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BioWorld - Thursday, May 14, 2026
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Microscope with laptop displaying histology image.
Cancer

Dual arginase inhibitor OATD-02 cleared to enter clinic for solid tumors

Nov. 29, 2022
Molecure SA has received clearance from the Polish Office for Registration of Medicinal Products, Medical Devices and Biocidal Products to conduct the first clinical trial of OATD-02.
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Breast cancer tumor and its microenvironment obtained from a live mouse model.
Cancer

PH-109 demonstrates antitumor activity in a mouse model of metastatic breast cancer

Nov. 29, 2022
Researchers from Phio Pharmaceuticals Corp. presented preclinical data for PH-109, a novel self-delivering RNAi targeting connective tissue growth factor (CTGF), which was originally developed and assessed in early clinical trials as potential treatment of dermal hypertrophic scarring and subretinal fibrosis. The current study evaluated PH-109 in a mouse model of metastatic breast cancer.
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Chikungunya-virus
Immune

Emergex advances chikungunya vaccine development with generation of CHIKV ligandome

Nov. 29, 2022
Emergex Vaccines Holding Ltd. has generated a chikungunya virus (CHIKV) ligandome, the first major milestone in the development of the company's CD8+ T-cell CHIKV adaptive vaccine candidate. Using an immunoproteomics approach, naturally presented MHC Class I-restricted peptides on the surface of a human leukocyte antigen (HLA)-typed cell line infected with CHIKV virus were extracted and identified.
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3D illustration of heart cross section
Cardiovascular

Gene therapy TN-401 designated US orphan drug for arrhythmogenic right ventricular cardiomyopathy

Nov. 29, 2022
The FDA has awarded orphan drug designation to Tenaya Therapeutics Inc.'s gene therapy product candidate, TN-401, for the treatment of arrhythmogenic right ventricular cardiomyopathy (ARVC). TN-401 is an adeno-associated virus (AAV)-based gene therapy being developed for the treatment of genetic ARVC caused by plakophilin-2 (PKP2) gene mutations.
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Cancer

Ikena nominates next-generation MEK-RAF complex inhibitor IK-595 as development candidate

Nov. 29, 2022
Ikena Oncology Inc. has nominated a next-generation mitogen-activated protein kinase (MEK)-RAF complex inhibitor, IK-595, as the company's first development candidate in the RAS pathway. IK-595 traps MEK and RAF in an inactive complex, more completely inhibiting RAS signals than existing inhibitors.
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Colon cancer illustration
Immuno-oncology

YH-38560 shows promise for the treatment of solid cancers

Nov. 29, 2022
Trophoblast glycoprotein, also known as 5T4, is widely expressed in several solid tumors; cluster of differentiation 47 (CD47) is an ubiquitous immune checkpoint receptor that is also overexpressed in many solid tumors as well as in hematological cancers. A Yuhan Corp. research team has presented preclinical results on YH-38560, a bispecific fusion protein that targets both 5T4 and CD4 for the potential treatment of solid tumors.
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Neurons
Endocrine/Metabolic

MYT-109, a promising treatment for Leigh syndrome

Nov. 29, 2022
Leigh syndrome is a rare neurometabolic disorder that causes the CNS to degenerate. Investigators from the University of California, Davis, and Myto Therapeutics Inc. noted that the NDUFS4-knockout (KO) mouse is a well-characterized model for this disease and shared results on the effects of monomethyl fumarate prodrug MYT-109 in this murine model.
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Neurology/Psychiatric

ELB-00824 prevents oxaliplatin-induced pain and oxidative stress in vivo

Nov. 29, 2022
Scientists at USA Elixiria Biotech Inc. and colleagues described data from preclinical studies evaluating the potential of the peroxisome proliferator-activated receptor γ (PPARγ) agonist, ELB-00824, for protection against chemotherapy-induced neuropathic pain (CINP).
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Cancer

Voronoi presents new HER2 and/or HER4 inhibitors

Nov. 28, 2022
Voronoi Inc. has identified heteroaryl compounds acting as HER2 (erbB2) and/or HER4 (erbB4) inhibitors reported to be useful for the treatment of cancer.
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Cancer

Nuvation Bio discovers new PARP inhibitors

Nov. 28, 2022
Nuvation Bio Inc. has disclosed drug conjugates comprising a nuclear receptor-targeting moiety covalently linked to a poly(ADP-ribose) polymerase 1 (PARP1) and/or PARP2 inhibitor though a linker. They are reported to be potentially useful for the treatment of cancer.
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