Biosimilars Market Size, Growth, Trends, Expected CAGR of 31.5% over the Forecast 2019-2025

Global Biosimilars Market

Global Biosimilars Market Overview:

Several blockbuster biologics of significant pharmaceutical companies, such as Remicade, Rituxan, Herceptin, Enbrel, Lantus, and others, have expired in latest years. In the coming decade, there would be an increase in the patent expiry of several current biological drugs, such as Erbitux, Avastin, Orencia, and others, which would provide a chance for many innovative businesses and generic suppliers to offer services specifically adapted to biosimilars. In addition, factors such as the cost-effectiveness nature of biosimilars, increased recognition and adoption by multiple stakeholders with the need for diversification in technology and business models are anticipated to drive the worldwide biosimilar market. At the same moment, with variables such as absence of definitive approval norms and appropriate profitability, considering the increased danger with worries about replaceability and interchangeability, many firms are discouraged from investing in this industry, thus impeding market growth.

Global Biosimilars Market Scope of the Report:

A biosimilar is a biologic “comparable” to another biologic medicine known as a reference item already authorized by the U.S. Food Administration FDA. Biosimilars are comparable in security, purity and potency to the reference product, but may have minor variations in clinically inactive parts. The FDA may require that producers perform a clinical survey or surveys to identify safety, purity or potency in one or more uses for which the reference item is authorized and the biosimilar seeks licensing.

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Global Biosimilars Market Key trends:

Oncology segment maintains a significant share in the global bio-like industry Market segment applications are segmented as Blood Disorders, Growth Hormonal Deficiency, Chronic and Autoimmune Disorders, Oncology, Others. The oncology segment dominates the worldwide biosimilar market in income due to elevated cancer incidence including lung, liver, colorectal, stomach, breast, and blood cancer. According to the National Cancer Institute NCI report, in 2018 1,735,350 fresh cancer cases are identified in the US and 609,640 individuals will die from the disease. Amelita, Amgen s Humira variant is the first adalimumab biosimilar authorized by the US FDA in September 2016. Two European variants, Amgevita and Solymbic, were suggested in January 2017 in the EU.

North America Dominated Biosimilar Market Development:

In 2017, North America accounted for the biggest share, accounting for about 30% of the worldwide market. The North American market segment studied is motivated by the existence of many big study laboratories such as Sandoz, Amgen, Teva Pharmaceutical, and others. According to a latest study, more than 40 biosimilars are under growth, including about 20 ready-to-market biosimilars, and a substantial amount of biosimilars are in the pipeline. Due to the region s enormous financial advances and booming biotechnology businesses, solid growth over the forecast period is also anticipated in Asia-Pacific. In addition, variables such as high demand for low-cost therapy and treatment, elevated prevalence and incidence of multiple chronic diseases, increased R&D spending by industry players in emerging markets such as India, South Korea and China are also driving development in the Asia Pacific economy.

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Global Biosimilars Market Competitive Landscape:

Biosimilar market has huge competition. With many national and foreign market players. Most market players adopt multiple development strategies such as acquisitions, alliances, fresh product launches for market survival.

For example,
In 2018 Mylan NV launched HulioTM, biosimilar to AbbVie s Humira ® adalimumab , across main European markets.

In October 2018, Sandoz, a Novartis biosimilar subsidiary, received permission from the US Food and Drug Administration FDA for its biosimilar, HyrimozTM adalimumab-adaz therapy of rheumatoid arthritis, adolescent idiopathic arthritis in patients four years of age and older.

In November 2018, Teva received HERZUMA ® trastuzumab-pkrb, a biosimilar to HERCEPTIN ® for the treatment ofHER2-Over-expressing breast cancer, for certain indications.

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