The FDA on 27 May approved Actavis' and Patheon Pharmaceuticals' Viberzi (eluxadoline) and Valeant's and its subsidiary Salix's Xifaxan (rifaximin) to treat adults with irritable bowel syndrome with diarrhea (IBS-D).
The FDA on 27 May approved Actavis' and Patheon Pharmaceuticals' Viberzi (eluxadoline) and Valeant's and its subsidiary Salix's Xifaxan (rifaximin) to treat adults with irritable bowel syndrome with diarrhea (IBS-D).
As many as 35 million adult Americans may have IBS, with 40% of those experiencing the subtype with diarrhea symptoms,...
The CEO of South Korean biotech shares how his company was able to reach a partnership with Rani so quickly and why it is confident in its GLP-1/GLP-2 dual agonist for obesity and diabetes, despite recent disappointing clinical results for its sole rival.
Chinese firm Sciwind has revealed additional Phase III findings for its promising once-weekly GLP-1 agonist ecnoglutide, just one asset in a burgeoning Chinese sector that could see the emergence of new rivals to current global leaders in obesity and diabetes.
2030 sales forecasts for Novo’s obesity hope are an order of magnitude larger than its closest rival among 2025’s expected debutantes.
GLP-1 receptor agonists could play a big role in tackling neurodegeneration and a new academic study has raised expectations of Novo Nordisk’s latest semaglutide Phase III results
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Pipelines in bioconjugates continue to develop, from ADCs to XDCs, with radionuclide drug conjugates (RDCs) and antibody-oligonucleotide conjugates (AOCs) leading the expansion.
Interim results from the Phase III REMARK study presented at WCLC showed the Chinese company’s second-generation ALK/ROS1 inhibitor met its primary endpoint as a first-line therapy in ALK-positive advanced NSCLC.
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