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BioWorld - Saturday, December 6, 2025
Home » Newsletters » BioWorld Science

BioWorld Science

Nov. 19, 2024

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Chinese flag and microscopes

‘A decade of innovation, a decade to come’ for China pharma

As China rises to second place, next only to the U.S., for innovative new drugs, a new report by Clarivate – A Decade of Innovation, A Decade to Come – outlines key policy reforms and regulatory, R&D and investment trends driving past and future growth of Chinese biopharmaceuticals. Read More

Novel Pin1 degraders act as ‘molecular crowbars’

Targeted protein degradation has gained attention in recent years due to its potential to hit proteins that are difficult to engage with conventional small molecules. Pin1 is an enzyme associated with tumor formation overexpressed in pancreatic cancer cells or cancer-associated fibroblasts in particular. Read More
Hands illustrating pain and inflammation

Deepcure’s DC-9476 ameliorates rheumatoid arthritis scores

The bromodomain and extra terminal domain (BET) family of proteins, including BRD4, regulates the transcription of multiple proinflammatory and immunoregulatory genes. BRD4 is involved in immune-related disorders such as rheumatoid arthritis (RA). Read More
Pipet, test tubes, chemical structures

Siren Biotechnology names SRN-101 as lead asset for high-grade gliomas

Siren Biotechnology Inc. has unveiled its lead asset, SRN-101, for the treatment of high-grade gliomas. The FDA has granted orphan drug and rare pediatric disease designations to SRN-101 for high-grade gliomas and pediatric-type diffuse high-grade gliomas, respectively. Read More

Telix signs purchase, license agreements for FAP-targeting compounds

Telix Pharmaceuticals Ltd. is expanding its theranostic pipeline with new assets targeting fibroblast activation protein (FAP). The company has entered into asset purchase and exclusive worldwide in-license agreements for a suite of clinically validated FAP-targeting therapeutic and precision medicine (diagnostic) radiopharmaceutical candidates developed at Johannes Gutenberg-Universität Mainz. Read More
Illustration of retinal detachment

VSX2 variant linked to retinal detachment risk

Researchers from the U.K. have analyzed whole-genome sequencing data from 7,276 cases and 236,741 controls in the UK Biobank to perform gene-level and a variant-level exome-wide association study analysis to identify variants related to retinal detachment. Read More

Verge Analytics patents new PIKfyve inhibitors

Verge Analytics Inc. (dba Verge Genomics) has prepared and tested new hydrazone and pyrazole 3H-imidazo(4,5-b)pyridine compounds acting as 1-phosphatidylinositol 3-phosphate 5-kinase (PIKfyve) inhibitors. Read More

Novel KDM3B variant found in atypical Diets-Jongmans case

The KDM3B gene encodes the histone lysine demethylase lysine-specific demethylase 3B, which is involved in the regulation of transcription. Read More

NY-303 is first-in-class NK cell engager

Researchers from Naya Biosciences Inc. and collaborators presented preclinical data on NY-303, a natural killer (NK) cell engager bispecific antibody targeting both GPC3 and NKp46. NKp46 is a cell surface receptor involved in NK cell activation and the elimination of target cancer cells. Read More
Lab glassware and antibodies art concept

BB-201, a potent first-in-class anti-Her2/anti-Trop2 bispecific ADC candidate

Researchers from Bright Biologics LLC presented the discovery and preclinical characterization of a novel bispecific anti-Her2/anti-Trop2 antibody-drug conjugate (ADC), BB-201. Read More

Imhotex identifies new NOD2 activators for treatment of Crohn’s disease

Several recent Imhotex Ltd. patents describe novel analogues of muramyl dipeptide (MDP), desmuramylpeptides (DMPs), acting as nucleotide-binding oligomerization domain-containing protein 2 (NOD2) activators potentially useful for the treatment of Crohn’s disease. Read More

Arkuda Therapeutics reports new mucolipin-1 blockers

Arkuda Therapeutics Inc. has patented new fused tricyclic mucolipin-1 (MCOLN1; TRPML1) blockers reported to be useful for the treatment of cancer, liver diseases, amyotrophic lateral sclerosis, cardiovascular disorders, frontotemporal dementia, Alzheimer’s, Huntington’s and Parkinson’s disease. Read More
Photomicrograph of hepatocellular carcinoma

MT-303 exerts antitumoral activity in liver cancer

Hepatocellular carcinoma (HCC) is the most common type of liver cancer, with a 5-year survival rate of 18%. Glypican-3 (GPC3) is a protein with high expression in HCC but not in healthy tissue, making it an interesting target for therapy. Read More

XPR1 unveiled as therapeutic target in lung cancer

Tumor cell survival is dependent on phosphate homeostasis, which requires high amounts of energy. Researchers have demonstrated that the silencing of xenotropic and polytropic retrovirus receptor 1 (XPR1) led to reduced tumor growth in an ovarian cancer cell line xenograft, and similar vulnerability was found in lung cancer. Read More

Gilead discloses GS-441524 prodrugs for treatment of viral infections

Gilead Sciences Inc. has synthesized 4-aminopyrrolo[2,1-F][1,2,4]triazine C-nucleoside analogues acting as prodrugs of GS-441524 and reported to be useful for the treatment of viral infections. Read More
Chemical structure research concept image

Synrx Therapeutics reports new PARG inhibitor

Hangzhou Synrx Therapeutics Biomedical Technology Co. Ltd. recently presented the development and characterization of a novel PARG inhibitor, SYN-608, for the potential treatment of tumors with/without homologous recombination deficiency (HRD). Read More

GSPT1 degradation inducers described in Beijing Innovare patent

Beijing Innovare Pharma Tech Co. Ltd. has reported heterocyclic molecular glue degrader compounds acting as eukaryotic peptide chain release factor GTP-binding subunit ERF3A (GSPT1) degradation inducers. Read More

Other news to note for Nov. 19, 2024

Additional early-stage research and drug discovery news in brief, from: Abelzeta Pharma, Carisma Therapeutics, Innate Pharma, Neurizon Therapeutics, Precision Biosciences, Silo Pharma, Ziccum. Read More

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