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BioWorld - Thursday, March 19, 2026
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Home » Topics » BioWorld Science, Endocrine/metabolic

BioWorld Science, Endocrine/metabolic
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Endocrine/metabolic

Aché Laboratórios Farmacêuticos describes new SGLT-1, SGLT-2 and DPP4 inhibitors

Dec. 22, 2025
Aché Laboratórios Farmacêuticos SA has identified compounds acting as sodium/glucose cotransporter 1 (SGLT-1), SGLT-2 and dipeptidyl peptidase 4 (DPP4; CD26) inhibitors reported to be useful for the treatment of cardiovascular, renal and metabolic diseases.
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Feet and scale
Endocrine/metabolic

Enveda’s ENV-308 advances into clinic for obesity

Dec. 22, 2025
No Comments
Enveda has obtained IND clearance from the FDA and commenced dosing in a phase I study of ENV-308, a once-daily oral therapy designed for chronic weight management.
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Cardiovascular

Rona Therapeutics seeks clinical trial clearance for RN-5681

Dec. 18, 2025
No Comments
Rona Therapeutics Co. Ltd. has announced the submission of RN-5681 to the Australian Human Research Ethics Committee (HREC), and anticipates dosing to begin in a phase I trial in the first quarter of next year.
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Concept art for blood sugar.
Endocrine/metabolic

Confo Therapeutics selects CFTX-2034 as development candidate

Dec. 18, 2025
No Comments
Confo Therapeutics NV has nominated CFTX-2034 as a development candidate to treat conditions linked to hyperinsulinemic hypoglycemia, specifically post-bariatric hypoglycemia (PBH). The company is now advancing CFTX-2034 through IND-enabling studies.
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Tape measure wrapped around scale
Endocrine/metabolic

Sanegenebio’s SGB-7342 cleared to enter clinic for obesity

Dec. 17, 2025
No Comments
Sanegenebio has obtained clinical trial clearance in China for SGB-7342, an siRNA medicine targeting inhibin β E (INHBE) for the treatment of obesity. A phase I trial is scheduled to begin early next year.
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Missing puzzle piece and broken DNA chain
Endocrine/metabolic

Immusoft’s ISP-002 designated US orphan drug for MPS II

Dec. 16, 2025
No Comments
Immusoft of CA Inc., a wholly owned subsidiary of Immusoft Corp., has announced that the FDA has granted orphan drug designation to ISP-002, the company’s investigational engineered B-cell therapy for the treatment of mucopolysaccharidosis type II (MPS II), also known as Hunter syndrome.
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Neutrophils in the bloodstream
Endocrine/metabolic

Neutrophils put the brakes on fat loss

Dec. 16, 2025
By Coia Dulsat
No Comments
Fat tissue balances energy by storing lipids during times of abundance and mobilizing them when needed, yet sustained metabolic stress demands mechanisms that limit excessive lipid loss. Researchers at the University of California San Diego (UCSD) report that stress-induced fat breakdown triggers a neutrophil response in visceral adipose tissue that feeds back to restrain lipolysis and preserve lipid reserves.
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Illustration of transfer RNA (tRNA)
Drug design, drug delivery & technologies

Alltrna advances tRNA-based strategy for stop codon diseases

Dec. 15, 2025
By Mar de Miguel
No Comments
Gene editing can repair mutations that prematurely halt protein synthesis, resulting in incomplete peptides that cause various diseases. However, other approaches achieve the same effect without altering the genome. Startup Alltrna Inc. has developed a strategy based on transfer RNA (tRNA) to bypass the premature stop codons that end early protein translation. The company already has a first clinical candidate that could treat metabolic diseases such as methylmalonemia (MMA) or phenylketonuria (PKU).
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Endocrine/metabolic

Hansoh discovers new GIPR, GCGR and GLP-1R agonists

Dec. 12, 2025
Jiangsu Hansoh Pharmaceutical Group Co. Ltd. and Shanghai Hansoh Biomedical Co. Ltd. have described compounds acting as gastric inhibitory polypeptide receptor (GIPR), glucagon receptor (GCGR) and glucagon-like peptide-1 receptor (GLP-1R) agonists reported to be useful for the treatment of metabolic dysfunction-associated steatotic liver disease (MASLD, NAFLD), diabetes and obesity.
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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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