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BioWorld - Thursday, April 30, 2026
Home » Topics » Immuno-oncology, BioWorld Science

Immuno-oncology, BioWorld Science
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Art concept for tumor
Immuno-oncology

Neok Bio’s bispecific ADC NEOK-001 gains IND clearance

Jan. 22, 2026
No Comments
Neok Bio Inc. has obtained IND clearance from the FDA for NEOK-001, enabling initiation of a phase I trial for solid tumors. Dosing is expected to begin in the coming months, and initial clinical data are anticipated next year.
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Red and blue bispecific antibodies
Immuno-oncology

First-in-class ADC targeting DEM-TXX shows high preclinical efficacy

Jan. 21, 2026
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Researchers at DEM Biopharma Inc. reported preclinical findings demonstrating the efficacy of DEM-301, a bifunctional antibody-drug conjugate (ADC) engineered to selectively recognize and eliminate tumor cells that express DEM-TXX.
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Blue gloved hand holding a syringe
Immuno-oncology

FDA clears IND for Immunomic’s ITI-5000

Jan. 21, 2026
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Immunomic Therapeutics Inc. has received FDA clearance of its IND application for ITI-5000, enabling initiation of a first-in-human study.
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Immuno-oncology

University of Washington discovers HER2-targeting ADCs for cancer

Jan. 20, 2026
The University of Washington has divulged antibody-drug conjugates (ADCs) comprising an antibody targeting HER2 (erbB2) linked to monomethyl auristatin E (MMAE) through a linker. They are described as useful for the treatment of cancer.
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Immuno-oncology

Sanofi’s TPP-45142 shows efficacy for HER2-low tumors

Jan. 20, 2026
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Unlike patients with HER2+ tumors, there is an unmet clinical need for patients with HER2-low expression cancers, which are refractory to trastuzumab. Sanofi SA has developed TPP-45142, a T-cell engager consisting of two nanobody domains targeting HER2 and T-cell receptor (TCR) fused to an Fc region harboring the F234A and L235A mutations to inhibit effector function.
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Immuno-oncology

GT Biopharma files IND for GTB-5550 TriKE

Jan. 16, 2026
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GT Biopharma Inc. has filed an IND application with the FDA for GTB-5550 TriKE, a B7-H3-targeted natural killer (NK) cell engager for the treatment of B7-H3-expressing solid tumor cancers. Pending approval, the planned phase I basket trial will evaluate GTB-5550 administered subcutaneously in solid tumors.
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Test tubes, dropper
Immuno-oncology

Medicenna advances MDNA-113 toward IND filing

Jan. 16, 2026
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Medicenna Therapeutics Corp. is advancing MDNA-113, a first-in-class, IL-13-directed and conditionally activated PD-1 x IL-2 bifunctional superkine, through preclinical development toward a planned IND filing in the second half of this year.
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3D illustration of tumor
Immuno-oncology

TCR-NK cells targeting MAGE-A4 to combat solid tumors

Jan. 15, 2026
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CAR T cells have made headlines for their ability to fight hematological cancers, but they have proven largely ineffective against solid tumors. To fight such tumors, many groups have engineered T cells to carry T-cell receptors (TCRs) that target cancer antigens, but this approach requires using T cells taken from the patient and it is ineffective against parts of the tumor that have lost expression of the target antigen. As an alternative strategy, researchers at Zelluna ASA in Norway have engineered natural killer (NK) cells to express TCRs against solid tumor antigens.
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Liver tumor treatment conceptual illustration
Immuno-oncology

Chi-NPB40 exerts antitumoral activity in HCC

Jan. 14, 2026
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CD276, also known as B7-H3, is an antigen highly expressed in several cancer types, including hepatocellular carcinoma (HCC, 79%-94% expression) and closely tied to aggressiveness and poor survival, but shows very low expression in normal tissues. Increasing evidence exists indicating B7-H3 has immune inhibitory functions, thus reducing interferon levels released by T cells and suppressing cytotoxic activity of natural killer cells, thereby aiding in tumor immune evasion.
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T cells attacking cancer
Immuno-oncology

First T-cell engager expressed locally from nanoparticle-delivered mRNA against HCC

Jan. 14, 2026
No Comments
Bispecific T-cell engagers (TCEs) aim to combat cancer by simultaneously binding T cells and tumor cells in order to induce the first to kill the second. This approach has failed to work effectively against many solid tumors because the exogenous engager proteins do not penetrate into tumors at sufficiently high concentrations.
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