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BioWorld - Friday, April 24, 2026
Home » Newsletters » BioWorld Science

BioWorld Science

Sep. 18, 2024

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Juleen Zierath on stage at EASD 2024

Studies on exercise and health win EASD prize

How do exercise and insulin collaborate in metabolism? The European Association for the Study of Diabetes (EASD) and the Novo Nordisk Foundation recognized the work of Juleen Zierath in this topic with the Diabetes Prize for Excellence at their recent annual meeting. Read More

RKER-065 fights fat, preserves muscle in mice on semaglutide

Incretin therapies based on GLP-1 receptor agonism aid in the loss of weight in obesity, but a relevant part of this loss (25%-40%) is attributed to loss of lean muscle mass, which raises the risk of sarcopenia. Keros Therapeutics Inc. has presented data on RKER-065, a novel modified ActRII-Fc ligand trap that inhibits myostatin and activins and promotes muscle formation. Read More
Malaria-infected-red-blood-cell

Novartis synthesizes fast-acting intravenous agents for malaria

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. Read More
Cell research illustration

PPL-001 gets US orphan drug designation for Friedreich’s ataxia

Papillon Therapeutics Inc.’s PPL-001 has been awarded orphan drug designation by the FDA for Friedreich’s ataxia. PPL-001 is an experimental gene-corrected CD34+ hematopoietic stem and progenitor cell (HSPC) therapy. Read More

CID-078 has activity in small, non-small-cell lung cancer models

Researchers from Circle Pharma Inc. have presented preclinical data for CID-078, a novel orally bioavailable cyclin A/B Rxl macrocycle being developed for the treatment of patients with lung cancer. CID-078 was developed as a macrocycle that binds to the hydrophobic patch of cyclins A and B and blocks RxL-dependent interactions of proteins, such as that of E2F1 with cyclin A-CDK2 and Myt1 with cyclin B-CDK1. Read More
Illustration of DNA double helix, DNA damage with TCGA letters flying around

Rakovina, Variational AI to target DNA damage response

Rakovina Therapeutics Inc. and Variational AI Inc. have entered into a research collaboration to identify and develop novel small-molecule therapies against DNA damage response (DDR) targets for the treatment of cancer. Read More

KU Leuven patents new exportin-1 receptor antagonists

KU Leuven has disclosed exportin-1 (CRM1; XPO1) receptor antagonists reported to be useful for the treatment of cancer, among others. Read More

Orbis to use Vivtex platform for gut permeability screening

Orbis Medicines SA has announced a research collaboration and option to an exclusive license with Vivtex Corp. Read More
Prostate-cancer-cells

Inhibiting miR-1271-5p reduces growth of hormone sensitive prostate cancer cell lines

Researchers from Imperial College London presented data from a study that aimed to assess the role of miR-1271-5p in prostate cancer (PCa) progression. Read More

Rutgers University divulges new PL-pro inhibitors

The State University of New Jersey (Rutgers) has synthesized non-structural protein 3 (nsp3; PL-pro) (SARS-CoV-2; COVID-19 virus) inhibitors reported to be useful for the treatment of viral infections. Read More

Chinese and US researchers describe new CDK12/13 degradation inducers

Scientists at Livzon Pharmaceutical Group Inc., Shanghai Institute of Organic Chemistry and the University of Michigan have identified proteolysis targeting chimeras (PROTACs) comprising an E3 ubiquitin ligase binding moiety covalently bound to a cyclin-dependent kinase 12 (CDK12) and 13 (CDK13) targeting moiety through a linker reported to be useful for the treatment of cancer. Read More
Molecular research art concept

Candidate milestone achieved under X-Chem’s collaboration with Astrazeneca

X-Chem Inc. has announced the achievement of a drug discovery milestone under its collaboration agreement with Astrazeneca plc. Read More

New TEAD inhibitors disclosed in Signet Therapeutics patent

Signet Therapeutics Co. Ltd. has divulged α, β-unsaturated amide compounds acting as transcriptional enhancer factor (TEAD) inhibitors reported to be useful for the treatment of cancer. Read More

Turkish researchers discover new EGFR inhibitors and apoptosis inducers for lung cancer

Researchers at Anadolu University and Bilecik Seyh Edebali University have described quinazolinone derivative compounds acting as EGFR (HER1; erbB1) inhibitors and apoptosis inducers reported to be useful for the treatment of lung cancer. Read More
Test-tubes_dropper.png

Astrazeneca’s AZD-6234 prompts body weight loss due to reduced food intake

Amylin is a hormone co-secreted with insulin in the pancreas that has anorexigenic effects, since it promotes satiety and reduces food intake. Amylin analogs and dual agonists of the amylin and calcitonin receptors have been developed for treating obesity. Astrazeneca plc reported results with their AMYR3 agonist AZD-6234. Read More

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