Abstract:
In view of the global changes in disease pattern, reduced health budget in developed countries,
increasing health budget in developing countries, patent expiry of some high valued products,
transformations in R&D productivities and side effects of chemical drugs global pharmaceutical
giants are concentrating on biologic products among which anticancer, antidiabetic, antiarthritic,
cardiovascular products are especially important. However, developing a biotech product involved
huge cost which is possible only by research based top companies. Realizing the fact, many
pharmaceutical companies tried to imitate the original biotech products after patent expiry and
became successful which bring a breakthrough in terms of health cost. These imitated products are
termed as biosimilar products. Although the history of biosimilars started at European Union (EU)
in 2006 with single product but currently it has been recognized everywhere in the world and EU
have highest 19 biosimilar products. United States Food & Drug Administration (USFDA) was
little conservative with biosimilars; nevertheless, they approved the first biosimilar 09 years after
EU approval and presently they have three biosimilars which are playing significant role in price
cutting of branded biologics. They also have so many biosimilars in pipelines. Emerging
economies especially South Africa, China & India are very aggressive with biosimilars. Under
Pharmaceutical Benefits Scheme Australian government is promoting biosimilars and they already
approved 09 biosimilars. Japan, Korea, Canada are also encouraging biosimilars. Bangladesh isthe only Least Development Countries (LDCs) that have very strong pharmaceutical sector; there
are so many manufacturing facilities with global standard and approved by USFDA and
UKMHRA. Bangladesh pharmaceuticals industry worth $ 2 billion and have a long history success
in both domestic and international markets with generic products. Unlike global giants very few
Bangladeshi companies are putting concentration on biosimilars. Till to date one pharmaceutical
claimed them as true biosimilar company without any product in the market. 08 other
pharmaceutical companies are offering Non-Comparable Biologics (NCBs) which is below 5% of
the total domestic revenue although biologics accounts for more than 22% of the global total.
Considering huge number of patients with chronic diseases, increasing access to biologic treatment
due to changes in income level, improving access to medical services and diagnostic facilities,
easy regulations, cheap labor and related cost factors, geographical location, availability of
trainable manpower, raising patient awareness, price sensitivity, strong entrepreneurial skills
Bangladesh is in little advantageous position with biosimilars. However, success of biosimilars in
Bangladesh is mostly depends on the acceptance by the physicians, reduction of treatment cost,
increasing life expectancy, easy availability at the drug stores, trust on manufacturers, various
promotional and disease awareness campaigns, dissemination of proper information towards
doctors and patients, monitoring by the regulatory bodies, government patronization, drug
substitution, efficacy and safety of the individual product, technical collaboration with the experts,
export possibilities etc. Therefore, this study identifies the growth potential of biosimilar products
in Bangladesh.