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BioWorld - Thursday, May 28, 2026
Home » Topics » Disease categories and therapies » Endocrine/metabolic

Endocrine/metabolic
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Endocrine/metabolic

Terns Pharmaceuticals patent discloses GIPR antagonists

Jan. 30, 2026
Terns Pharmaceuticals Inc. has reported triazole compounds acting as gastric inhibitory polypeptide receptor (GIPR) antagonists. They are intended for use in the treatment of diabetes, obesity, liver diseases and cardiometabolic syndrome.
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Connecting puzzle pieces
Endocrine/metabolic

Astrazeneca and CSPC collaborate in obesity and type 2 diabetes

Jan. 30, 2026
No Comments
Astrazeneca plc has signed a new strategic collaboration agreement with CSPC Pharmaceutical Group Ltd. to advance the development of next-generation therapies for obesity and type 2 diabetes across eight programs.
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Dollar sign in light bulb on yellow background
Endocrine/metabolic

Grant supports Ahead Therapeutics’ platform for type 1 diabetes

Jan. 30, 2026
No Comments
Ahead Therapeutics SL has been awarded an Industry Discovery and Development Partnership (IDDP) grant from Breakthrough T1D to support progression of the company’s proprietary Mimi-Top (mimicking tolerogenic particles) platform.
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Purple-tinted test tubes and dropper
Endocrine/metabolic

Insilico Medicine nominates ISM-0676 as preclinical candidate

Jan. 30, 2026
No Comments
Insilico Medicine Cayman Topco has nominated ISM-0676 as a preclinical candidate targeting the glucose-dependent insulinotropic polypeptide receptor (GIPR).
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Art concept for gene therapy

Regenxbio wrestling holds on MPS I, II gene therapy trials

Jan. 28, 2026
By Randy Osborne
No Comments
With the PDUFA date fast approaching for Regenxbio Inc.’s gene therapy RGX-121, the U.S. FDA placed the drug on clinical hold along with another, RGX-111, after preliminary analysis of a single case of neoplasm (specifically, an intraventricular central nervous system tumor) in a participant treated in the phase I/II study with the latter treatment.
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Endocrine/metabolic

Di’ao Group Chengdu Pharmaceutical identifies GLP-1R agonists

Jan. 28, 2026
Di’ao Group Chengdu Pharmaceutical Co. Ltd. has synthesized glucagon-like peptide-1 receptor (GLP-1R) agonists. They are reported to be useful for the treatment of hypertension, diabetes type 1, cerebral infarction, metabolic dysfunction-associated steatohepatitis (MASH; NASH), metabolic syndrome, obesity, arteriosclerosis and Parkinson’s disease, among others.
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Endocrine/metabolic

MGAT2 inhibitors divulged in Evopoint Biosciences patent

Jan. 28, 2026
Evopoint Biosciences Co. Ltd. has patented 2-acylglycerol O-acyltransferase 2 (MGAT2, MOGAT2) inhibitors. They are described as potentially useful for the treatment of obesity, metabolic syndrome, hyperlipidemia, hypertriglyceridemia, diabetes and arteriosclerosis.
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Man measuring waist
Endocrine/metabolic

Tetrapharm advances TPC-026 for chronic use in obesity

Jan. 28, 2026
No Comments
Tetrapharm (Tetra Pharm Technologies ApS) has announced promising preclinical data for TPC-026 for the chronic treatment and long-term management of metabolic disorders, including obesity. The preclinical findings support TPC-026 as a differentiated therapeutic candidate, designed to address underlying disease mechanisms, rather than symptoms alone.
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Endocrine/metabolic

Novo Nordisk patents new GLP-1R agonists

Jan. 27, 2026
Novo Nordisk A/S has disclosed GLP-1 polypeptide analogues acting as glucagon-like peptide-1 receptor (GLP-1R) agonists. As such, they are reported to be useful for the treatment of obesity and diabetes.
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Art concept for liver damage, such as fatty liver, fibrosis or cirrhosis
Drug design, drug delivery & technologies

In vivo CAR T cells reduce liver fibrosis

Jan. 27, 2026
By Mar de Miguel
No Comments
Liver fibrosis in the course of metabolic dysfunction-associated steatohepatitis (MASH) could be significantly reduced using CAR T-cells generated in vivo. Scientists at the Icahn School of Medicine at Mount Sinai have developed an experimental cell therapy that eliminates only one type of liver cell, the stellate cells that express fibroblast activation protein alpha (FAP). This strategy not only reduced fibrosis but also reversed liver damage.
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