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pharmaphorum
12d
Are timely access and robust safety mutually exclusive?
They found that the FDA approved 85 (95%) of the drugs before the EMA, with the latter clocking up a median delay of 241 (150-370) days. But while the figures may sound stark, they come as no ...
Targeted Oncology
4d
FDA Approves Axatilimab for Chronic GVHD in New Vial Sizes
Axatilimab has gained FDA approval in 9 mg and 22 mg vials, expanding treatment options for patients with chronic GVHD after ...
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