Merck's HCV Strategy Might Be: Get To Market, Then Improve Incrementally

Labeling for intravenous drug users with hepatitis C might be an important niche indication while Merck gets triple combination NDA ready.

Merck & Co. Inc. is nearing approval of its two-drug direct-acting antiviral combo for hepatitis C heading into the American Association for the Study of Liver Disease conference, but its commercial strategy seems already to be looking past the so-called "doublet" to several therapeutic improvements that a triple-combination therapy in Phase II could offer.

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Antabio’s next-generation, broad-spectrum antibacterial, MEM-ANT3310, has made it onto the European Medicines Agency’s priority medicines scheme. The company says its product is designed to make a significant impact on the growing problem of antimicrobial resistance.

New Carbon Monitoring Initiative Could Help Future Proof Clinical Research

 

A new European initiative will help trial sponsors better understand whether digitization and decentralized clinical trials of drugs generate less carbon than traditional methods.

Major Analysis To Help MHRA Fill Gaps In UK Clinical Trials Landscape

 
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A first-of-its-kind review of clinical trial applications submitted to the UK medicines regulator, the MHRA, shows there is a concentration of research in certain disease areas and identifies opportunities to enhance the representation of specific patient groups.