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Illustration of antibodies attacking nerve cells
Immune

Indupro and Sanofi to advance bispecific for autoimmune diseases

Dec. 12, 2025
No Comments
Indupro Inc. has announced a strategic equity investment and research collaboration with Sanofi SA. The agreement with Sanofi includes the right of first negotiation for Indupro’s bispecific PD-1 agonist program.
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Medical illustration showing cross section of skin with hair follicles
Dermatologic

Absci’s ABS-201 stimulates human hair follicle growth ex vivo

Dec. 12, 2025
No Comments
Absci Corp. has released new preclinical data for ABS-201, an AI-designed antibody targeting the prolactin receptor (PRLR) designed to stimulate hair follicle regeneration and promote durable hair regrowth for the potential management of androgenetic alopecia.
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Person with chest pain after receiving a COVID-19 vaccine
Inflammatory

Research unpicks molecular mechanism of vaccine-induced cardiac inflammation

Dec. 12, 2025
By Anette Breindl
No Comments
The cardiomyositis that is a rare adverse effect of mRNA-based COVID vaccines is due to immune cell activity as a result of increased levels of the chemokines CXCL10 and interferon-γ (IFN-γ). Blocking CXCL10 and IFN-γ could prevent muscle cell damage in cell culture, and cardiomyositis in animal models. The findings, reported in the Dec. 10, 2025, issue of Science Translational Medicine, suggest a way of mitigating the risk of cardiomyositis.
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Brain and DNA
Neurology/psychiatric

Epilepsygtx's $33M advances focal epilepsy gene therapy

Dec. 11, 2025
By Nuala Moran
No Comments
Epilepsygtx Ltd. has raised a $33 million series A to fund a phase I/IIa trial of EPY-201, a gene therapy for treating drug-resistant focal epilepsy. EPY-201 uses an adeno-associated viral vector to deliver KCNA1, the gene encoding Kv1.1, a potassium ion channel that modulates neuronal excitability.
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Cancer

Shanghai Best-Link Bioscience discovers new polymer-drug conjugates

Dec. 11, 2025
Shanghai Best-Link Bioscience LLC has described polymer-drug conjugates comprising a polymer covalently linked to a cytotoxic drug through a linker and its nanoparticles reported to be useful for the treatment of cancer.
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Neurology/psychiatric

New opioid receptor agonists disclosed in Alphamol Science patent

Dec. 11, 2025
Alphamol Science Ltd. has divulged opioid receptor agonists reported to be useful for the treatment of pain.
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Immuno-oncology

Chinese scientists describe new CEACAM5-targeting antibody-drug conjugates

Dec. 11, 2025
Chengdu Kangnuoxing Biopharma Inc. and Keymed Biosciences Co. Ltd. have identified antibody-drug conjugates comprising antibodies targeting carcinoembryonic antigen-related cell adhesion molecule 5 (CEACAM5; CEA; CD66e) covalently linked to a cytotoxic drug through a linker reported to be useful for the treatment of cancer.
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Endocrine/metabolic

Meta Pharmaceutical and Moyuan Pharmaceuticals divulge new LDHA inhibitors

Dec. 11, 2025
Meta Pharmaceutical (HK) Ltd. and Shenzhen Moyuan Pharmaceuticals Co. Ltd. have synthesized lactate dehydrogenase A (LDHA) inhibitors reported to be useful for the treatment of primary hyperoxaluria.
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Immuno-oncology

Hangzhou Zhongmei Huadong Pharmaceutical patents new antibody-drug conjugates

Dec. 11, 2025
Hangzhou Zhongmei Huadong Pharmaceutical Co. Ltd. has disclosed antibody-drug conjugates consisting of antibodies covalently linked to a cytotoxic drug through a linker reported to be useful for the treatment of cancer.
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HIV-1 virus particle
HIV/AIDS

Peptidomimetic against drug-resistant HIV-1

Dec. 11, 2025
No Comments
Many cases of human immunodeficiency virus (HIV)-1 infection can be effectively treated with existing drugs, but they can lose efficacy over time because of the emergence of resistance. In an effort to generate next-generation drugs, Chinese researchers at the Chinese Academy of Medical Sciences & Peking Union Medical College and other institutions synthesized a series of peptidomimetics against the viral protease, in which they extended the therapeutically effective hydroxyethyl sulfonamide scaffold using an amino acid linker. They reasoned that the linker could allow the drug to make additional contacts with the protease.
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