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BioWorld - Monday, August 3, 2026
Home » Newsletters » BioWorld Science

BioWorld Science

July 20, 2026

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Click chemistry drug bound to pancreatic cancer cells from mice

In vivo click ADCs could address tumor heterogeneity

Researchers at Washington University in St. Louis have used click chemistry to link a second antibody to a pre-existing antibody-drug conjugate (ADC) in vivo. In preclinical models of HER2 and EGFR co-expressing pancreatic, breast and gastric tumors, sequential administration of the ADC and the second antibody was better at shrinking tumors than either ADC monotherapy or a combination of antibody and ADC treatment. Read More
Ovarian cancer

CD98hc as promising target for ADC therapy in ovarian cancer

In a recently published study, researchers from the Institute of Biomedical Research of Salamanca and collaborators investigated the potential of CD98hc as a novel antibody-drug conjugate (ADC) target in ovarian cancer. CD98hc, encoded by the SLC3A2 gene, is a transmembrane glycoprotein involved in amino acid transport, cell adhesion and signal transduction, among other biological activities. Read More
T cells attacking cancer

Veraxa Biotech receives feedback on BiTAC-TCE program

Veraxa Biotech AG has received scientific advice from the German regulatory authority, the Paul-Ehrlich-Institute (PEI), regarding the underlying biology and proposed nonclinical development plan for its most advanced development program based on its proprietary BiTAC-TCE (bi-targeted tumor-associated cytotoxicity T-cell engager) technology. Read More
Green money bag tiles stacked on tile with microscope icon

Funding to expand Sightera Biosciences’ AI-discovered programs

Sightera Biosciences BV announced it has raised €3 million (US$3.5 million) in pre-seed funding. The funding will be used to extend the company’s platform technology and asset portfolio, including its lead program in oncology, SIGHT-001. Read More

Teikyo University discloses new neutrophil elastase inhibitors

Teikyo University has synthesized new neutrophil elastase (ELANE; leukocyte elastase) inhibitors potentially useful for the treatment of acute lung injury. Read More
Cancer tumor in breast illustration

New PROTAC tackles ESR1-mutated breast cancer

Researchers from Wuhan University and collaborators reported the synthesis and preclinical characterization of NCP07, a novel ERα PROTAC degrader designed to treat endocrine therapy-resistant tumors. Read More
Microscopic cross section of skin

Study identifies ampyrone as direct tyrosinase activator for treating hypopigmentation

Tyrosinase (TYR) is the key enzyme in melanin synthesis because it catalyzes the first and rate-limiting step of melanin synthesis. TYR inhibitors are used clinically for hyperpigmentation, but there are few direct TYR activators for treating hypopigmentation. Read More

Merck KGaA identifies new KRAS mutant degradation inducers

Merck KGaA has discovered new GTPase KRAS mutant degradation inducers potentially useful for the treatment of cancer. Read More

Gan & Lee Pharmaceuticals synthesizes new CK1α molecular glue degraders

Gan & Lee Pharmaceuticals Co. Ltd. has divulged new molecular glue degraders comprising cereblon (CRBN)-binding agents and casein kinase 1 isoform α (CK1α, CSNK1A1) degradation moieties potentially useful for the treatment of cancer. Read More
Tree in the shape of human head losing leaves

KBN-2201 reverses key features of Alzheimer’s in mice

Researchers from Ajou University School of Medicine reported the preclinical efficacy of KBN-2201 in a mouse model of late-stage Alzheimer’s disease. Read More

CRF2 receptor agonists detailed in Sciwind patent

Beijing Sciwind Biotechnology Co. Ltd. and Sciwind Biosciences Co. Ltd. have disclosed new corticotropin-releasing factor CRF2 receptor (CRFH2) agonists potentially useful for the treatment of heart failure, hypertension, obesity, sarcopenia, diabetes and chronic kidney diseases. Read More

Hansoh patents new dopamine D1/5 receptor partial agonists

Jiangsu Hansoh Pharmaceutical Group Co. Ltd. and Shanghai Hansoh Biomedical Co. Ltd. have reported new dopamine D1 and/or D5 receptor partial agonists. As such, they are reported to be useful for the treatment schizophrenia, attention deficit hyperactivity disorder (ADHD), Tourette disease, sleep disorder, pain, autism spectrum disorder, Parkinson’s and Alzheimer’s disease, among others. Read More
Pediatric brain illustration

CDKL5 gene therapy rescues behavioral, cognitive and synaptic deficits in CDD mice

Researchers from the Universities of Bologna and Torino recently presented their hematopoietic stem cell gene therapy (HSC-GT) strategy based on microglia-mediated delivery using a lentiviral vector encoding a secretable, cell-penetrating CDKL5 protein (Igκ-TATk-CDKL5). Read More

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