Novartis
advances with push on cancer and liver disease
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[April 18, 2017] ZURICH
(Reuters) - Novartis's push into oncology and liver disease, two of its
treatment priorities, advanced on Monday as the Swiss drugmaker won a
second U.S. breakthrough tag for its cancer gene therapy while striking
a separate pact with Allergan.
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The Basel-based drugmaker's chimeric antigen receptor therapy
(CAR-T) treatment, called CTL019, was awarded the U.S. Food and Drug
Administration's breakthrough therapy designation for adults with
relapsed/refractory (r/r) diffuse large B-cell lymphoma, a common
blood cancer.
Novartis also said it will combine one of its investigational drugs
with Allergan's cenicriviroc in a mid-stage trial against liver
disease known as non-alcoholic steatohepatitis, or NASH, that is
growing more prevalent due in large part to obesity.
Novartis's drug development head Vas Narasimhan has highlighted
oncology and NASH as two pillars of his strategy to ensure growth.
Narasimhan expects CTL019 to eventually top $1 billion in sales for
multiple cancer types and also has high hopes for his NASH
treatments, in particular in concert with other companies.
"Collaboration is key to developing the best possible treatments
that are urgently needed for NASH patients," Narasimhan said in a
statement.
Late last year, Novartis struck a $50 million licensing deal with
Conatus Pharmaceuticals for a separate treatment for NASH, an area
that has also been tagged as a focus by industry rivals including
Gilead and Bristol-Myers Squibb.
CTL019 previously won accelerated FDA review for treating young
people with acute lymphoblastic leukemia (ALL).
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Last month, Novartis submitted CTL019 for FDA review in young ALL
patients as it races rivals including Kite Pharma to become the
first to secure regulators' approval for a CAR-T treatment, where T
cells are removed from patients, re-engineered to fight their
cancers, then reinfused.
(Reporting by John Miller; Editing by Tom Heneghan)
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