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BioWorld - Sunday, June 14, 2026
Home » Topics » Drugs » Antibody-drug conjugate

Antibody-drug conjugate
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Tot Biopharm’s first ADC bevacizumab gets China lung cancer approval

Dec. 7, 2021
By Doris Yu
Tot Biopharm International Co. Ltd.’s self-developed Pusintin (bevacizumab), a biosimilar to Roche Holding AG’s Avastin, has won marketing approval from China’s NMPA. It was approved for the treatment of patients with advanced, metastatic, or recurrent non-squamous non-small-cell lung cancer and those with metastatic colorectal cancer.
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Aiming to build a better ADC, Emergence raises $98M in series A

Dec. 7, 2021
By Nuala Moran
LONDON – Europe’s latest antibody-drug conjugate (ADC) specialist, Emergence Therapeutics AG, will be going head to head with pioneer Seagen Inc.’s approved ADC, Padcev, after raising €87 million (US$97.9 million) in a series A round.
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Tot Biopharm’s first ADC bevacizumab gets China lung cancer approval

Dec. 2, 2021
By Doris Yu
Tot Biopharm International Co. Ltd.’s self-developed Pusintin (bevacizumab), a biosimilar to Roche Holding AG’s Avastin, has won marketing approval from China’s NMPA. It was approved for the treatment of patients with advanced, metastatic, or recurrent non-squamous non-small-cell lung cancer and those with metastatic colorectal cancer.
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Soraya hope in resistant ovarian cancer: Immunogen unveils top-line phase III data with ADC

Nov. 30, 2021
By Randy Osborne
Ursula Matulonis, a co-principal investigator in the latest study with Immunogen Inc.’s antibody-drug conjugate mirvetuximab soravtansine in stubborn ovarian cancer, said the top-line data are “truly spectacular” and bring “the potential to be transformative for patients.”
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Antibodies

Expanded cancer ADC deal between Synaffix and Mersana could be worth $1B

Nov. 30, 2021
By Richard Staines
The Netherlands-based Synaffix BV has expanded a deal focusing on its antibody-drug conjugate (ADC) linker tech with U.S. cancer biotech Mersana Therapeutics Inc., with the revised contract potentially paying out more than $1 billion. Privately owned Synaffix is hoping to ride a wave of interest in ADC technology, which is finally coming of age more than two decades after the first drug of this type was approved.
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Sotio places billion dollar bet on Legochem’s ADC tech

Nov. 23, 2021
By David Ho and Gina Lee
Sotio Biotech AS has licensed Legochem Biosciences Inc.’s technology for five new antibody-drug conjugates (ADC) in a deal that could bring the latter over $1 billion. Prague, Czech Republic-based Sotio will have the rights to deploy Legochem’s Conjuall and potent linker-payload platform, including multiple different payloads, for five therapeutic programs targeting solid tumors and combine its proprietary antibodies with it.
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Antibody-drug conjugate

Antengene partners with Legochem Biosciences to co-develop ADCs

Nov. 2, 2021
By Doris Yu
Antengene Corp. Ltd. has formed a partnership with Legochem Biosciences Inc. to jointly develop new antibody-drug conjugates (ADCs) primarily for cancer. The partners will integrate antibodies from Antengene with Legochem’s ADC technology.
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Antengene partners with Legochem Biosciences to co-develop ADCs

Oct. 27, 2021
By Doris Yu
Antengene Corp. Ltd. has formed a partnership with Legochem Biosciences Inc. to jointly develop new antibody-drug conjugates (ADCs) primarily for cancer. The partners will integrate antibodies from Antengene with Legochem’s ADC technology.
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Antibody-drug conjugate

Third ADC candidate with Synaffix’s tech enters clinic as Miracogen kicks off phase I

Oct. 12, 2021
By David Ho
It looks like Shanghai Miracogen Inc.’s antibody-drug conjugate (ADC) partnership with Synaffix BV is paying off as MRG-004A, an ADC designed to treat solid tumors, has entered a U.S. phase I/II trial to treat solid tumors.
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Third ADC candidate with Synaffix’s tech enters clinic as Miracogen kicks off phase I

Oct. 8, 2021
By David Ho
It looks like Shanghai Miracogen Inc.’s antibody-drug conjugate (ADC) partnership with Synaffix BV is paying off as MRG-004A, an ADC designed to treat solid tumors, has entered a U.S. phase I/II trial to treat solid tumors.
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