Biosimilars are biological products that
are similar to FDA-approved drug known as branded drug. Biosimilars are
drugs licensed by the European Medicines Agency (EMA) and the U.S. FDA.
These do not have significant differences from the reference products in
terms of purity, effectiveness, and safety. Biosimilar drugs can only
be permitted for conditions and indications that have been formerly
accepted for the reference product by government regulatory agencies and
organizations, when the original products patents expires. Compared to
generic drugs, biosimilars show more molecular complexity. These are
also quite sensitive to modifications in the manufacturing process.
Report Overview @ https://www.transparencymarketresearch.com/infliximab-market.html
The global infliximab market is projected
to grow at a rapid pace in the next few years. Increase in incidence of
hereditary and autoimmune diseases such as plaque psoriasis and
rheumatoid arthritis drive the global market. The number of people
suffering from Crohn’s disease and ulcerative colitis (UC) has increased
in various regions in the past few years. All the inflammatory bowel
diseases (IBD) are associated with considerable morbidity cases with
substantial use of health care resources. Early patent expiry,
discounted pricing on branded drugs, and quick response time due to
intravenous mode of administration propel the market. Additionally,
entry of biosimilars into the market has the ability to provide
significant financial relief to the current health care systems.
However, side effects of the drug treatment such as histoplasmosis
(fungal infection), tuberculosis (TB), bacterial sepsis, and others
restrain the global infliximab market. Hence, manufacturers of the drug
have been mandated to include warnings to alert both patients and health
care professionals. Additionally, lack of FDA-approved facilities,
especially in developing countries, to manufacture the drug are the
factors expected to restrain the market.
Geographically, the global infliximab
market can be segmented into North America, Europe, Asia Pacific, Latin
America, and Middle East & Africa. North America and Europe are
projected to dominate the market, followed by Asia Pacific and Latin
America. Dominance of North America and Europe is attributed to launch
of biosimilars after patent expiry. The market in Asia Pacific is
anticipated to grow at a rapid pace in the next few years. This is due
to presence of rapidly developing economies such as China and India,
increase in awareness about health and hygiene, enhanced health care
infrastructure, and unexploited market as increase in geriatric
population that lacks adequate diagnostic & treatment solutions.
Additionally, rise in government support for the manufacture of
biosimilars drugs and increase in awareness and adoption of biosimilars
is anticipated to drive the global infliximab market.
Key players in the global infliximab market are Merck & Co., Celltrion, Inc., Alvogen, Janssen Biotech, Inc., NAPP Pharmaceuticals, Nippon Kayaku, and Pfizer, Inc. (AC. Hospira), among others.
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