The global antibody drug conjugates market size was valued at USD 5.81 billion in 2021 and is expected to expand at a compound annual growth rate (CAGR) of 16.4% from 2022 to 2030. The market is primarily driven by globally rising incidences of cancer. According to Cancer Research UK estimates the number of new cancer cases worldwide is expected to reach 27.5 million by 2040. Factors such as smoking, unhealthy diet, obesity, and alcohol are the major cause of rising cancer cases, worldwide. The COVID-19 pandemic had a negative impact on the product sale due to the loss of health insurance coverage, decrease in hospital visits, and lower diagnosis rates. The unavailability of participants for clinical trial studies led to a delay in the potential approval of ADCs such as Adcetris for other indications.
Increasing investment in this field by the key players such as Piramal Pharma Solution, Pfizer Inc., Seagen Inc., and F. Hoffman La-Roche Ltd for the development of new ADCs intended for the treatment of cancer is expected to drive the market growth. For instance, in February 2022, CDMO Piramal Pharma Solutions (PPS) invested about USD 74.6 million in the development of two new antibody-drug conjugates (ADC) production facilities at its existing sites in Grange mouth, Scotland to fulfill the growing demand for commercial ADCs in UK. This investment strengthens PPS’ position in the market, significantly, by increasing ADC manufacturing capacity.
Most of the companies are conducting clinical trials to bring new products to the market and to gain label expansion for their already approved products. For instance, in January 2022, Seagen initiated phase-1 clinical trials of two novel antibody-drug conjugates such as SGN-B7H4V & SGN-PDL1V in patients with advanced solid tumors. In addition, the company in collaboration with Astellas completed enrollment of the patients for cohort K EV-103 trial used for the treatment of First-Line Metastatic Urothelial Cancer (mUC). Successful completion of the clinical trial study and subsequent approval of the products is expected to drive market growth.
Breast cancer accounted for the largest revenue share in 2021 owing to the relatively high prevalence of the disease worldwide. According to WHO, there were around 2.26 million new breast cancer cases diagnosed worldwide in 2020, and estimated deaths due to cancer were 685,000. There are three antibody-drug conjugate products available for the treatment of breast cancer as; Trodelvy from Gilead Sciences, Inc.; Enhertu from AstraZeneca; and Kadcyla from Hoffmann-La Roche Ltd. Providing these drugs under the patient assistance program is expected to drive the market growth. Kadcyla offers financial assistance to eligible patients, who are publicly and commercially insured.
The blood cancer segment is expected to increase by the 15.4% CAGR during the forecast period. Blood cancer is the fifth most common cancer and is the second leading cause of cancer deaths, globally. According to the National Foundation of Cancer Research, in the U.S., a total of 186,400new cases of leukemia, lymphoma, and myeloma were diagnosed in 2021. Furthermore, the approval for multiple products during the forecast period is expected to drive market growth. For instance, in October 2019, a new product, Polivy, was launched in the market, for the treatment of diffuse large B-cell lymphoma (DLBCL).
The cleavable linker segment accounted for the largest revenue share, in2021. The ability of cleavable linkers to remain stable in the bloodstream for longer duration & release of a cytotoxin from ADCs makes them the most popular used technology for an effective outcome of ADCs in cancer treatment. For instance, in 2020, Seagen’s & Takeda’s Adcetris was approved by NMPA for use in the treatment of relapsed Hodgkin's lymphoma and relapsed systemic anaplastic large cell lymphoma sALCL in China. Such factors are expected to drive the cleavable linker market segment, during the forecast period.
Non-cleavable linker was the second largest revenue-generating segment in 2021 owing to the increase in usage of Kadcyla, which contains a non-cleavable linker. Non-cleavable linker is used for the production of ADCs that are reliant on the ADC’s lysosomal degradation and prevents the non-specific release of the drug, thus reducing the overall cytotoxicity of the ADC to surrounding healthy cells. This is expected to drive the segment during the forecast period. Currently, only FDA approved ADCs such as Kadcyla and Blenrep use non-cleavable linkers for binding the antibody and cytotoxic molecule
Linker is the key component of ADCs and it connects the antibody & cytotoxic payload. It imparts the characteristics to ADCs such as high stability in circulation and specific release of payload in the target tissue. There are number of linkers available in the market which includes VC, Sulfo-SPDB, VA, Hydrazone, SMCC, SPP, MCC, maleimide tetrapeptide, CL2A, and MC are used to deliver payloads to their target sites.
Payloads are cytotoxic agents that are used to kill target cancerous cells. Currently, there are many payloads available in the market including microtubuline inhibitors (Vinorelbine, Paclitaxel, Epothilone B, Tubulysins (IM-2, B), DNA cleavers (Bleomycin A2), Akt inhibitors (GDC - 0068), DNA intercalators (Doxorubicin hydrochloride, Epirubicin hydrochloride, Duocarmycins, PBD dimers), MMAF & MMAE. Currently, Blenrep (belantamab mafodotin-blmf) developed by GlaxoSmithKline plc. utilizes MMAF, protease linker, and anti-CD38 monoclonal antibody to kill target cell in adult patients with relapsed multiple myeloma.
North America dominated the market in terms of revenue in 2021. The well-established research facilities for the development of novel ADCs, rising per capita healthcare expenditure, and increasing prevalence of cancer are the major factors responsible for the dominance of the region. As per the American Cancer Society estimates, the incidence of cancer reached 1.9 million in 2022 and around 609,360 deaths in the U.S. The approval of new ADCs in the region is expected to drive market growth. For instance, in September 2021, the U.S. FDA approved Tidvak for the treatment of adult patients with metastatic or recurrent cervical cancer.
Asia Pacific antibody-drug conjugates market is expected to witness a CAGR of 18.7% during the forecast period. The growth of the region is attributable to the approval of new ADCs in the region. For instance, in May 2021, Japan’s MHLW granted priority review to Astellas’s enfortumab vedotin for the treatment of metastatic or locally advanced urothelial cancer.
The leading players are focusing on growth strategies, such as innovations in the existing product, approval of new products, and mergers & acquisitions to gain market share. For instance, in October 2020, Gilead completed the acquisition of Immunomedics, Inc. for around USD 21.0 billion. Additionally, in May 2020, Takeda’s Adcetris received approval from China’s NMPA for the treatment of adult patients with ALCL or systemic Hodgkin lymphoma.
Some of the prominent players in the global antibody drug conjugates market include:
Seagen, Inc.
Takeda Pharmaceutical Company Limited
AstraZeneca
F. Hoffmann-La Roche Ltd.
Pfizer, Inc.
Gilead Sciences, Inc.
Daiichi Sankyo Company Limited
GlaxoSmithKline plc
Astellas Pharma, Inc.
ADC Therapeutics SA
Report Attribute |
Details |
Market size value in 2022 |
USD 8.08 billion |
Revenue forecast in 2030 |
USD 22.87 billion |
Growth Rate |
CAGR of 16.4% from 2021 to 2030 |
Base year for estimation |
2021 |
Historical data |
2017 - 2020 |
Forecast period |
2022 - 2030 |
Quantitative units |
Revenue in USD Million, CAGR from 2021 to 2030 |
Report coverage |
Revenue forecast, company ranking, competitive landscape, growth factors, trends |
Segments covered |
Application, technology, region |
Regional scope |
North America; Europe; Asia Pacific; Latin America; MEA |
Country scope |
U.S.; Canada; UK; Germany; France; Spain; Italy; Russia; China; Japan; India; Australia; South Korea; Singapore; Brazil; Mexico; Argentina; South Africa; Saudi Arabia; UAE |
Key companies profiled |
Takeda Pharmaceutical Company Limited; F. Hoffmann-La Roche Ltd; Pfizer, Inc.; AstraZeneca; Gilead Sciences, Inc.; Astellas Pharma; Seagen, Inc.; Daiichi Sankyo Company Limited; GlaxoSmithKline Plc; ADC Therapeutics SA |
Customization scope |
Free report customization (equivalent up to 8 analyst’s working days) with purchase. Addition or alteration to country, regional & segment scope. |
Pricing and purchase options |
Avail customized purchase options to meet your exact research needs. Explore purchase options |
This report forecasts revenue growth and provides an analysis of the market trends in each of the sub-markets from 2017 to 2030. For this study, Grand View Research has segmented the global antibody drug conjugates market report based on the application, technology, and region:
Application Outlook (Revenue, USD Million; 2017 - 2030)
Blood Cancer
Leukemia
Lymphoma
Multiple Myeloma
Breast Cancer
Urothelial Cancer & Bladder Cancer
Other Cancer
Technology Outlook (Revenue, USD Million; 2017 - 2030)
Type
Cleavable Linker
Non- cleavable Linker
Linkerless
Linker Type
VC
Sulfo-SPDB
VA
Hydrazone
Others
Payload Type
MMAE
MMAF
DM4
Camptothecin
Others
Regional Outlook (Revenue, USD Million; 2017 - 2030)
North America
U.S.
Canada
Europe
Germany
UK
France
Italy
Spain
Russia
Asia Pacific
Japan
China
India
Australia
South Korea
Singapore
Latin America
Brazil
Mexico
Argentina
MEA
South Africa
Saudi Arabia
UAE
b. The global antibody-drug conjugates market is expected to grow at a compound annual growth rate of 16.4% from 2022 to 2030 to reach USD 22.87 billion by 2030.
b. Based on application, the breast cancer segment dominated the antibody-drug conjugate market with a share of 54.48% in 2021. A higher number of approved products and label expansion of currently approved products for early-stage breast cancer are some of the key factors driving the growth of this segment.
b. Some key players operating in the antibody-drug conjugates market include Seagen, Inc.; Takeda Pharmaceutical Company Limited; AstraZeneca Plc, F. Hoffmann-La Roche Ltd.; Pfizer, Inc.; ADC Therapeutics; Astellas Pharma; Gilead Sciences, Inc.; GlaxoSmithKline Plc; and Daiichi Sankyo Company Limited.
b. Key factors that are driving the antibody-drug conjugates market growth include the increasing prevalence of cancer and the impending approval of new products such as Tisotumab Vedotin, Camidanlumab Tesirine, and trastuzumab Duocarmazine amongst others.
b. The global antibody-drug conjugates market size was estimated at USD 5.81 billion in 2021 and is expected to reach USD 8.08 billion in 2022.
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Multiple therapeutic regimens are being followed across the globe in attempts to come up with a reliable treatment for Covid-19. One line of treatment includes the use of hydroxychloroquine, while a second treatment line focuses to use antiviral drugs used in the disease management of HIV. Both these approaches have surged demand from advanced antivirals and antimalarial drugs. This impacts the drug manufacturers as an off label indication for these drug classes has to be worked upon. At the moment, the WHO has not prescribed any of these approaches, neither they have commented if one is better than the other. The report will account for COVID-19 as a key market contributor.
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