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BioWorld - Saturday, June 20, 2026
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Cancer

Chia Tai Tianqing Pharmaceutical divulges new GSPT1 degradation inducers

Aug. 27, 2025
Chia Tai Tianqing Pharmaceutical Group Co. Ltd. has synthesized proteolysis targeting chimera (PROTAC) compounds comprising an E3 ubiquitin ligase binding moiety covalently linked to a eukaryotic peptide chain release factor GTP-binding subunit ERF3A (GSPT1) targeting moiety via a linker reported to be useful for the treatment of cancer.
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Cancer

Ensem Therapeutics patents new PI3Kα inhibitors

Aug. 27, 2025
Ensem Therapeutics Inc. has disclosed phosphatidylinositol 3-kinase α (PI3Kα) inhibitors, particularly PI3Kα mutant inhibitors, reported to be useful for the treatment of cancer.
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Illustration of lungs with cancer inset
Cancer

USP3-MIC19 axis is an approach for treating NSCLC

Aug. 27, 2025
No Comments
Hypoxia is a common event in the microenvironment of solid tumors, triggering some changes in gene expression profiles to adapt to low-oxygen levels. Increasing evidence exists regarding hypoxia and mitochondrial dysfunction to play a role in the progression of non-small-cell lung cancer (NSCLC).
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Illustration of brain degeneration
Aging

MED15 T603 phosphorylation controls SASP production in aging

Aug. 27, 2025
No Comments
Aging is marked by a gradual decline in body function, partly driven by the buildup of senescent cells. These cells stop dividing but release a mix of inflammatory and tissue-remodeling factors, known as the senescence-associated secretory phenotype (SASP).
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Illustration demonstrating parts of the ear
Ear, nose & throat

Lineage enters collaboration for ANP-1 for hearing loss

Aug. 27, 2025
No Comments
Lineage Cell Therapeutics Inc. has entered into a research collaboration with William Demant Invest A/S to develop Lineage’s auditory neuronal cell transplant Resonance (ANP-1) for hearing loss.
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3D illustration of human digestive system
Gastrointestinal

Preclinical profile of colon-targeted, pan-SIK inhibitor for IBD

Aug. 27, 2025
No Comments
Pfizer Inc. provided details on the discovery and in vitro/in vivo characteristics of SIK inhibitor PF-07899895 for the treatment of inflammatory bowel disease (IBD). Pfizer’s program focused on pan-SIK inhibition to regulate cytokine production in immune cells based on the hypothesis that this approach could suppress pro-inflammatory cytokines/chemokines and promote an anti-inflammatory phenotype.
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Scientist, microscope and dropper
Drug design, drug delivery & technologies

New biological target and indication identified for AZD-1656

Aug. 27, 2025
No Comments
CDT Equity Inc. has deployed an AI-led drug repurposing strategy for its portfolio and identified a new biological target and novel therapeutic indication for its lead program, AZD-1656 (and its derivatives).
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Blood cells and bacteria
Infection

Grant supports Phiogen’s phage therapy for E. coli infections

Aug. 27, 2025
No Comments
Combating Antibiotic-Resistant Bacteria Biopharmaceutical Accelerator (CARB-X) has awarded $1.1 million to Phiogen Inc. to evaluate PHI-BI-01, the company’s dual-action therapeutic designed to treat and prevent extraintestinal pathogenic Escherichia coli (ExPEC) bloodstream infections.
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Cancer

LRK-4189 shows promise for microsatellite stable CRC

Aug. 27, 2025
No Comments
It is known that phosphatidylinositol 5-phosphate 4-kinase, type II, γ (PIP4K2C) is a lipid kinase tied to poor outcomes in a variety of cancers, such as colorectal (CRC) and breast cancers. In the search for PIP4K2C degraders, researchers from Larkspur Biosciences Inc. discovered LRK-4189, a cereblon-mediated PIP4K2C degrader.
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Stem cells
Aging

ARDD 2025: Hitting rewind, not reset, for in vivo rejuvenation

Aug. 27, 2025
By Anette Breindl
No Comments
At the 12th Aging Research & Drug Discovery (ARDD) Meeting, which is being held this week in Copenhagen, Life Biosciences Inc. announced that it is developing its partial epigenetic reprogramming technology for liver disease as well as optic neuropathies. The company’s chief scientific officer Sharon Rosenzweig-Lipson estimated that its ER-100 would enter clinical trials in early 2026, putting it on track to be the first application of partial epigenetic reprogramming to enter the clinic.
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