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BioWorld - Wednesday, January 28, 2026
Home » Newsletters » BioWorld Science

BioWorld Science

Jan. 4, 2023

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Human T cell under attack by HIV.

Latently HIV-infected T cells sleep with one eye open

A multiomic analysis of the HIV reservoir has characterized the phenotypic and epigenetic heterogenicity of the virus-infected memory CD4+ T-cell population in people living with HIV taking antiretroviral therapy (ART-PLWH). This is the step towards an ex vivo single-cell atlas for these cells, which could help to design new strategies to eliminate the reservoir. Read More

Hotspot cleared to enter clinic with small-molecule allosteric CBL-B inhibitor HST-1011 for solid tumors

Hotspot Therapeutics Inc. has received FDA clearance of its IND application for HST-1011, the company's investigational small-molecule allosteric inhibitor of casitas B-lineage lymphoma-B (CBL-B), an E3 ubiquitin protein ligase critically involved in immune cell response. Read More
Parkinsons-neurons-Lewy-bodies.png

Golexanolone improves symptoms of Parkinson's disease in preclinical model

Umecrine Cognition AB has announced results showing that its GABA-A receptor-modulating steroid antagonist golexanolone reversed fatigue, anxiety, depression, and some cognitive and motor alterations in a preclinical model of Parkinson's disease. Compared to a control-operated group, models with Parkinson's disease showed increased fatigue in the treadmill test and anxiety in the open field test. Read More
Light micrograph of skeletal muscle.

Satellos designates SAT-3153 as development candidate for Duchenne muscular dystrophy

Satellos Bioscience Inc. has designated SAT-3153 as a development candidate for Duchenne muscular dystrophy and will move the candidate into pre-IND-enabling studies and toward an IND filing. SAT-3153 is a small molecule designed to inhibit a particular kinase protein which the company believes controls Notch polarity within muscle stem cells. Read More

Genfleet Therapeutics discloses new RIPK1 inhibitors

Genfleet Therapeutics (Shanghai) Inc. has patented receptor-interacting serine/threonine-protein kinase 1 (RIPK1) inhibitors reported to be useful for the treatment of stroke, rheumatoid arthritis, psoriasis, heart failure, nonalcoholic steatohepatitis and inflammatory bowel disease. Read More
3D illustration of B-cell lymphoma

Oncopeptides presents peptide-drug conjugate for hematological cancer

Peptide-drug conjugates are an emerging class of molecules that allow efficient targeted drug delivery into tumors. Researchers from Oncopeptides AB and their collaborators presented data on the novel peptide-drug conjugate OPDC3, which has a novel alkylating payload, in models of diffuse large B-cell lymphoma (DLBCL) and acute myeloid leukemia (AML). Read More

Hangzhou Zhongmei Huadong Pharmaceutical patents new MAP4K1 inhibitors

Hangzhou Zhongmei Huadong Pharmaceutical Co. Ltd. has divulged pyrrolopyridines acting as mitogen-activated protein kinase kinase kinase kinase 1 (MAP4K1) inhibitors reported to be useful for the treatment of cancer. Read More

Avelos Therapeutics presents new MASTL inhibitors

Avelos Therapeutics Inc. has identified substituted 1,2-diaminoheterocyclic compound derivatives acting as serine/threonine-protein kinase greatwall (MASTL) inhibitors reported to be useful for the treatment of cancer, diabetes, obesity, stroke, thrombosis deep venous, thrombocytopenia and cardiovascular disorders. Read More
Multiple myeloma illustration

Dual GPRC5D/CD38-targeting agent FT-555 shows promise for treating multiple myeloma

G-protein coupled receptor family C group 5 member D (GPRC5D) is a tumor-associated receptor that is highly expressed in multiple myeloma (MM) and is a potential target for therapy in MM. Preclinical data have been presented for FT-555, an induced pluripotent stem cell (iPSC)-derived CAR-NK (CAR-iNK) cell product that exerts dual targeting on GPRC5D and CD38 in combination with daratumumab. Read More

University of Maryland describes new PROTACs for cancer

University of Maryland has presented proteolysis targeting chimeras (PROTACs) comprised of E3 ubiquitin ligase cereblon (CRBN)-binding moiety covalently linked to induced myeloid leukemia cell differentiation protein Mcl-1-binding moiety through a linker reported to be useful for the treatment of cancer. Read More

US researchers synthesize new BRD4 BD2 inhibitors

Poseidon Innovation LLC and the University of California have patented bromodomain-containing protein 4 (BD2 domain) (BRD4 BD2) inhibitors reported to be useful for the treatment of cancer, viral infections and acute renal disorders, among others. Read More
Liver anatomy illustration

Zebrafish model of Alagille syndrome supports role of Sox9

Alagille syndrome (ALGS) is a rare JAG1 (encodes for a Notch ligand) autosomal dominant disease affecting approximately 1 in 30,000-40,000 individuals. ALGS developmental defects cause an absence of bile ducts (intrahepatic duct paucity, IHDP) with an inability to transport bile from the liver to bile ducts (cholestasis) as well as heart problems. Read More

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