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BioWorld - Saturday, April 11, 2026
Home » Topics » Immuno-oncology, BioWorld Science

Immuno-oncology, BioWorld Science
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Lab glassware and antibodies art concept
Immuno-oncology

Crescent and Kelun announce IND approvals for CR-001, CR-003

Jan. 7, 2026
No Comments
Crescent Biopharma Inc. has announced regulatory clearances of IND applications for CR-001 (SKB-118), a PD-1 x VEGF bispecific antibody, and CR-003 (SKB-105), an integrin β-6 (ITGB6)-targeted antibody drug-conjugate (ADC), both being developed for the treatment of advanced solid tumors.
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Immuno-oncology

Ernexa completes pre-IND meeting toward ovarian cancer trial

Jan. 7, 2026
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Ernexa Therapeutics Inc. has successfully completed a pre-IND meeting with the FDA, setting a pathway toward submitting an IND and initiating a first-in-human trial for the treatment of ovarian cancer, expected in the second half of this year.
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Immuno-oncology

Innolake Biopharm patents new antibody-drug conjugates

Jan. 5, 2026
Innolake Biopharm (Hangzhou) Co. Ltd. has disclosed antibody-drug conjugates comprising bispecific antibodies covalently bound to exatecan through a linker reported to be useful for the treatment of cancer.
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Immuno-oncology

Hainan Simcere Pharmaceutical divulges new antibody-drug conjugates

Dec. 31, 2025
Hainan Simcere Pharmaceutical Co. Ltd. has disclosed antibody-drug conjugates comprising a glycoengineered antibody covalently linked to a cytotoxic drug through a linker reported to be useful for the treatment of cancer.
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Breast cancer illustration
Immuno-oncology

Anti-ROR1 scFv shows preclinical activity in triple-negative breast cancer

Dec. 31, 2025
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The receptor tyrosine kinase-like orphan 1 (ROR1) is a transmembrane protein expressed during embryonic development. Moreover, it is highly expressed on the surface of several cancer cell types, including B-cell malignancies and solid tumors such as triple-negative breast cancer (TNBC). Researchers from The University of Queensland and collaborating institutions recently reported the development of a single-chain fragment variable (scFvs) specifically targeting the membrane proximal region of ROR1 rather than the Ig-like domain, aiming to reduce cross-reactivity with other surface proteins expressed in normal tissues.
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Illustration of cancer cell in crosshairs being destroyed
Immuno-oncology

Three Helius solid tumor candidates gain clinical trial clearance

Dec. 31, 2025
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Shanghai Henlius Biotech Inc. has announced acceptance of IND applications by China’s National Medical Products Administration (NMPA) for three differentiated candidates for the treatment of solid tumors.
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3D rendering of antibody drug conjugated with cytotoxic payload
The year in review

ADCs’ breakout 2025 and their still-unfinished potential

Dec. 30, 2025
By Coia Dulsat
No Comments
Over the course of the year, and continuing into the latest scientific meetings, an extraordinary breadth of new antibody-drug conjugate (ADC) designs was reported, with innovations spanning targets, linkers, payloads, conjugation chemistries and overall architectures. Once defined by a simple “one target, one payload” model, the field is lately expanding into a more versatile and diverse therapeutic space.
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Immuno-oncology

Hanx Biopharmaceuticals describes new TRBV12-targeting ADCs

Dec. 29, 2025
Hanx Biopharmaceuticals Inc. has identified antibody-drug conjugates (ADCs) consisting of an antibody targeting TRBV12 covalently linked to cytotoxic drugs through linkers reported to be useful for the treatment of T-cell leukemia and T-cell lymphoma.
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CAR T cell attacking cancer cells
Immuno-oncology

Development and characterization of anti-CD19 in vivo CAR T therapy

Dec. 29, 2025
No Comments
Shenzhen Grit Biotechnology Co. Ltd. and Shanghai Vitalgen Biopharma Co. Ltd. recently presented their work to develop and evaluate a novel anti-CD19 in vivo CAR T candidate, named GT-801.
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Immuno-oncology

Jiangsu Simcere Biologics patents new antibody-drug conjugates

Dec. 24, 2025
Jiangsu Simcere Biologics Co. Ltd. has disclosed antibody-drug conjugates (ADC) comprising an antibody huAb-H3aL3-IgG1 targeting cadherin-17 (CDH17) covalently linked to a camptothecin derivative through a linker reported to be useful for the treatment of cancer.
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