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BioWorld - Saturday, July 4, 2026
Home » Topics » Antibody-drug conjugate, BioWorld Science

Antibody-drug conjugate, BioWorld Science
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3D illustration demonstrating antibody-drug conjugate.
Cancer

TROP-2-targeting ADCs show antiproliferative effects in models of penile squamous cell carcinoma

June 4, 2024
Researchers from Sun Yat-sen University Cancer Center (SYSUCC) presented data from a study that aimed to assess the role of trophoblast cell-surface antigen-2 (TROP-2) in penile squamous cell carcinoma (PSCC).
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3D rendering of drug linked to antibody
Immuno-oncology

Merck KGaA advances anti-GD2 ADC toward clinic for solid tumors

June 4, 2024
Merck KGaA has announced it is advancing M-3554, a potential first-in-class anti-GD2 antibody-drug conjugate (ADC), toward the clinic. M-3554 links an exatecan payload with an anti-GD2 antibody.
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Lung cancer illustration
Immuno-oncology

Almac Discovery nominates bispecific ADC for refractory lung cancer

May 31, 2024
Almac Discovery Ltd. has nominated a new preclinical candidate molecule, ALM-401, a first-in-class bispecific antibody-drug conjugate (ADC) targeting EGFR/ROR1. It is being developed for the treatment of refractory lung cancer characterized by dual expression of ROR1 and EGFR.
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Blood cells and destruction of cancer cell
Cancer

A pan-approach against blood cancer preserving hematopoiesis

May 29, 2024
By Mar de Miguel
A group of scientists from Basel University Hospital have designed an antibody-drug conjugate (ADC) that eliminated blood cancer cells without attacking healthy hematopoietic stem cells (HSCs), which they modified by base editing and transplanted to renew an altered blood system. They achieved this by focusing on the panhematopoietic marker CD45.
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Antibody-drug conjugate illustration
Immuno-oncology

Pheon Therapeutics raises series B financing to advance ADCs for cancer

May 21, 2024
Pheon Therapeutics Ltd. has completed a $120 million series B financing to fund the development of its pipeline of differentiated antibody-drug conjugates (ADCs) for cancer through clinical proof of concept.
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HER3 protein
Immuno-oncology

HER3-targeting ADC, DB-1310, has efficacy and bystander antitumor effect in preclinical models

May 17, 2024
Even though HER3 is validated as a promising therapeutic target for cancer therapy, no HER3-targeting antibodies or antibody-drug conjugates (ADCs) have been approved for clinical use. Investigators at Duality Biologics (Suzhou) Co. Ltd. have developed DB-1310, a new HER3-targeting ADC being studied for the treatment of solid tumors, and published findings from preclinical characterization.
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Antibody-drug conjugate
Cancer

BL-M11D1 shows antitumor activity in AML xenograft models

May 9, 2024
Researchers from Sichuan Baili Pharmaceutical Co. Ltd. and Systimmune Inc. presented preclinical data for the novel CD33-targeting antibody-drug conjugate (ADC) being evaluated for the treatment of hematologic malignancies.
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AI-generated image for cancer cells observed under a microscope
Immuno-oncology

Bioatla’s anti-Nectin-4 ADC gains IND clearance

May 7, 2024
Bioatla Inc. has received FDA clearance of its IND application for BA-3361, a conditionally active biologic (CAB)-Nectin-4 antibody-drug conjugate (ADC) for the treatment of multiple tumor types.
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3D illustration demonstrating antibody-drug conjugate.
Immuno-oncology

GB01-VA-PL2202, a Claudin-6-targeting ADC with potent antitumor efficacy and bystander killing activity

May 7, 2024
Researchers from ADC Therapeutics SA presented the discovery and preclinical evaluation of a novel camptothecin-based Claudin-6-specific antibody-drug conjugate (ADC), GB01-VA-PL2202.
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Hand holding dollar sign
Cancer

Covalent proteins? Enlaza views opportunity with $100M series A

May 6, 2024
By Jennifer Boggs
“A white space opportunity.” That’s how Enlaza Therapeutics Inc. co-founder and CEO Sergio Duron described to BioWorld the company’s efforts to develop the first covalent biologics, an endeavor that has gained the backing of an impressive group of investors in a recently closed $100 million series A round.
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