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Novartis seeks accelerated FDA approval for pelabresib

诺华目前预计将在年底前与FDA讨论 pelabresib 可能获得加速批准一事,首席执行官瓦斯·纳拉西姆汉在周二的电话会上对投资者表示。

English original

Novartis now expects to speak with the FDA about a potential accelerated approval of pelabresib before the end of the year, CEO Vas Narasimhan told investors on a call Tuesday.

在周二的投资者电话会上

V
瓦斯·纳拉辛汉Novartis · 首席执行官

报道摘要

For that indication, Rytelo is dosed at 7.1 mg/kg administered as an intravenous infusion every four weeks. Thrombocytopenia and neutropenia are among some serious side effects tied to the drug that ...

fiercepharma.com

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