Bayer Receives FDA Priority Review For Investigational Anti-Cancer Compound Copanlisib (for specialized target groups only)

Regulatory submission based on data from the Phase II CHRONOS-1 study, in which copanlisib showed objective response rate of 59% and a manageable safety profile in patients with follicular lymphoma (FL) / Copanlisib is an intravenous pan-class I phosphatidylinositol-3-kinase (PI3K) inhibitor with predominant activity against PI3K-α and PI3K-δ isoforms / Copanlisib granted Fast Track and Orphan Drug Designation in the U.S. for FL
Source: Bayer Company News - Category: Pharmaceuticals Source Type: news