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BioWorld - Monday, December 15, 2025
Home » Topics » Drugs » Peptide

Peptide
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EMA investigating potential semaglutide link to eye disease

Jan. 17, 2025
By Nuala Moran
The EMA has started a review of Novo Nordisk A/S’ GLP-1 receptor agonist, semaglutide, after the Danish regulatory agency raised the possibility it causes an increased risk of suffering from an acute eye condition. After the first report in July 2024, the Danish regulator had received, by Dec. 10, 2024, a total of 19 reports of non-arteric anterior ischemic neuropathy, a rare condition that affects the small blood vessels at the front of the optic nerve. This can lead on to sudden vision loss and visual field defects.
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Targets with arrows

Biotech Showcase: GLP-1s and the search beyond obesity

Jan. 15, 2025
By Lee Landenberger
Can the market justify the hundreds of GLP-1 developers that are working to eventually reach the market? When the dust settles, Minji Kim, CEO of Cross Border Partners and Advisory Service, told attendees at the Biotech Showcase in San Francisco, only a few leading companies will end up dominating the field.
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Close-up of injector pen in hands

Amid booming market, US FDA advises on obesity drug development

Jan. 8, 2025
By Mari Serebrov
With obesity drugs taking the U.S. and global markets by storm and more than 100 clinical programs currently in progress for the drugs, the U.S. FDA released a draft guidance Jan. 7 to help sponsors develop drugs and biologics for weight reduction and long-term maintenance of body weight.
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Purple-tinted test tubes and dropper
Endocrine/metabolic

Amylyx and Gubra collaborate to develop long-acting GLP-1 receptor antagonist

Dec. 31, 2024
Amylyx Pharmaceuticals Inc. and Gubra A/S have established a collaboration for the development of a novel long-acting GLP-1 receptor antagonist.
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CRL for Zealand Pharma's glepaglutide; Novo’s Cagrisema disappoints

Dec. 20, 2024
By Nuala Moran
Shares in Zealand Pharma A/S (CO:ZEAL) dropped 22.4% to as low as DKK587 (US$82.16) on Dec. 20, after the U.S. FDA issued a complete response letter (CRL) for glepaglutide in the treatment of short bowel syndrome.
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Ozempic pen and packaging

Danish regulators question possible Ozempic link to rare eye condition

Dec. 17, 2024
By Nuala Moran
The Danish Medicines Agency is to ask the EMA’s pharmacovigilance committee to investigate a potential increased risk of an acute eye condition in diabetic patients being treated with the glucagon-like peptide-1 receptor agonist Ozempic (semaglutide).
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Man measuring waist
Endocrine/metabolic

Peptidream’s oral myostatin inhibitors show lean body mass preservation in obesity model

Dec. 13, 2024
Peptidream Inc. has released promising results from preclinical testing of its oral myostatin inhibitors, administered in combination with semaglutide, in a mouse model of obesity.
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3D rendering conceptualizing theranostics
Diagnostics

Peptidream announces new peptide radiopharmaceutical development candidate targeting CLDN12.8

Dec. 13, 2024
Peptidream Inc. has announced a new peptide radiopharmaceutical development candidate, PD-29875, a novel first-in-class highly selective macrocyclic peptide-radioisotope conjugate against Claudin 18.2 (CLDN18.2).
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European Commission clears Novo’s Catalent buy

Dec. 6, 2024
The European Commission approved Novo Holding A/S’ acquisition of Catalent Inc., a global contract development and manufacturing organization expected to help Novo Nordisk A/S keep up with increasing demand for its GLP-1 drug, Wegovy (semaglutide).
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Acinetobacter baumannii
Infection

Peptide P92 targets A. baumannii OmpA, reducing pathogenicity and exhibiting antibacterial activity

Dec. 5, 2024
Researchers from the Fourth Military Medical University (Air Force Medical University) have identified novel antimicrobial molecules.
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