Is Oncology Biosimilars Market Trapped Between Growth Expectations and Uncertainty?

According to the World Health Organization (WHO), Cancer accounts for one in six deaths globally, claiming more lives than AIDS, tuberculosis, and malaria combined. This disease represents a big burden on the healthcare systems worldwide due to high-cost factor for treatment and therapeutics. The patent expiry of several cancer therapeutics has resulted in the entry of Biosimilars which are being incorporated in the treatment of oncology. Due to the high incidence of cancer, the market of Oncology Biosimilars is providing huge growth opportunity to the key vendors. According to the U.S. Food and Drug Administration (FDA), Biosimilars is a biological product that is highly similar to an existing, approved reference product and has no clinically meaningful differences. These are manufactured by different companies on being approved officially for cancer treatment. Oncologic Biosimilars are cost-effective molecules with the same efficacy and potency as original biologics.

Latest Research Study on Global Oncology Biosimilars Market published by AMA, offers a detailed overview of the factors influencing the global business scope. Oncology Biosimilars Market research report shows the latest market insights with upcoming trends and breakdown of the products and services. The report provides key statistics on the market status, size, share, growth factors, Challenges and Current Scenario Analysis of the Oncology Biosimilars. This Report also covers the emerging player’s data, including: competitive situation, sales, revenue and global market share of top manufacturers are Biocon (India), Celltrion (South Korea), Dr Reddy laboratories (India), F Hoffman-La Roche (Switzerland), Mylan (United States), Sandoz (Germany), Teva Pharmaceuticals Ltd.(Israel), STADA Arzneimittel AG (Germany), Pfizer Inc. (United States), BIOCAD (United States) and Sanofi (France).

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Market Drivers

• Increased prevalence of cancer leading to demand for affordable therapies to treat cancer
• Patent expiry of existing biologics
• Increasing number of alliances for the development of Biosimilars.

Market Trend

• The number of FDA approved cancer therapies continues to rise, with 63 cancer drugs launching within the past five years
• Over one-third of trials are using biomarkers to stratify patients, pointing to even more personalized cancer treatments in the future.

Restraints

• Adoption of Biosimilars by many oncologists due to high cost.

Opportunities

• Patent expiry will provide an opportunity to the pharmaceutical companies to manufacture more Biosimilars leading to fuel the market.

Challenges

• Potential of Biosimilars to mitigate rising health care cost while improving highly effective therapies.

Region Included are: North America, Europe, Asia Pacific, Oceania, South America, Middle East & Africa

Country Level Break-Up: United States, Canada, Mexico, Brazil, Argentina, Colombia, Chile, South Africa, Nigeria, Tunisia, Morocco, Germany, United Kingdom (UK), the Netherlands, Spain, Italy, Belgium, Austria, Turkey, Russia, France, Poland, Israel, United Arab Emirates, Qatar, Saudi Arabia, China, Japan, Taiwan, South Korea, Singapore, India, Australia and New Zealand etc.

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Extracts from Table of Contents
Chapter 1: Oncology Biosimilars Market Overview
Chapter 2: Global Oncology Biosimilars Market Share and Market Overview
Chapter 3: Oncology Biosimilars Market Manufacturers/Players Analysis
3.1 Market Concentration Rate
3.2 Competition Scenario: BCG Matrix [Relative Market Share v/s Revenue Growth Rate]
3.3 Heat Map Analysis
3.4 Comparative Market Share Analysis by Players (2018-2019) Rank, [% Market Share, Market Revenue]
3.5 Company Profile – Business Distribution by Region, Interview Record, Business Profile, Product/Service Specification, Price, Revenue and Gross profit 2017-2019
3.6 Price Benchmarking (2017-2019)
Chapter 4: Global Oncology Biosimilars Market Segmentation (Country Level Breakdown) (2014-2025)

• North America: United States, Canada, and Mexico.
• South & Central America: Argentina, Chile, and Brazil.
• Middle East & Africa: Saudi Arabia, UAE, Turkey, Egypt and South Africa.
• Europe: United Kingdom, France, Italy, Germany, Spain, Belgium, Netherlands, Poland and Russia.
• Asia-Pacific: India, China, Japan, South Korea, Indonesia, Singapore, and Australia.

Chapter 5: Global Oncology Biosimilars Market Breakdown by Segments (by Type (G-CSF, Hematopoietic Agents, Monoclonal Antibodies), Application (Cancer Treatment Drugs, Supportive Care Drugs), Drug type (Monoclonal antibody (mAb), Immunomodulators, Hematopoietic agents, G-CSF, Others), Cancer type (Lung Cancer, Colorectal cancer, Cervical Cancer, Breast Cancer, Kidney cancer, Stomach cancer, Brain Cancer, Others), End user (Retail Pharmacies, Hospitals), Distribution channel (Hospital Pharmacies, Online Pharmacies, Retail Pharmacies))
5.1 Global Oncology Biosimilars Market Segmentation (Product Type) Market Size 2014-2025
5.2 Different Oncology Biosimilars Price Analysis by Product Type (2014-2025)
5.3 Global Oncology Biosimilars Market Segmentation (Product Type) Analysis
5.4 Global Oncology Biosimilars Market by Application/End users Market Size 2014-2025
5.5 Global Oncology Biosimilars Market Segmentation (other segments) Analysis
Chapter 6: Methodology/Research Approach, Data Source, Disclaimer

Data Sources & Methodology

The primary sources involves the industry experts from the Global Oncology Biosimilars Market including the management organizations, processing organizations, analytics service providers of the industry’s value chain. All primary sources were interviewed to gather and authenticate qualitative & quantitative information and determine the future prospects.

In the extensive primary research process undertaken for this study, the primary sources – Postal Surveys, telephone, Online & Face-to-Face Survey were considered to obtain and verify both qualitative and quantitative aspects of this research study. When it comes to secondary sources Company’s Annual reports, press Releases, Websites, Investor Presentation, Conference Call transcripts, Webinar, Journals, Regulators, National Customs and Industry Associations were given primary weight-age.

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