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BioWorld - Thursday, December 18, 2025
Home » Topics » Drugs » Antibody-drug conjugate

Antibody-drug conjugate
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Antibody-drug conjugate

Adcendo licenses Multitude’s phase I-ready ADC for $1B+

Aug. 27, 2024
By Tamra Sami
Adcendo ApS has inked a deal with Multitude Therapeutics Inc. and is licensing Multitude’s phase I-ready antibody-drug conjugate (ADC), ADCE-T02, which targets tissue factor. Under the deal, Copenhagen, Denmark-based Adcendo gains exclusive development and commercialization rights for the ADC globally, excluding greater China (mainland China, Hong Kong, Macao and Taiwan) where Multitude retains all rights.
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Antibody-drug conjugate

Adcendo licenses Multitude’s phase I-ready ADC for $1B+

Aug. 21, 2024
By Tamra Sami
Adcendo ApS has inked a deal with Multitude Therapeutics Inc. and is licensing Multitude’s phase I-ready antibody-drug conjugate (ADC), ADCE-T02, which targets tissue factor. Under the deal, Copenhagen, Denmark-based Adcendo gains exclusive development and commercialization rights for the ADC globally, excluding greater China (mainland China, Hong Kong, Macao and Taiwan) where Multitude retains all rights.
Read More
Immuno-oncology

Chengdu Duote Antibody Pharmaceutical discovers new antibody-drug conjugates

Aug. 20, 2024
Chengdu Duote Antibody Pharmaceutical Co. Ltd. has described antibody-drug conjugates comprising antibody or antigen-binding fragments covalently linked to eribulin derivatives through a linker reported to be useful for the treatment of cancer.
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Lab glassware and antibodies art concept
Immuno-oncology

Adcendo licenses rights to Multitude’s ADC targeting tissue factor

Aug. 20, 2024
Adcendo ApS and Multitude Therapeutics Inc. have signed a licensing agreement for the development of a highly differentiated antibody-drug conjugate (ADC) targeting tissue factor, designated ADCE-T02.
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Cancer

Yarrow Therapeutics synthesizes ecteinascidin derivative ADCs

Aug. 14, 2024
Yarrow Therapeutics Inc. has divulged antibody-drug conjugates comprising antibody or antigen binding fragments covalently linked to ecteinascidin derivatives through linkers reported to be useful for the treatment of cancer.
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Cancer

Otsuka Pharmaceutical patents new antibody-drug conjugates

Aug. 13, 2024
Otsuka Pharmaceutical Co. Ltd. has disclosed antibody-drug conjugates comprising humanized monoclonal antibody targeting syndecan-1 (SDC1; SYND1; CD138) covalently linked to anticancer and/or cytotoxic agents through linkers reported to be useful for the treatment of cancer.
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Ideaya nabs Biocytogen’s bispecific ADC program for $406M

Aug. 6, 2024
By Marian (YoonJee) Chu
Ideaya Biosciences Inc. bought global rights to Biocytogen Pharmaceuticals Co. Ltd.’s cancer-targeting bispecific antibody-drug conjugate (bsADC) program in a deal reaching up to $406.5 million.
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Phase I gastric data lower Elevation in crowdin’ Claudin space

Aug. 6, 2024
By Randy Osborne
Closely watched-for phase I data from Elevation Oncology Inc. in the Claudin 18.2 space sent shares of the Boston-based firm (NASDAQ:ELEV) down 63%, or $1.35, to close Aug. 6 at 78 cents. Elevation provided initial data from the dose-escalation portion of the ongoing experiment with antibody-drug conjugate (ADC) EO-3021 in patients with advanced, unresectable or metastatic solid tumors likely to express Claudin 18.2, including gastric, gastroesophageal junction (GEJ), pancreatic or esophageal cancers.
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Antibodies attacking cancer cell
Cancer

Salubris gets EMA clearance for basket trial

Aug. 5, 2024
Salubris Biotherapeutics Inc. has received clearance by the European Medicines Agency (EMA) to begin a first-in-human basket trial of JK-06.
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Ideaya nabs Biocytogen’s bispecific ADC program for $406M

Aug. 1, 2024
By Marian (YoonJee) Chu
Ideaya Biosciences Inc. bought global rights to Biocytogen Pharmaceuticals Co. Ltd.’s cancer-targeting bispecific antibody-drug conjugate (bsADC) program in a deal reaching up to $406.5 million. Announced July 31, San Francisco-based Ideaya agreed to license-in global rights to Biocytogen’s B7H3/PTK7 bispecific ADC program with topoisomerase-I (TOP1) payload to develop as either a monotherapy or combination therapy for solid tumors.
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