By Barbara Obstoj-Cardwell. Editor
Negative research news last week included France’s Genfit adding to the list of failures in non-alcoholic steatohepatitis (NASH) last week with Phase III data on its elafibranor. On a positive note, US firm MyoKardia posted promising results from a Phase III study of its mavacamten for the treatment of hypertrophic cardiomyopathy. Regulatory developments included a setback for US biotech bluebird bio and its partner Bristol-Myers Squibb with the US Food and Drug Administration refusing to review their Biologic License Application for their CAR-T therapy immune-oncology drug lisocabtagene maraleucel. Elsewhere, US biotech Novavax last week announced additional funding of $384 million from the CEPI to advance development of its COVID-19 vaccine candidate NVX-CoV2373.
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