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BioWorld - Sunday, December 28, 2025
Home » Newsletters » BioWorld Science

BioWorld Science

Oct. 10, 2024

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Clostridium difficile bacteria

A novel mRNA-LNP vaccine facilitates Clostridioides difficile control

Clostridioides difficile has been traditionally isolated from healthcare facilities' inpatients, but it is increasingly being identified in people who have not recently been hospitalized and is more and more found in community settings. Investigators from Perelman School of Medicine at University of Pennsylvania have developed an mRNA-LNP vaccine with promising results in preventing and controlling C. difficile infection. Read More
Illustration of kidney with DNA structures

Advancing gene therapy for kidney disease, Purespring adds £80M

Purespring Therapeutics Ltd. has raised £80 million (US$104.6 million) in a series B, putting it on course to be the first to take a gene therapy for a kidney disease into the clinic. The money enables the company to move the lead program, PS-002, for the treatment of IgA nephropathy to clinical proof of concept and advance programs in other complement-mediated kidney diseases, and in an undisclosed glomerular kidney disease. Read More
Illustration of motor neuron connecting to muscle fiber

ENTR-601-45 restores dystrophin in Duchenne muscular dystrophy models

Duchenne muscular dystrophy is a severe and progressive disorder caused by mutations in the dystrophin (DMD) gene that lead to malfunction or absence of dystrophin. This protein stabilizes the sarcolemma and protects muscle cells during contraction. Read More
Illustration of male vs. female bodies showing organs

Sex-specific model of lupus-like cardiovascular disease

Clinical research has shown that patients with systemic lupus erythematosus (SLE) are more likely to develop cardiovascular disease (CVD), including cardiac and vascular dysfunction. In the current study, researchers from Medical University of South Carolina developed and characterized a novel preclinical model of SLE-like CVD. Read More

Kymera’s oral STAT degrader KT-621 gains IND clearance from FDA

Kymera Therapeutics Inc. has received IND clearance from the FDA for KT-621, an investigational first-in-class, once-daily, oral STAT6 degrader. Read More
Concept art for targeting cancer

Ono and Ligachem sign licensing agreement for ADC LCB-97 for solid tumors

Ono Pharmaceutical Co. Ltd. has entered into a license agreement with Ligachem Biosciences Inc. for LCB-97, a preclinical stage antibody-drug conjugate (ADC) for solid tumors. Read More

Chengdu Zeling Biomedical Technology patents NLRP3 inflammasome inhibitors

Chengdu Zeling Biomedical Technology Co. Ltd. has identified triazine compounds acting as NLRP3 inflammasome inhibitors. Read More

SYT4 expression is needed for axonal regeneration after spinal cord injury

Axonal regrowth is a crucial process for forming a compensatory neuronal network after spinal cord injury (SCI), but this is very limited in the adult mammalian central nervous system. Read More

New murine chronic skin fibrosis model developed by Rubedo

Many cancer patients receive radiation therapy or DNA-damaging agents that induce skin damage, and more rarely, chronic skin fibrosis. Read More
Cancer cells under magnifying glass

MMV-1645152 blocks the KSHV lytic lifecycle

Researchers from Rhodes University and collaborators identified MMV-1645152 after screening the Medicines for Malaria Venture (MMV) pandemic response box for non-cytotoxic inhibitors of Kaposi's sarcoma-associated herpesvirus (KSHV) replication. Read More

D3 Bio discloses GTPase KRAS (G12D mutant) inhibitors

A D3 Bio (Wuxi) Co. Ltd. patent describes heterocyclic-substituted pyrimidopyran compounds acting as GTPase KRAS (G12D mutant) inhibitors reported to be useful for the treatment of cancer. Read More

PI3Kα (H1047R mutant) inhibitors reported in Reactive Biosciences patent

Work at Reactive Biosciences Inc. has led to the discovery of new phosphatidylinositol 3-kinase α (PI3Kα) (H1047R mutant) inhibitors reported to be useful for the treatment of cancer. Read More
fatty-liver-disease.png

SPTBN1 is therapeutic target in MASH, other metabolic disorders

The identification of non-toxic targets for the treatment of metabolic disorders would allow the development of therapies for the harmful effects of impaired metabolism of reactive aldehydes, among others, which is challenging for drug development due to short half-life and lack of tissue specificity. Read More

Insitro and Lilly take aim at metabolic diseases through new agreements

Insitro Inc. has signed three strategic agreements with Eli Lilly & Co. focused on advancing potential new medicines for metabolic diseases, including metabolic dysfunction-associated steatotic liver disease (MASLD), based on targets identified by Insitro using its artificial intelligence/machine learning-based platform. Read More

Ono Pharmaceutical identifies new EP3 receptor agonists

Ono Pharmaceutical Co. Ltd. has patented tricyclic prostaglandin E2 receptor EP3 subtype (PTGER3; EP3) agonists potentially useful for the treatment of renal diseases. Read More
Multiple myeloma cells in the bone marrow.

Mcl-1 inhibitor KS-18 fights resistance in multiple myeloma models

Researchers from Rowan University, Pennsylvania State University, and affiliated organizations presented preclinical data for the selective Mcl-1 inhibitor, KS-18, in models of multiple myeloma (MM). Read More

Haisco Pharmaceutical patent describes Nav1.8 channel blockers for pain

Haisco Pharmaceutical Group Co. Ltd. has disclosed new tetrahydrofuran derivatives acting as sodium channel protein type 10 subunit alpha (SCN10A; Nav1.8) blockers reported to be useful for the treatment of pain. Read More

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