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BioWorld - Wednesday, December 31, 2025
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3D illustration of T cells fighting cancer
Immuno-oncology

Preclinical data on bispecific TCE support further development

Dec. 1, 2025
No Comments
HER2-targeted antibody-drug conjugates (ADCs) have significantly improved cancer therapy in recent decades. However, ADCs can cause toxicity and resistance, while T-cell engagers (TCEs) show promising antitumor activity in solid tumors but are limited by substantial adverse effects.
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Gene editing illustration
Immuno-oncology

CRAFT CAR T cells: Using CRISPR with reduced off-target risks

Dec. 1, 2025
No Comments
Allogeneic CAR T-cell therapy offers several advantages over an individualized autologous CAR T approach, thanks to the use of readily available, higher quality and quantity of starting donor T cells and the potential to generate multiple doses from a single manufacturing process.
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Concept art for targeting cancer
Cancer

Ideaya’s IDE-034 gains IND clearance for solid tumors

Dec. 1, 2025
No Comments
Ideaya Biosciences Inc. has received IND clearance from the FDA for the initiation of a phase I trial to evaluate IDE-034, a bispecific B7H3/PTK7 TOP1 antibody-drug conjugate.
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Immuno-oncology

STK-012 boosts T-cell activation while minimizing side effects

Dec. 1, 2025
No Comments
Researchers from Synthekine Inc. presented preclinical efficacy data on STK-012, a first-in-class IL-2 partial agonist engineered for preferential binding to the IL-2Rαβγ receptor.
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Handshake with DNA, molecules
Endocrine/metabolic

Regeneron and Tessera collaborate on TSRA-196

Dec. 1, 2025
No Comments
Regeneron Pharmaceuticals Inc. and Tessera Therapeutics Inc. have established a global collaboration to develop and commercialize TSRA-196, Tessera’s lead investigational in vivo gene editing program for the treatment of α-1 antitrypsin deficiency (AATD).
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Obesity, fat cell research concept image
Endocrine/metabolic

Ascletis selects ASC-37 as development candidate for obesity

Dec. 1, 2025
No Comments
Ascletis Pharma Inc. has selected ASC-37 oral tablets as a clinical development candidate for the treatment of obesity. The company expects to submit an IND application to the FDA in the second quarter of next year.
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Cancer

XRD-0394 exhibits efficacy against glioma in vitro

Dec. 1, 2025
No Comments
High-grade gliomas, including glioblastomas, are aggressive cancers of the brain that usually recur despite standard treatment, including radiation therapy. These mechanisms conferring persistence to tumor cells may be explained by DNA damage response pathways, especially those relying on ataxia-telangiectasia mutated (ATM) and DNA-dependent protein kinase (DNA-PK), which induce the repair of radiation-induced DNA damage. The effects of the ATM/DNA-PK inhibitor XRD-0394 were evaluated in in vitro models of glioma.
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Illustration of HIV/AIDS virus in the bloodstream
HIV/AIDS

HIV remission after heterozygous CCR5Δ32 stem cell transplant

Dec. 1, 2025
By Mar de Miguel
No Comments
2025 has been the most challenging year in the efforts to fight HIV since at least the advent of antiretroviral therapy. In a report on “Overcoming disruption, transforming the AIDS response,” released last week ahead of World AIDS Day on Dec. 1, the Joint United Nations Program on HIV/AIDS (UNAIDS) described “a global system in shock” by sharply reduced funding from the U.S. and other wealthy nations. Scientifically, for now, progress is ongoing. To mark World AIDS Day, Nature published three independent studies on HIV.
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Respiratory

Boehringer Ingelheim discovers new cGAS inhibitors

Nov. 28, 2025
Boehringer Ingelheim Pharma GmbH & Co. KG has described cyclic GMP-AMP synthase (MB21D1; cGAS) inhibitors reported to be useful for the treatment of autoinflammatory interferonopathy, idiopathic pulmonary fibrosis, cirrhosis, metabolic dysfunction-associated steatohepatitis (MASH), interstitial lung diseases, systemic scleroderma (systemic sclerosis) and systemic lupus erythematosus.
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Cancer

New EGFR inhibitors disclosed in Schrodinger patent

Nov. 28, 2025
Schrodinger Inc. has divulged EGFR (HER1; erbB1) mutant inhibitors reported to be useful for the treatment of cancer.
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