By Robert King
The Senate passed a $1.9 trillion COVID-19 package that temporarily boosts ACA subsidies and gives more money to rural hospitals but doesn't include several priorities for hospitals.
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By Angus Liu
Moderna has recruited a new chief legal officer with a decade of Big Pharma experience as its COVID-19 vaccine rollout kicks into gear. Shannon Thyme Klinger, the Novartis chief legal officer who stepped in after the Swiss pharma's Michael Cohen scandal, will become Moderna’s legal mastermind on June 1.
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By Conor Hale
One year into the pandemic, the FDA has authorized its first molecular COVID-19 diagnostic that can be performed completely at home and purchased without a prescription.
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By Ben Adams
Johnson & Johnson recently nabbed an emergency use authorization from the FDA for its single-shot COVID-19 vaccine, but today it said its trials for the shot had largely been done virtually through IQVIA.
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By Robert King
Trinity Health posted net earnings of $2.7 billion for the second half of 2020 as the system was able to weather major declines in net patient service revenue caused by COVID-19.
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By Nick Paul Taylor
A phase 3 clinical trial of CytoDyn’s leronlimab in COVID-19 patients has missed its primary and all major secondary endpoints. However, CytoDyn zeroed in on a subgroup of patients and performed an “age adjustment” analysis to hail the study as evidence of the efficaciousness of leronlimab.
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By Kevin Dunleavy
Matica, a subsidiary of South Korea-based CHA Biotech, will carry the hopes of the parent company to establish a CDMO business in the United States. One thing's for sure: Between the burgeoning gene therapy pipeline and the surge of pandemic vaccines, there will be demand for its viral vectors.
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By Kevin Dunleavy,Fraiser Kansteiner,Eric Sagonowsky,Angus Liu,Conor Hale
Russia is promoting its coronavirus vaccine Sputnik V, while also mounting a campaign to undermine confidence in Western vaccines. Merck got a positive bit of good news in testing for a COVID-19 drug. Amid poor results for its COVID-19 drug, CytoDyn found hope by focusing on a subgroup.
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By Nick Paul Taylor
Seres Therapeutics has stopped enrollment in a metastatic melanoma clinical trial and deprioritized the drug. The microbiome specialist attributed the actions to slow enrollment during the pandemic and the progress of its preclinical oncology pipeline.
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