Market ExpansionThe market opportunity for CD388 continues to strengthen, with the expanded patient population bringing the addressable target population from ~50 million to over ~100 million in the U.S. alone.
Regulatory ApprovalsThe FDA has guided that if successful, a single trial of CD388 will be sufficient for a BLA submission.
Strategic PartnershipsCidara Therapeutics announced that it received an award valued up to $339M from the Biomedical Advanced Research and Development Authority (BARDA), which validates both the clinical utility and strategic importance of CD388.