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BioWorld - Friday, December 5, 2025
Home » Newsletters » BioWorld Science

BioWorld Science

April 11, 2024

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The calcitonin gene related peptide (CGRP, yellow) bound to its receptor

Neuropeptide released by pain neurons promotes wound healing by interacting with immune system

Wound healing is a highly specialized dynamic process for the repair of damaged/injured tissues through an intricate mechanism. Any failure in the normal wound healing process results in abnormal scar formation, and a chronic state which is more susceptible to infections. Researchers from Monash University in Australia and Osaka University in Japan have demonstrated that the removal of a specific subtype of sensory neurons containing the Nav1.8+ ion channel significantly impairs skin wound repair and muscle regeneration following injury. Read More

GC Cell reports data on anti-CD5 CAR-NK therapy with potent efficacy, long-term in vivo persistence in blood

A team from GC Cell Corp. reported preclinical data on GL-205, a novel allogeneic anti-CD5 CAR-NK being developed for the treatment of T-cell malignancies. GL-205 was developed using cord blood-derived NK cells that were genetically modified to express CD5-directed CAR and simultaneously produce IL-15 to support NK cell survival and proliferation. Read More
3D illustration of the cross-section of skin layers with atopic dermatitis

Sitryx names first clinical development candidate for atopic dermatitis

Sitryx Therapeutics Ltd. has nominated SYX-5219 as the first candidate from its proprietary pipeline to progress to regulatory nonclinical studies to support a clinical trial authorization (CTA). SYX-5219 has the potential to address a broad range of inflammatory diseases and will advance into the clinic for the treatment of atopic dermatitis. Read More
Blood clot under microscope.

Cereno Scientific submits CTA in Europe for phase I study of new antithrombotic treatment

Cereno Scientific AB has submitted a clinical trial application (CTA) to the EMA seeking approval for a first-in-human, phase I study of CS-014, a novel histone deacetylase (HDAC) inhibitor drug candidate under development as an antithrombotic treatment. Read More

Cullgen patents new DCAF1-binding PROTACs for cancer

Cullgen (Shanghai) Inc. has disclosed proteolysis targeting chimera (PROTAC) compounds comprising a DDB1- and CUL4-associated factor 1 (DCAF1) binding moiety covalently linked to target protein moiety (such as bromodomain-containing protein 4 [BRD4; HUNK1], cyclin-dependent kinase 4 [CDK4] and estrogen receptor α [ER-α; ESR1]) through a linker reported to be useful for the treatment of cancer. Read More
Illustration of antibodies binding to human cell receptors

Dual TfR1- and EGFR-targeting KK-2260 has antitumoral activity in EGFR-expressing tumors

The overexpression of transferrin receptor 1 (TfR1) has been reported in several cancer types but is also expressed in normal cell types such as erythroblasts. On the other hand, epidermal growth factor receptor (EGFR) is highly expressed in epithelial carcinomas. Read More
stem-cells

Tr1x’s TRX-103 to enter phase I following IND clearance

The U.S. FDA has cleared Tr1x Inc.’s IND application for TRX-103 for the prevention of graft-vs.-host disease (GVHD) in patients undergoing HLA-mismatched hematopoietic stem cell transplantation (HSCT). Read More

New SLC6A19 inhibitors divulged in Jnana Therapeutics patents

Jnana Therapeutics Inc. has synthesized sodium-dependent neutral amino acid transporter B(0)AT1 (SLC6A19) inhibitors reported to be useful for the treatment of amino acid metabolism disorders, amino acid transport disorders and metabolic and nutritional genetic disorders, among others. Read More

Chinese scientists describe new RSK4 inhibitors for cancer

Scientists at East China Normal University, East China University of Science & Technology, Jinfeng Laboratory and Zhengzhou University have identified ribosomal protein S6 kinase α-6 (RPS6KA6; RSK-4) inhibitors reported to be useful for the treatment of cancer. Read More
Lab glassware and scientist

HSN-002066, a novel PARP7 inhibitor with improved potency and selectivity

Researchers from Beijing Pharscin Innobio Co. Ltd. presented the discovery and preclinical characterization of a novel highly selective poly (ADP-ribose) polymerase 7 (PARP7) inhibitor, HSN-002066, being developed for the treatment of cancer. Read More

Lundbeck and Vernalis present new LRRK2 and LRRK2 G2019S mutant inhibitors

Scientists at H. Lundbeck A/S and Vernalis (R&D) Ltd. have divulged leucine-rich repeat kinase 2 (LRRK2; Dardarin) and LRRK2 G2019S mutant inhibitors reported to be useful for the treatment of Parkinson’s disease, Lewy body dementia and multiple system atrophy. Read More

SPX-303, an LILRB2/PD-L1 bispecific antibody, enhances antitumor immunity in preclinical models

Sparx Biopharmaceutical Corp.’s SPX-303, is an anti-LILRB2/PD-L1 bispecific antibody (bsAb) being developed as an anticancer agent. Read More
Dividing breast cancer cell.

ZCCHC3 is a prognostic marker in TNBC

Triple-negative breast cancer (TNBC) is an aggressive type of breast cancer with poor prognosis and limited therapeutic options, and it accounts for 15%-20% of female invasive breast cancers. Read More

Schrodinger and Takeda scientists discover new 3CLpro inhibitors

Researchers at Schrodinger Inc. and Takeda Pharmaceutical Co. Ltd. have described 3C-like proteinase (3CLpro; Mpro; nsp5) inhibitors reported to be useful for the treatment of coronavirus acute respiratory syndrome. Read More

Other news to note for April 11, 2024

Additional early-stage research and drug discovery news in brief, from: Cantargia, Compugen, Moleculin, Revolution, Vesicure. Read More

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