Novartis is securing global rights to a PTC Therapeutics Huntington's disease drug candidate that has encouraging Phase 2 data that will be discussed with the FDA to plan a pivotal study. Last year, Novartis discontinued its Huntington's program after safety issues emerged in Phase 2 testing.
In this new episode of the MedCity Pivot Podcast, Chief Medical Officer Jeff Jacques offers a window into companies' strategies for including GLP-1 drugs in their health benefits.
Philips is showcasing its partnerships and new products at RSNA 2024, including an expanded collaboration with AWS and a CT scanner that the company said uses up to 80% less radiation than traditional systems.
The FDA cited deficiencies in govorestat's application in galactosemia, a rare metabolic disease, Applied Therapeutics said. The biotech is still on track to submit a separate application for the drug in sorbitol dehydrogenase (SORD) deficiency, another rare disease that has no FDA-approved therapies.
Besides the impact to physician satisfaction, the cost of this administrative burden is staggering: Organizations spend $82.7 billion annually on documentation, coding, and other administrative tasks, straining both budgets and staff.
In this episode, we're joined by Dr. Tiffany Inglis, national medical director for women and children's health at Carelon Health, a subsidiary of Elevance Health. Inglis discusses a paper Elevance Health Public Policy Institute recently published about doulas.
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