FDA Panel Votes 9-3 Against Capricor’s Duchenne Heart Therapy Over Weak Evidence
Final decision due Aug. 22.
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Final decision due Aug. 22.
FDA review papers reveal encouraging Week 52 eGFR findings (+5.2 placebo-adjusted) for TRUTAKNA in primary IgA nephropathy patients.
Key reason: rapid shift to >90% AI revenue and exclusive position in high-power reliability testing for advanced chips.
Backlog hits $1.76B (4.5x book-to-bill), implying ~48% upside despite Q2 miss.