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BioWorld - Wednesday, July 8, 2026
Home » Topics » Drugs » Antibody-drug conjugate

Antibody-drug conjugate
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3D illustration demonstrating antibody-drug conjugate.
Immuno-oncology

Ajinomoto and Exelixis sign license agreement to incorporate AJICAP technology into Exelixis ADCs

Jan. 11, 2023
Ajinomoto Co. Inc.'s Ajinomoto Bio-Pharma Services has announced a license agreement with Exelixis Inc. to incorporate AJICAP, Ajinomoto's proprietary site-specific bioconjugation and linker technologies, in the development of certain of Exelixis' antibody-drug conjugate (ADC) programs for cancer.
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Immuno-oncology

Minghui Pharmaceutical divulges new antibody-drug conjugates for cancer

Jan. 10, 2023
Minghui Pharmaceutical (Hangzhou) Ltd. and Minghui Pharmaceutical (Shanghai) Ltd. have synthesized antibody-drug conjugates consisting of an antibody covalently linked to exatecan derivatives through a linker.
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Immuno-oncology

Ammax signs option agreement with Evopoint for ADC for solid tumors

Jan. 10, 2023
Ammax Bio Inc. has entered into an exclusive option with Evopoint Biosciences Co. Ltd. for a worldwide license, excluding Greater China, for the development and commercialization of a novel antibody-drug conjugate (ADC) for treating solid tumors.
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Concept of business partnership

Legochem out-licenses ADC targets to Amgen in ₩1.6 trillion deal

Dec. 27, 2022
By Tamra Sami
South Korea’s Legochem Bioscience Inc. inked a licensing deal with Amgen Inc. on Dec. 23 for five undisclosed antibody drug conjugate (ADC) targets worth up to ₩1.6 trillion (US$1.24 billion). Under the terms of the deal, Legochem will out-license global rights to Amgen for five undisclosed ADC targets and will receive an undisclosed up-front payment as well as development milestones and sales royalties. The companies did not disclose additional details.
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Antibody-drug conjugate illustration

The year’s biggest deal: Merck and Kelun enter $9.3B alliance

Dec. 27, 2022
By Lee Landenberger
Two deals for antibody-drug conjugates inked since May between Merck & Co. Inc. and Sichuan Kelun-Biotech Pharmaceutical Co. Ltd. have blossomed eight months later into the year’s biggest agreement, one that could bring Kelun-Biotech up to $9.3 billion in development, regulatory and sales milestones. The exclusive license and collaboration deal has Merck paying an up-front $175 million to Kelun-Biotech plus promising to make an equity investment in the Sichuan, China-based company.
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Immuno-oncology

Merck KGaA and Mersana collaborate on novel ADCs using Immunosynthen STING-agonist ADC platform

Dec. 23, 2022
Merck KGaA has entered into a research...
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Antibody-drug conjugate
Immuno-oncology

Merck & Co. and Kelun-Biotech partner on preclinical ADCs for cancer

Dec. 23, 2022
Merck & Co. Inc. and Kelun-Biotech, a holding...
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Antibody-drug conjugate illustration

The year’s biggest deal: Merck and Kelun enter $9.3B alliance

Dec. 22, 2022
By Lee Landenberger
Two deals for antibody-drug conjugates inked since May between Merck & Co. Inc. and Sichuan Kelun-Biotech Pharmaceutical Co. Ltd. have blossomed eight months later into the year’s biggest agreement, one that could bring Kelun-Biotech up to $9.3 billion in development, regulatory and sales milestones.
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Pinotbio, Conjugatebio strike $250M deal for 10 ADC targets

Dec. 21, 2022
By Marian (YoonJee) Chu
South Korean biotech Pinotbio Co. Ltd. inked a $250 million (₩320 billion) licensing deal with Princeton, N.J.-based Conjugatebio Inc. to develop 10 antibody-drug conjugate (ADC) targets with Pinotbio’s ADC platform technology. The deal announced on Dec. 21 adds to a previous agreement between the two companies last year. Pinotbio and Conjugate first teamed up to discover and develop five ADC targets in June 2022.
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Post-dose escalation SAEs vex Magenta in phase I/II trial

Dec. 20, 2022
By Michael Fitzhugh
Magenta Therapeutics Inc., the developer of an antibody-drug conjugate intended to help prep certain relapsed/refractory acute myeloid leukemia and myelodysplastic syndrome patients for stem cell transplant or gene therapy, has stopped dosing the drug in part of an ongoing trial after observing two cases of serious adverse events (SAEs) possibly related to the candidate.
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