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BioWorld - Sunday, April 26, 2026
Home » Newsletters » BioWorld Science

BioWorld Science

Dec. 31, 2025

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Science in 2025: the best of the rest

A review of 2025's noteworthy advances in medical research, including GLP-1 receptor agonists as anti-aging drugs, tumor-agnostic therapies and xenotransplants. Read More

Bayosthiti AI to build India-specific RNA sequencing ecosystem

Bayosthiti AI Pvt Ltd. aims to make RNA sequencing and AI-based preventive health care affordable and accessible for the Indian market, leveraging intellectual property from its parent company, Biostate AI Inc. Read More
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Three Helius solid tumor candidates gain clinical trial clearance

Shanghai Henlius Biotech Inc. has announced acceptance of IND applications by China’s National Medical Products Administration (NMPA) for three differentiated candidates for the treatment of solid tumors. Read More
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BioWorld Science 2025 Year in Review

BioWorld Science looks back at the year’s biggest stories in research. Find all of our 2025 Year in Review articles here. Read More

Holiday notice

In accordance with the publishing schedule, BioWorld Science will not be published on Thursday, Jan. 1, 2026, and Friday, Jan. 2, 2026. Read More
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Notice of email fulfillment change

Effective Jan. 5, 2026, BioWorld is switching email fulfillment services. While we have made every effort to ensure that all current user subscription details — as well as information on users who have unsubscribed — have been migrated accurately to the new system, there may be a few instances where certain information may not have carried over as expected. If you have any concerns that you received a newsletter in error or if a colleague has not received an expected newsletter, do not hesitate to reach out to our customer care team. Call us:
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Going forward, if you would like to be unsubscribed, click on the ‘Unsubscribe’ link at the bottom of the emailed newsletter.
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Hainan Simcere Pharmaceutical divulges new antibody-drug conjugates

Hainan Simcere Pharmaceutical Co. Ltd. has disclosed antibody-drug conjugates comprising a glycoengineered antibody covalently linked to a cytotoxic drug through a linker reported to be useful for the treatment of cancer. Read More
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Gene therapy restores SynGAP1 function, rescues epilepsy and behaviors

SYNGAP1-related disorders (SRDs) are rare neurodevelopmental conditions characterized by a wide range of symptoms, including intellectual disability, epilepsy, motor deficits and increased risk-taking behavior. Read More

Shanghai Xianxiang Medical Technology patents new CDK2/cyclin E1 inhibitors

Shanghai Xianxiang Medical Technology Co. Ltd. has synthesized CDK2/cyclin E1 inhibitors reported to be useful for the treatment of cancer. Read More

Guangzhou Runer Ophthalmic Biotechnology describes new complement factor B inhibitors

Guangzhou Runer Ophthalmic Biotechnology Co. Ltd. has identified complement factor B (CFB) inhibitors reported to be useful for the treatment of age-related macular degeneration, asthma, atherosclerosis, Crohn’s disease, glomerular disorders, hemolytic uremic syndrome, neurological disorders and diabetic retinopathy, among others. Read More
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Anti-ROR1 scFv shows preclinical activity in triple-negative breast cancer

The receptor tyrosine kinase-like orphan 1 (ROR1) is a transmembrane protein expressed during embryonic development. Moreover, it is highly expressed on the surface of several cancer cell types, including B-cell malignancies and solid tumors such as triple-negative breast cancer (TNBC). Researchers from The University of Queensland and collaborating institutions recently reported the development of a single-chain fragment variable (scFvs) specifically targeting the membrane proximal region of ROR1 rather than the Ig-like domain, aiming to reduce cross-reactivity with other surface proteins expressed in normal tissues. Read More

New AT2 receptor agonists disclosed in Jiangsu Carephar Pharmaceutical patent

Jiangsu Carephar Pharmaceutical Co. Ltd. has divulged angiotensin AT2 receptor (AGTR2) agonists reported to be useful for the treatment of idiopathic pulmonary fibrosis. Read More

Convergen (Suzhou) Pharmaceutical discovers new PAK4 degradation inducers

Convergen (Suzhou) Pharmaceutical Co. Ltd. has described proteolysis targeting chimera (PROTAC) compounds comprising a cereblon (CRBN) E3 ubiquitin ligase-binding moiety coupled to a serine/threonine-protein kinase PAK4-targeting moiety through a linker reported to be useful for the treatment of cancer. Read More
Illustration of man holding magnifying glass to human body model showing muscle anatomy

SPAST-AAV9 gene therapy prevents hereditary spastic paraplegia symptoms

In a recent publication in Molecular Therapy, researchers from Drexel University College of Medicine and UMass Chan Medical School presented a silence-and-replace gene therapy strategy aiming to address both the gain-of-toxicity and loss-of-function components of the disease hereditary spastic paraplegia (HSP). Read More

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