Market Size in 2023 | Market Forecast in 2032 | CAGR (in %) | Base Year |
---|---|---|---|
USD 6.13 Billion | USD 28.26 Billion | 18.50% | 2023 |
The global oncology biosimilar market size was worth around USD 6.13 billion in 2023 and is predicted to grow to around USD 28.26 billion by 2032 with a compound annual growth rate (CAGR) of roughly 18.50% between 2024 and 2032.
The report covers forecast and analysis for the oncology biosimilar market on a global and regional level. The study provides historical data from 2018 to 2022 along with a forecast from 2024 to 2032 based revenue (USD Billion).
Biosimilar is a biological medical product which is an identical copy of the original product manufactured by the companies. Biosimilar is the approved version of innovative products and can only be manufactured after the patent expiry of the original product. Oncology biosimilar is different as compared to the biologics in terms of complexity and manufacturing process. The biosimilar is much cheaper as compared to branded and approved products which are available in the market. There are several biologics available in the market for oncology which is on its way of patent expiry. Patent expiry of branded biologics will increase the biosimilar market. Biosimilar can be used for the treatment of various types of cancer such as lung cancer, kidney cancer, and others which are expected to open the gates of opportunities for the biosimilar market in the near future.
One of the major factors driving the oncology biosimilar market is the increasing demand for affordable therapies due to the constant increase in cancer patients worldwide. Various pharmaceutical companies are involved in the development of oncology biosimilar and generic medicines for the treatment of cancer at all stages and early detection of cancer. Due to the high demand for the cancer treatment, there is a rapid rate of approval observed in past few years which are expected to drive the oncology biosimilar market. The first biosimilar was approved in 2006 in Europe, and in the U.S. first biosimilar was approved in 2015 after the approval of first biosimilar FDA has approved five biosimilars in 2017. There is a number of applications pending for the approval of oncology biosimilar and their approval in future are expected to support the growth of oncology biosimilar market.
The study provides a decisive view on the oncology biosimilar market by segmenting the market based on cancer type, drug type, distribution channel, and regions. All the segments have been analyzed based on present and future trends and the market are estimated from 2024 to 2032.
Based on cancer type, the oncology biosimilar market is segmented as breast cancer, colorectal cancer, blood cancer, neutropenia cancer, non-small cell lung cancer and others.
On the basis of drug type, oncology biosimilar market is segmented into mAb, immunomodulators, hematopoietic agents, G-CSF, and others. G-CSF segment is expected to grow at the fastest rate during the forecast period.
Based on the distribution channel, oncology biosimilar market is segmented into retail pharmacies, hospital pharmacy, and online pharmacy. Hospital pharmacy segment is expected to grow at the fastest rate during the forecast period.Increasing demand for affordable therapies due to the constant increase in cancer patients is one of the major driving factors of oncology biosimilar market. High medical expenses associated with cancer treatment; the lack of awareness and dearth of skilled personnel are factors that influence the market growth during the forecast period.
Report Attributes | Report Details |
---|---|
Report Name | Oncology Biosimilar Market Research Report |
Market Size in 2023 | USD 6.13 Billion |
Market Forecast in 2032 | USD 28.26 Billion |
Growth Rate | CAGR of 18.50% |
Number of Pages | 110 |
Key Companies Covered | Teva Pharmaceutical Industries Ltd., Biocon, STADA Arzneimittel AG, Sandoz International GmbH, Intas Pharmaceuticals Ltd., Celltrion Inc., Pfizer Inc., Apotex Inc., Dr. Reddy’s Laboratories Ltd., BIOCAD, and among others. |
Segments Covered | By Cancer Type, By Drug Type, By Distribution Channel, And By Region |
Regions Covered | North America, Europe, Asia Pacific (APAC), Latin America, Middle East, and Africa (MEA) |
Base Year | 2023 |
Historical Year | 2018 to 2022 |
Forecast Year | 2024 - 2032 |
Customization Scope | Avail customized purchase options to meet your exact research needs. Request For Customization |
The regional segmentation includes the current and forecast demand for North America, Europe, Asia Pacific, Latin America, and the Middle East & Africa with its further bifurcation into major countries, including the U.S., Canada, Mexico, Germany, Spain, Italy, France, UK, China, Japan, India, and Brazil. This segment includes demand for oncology biosimilar market based on individual segment and test types in all the regions and countries.
North America is expected to remain the dominant region over the forecast period which is closely followed by Europe. Due to the increased patent expiration and FDA approval of the new drugs the oncology biosimilar market is anticipated to grow rapidly over the forecast period. The Asia Pacific is expected to experience significant growth over the forecast period due to the increase in strategic collaboration in this region. Latin America and the Middle East & Africa are expected to experience a considerable growth over the forecast period. All the above-mentioned factors are responsible for the growth of oncology biosimilar market over the forecast period.
The report also includes detailed profiles of end players such as
By Cancer Type
By Drug Type
By Distribution Channel
By Region
FrequentlyAsked Questions
An oncology biosimilar is a biological product that is highly similar to an already approved reference biologic drug used in the treatment of cancer.
According to study, the global oncology biosimilar market size was worth around USD 6.13 billion in 2023 and is predicted to grow to around USD 28.26 billion by 2032.
The CAGR value of oncology biosimilar market is expected to be around 18.50% during 2024-2032.
North America has been leading the global oncology biosimilar market and is anticipated to continue on the dominant position in the years to come.
The global oncology biosimilar market is led by players like Teva Pharmaceutical Industries Ltd., Biocon, STADA Arzneimittel AG, Sandoz International GmbH, Intas Pharmaceuticals Ltd., Celltrion Inc., Pfizer Inc., Apotex Inc., Dr. Reddy’s Laboratories Ltd., BIOCAD, and among others.
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