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BioWorld - Tuesday, July 21, 2026
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Liver disease
Gastrointestinal

DGAT2 blockade ameliorates hepatic steatosis by rebalancing phosphatidylethanolamine

Feb. 12, 2024
Metabolic dysfunction-associated steatotic liver disease (MASLD), formerly known as nonalcoholic fatty liver disease (NAFLD), is characterized by accumulation of triglycerides (TGs) in liver hepatocytes, and which can progress into chronic liver disease or even hepatocellular carcinoma.
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CAR T cells attacking cancer cell
Immuno-oncology

Elicera’s CAR T-cell therapy ELC-301 cleared to enter clinic in Sweden for B-cell lymphoma

Feb. 12, 2024
Elicera Therapeutics AB has received approval from the Swedish Medical Products Agency to start a phase I/II study of chimeric antibody receptor (CAR) T-cell therapy ELC-301 in patients with refractory or relapsed B-cell lymphoma.
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Cancer

Targeting ANKRD1 reverts activation of cancer-associated fibroblasts

Feb. 12, 2024
Early steps in cancer development are closely linked to fibroblast senescence and their transformation into tumor-promoting cancer-associated fibroblasts (CAFs).
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3D illustration of the cross-section of skin layers with atopic dermatitis
Dermatologic

Alys Pharmaceuticals launches with focus on immuno-dermatology pipeline

Feb. 12, 2024
Alys Pharmaceuticals Inc. has launched with a focus in the field of immuno-dermatology. Supported by $100 million in financing from Medicxi, Alys was formed through the aggregation of six asset-centric Medicxi companies: Aldena Therapeutics Inc., Graegis Pharmaceuticals Ltd., Granular Therapeutics Ltd., Klirna Biotech Sàrl, Nira Biosciences Inc. and Vimela Therapeutics Inc.
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Brain and blood cells
Neurology/Psychiatric

JR-14a attenuates neuroinflammation and reduces brain infarction following stroke

Feb. 12, 2024
Researchers from the University of Queensland and affiliated organizations recently presented preclinical data for the novel C3a receptor (C3aR) antagonist JR-14a, being developed as a neuroprotective agent for the treatment of post-stroke neuroinflammation.
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Biomarkers

Novel heterozygous missense mutation in the FGG gene linked to hypodysfibrinogenemia

Feb. 12, 2024
The rare hereditary fibrinogen disorder hypodysfibrinogenemia is characterized by fibrinogen defects, which can cause thrombotic and hemorrhagic phenotypes that are not always predicted by routine coagulation tests. Researchers from Academic Hospital Maastricht aimed to characterize the genetic profile of a family with hypodysfibrinogenemia and predict bleeding and/or thrombotic phenotypes in asymptomatic family members using innovative testing.
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Immunofluorescence image shows small-cell lung cancer spreading throughout the bronchioles of a mouse lung.
Cancer

Study disentangles how cancers can metamorphosize

Feb. 12, 2024
By Coia Dulsat
Biopsies from up to 14% of patients with non-small-cell lung cancer (NSCLC) showing resistance to epidermal growth factor receptor (EGFR) tyrosine kinase therapy ascertain histologic transformation (HT) to SCLC, which is estimated to kill around 250,000 patients globally, every year. In a study published in Science on Feb. 9, 2024, researchers from Weill Cornell Medicine have dissected that complex process using a genetically engineered mouse model of pulmonary HT.
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Cancer

Roche identifies new TLR7 agonists

Feb. 9, 2024
F. Hoffmann-La Roche Ltd. and Hoffmann-La Roche Inc. have patented phosphorylpurinone compounds acting as Toll-like receptor 7 (TLR7) agonists reported to be useful for the treatment of cancer.
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Cancer

Incyte describes new GTPase KRAS mutant inhibitors

Feb. 9, 2024
Incyte Corp. has developed fused tricyclic compounds acting as GTPase KRAS (mutant) inhibitors. As such, they are reported to be useful for the treatment of cancer, inflammation and immunological disorders.
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Endocrine/Metabolic

SLC6A19 inhibitors disclosed in Jnana Therapeutics patent

Feb. 9, 2024
Work at Jnana Therapeutics Inc. has led to the identification of sodium-dependent neutral amino acid transporter B(0)AT1 (SLC6A19) inhibitors reported to be useful for the treatment of diabetes, chronic kidney disease, metabolic dysfunction-associated steatohepatitis (MASH), phenylketonuria, metabolic syndrome, obesity, neurodevelopmental and autism spectrum disorders, among others.
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