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3D illustration of a chain of amino acid or biomolecules called protein
Drug design, drug delivery & technologies

Omnigeniq’s journey from space science to drug design

Feb. 18, 2026
By Tamra Sami
No Comments
A project that started as a bioreactor to assist astronauts in deep space to keep medications safe in a microgravity environment could help pharma companies model how drugs behave in the human body. Omnigeniq unveiled at the J.P. Morgan Healthcare conference the first computer model of a human protein as it exists in the body, confirming that native protein topology can be calculated directly from physics.
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Cancer

Shenzhen Targetrx reports EGFR-targeted PROTACs

Feb. 18, 2026
Shenzhen Targetrx Inc. has designed new proteolysis targeting chimeric (PROTACs) compounds comprising cereblon (CRBN) ligands covalently bonded to an EGFR L858R-, L858R/T790M double mutant- and L858R/T790M/C797S triple mutant-targeting moiety through a linker reported to useful for the treatment of non-small-cell lung cancer.
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Cancer

Tyra Biosciences patents new FGFR inhibitors

Feb. 18, 2026
Tyra Biosciences Inc. has disclosed new indazole compounds acting as fibroblast growth factor receptor (FGFR) inhibitors. They are reported to be useful for the treatment of cancer and developmental disorders.
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Melanoma cells stained with an H & E stain and magnified to 320x.
Cancer

HOXD13 drives angiogenesis and immune evasion in melanoma

Feb. 18, 2026
No Comments
Although physiological immune responses require increased tissue vasculature, many solid tumors simultaneously activate angiogenesis to meet the increasing demand for oxygen and nutrients while excluding immune cells. The exact molecular mechanisms by which cancer cells control this immune-refractory angiogenic process remain widely unclear.
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Cancer

New compound against tumors with aberrant FGFR2 signaling

Feb. 18, 2026
No Comments
Fibroblast growth factor receptor 2 (FGFR2) is a transmembrane tyrosine kinase that regulates signaling pathways controlling cell survival and proliferation. Dysregulation of FGFR2, through amplification or activating mutations, contributes to tumor development, making it an attractive target for therapeutic intervention in oncology.
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Cancer and blood cells
Cancer

Omeros reports Oncotox-AML primate data

Feb. 18, 2026
No Comments
Omeros Corp. has successfully completed its initial study in nonhuman primates evaluating the efficacy and safety of its Oncotox-AML cancer therapeutic platform for acute myeloid leukemia (AML). Oncotox-AML is an engineered biologic designed to selectively kill both AML blasts and relapse-related leukemia stem cells.
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3D illustration of organoid models in a petri dish
Drug design, drug delivery & technologies

Human organoid mimics cancer-induced cachexia

Feb. 17, 2026
By Mar de Miguel
No Comments
The variety of organoids that can be developed in vitro is enabling major advances. Depending on the type of tissues and the research goals, these small 3D cell-based structures that mimic real tissue offer certain advantages over animal models. Scientists at the University of Padova in Italy have created human neuromuscular organoids to reproduce cancer-induced muscle cachexia, a condition that murine models do not accurately replicate.
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Cancer

Ascentage Pharma Group patents BTK PROTAC degraders

Feb. 17, 2026
Ascentage Pharma Group Corp. Ltd. and Ascentage Pharma (Suzhou) Co. Ltd. have disclosed proteolysis targeting chimera (PROTAC) compounds comprising E3 ubiquitin ligase-binding moiety covalently linked to a Bruton tyrosine kinase (BTK)-targeting moiety. They are reported to be useful for the treatment of cancer.
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Cancer

Merna Therapeutics prepares new polypeptides targeting sortilin

Feb. 17, 2026
Merna Therapeutics Inc. has discovered polypeptides targeting sortilin (neurotensin NTR3; NT3; Gp95) receptor. They are reported to be useful for the treatment of cancer.
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Cancer

French investigators identify new furin inhibitors

Feb. 17, 2026
The Institut National De La Santé et de la Recherche Médicale, Université de Bordeaux and Université de Paris Cité have synthesized N-phenyl-quinoline-4-carboxamide compounds acting as furin (PACE; PCSK3) inhibitors. They are reported to be useful for the treatment of cancer.
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