Amgen's Neulasta®).
The filgrastim study is to evaluate the efficacy and safety of Sandoz's biosimilar filgrastim versus Neupogen® in breast cancer patients eligible for myelosuppressive chemotherapy treatment. It is expected to support extension of commercialization to the US, the largest global market for biologics. Sandoz's filgrastim biosimilar is already marketed under the brand name Zarzio® in more than 30 countries outside the United States.
The pegfilgrastim study, which is being conducted in breast cancer patients undergoing myelosuppressive chemotherapy treatment, represents the next major step in the Sandoz global biosimilar development program.
"Sandoz is already the clear global leader in biosimilars overall and in each of our three marketed products, with approximately 50% total segment share in the highly regulated markets of North America, Europe, Japan and Australia", said Sandoz's global head, Jeff George. "These two development milestones demonstrate that we also continue our efforts to make good on the longer-term promise of our leading pipeline."
In addition to Zarzio, Sandoz markets biosimilar somatropin (Omnitrope®) and epoetin alfa (Binocrit®) in countries across Europe and elsewhere. Omnitrope is also marketed in the US, under a different approval pathway.
Ameet Mallik, global head of Sandoz Biopharmaceuticals, added: "The start of these two studies represents significant progress for our broad ongoing development program, which includes previously announced late-stage trials for biosimilar rituximab (Roche's Rituxan®). We will work to leverage our strong capabilities and our unique position within Novartis to drive the continued success of our biosimilar pipeline, with eight to 10 molecules at various stages of development."
As with all its biosimilar development programs, Sandoz has focused on using state-of-the-art analytical techniques and process development to produce molecules that are highly similar to their reference product, prior to launching tailored clinical programs to generate appropriate supportive data.
Zarzio is already the #1 filgrastim biosimilar worldwide, accepted in multiple markets as the first choice for primary prevention of febrile neutropenia (low white blood cell counts) and rapidly expanding global patient access to this essential biologic. Pegfilgrastim is a pegylated [2] form of recombinant human granulocyte-colony stimulating factor (G-CSF), or filgrastim, and Amgen's Neulasta® remains the best-selling G-CSF worldwide. It is the goal of Sandoz to create the #1 overall G-CSF franchise worldwide, with both its daily filgrastim and its once-per-cycle pegfilgrastim as the most-prescribed medicines in their respective areas.
Disclaimer
The foregoing release contains forward-looking statements that can
be identified by terminology such as "commitment," "expected,"
"longer-term promise," "pipeline," "plan," "goal," or similar
expressions, or by express or implied discussions regarding
potential future marketing approvals of follow-on versions of
filgrastim or pegfilgrastim or of other biosimilar products, or
regarding potential future revenues from filgrastim or
pegfilgrastim or other Sandoz biosimilar products. You should not
place undue reliance on these statements. Such forward-looking
statements reflect the current views of the Company regarding
future events, and involve known and unknown risks, uncertainties
and other factors that may cause actual results to be materially
different from any future results, performance or achievements
expressed or implied by such statements. There can be no guarantee
that filgrastim or pegfilgrastim will be submitted or approved for
sale in any market, or at any particular time. Neither can
there be any guarantee that Sandoz will succeed in developing and
bringing to market any additional biosimilar products. Nor
can there be any guarantee that filgrastim or pegfilgrastim or any
other biosimilar products will achieve any particular levels of
revenue in the future. In particular, management's expectations
regarding such products could be affected by, among other things,
unexpected clinical trial results including new clinical data and
additional analysis of existing clinical data; unexpected
regulatory actions or delays or government regulation generally;
unexpected development difficulties; unexpected manufacturing
difficulties; competition in general; government, industry and
general public pricing pressures; unexpected patent litigation
outcomes; the impact that the foregoing factors could have on the
values attributed to the Group's assets and liabilities as recorded
in the Group's consolidated balance sheet, and other risks and
factors referred to in Novartis AG's current Form 20-F on file with
the US Securities and Exchange Commission. Should one or more of
these risks or uncertainties materialize, or should underlying
assumptions prove incorrect, actual results may vary materially
from those anticipated, believed, estimated or expected. 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 Sandoz
Sandoz, a Division of the Novartis Group, is a global leader in the
field of generic pharmaceuticals, offering a wide array of
high-quality, affordable products that are no longer protected by
patents. It has a portfolio of approximately 1000 compounds
and sells its products in more than 130 countries. Key
product groups include antibiotics, treatments for central nervous
system disorders, gastrointestinal medicines, cardiovascular
treatments and hormone therapies. Sandoz develops, produces
and markets these medicines along with pharmaceutical and
biotechnological active substances. In addition to strong
organic growth in recent years, Sandoz has made a series of
acquisitions including Lek (Slovenia), Sabex (Canada), Hexal
(Germany), Eon Labs (US), and EBEWE Pharma (Austria). In
2009, Sandoz employed approximately 23,000 people worldwide and
posted sales of USD 7.5 billion.
For further information
Eric Althoff
Novartis Global Media Relations
+41 61 32 47999
eric.althoff@novartis.com
Chris Lewis
Sandoz Communications
+49 8024 476 2550
chris.lewis@sandoz.com
Novartis Investor Relations
International:
Susanne Schaffert
Pierre-Michel Bringer
Thomas Hungerbuehler
Isabella Zinck
Central phone no: +41 61 324 7944
E-mail: investor.relations@novartis.com
North America:
Richard Jarvis +1 212 830 2433
Jill Pozarek +1 212 830 2445
Edwin Valeriano +1 212 830 2456
E-mail: investor.relations@novartis.com
References:
[1] All registered trademarks named in this release are the property of the respective companies.
[2] Pegylation is the process of covalent attachment of
polyethylene glycol polymer chains to another molecule, normally a
drug or therapeutic protein.
Posted: January 2012
