By Barbara Obstoj-Cardwell. Editor
Last week saw Gilead Sciences’ chief executive outline pricing for developed countries for its remdesivir in the treatment of COVID-19, and the US Food and Drug Administration issue new clinical guidelines for drugmakers developing vaccines for the novel coronavirus. Heron Therapeutics had a major disappointment last Monday, when the FDA issued a complete response letter (CRL) regarding its post-operative pain candidate HTX-011. Intercept Pharmaceuticals also received a CRL the same day for its non-alcoholic steatohepatitis (NASH) candidate. There was better news for Akero Therapeutics, which presented encouraging new data on its NASH candidate AKR-001.
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