Facing
rival drugs, Novartis gets win with Afinitor in Europe
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[June 02, 2016]
ZURICH (Reuters) - Efforts by
Novartis to defend its blockbuster cancer drug Afinitor against
competitors got a boost on Thursday from European regulators, who
approved it for use on certain types of advanced gastrointestinal and
lung neuroendocrine tumors.
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Afinitor posted $1.61 billion in sales in 2015 but has been under
pressure in some areas of disease including kidney cancer as rivals
drugs have been shown in trials to be more effective.
Novartis Chief Executive Joe Jimenez has acknowledged competition
from Bristol-Myers Squibb's immunotherapy drug Opdivo and Exelixis's
Cometriq could temper Afinitor's growth, but has maintained the
drug's promise lies in multiple applications for different tumors.
That was underscored by Thursday's European approval for the drug to
be used against nonfunctional gastrointestinal and lung
neuroendocrine tumors, rare cancers that in many people are
diagnosed at advanced stages when they are difficult to fight.
"We are pleased that this latest milestone makes Afinitor available
to patients in the EU who previously had few or no approved
treatment options," Bruno Strigini, president of Novartis Oncology,
said in a statement.
Afinitor had been approved by the U.S. Food and Drug Administration
(FDA) in 2012 for a certain type of breast cancer and its label has
expanded since then.
In February, the FDA approved the drug for similar uses that on
Thursday were the subject of the European approval.
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Neuroendocrine tumors are a type of cancer that originate in
neuroendocrine cells, and most commonly arise in the GI tract, lungs
or pancreas. Symptoms include intestinal obstruction, pain and
bleeding, as well as asthma, chronic obstructive pulmonary disease
and pneumonia.
Consensus forecasts have pointed to Afinitor sales peaking at more
than $2 billion in 2018, according to Thomson Reuters Cortellis.
(Reporting by John Miller; Editing by David Holmes)
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