Antibody drug conjugates, or ADCs, are highly targeted biopharmaceutical drugs that mix monoclonal antibodies that are specific for surface antigens found on certain tumor cells with highly effective anticancer agents that are linked by chemical linkers. In simple terms, antibody-drug conjugates send "deactivated" cytotoxins to cancer cells. Once the cytotoxin gets inside the tumor cell, a process called "internalization," starts that can kill cancer cells again. Because of this, cell death happens quickly. There are thousands of naturally occurring or chemically made cellular toxins, but only a few of them can be used as parts of an antibody-drug complex (ADC). Chemotherapy drugs like doxorubicin and methotrexate were used to make some of the first ADCs.The increasing cases of breast cancer for which antibody drug conjugates are used as a treatment, is expected to drive growth of the market over the forecast period. The emerging prevalence of breast cancer is expected to bolster the growth of global antibody drug conjugates market.
The global Antibody Drug Conjugates Market is anticipated to grow at a CAGR of 14.0% during the period of forecast (2021-2028).
Major Players in the Antibody Drug Conjugates Industry:
F. Hoffmann-La Roche Ltd
F. Hoffmann-La Roche Ltd, commonly known as Roche, is a Swiss multinational healthcare company. It was founded in and headquartered in. It operates in more than 150 countries.
Gilead Sciences, Inc
Gilead Sciences, Inc is an American biopharmaceutical company, was founded in 1987 and headquartered in California, United States. It operates in more than 35 countries worldwide. In January 2022, Gilead and Merck will collaborate on clinical trials to evaluate Trodelvy® in combination with KEYTRUDA® in patients with metastatic non-small cell lung cancer in first-line treatment.
GlaxoSmithKline Plc
GlaxoSmithKline Plc is a British multinational pharmaceutical and biotechnology company, was founded in 2000 and headquartered in England, U.K. It operates in over 115 countries. In Nov 2022, following the FDA's request, GSK plc began the process of withdrawing Blenrep's US marketing authorization. The DREAMM-3phase III confirmatory study results did not meet FDA Accelerated Approval standards, hence this request was made. Blenrep is a monotherapy for adult RRMM patients who have received at least four prior therapies, including an anti-CD38 monoclonal antibody, a proteasome inhibitor, and an immunomodulatory drug.
