Teva, Mylan and Novartis’ Sandoz have announced significant steps to meet the “urgent demand” for off-patent hydroxychloroquine sulfate as a potential treatment option for the global COVID-19 pandemic, as the White House directed the US Food and Drug Administration to expedite testing and possible broader use of the drug alongside another anti-malarial drug, chloroquine phosphate.
Sandoz, Teva And Mylan Step Up On Hydroxychloroquine
As White House And FDA Ramp Up Coronavirus Research
To meet expected demand in the weeks and months ahead, Novartis' Sandoz has committed to donate up to 130 million doses of generic hydroxychloroquine – a treatment for malaria currently under investigation as a therapy to aid in the COVID-19 pandemic – while Teva and Mylan have also made strides, as the generics industry continues to play its part in tackling the coronavirus outbreak.

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Meitheal Pharmaceuticals said that its generic version of the GLP-1 agonist Victoza would be one of 22 planned launches during 2025, as the firm continues to build out its portfolio with the aid of its parent, Hong Kong King-Friend Industrial.
A UK High Court justice came down on the side of Glenmark in AstraZeneca’s bid to enjoin the firm from launching a generic version of its Forxiga blockbuster before judgment is delivered in the firms’ patent-litigation clash.