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BioWorld - Tuesday, February 24, 2026
Home » Newsletters » BioWorld Science

BioWorld Science

Feb. 6, 2026

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Illustration of SCAN in Parkinson’s vs healthy subcortex

SCAN is core circuit affected in Parkinson’s disease

Parkinson’s disease (PD) is a neurodegenerative disorder that affects movement, and tremor is one of its signatures. But it is a much more wide-ranging disorder, and patients experience problems with cognitive and emotional processes as well. SCAN, the somato-cognitive action network identified in 2023, could reshape the definition of PD. Treating this circuit can improve outcomes. Read More
Chromosome with shortened telomeres

ALTx formed to drug pathway by which cancer cells become immortal

Newco ALTx Therapeutics Ltd. has launched with a £12.55 million (US$17.1 million) seed round to develop inhibitors of the alternative lengthening of telomeres (ALT) pathway, by which 10% to 15% of cancers become immortal. Read More
NLRP3 inflammasome

Insilico Medicine selects NLRP3 inhibitor preclinical candidate

Insilico Medicine Cayman Topco has nominated ISM-5059, a peripherally restricted small-molecule NLRP3 inhibitor, as a preclinical candidate. Read More
Woman and 3D brain

Astellas’ ASP-2246 shows promise in stroke management

Astellas Pharma Inc. recently presented data regarding ASP-2246, a drug candidate comprised of an mRNA encoding the transcription factor NeuroD1 encapsulated in lipid nanoparticles. Read More

Nb20 nanobody reverses depressive-like behavior in mice

Researchers from the University of Miami Miller School of Medicine and collaborators described the preclinical efficacy of Nb20. Read More
3D illustration of platelets in the boodstream

Tangram’s TGM-148 demonstrates pan-bleeding disorder therapeutic potential

Researchers at Tangram Therapeutics Inc. have presented preclinical safety and efficacy data for TGM-148 in a model of von Willebrand disease. Read More

Jeil Pharmaceutical patents PDE4 inhibitors

Jeil Pharmaceutical Co. Ltd. has disclosed dihydrothiopyranopyrimidine compounds acting as phosphodiesterase PDE4 inhibitors reported to be useful for the treatment of inflammatory joint disease, neurological disorders and more. Read More
3D illustration showing DNA inside adenovirus

Dual AAV gene therapy improves LAMA2 muscular dystrophy in mice

Laminins are extracellular matrix (ECM) glycoproteins that preserve the structural and functional integrity of tissues. These heterotrimeric proteins, composed of one α, β and γ chain encoded by different genes, provide mechanical support, facilitate cell adhesion and maintain tissue organization and stability. Read More

French team discloses furin inhibitors

Researchers from the Institut National De La Sante Et De La Recherche Medicale, Universite de Bordeaux and Universite de Paris Cite have reported indane 1,3-dione derivatives acting as furin (PACE; PCSK3) inhibitors potentially useful for the treatment of cancer. Read More

O-GlcNAcase inhibitors reported in Tyk Medicines patent

Tyk Medicines Inc. has identified N-acetyl-β-D-glucosaminidase (O-GlcNAcase; OGA) inhibitors described as potentially useful for the treatment of cancer, metabolic diseases, Alzheimer’s disease and progressive supranuclear palsy. Read More
Hidradenitis suppurativa abscesses in the armpit

First evidence of GJB3 as a target in hidradenitis suppurativa

Hidradenitis suppurativa (HS) is a chronic autoinflammatory condition affecting the skin, the genetic mechanisms of which are not well understood. A group of researchers set out to explore the genetic background of familial HS by performing whole-exome sequencing on genomic DNA from patients. Read More

Abbisko Therapeutics identifies GTPase KRAS mutant inhibitors

Abbisko Therapeutics Co. Ltd. has synthesized new GTPase KRAS G12V and G12D mutant inhibitors designed for use in the treatment of cancer. Read More

Shenzhen Salubris Pharmaceuticals synthesizes dual PCSK9/HMG-CoA reductase inhibitors

Shenzhen Salubris Pharmaceuticals Co. Ltd. has discovered new proprotein convertase subtilisin/kexin-type 9 (PCSK9) and 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) reductase dual inhibitors. They are described as potentially useful for the treatment of hypercholesterolemia. Read More
Art concept for drug research

Gedeon Richter details discovery, preclinical characterization of RGH-706

The melanin-concentrating hormone (MCH) is one of the most potent central stimulators of feeding and regulates energy balance. Therefore, agonists of the melanin-concentrating hormone MCH1 receptor could offer potential for weight management. Moreover, the role of MCH1 receptor in syndromic obesity has recently been uncovered. Read More

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