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BioWorld - Sunday, June 21, 2026
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Art concept for tumor
Cancer

New selective pan-TEAD inhibitor exhibits antitumor activity in preclinical models

April 10, 2024
Insilico Medicine Inc. recently discussed the generative artificial intelligence (AI)-powered design of ISM-6331, a novel, potent, selective and non-covalent pan-TEAD inhibitor that blocks TEAD palmitoylation to suppress YAP/TAZ-TEAD transcriptional activity and shows strong antitumor activity in a preclinical model of Hippo pathway-dysregulated cancers and other solid cancers were discussed.
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Illustration of brain with electrical activity background
Neurology/Psychiatric

Teijin Pharma grants Bioprojet rights to OX2 receptor agonist for narcolepsy

April 10, 2024
Teijin Pharma Ltd. has entered into an exclusive global licensing agreement with Bioprojet under which Teijin Pharma grants Bioprojet Pharma SAS exclusive worldwide rights to research, develop, manufacture and commercialize an investigational candidate for narcolepsy.
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Antibodies attacking cancer cell
Immuno-oncology

FDA clears IND for Biocity Biopharma’s BC-2027

April 10, 2024
The U.S. FDA has cleared Biocity Biopharma Co. Ltd.’s IND application for a phase I study of BC-2027. This is the company’s second first-in-class antibody-drug conjugate (ADC) to be approved for clinical trials, following BC-3195, which is directed against placental-cadherin (CDH3).
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Immuno-oncology

Hangzhou’s DXC-006 ADC shows antitumor activity in preclinical models

April 10, 2024
DXC-006 (Hangzhou DAC Biotechnology Co. Ltd.) is an antibody-drug conjugate (ADC) that targets CD56, a molecule involved in cell-cell adhesion and cell-matrix adhesion that is overexpressed in neuroblastoma, small-cell lung cancer and multiple myeloma, but less frequently expressed in normal tissues. DXC-006 consists of an anti-CD56 antibody (DXA-006) linked to the topoisomerase 1 (TOP1) inhibitor CPT-116 through a linker.
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Cell research illustration
Cancer

Oric Pharmaceuticals reports on highly potent, selective and orally bioavailable PLK4 inhibitor

April 10, 2024
The discovery of a potent, selective and orally bioavailable serine/threonine-protein kinase PLK4 (STK18) inhibitor with synthetic lethality in TRIM7-amplified cancers was reported by Oric Pharmaceuticals Inc. at the ongoing AACR meeting in San Diego.
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3D Rendering of tumor microenvironment
Cancer

PH027-1, a potent WRN inhibitor with a wide safety margin and efficacy against MSI-H tumors

April 10, 2024
Researchers from Puhe Biopharma Co. Ltd. presented the discovery and preclinical evaluation of PH027-1, a novel small-molecule Werner syndrome protein (WRN) inhibitor targeting microsatellite instability high (MSI-H) tumors.
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Cardiovascular

Cathepsin C inhibitor suppresses NET formation in MPO-ANCA vasculitis

April 10, 2024
Myeloperoxidase-antineutrophil cytoplasmic antibody (MPO-ANCA)-associated vasculitis is a systemic condition affecting the small vessels with production of MPO-ANCA in serum. It has been suggested that the formation of neutrophil extracellular traps (NETs) induced by MPO-ANCA is a driver of pathogenesis, with involvement of neutrophil elastase (NE), which in turn is activated by the enzyme cathepsin C.
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Illustration of cancer cells entering the bloodstream.
Cancer

AACR 2024: New concepts suggest new targets for metastatic disease

April 10, 2024
By Anette Breindl
Prior to this year’s Annual Meeting of the American Association for Cancer Research (AACR), it had been 14 years since metastasis had been the subject of a plenary session. So, the Tuesday session on “Evolution of the genome, microenvironment, and host through metastasis” had plenty of new insights to share.
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Cancer

Chengdu Origiant Pharmaceutical discovers new GTPase KRAS mutant inhibitors

April 9, 2024
Chengdu Origiant Pharmaceutical Co. Ltd. has described GTPase KRAS (G12D mutant) inhibitors reported to be useful for the treatment of cancer.
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Infection

New C5aR antagonists described in Vanqua Bio patent

April 9, 2024
Vanqua Bio Inc. has divulged C5a anaphylatoxin chemotactic receptor 1 (C5aR; CD88) antagonists reported to be useful for the treatment of autoimmune disease, cancer, infections and cardiovascular, inflammatory and neurological disorders.
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