The global antibody drug conjugates market size is valued at USD 13.63 billion in 2025 and is anticipated to grow from USD 15.41 billion in 2026 to USD 34.87 billion by 2034, growing at a CAGR of 11.04% from 2026 to 2034. Increasing approvals of HER2-targeted therapies, strategic ADC development partnerships across Asia Pacific, and rising adoption of antibody drug conjugates for cancer treatment are driving robust growth in the market.
Antibody drug conjugates are becoming highly valuable in the market, with currently 15 approved ADCs targeting 16 different indications for hematological and solid tumor malignancies as of June 2025. Pfizer Inc., AstraZeneca, Gilead Sciences, F. Hoffmann-La Roche Ltd., along with other pharmaceutical companies, are significantly investing in ADCs. Thus, market consolidation is a major driver boosting the revenue of global manufacturers.
Table: Top 5 Antibody Drug Conjugate Manufacturers
|
Manufacture |
ADC |
Revenue 2024 (USD Million) |
|
F. Hoffmann La-Roche Ltd. |
Kadcyla |
2,270.9 |
|
Polivy |
1,274.1 |
|
|
Pfizer Inc. |
Adcetris |
1,089.0 |
|
Padcev |
1,588.0 |
|
|
AstraZeneca |
Enhertu |
1,982.0 |
|
Gilead Sciences |
Trodelvy |
1,315.0 |
|
AbbVie Inc. |
Elahere |
479.0 |
Source: Company Annual Reports & Straits Analysis

Source: Straits Research Analysis
The use of Enhertu through advancing payloads is a key trend in the U.S. market. For example, Enhertu with pertuzumab has delivered a 40.7-month progression-free survival compared to 26.9 months for standard chemotherapy. This showcases ADCs as a potential first line treatment of care in HER2+ metastatic breast cancer across North America.
This fuels the demand for Enhertu in North America, which, in turn, contributes to the market growth.
Global manufacturers are taking the ADC market towards consolidation by acquiring smaller companies to advance their clinical cancer pipelines. This highlights the importance of ADC innovation in the U.S.
Elahere 2024 Journey
|
Date |
Elahere Development |
|
November 2024 |
CE grant marketing authorization to treat adult patients with FRα-positive, serious epithelial ovarian and fallopian tube cancer. |
|
June 2024 |
Positive phase 2 results from PICCOLO trial, where Elahere was evaluated as monotherapy in patients with platinum-sensitive ovarian cancer. |
|
March 2024 |
U.S. FDA approval for the indication of epithelial ovarian and fallopian tube cancer |
Source: AbbVie Form 10 K
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The surge in ADC approvals has created supply challenges in the market. To overcome this, in January 2024, Samsung Biologics launched a new ADC facility, and Lonza also acquired Genentech's large-scale biologics manufacturing site in Vacaville in October 2024. These development shows that manufacturers are making production a strategic priority. Thus, manufacturers are scaling up production and securing supply chains to prepare for global demands and reduce the risk of shortage, thereby driving the market growth for ADCs.
Global manufacturers are focusing on replacing chemotherapy with ADCs is a major factor supporting the adoption of ADCs in cancer therapy.
Thus, by replacing chemotherapy, ADC manufacturers are developing new standards of care, where ADC is becoming a first-line treatment, which will boost the company’s revenue growth in the long run.
Pricing, reimbursement, and competitive pressure reduce the revenue per unit, even when the product volume rises are a major restraint for ADC manufacturers. Gilead’s public filings and quarterly reporting for 2024 call out reimbursement pressures, rebates, and competition as explicit risks that are lowering prices of branded ADCs.
Breast cancer is a major indication for ADC use; manufacturers are focusing on extending it into other solid tumors.
Thus, expanding into multiple cancers will help manufacturers to diversify revenue generation and gain a strong foothold in the market.
North America dominated the antibody drug conjugates market in 2025, accounting for 44.87% market share. This dominance is attributed to strong clinical trial leadership, high uptake of ADCs, and a growing number of antibody approvals in the U.S. Furthermore, strong reimbursement support for high-cost oncology drugs is making ADCs available at low cost, leading to increased consumption. For instance, Trodelvy’s U.S. sales nearly doubled in 2024, showcasing high market uptake. Moreover, the region also benefits from a strong supply chain network, developed clinical infrastructure, and faster adoption of ADCs as compared to other regions.
Asis Pacific is emerging as the fastest-growing region with a CAGR of 12.7% from 2026-2034, owing to increasing local innovations, strong regulatory support, and expanding patient access. In this region, countries such as China, Japan, and South Korea are developing their own ADCs. For example, in May 2025, RemeGen’s disitamab vedotin became the first China-approved ADC signaling domestic innovations. In addition, the growing cancer incidences and large patient population are also making the Asia Pacific the fastest-growing region. For example, in 2025, Daiichi Sankyo’s Datroway (datopotamab deruxtecan) was approved in Japan to treat the highly prevalent breast cancer.

Source: Straits Analysis
U.S. accounts for the dominant share in the antibody drug conjugates market, driven by the highest number of ADC approvals, the development of novel ADCs through key market players, and a surge in patent application filing for ADCs. The table below highlights the number of ADC patents filed by various countries.
Table: Countries Holding ADC Patent
|
Country |
*No.Of Patents |
|
U.S. |
6741 |
|
Canada |
346 |
|
UK |
543 |
|
Germany |
525 |
|
France |
372 |
|
Italy |
138 |
|
Switzerland |
392 |
|
China |
2445 |
|
Japan |
502 |
|
India |
85 |
|
South Korea |
399 |
|
Israel |
187 |
Source: American Chemical Society
U.S. is the highest ADC patent-holding country, attributed to various factors such as high government investments (NIH Investment USD 47 Billion in 2024), which fuels the novel research that needs intellectual rights. Moreover, FDA’s leadership in approving ADCs like Trodelvy, Enhertu, and Padcev are making a big commercial market, giving manufacturers a strong motive to secure their drug with a patent.
China antibody drug conjugates market growth is driven by a surge in ADC clinical trials, increasing prevalence of cancers and autoimmune diseases, and accelerated development of domestic ADCs. Furthermore, China is also becoming the largest filer of patents across the globe through companies such as RemeGen, taking the lead with its ADC disitamab vedotin, being among the first approved in China. Moreover, the Chinese government has also prioritized biotech in its national policies, making funding and approvals faster for ADCs.
Germany's market is witnessing significant growth due to strong demand for targeted therapies and rising cancer incidences. Additionally, innovation in linker technologies for non-cleavable linkers, as in Kadcyla, further supports the market growth. Moreover, local manufacturing hubs are expanding ACD pipelines by raising funding for ADC research, thus creating new opportunities for market growth.
Switzerland’s advancement is driven by Roche’s ADCs, such as Kadcyla, and Lonza, known as one of the largest ADC manufacturing hubs in the country. These factors are collectively driving the ADC market growth in Switzerland. Moreover, growing R&D investment by domestic players to support ADC pipelines and a favorable European regulatory framework drive the market growth for antibody drug conjugates.
Japan is an emerging country in the antibody drug conjugates market, due to strong regulatory support leading to new ADC approvals. For instance, Japanese company Daiichi Sankyo significantly contributes to ADC innovations and currently has 3 candidates in the clinical pipeline. The company is also partnered with AstraZeneca for Enhertu. All the aforementioned factors position Japan as an emerging player in the market.
The Kadcyla segment dominated the market with a revenue share of 28.86% in 2025. This growth is attributed to its highest sales in the U.S. and the rest of the world. Additionally, in 2025, Roche expanded global access programs, showcasing Kadcyla in new healthcare systems across the Asia Pacific and Latin America, which led to increased market adoption. Moreover, the expanding application of Kadcyla for HER2-positive early breast cancer further drives the market penetration.

Source: Straits Analysis
The breast cancer segment dominated the market in 2025 and is anticipated to register the fastest CAGR of 12.4% during 2026-2034. This dominance is attributed to the high prevalence of breast cancer worldwide and the increasing number of ADC approvals for breast cancer treatment. Currently, Kadcyla, Trodelvy, and Enhertu are highly revenue-generating ADCs that are primarily approved for the treatment of Breast cancer. Thus, all aforementioned factors support segmental market growth.
The HER2 segment dominated the market in 2025, as it is one of the best biomarkers in oncology treatment. Recently, Enhertu’s approval for HER2-positive targets has built physician trust, making HER2-targeted ADC a first choice in the treatment. Moreover, a high clinical trial success rate compared to other targets such as Trop-2 and CD30 has supported the positive clinical trial results of the HER2 target.
The global antibody drug conjugates market is highly consolidated, with fewer players accounting for the maximum market share. The major key players in the market are Pfizer Inc., F. Hoffmann-La Roche Ltd., AstraZeneca, AbbVie Inc., Gilead Sciences, and others.
These players are actively engaged in various market strategies such as product approval, partnership, acquisition, and product launch to remain competitive in the market.
RemGen is a domestic manufacturer and developer of ADCs in China. The company is actively engaged in novel ADC development through partnerships with global companies. The company is emerging as a significant player in the market through its recent ADC approval.
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As per the analyst's opinion, the ADC market is gaining strong momentum as the pharmaceutical companies push for more precise and effective cancer treatments. The shift from traditional chemotherapy towards targeted therapies is the major factor supporting the ADC adoption for cancer therapies. Moreover, ongoing ADC approvals, with expanding applications in hematology and solid tumors, reflect growing clinical acceptance.
| Report Metric | Details |
|---|---|
| Market Size in 2025 | USD 13.63 Billion |
| Market Size in 2026 | USD 15.41 Billion |
| Market Size in 2034 | USD 34.87 Billion |
| CAGR | 11.04% (2026-2034) |
| Base Year for Estimation | 2025 |
| Historical Data | 2022-2024 |
| Forecast Period | 2026-2034 |
| Report Coverage | Revenue Forecast, Competitive Landscape, Growth Factors, Environment & Regulatory Landscape and Trends |
| Segments Covered | By Product Type, By Application, By Target, By Region. |
| Geographies Covered | North America, Europe, APAC, Middle East and Africa, LATAM, |
| Countries Covered | U.S., Canada, U.K., Germany, France, Spain, Italy, Russia, Nordic, Benelux, China, Korea, Japan, India, Australia, Taiwan, South East Asia, UAE, Turkey, Saudi Arabia, South Africa, Egypt, Nigeria, Brazil, Mexico, Argentina, Chile, Colombia, |
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Mitiksha Koul is a Research Associate with 2 years of experience in market research. She focuses on analyzing industry trends, competitive landscapes, and growth opportunities to support strategic decision-making. Mitiksha’s strong analytical skills and research expertise enable her to deliver actionable insights that help businesses adapt to evolving market dynamics and achieve sustainable growth.
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