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Mashup Score: 6FDA approves KalVista's Ekterly for hereditary angioedema - 1 month(s) ago
The FDA has approved Ekterly (sebetralstat) as the first and only oral on-demand medication for acute attacks of hereditary angioedema (HAE).
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Mashup Score: 3Flu vaccine strategy on the line as new US leaders anticipated to take charge - Pharmaceutical Technology - 8 month(s) ago
Public health experts are anticipating a changing discourse following RFK Jr’s appointment as head of HHS.
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Mashup Score: 0PrEP therapies offer new hope in HIV preventive landscape as vaccine failures amass - Pharmaceutical Technology - 9 month(s) ago
The HIV vaccine space has seen dwindling research activity as drug manufacturers turn to PrEP therapies for preventive treatment.
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Mashup Score: 28Insulin pricing: could an e-commerce approach cut costs? - 11 month(s) ago
An e-commerce drug delivery approach could put a dent in upward spiraling insulin prices, but uptake challenges loom large.
Categories: General Medicine News, Hem/OncsTweet
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Mashup Score: 8NICE recommends BeiGene’s marginal zone lymphoma tablet - 1 year(s) ago
The UK NICE has recommended BeiGene’s Zanubrutinib for marginal zone lymphoma (MZL) for use on the National Health Service (NHS).
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Mashup Score: 0How NVIDIA grew with the healthcare market instead of pushing into it - Pharmaceutical Technology - 1 year(s) ago
As the use of AI soared across healthcare, NVIDIA fit the bill in providing the necessary technology – and its stock tells the same story.
Categories: General Medicine News, General HCPsTweet
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Mashup Score: 0Outrun Therapeutics announces launch with $10m seed funding - 1 year(s) ago
Outrun Therapeutics announced its launch with $10m seed funding to advance a protein stabilisation pipeline focused on E3 ligase inhibitors.
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Mashup Score: 33
There has been several developments in the KRAS inhibitor space, shaping the KRAS inhibitors of the future.
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Mashup Score: 2Norgine seeks approval for high-risk neuroblastoma treatment - 1 year(s) ago
Norgine has sought approval for eflornithine (DFMO) for the treatment of patients with high-risk neuroblastoma (HRNB).
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Mashup Score: 1Gilead's Biktarvy receives FDA expanded approval for HIV - 1 year(s) ago
Gilead Sciences has received FDA approval for an expanded indication for Biktarvy to treat HIV patients with M184V/I resistance mutations.
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FDA approves KalVista's Ekterly for #hereditary #angioedema: Ekterly’s efficacy was demonstrated through data from KalVista’s Phase III KONFIDENT clinical trial. https://t.co/SZ4i3pZ7rR https://t.co/rMees0J1r2