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BioWorld - Wednesday, April 8, 2026
Home » Topics » Science » New compound

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Lung cancer illustration
Cancer

New eIF4E inhibitor shows efficacy with SOC in KRAS-mutant NSCLC

Sep. 25, 2024
Ribometrix Inc. recently discussed the discovery and preclinical evaluation of a novel potent and selective eukaryotic translation initiation factor 4E (eiF4E) inhibitor, RBX-6610, being developed for the treatment of KRAS-mutant non-small-cell lung cancer (NSCLC).
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Elderly woman holding illustration of brain with missing puzzle piece
Neurology/psychiatric

FO-4-15, an anti-AD candidate with reduced neurotoxicity and enhanced neuroprotective effects

Sep. 20, 2024
Researchers from the Chinese Academy of Medical Sciences reported the discovery of the 1,2,4-oxadiazole derivative FO-4-15 for the treatment of Alzheimer’s disease (AD).
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Red blood cell infected with malaria parasites
Infection

Novartis synthesizes fast-acting intravenous agents for malaria

Sep. 18, 2024
The increasing resistance to intravenous artemisinin therapy for malaria highlights the urgent need for new treatments that offer better patient compliance and a single-dose cure to address this global health threat. Novartis AG recently presented the discovery, development and evaluation of aminoisoquinolines as fast-acting intravenous therapeutic agents for severe malaria treatment.
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Cancer

BRD9 PROTAC degrader shows efficacy in model of synovial sarcoma

Sep. 16, 2024
The University of Michigan has published details on the discovery and preclinical characterization of a new potent and selective proteolysis targeting chimera (PROTAC) degrader of BRD9, CW-3308. Synthesis and optimization of two different cereblon ligands led to the discovery of a novel series of highly potent BRD9 degraders, with CW-3308 selected as the lead candidate.
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Profile view of the human head highlighting the eye
Ocular

Partial epigenetic reprogramming to treat ischemic optic neuropathy

Sep. 12, 2024
By Mar de Miguel
A novel gene therapy that leads to cellular rejuvenation could restore vision after non-arteritic anterior ischemic optic neuropathy (NAION) and glaucoma. The technique is based on a reprogramming process that reverses the epigenetic DNA alterations caused by aging. Preclinical studies in glaucoma mice and nonhuman primates (NHP) models for this stroke-like disorder that affects the eye, showed an improvement of vision and restoration of the damaged axons of the optic nerve.
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Illustration of leg anatomy with target around knee
Musculoskeletal

Novel TAK1 inhibitor from Novartis for treating osteoarthritis

Sep. 6, 2024
Novartis AG described the identification and activity of TAK-756, a novel, selective and potent TAK1 inhibitor, as a potential intra-articular therapy for the treatment of osteoarthritis. Previous studies demonstrated that TAK1 appears to be a potential target for controlling inflammation and catabolism through NF-κB and MAPK pathways.
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Art concept for hematologic cancer
Cancer

Identification of highly potent, orally bioavailable BCL6 ligand-directed degraders

Aug. 23, 2024
At the recently concluded ACS Fall meeting, Bristol Myers Squibb Co. reported the discovery of potent orally bioavailable B-cell lymphoma 6 protein (BCL6) ligand-directed degraders (LDDs).
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Woman with blanket on couch blowing her nose with a tissue
Infection

New antirhinoviral compound with broad-spectrum activity described

Aug. 20, 2024
Human rhinoviruses (hRVs) are associated with upper respiratory tract infections such as the common cold, otitis media or sinusitis. In immunocompromised individuals or older people, hRVs can exacerbate existing pulmonary conditions such as asthma or chronic obstructive pulmonary disease.
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Cross section illustration of ion channel in cell membrane
Neurology/psychiatric

Nav1.8 inhibitor MSD-199 has activity in inflammatory, neuropathic pain models

Aug. 7, 2024
Researchers from Merck & Co Inc. have presented preclinical data for the novel Nav1.8 inhibitor MSD-199, being developed for the treatment of inflammatory and neuropathic pain.
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Kidney illustration
Nephrology

META-001-PH gets rare pediatric disease designation

Aug. 6, 2024
Meta Pharmaceuticals Inc. announced that the FDA has granted rare pediatric disease designation to its investigational new drug META-001-PH for the treatment of primary hyperoxaluria (PH), an autosomal recessive metabolic disorder in which oxalate is overproduced and deposited in the body.
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