Incyte Corporation is hoping that mixed Phase III data for Jakafi (ruxolitinib) in patients with severe COVID-19 will pass muster with the US Food and Drug Administration and lead to its availability under compassionate use. But the disease area it is attempting to tackle has been a difficult one.
The Wilmington, DE-based drug maker announced 18 March results from the placebo-controlled Phase III DEVENT trial comparing the JAK inhibitor...





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