Bangalore-headquartered biotechnology company Biocon
today announced the launch of a biological drug researched, developed
and manufactured in the country to treat chronic plaque psoriasis and
said it is in discussions to finalise a global partner to take it
worldwide.
Alzumab, now commercially available in the
country for treating patients with chronic plaque psoriasis, was priced
at least 50 per cent lower than similar drugs in the market, the
company’s Chairperson and Managing Director, Kiran Mazumdar—Shaw told a
news conference here.
”....we will be addressing the
global opportunity through partnering the molecule (the infusion drug)
globally”, she said, adding, Biocon was currently engaged in discussions
with a large number of companies in this regard.
“This
is a breakthrough innovation and it has potential to make huge global
impact”, Shaw said adding that it is a matter of time before Biocon inks
partnership deal to take it worldwide.
Biocon, which
started developing Alzumab in 2006, estimates psoriasis treatment will
have a global market size of $8 billion by 2016.
Psoriasis is a socially-debilitating disease affecting an estimated 2—3 per cent of the world population.
Shaw
also said Biocon would soon file for an investigational new drug (IND)
application with US FDA (Food and Drug Administration) for Alzumab,
which is indicated for the treatment of moderate-to-severe psoriasis.
“We
have had discussions with regulators...US FDA.. and they are also very
excited about the promise of this drug and we are planning to file an
IND very soon (within the current fiscal)”, Mazumdar-Shaw said.
Biocon
said Alzumab (Itolizumab) has demonstrated preclinical and clinical
evidence in treating other auto—immune diseases such as rheumatoid
arthritis, psoriatic arthritis and multiple sclerosis.
Rakesh
Bamzai, President—Marketing, Biocon said, “We are committed to address
the huge unmet need of patients suffering from psoriasis through its
‘first in class’ biologic Alzumab.
“Compared to
existing therapies, it offers a better safety and efficacy profile to
the patients with longer remission periods and lower infection rates
that will lead to better patient compliance and overall reduction in the
cost burden to the patient,” he said.
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