Shionogi Announces Positive Top-Line Results For Cefiderocol Pivotal cUTI Clinical Trial

Shionogi & Co., Ltd. has announced that cefiderocol (S-649266), a novel siderophore cephalosporin in late-stage development, met the FDA pre-specified primary endpoint for non-inferiority vs imipenem/cilastatin (IPM/CS) in patients with serious complicated urinary tract infection (cUTI) with Gram-negative bacteria. Cefiderocol was superior to IPM/CS at test of cure (TOC).

The study APEKs-cUTI* enrolled 452 patients with cUTI. The median duration of treatment was nine days for both cefiderocol and IPM/CS for all populations. Cefiderocol met the FDA primary efficacy endpoint of composite of clinical cure and microbiologic eradication at test of cure (TOC) in 72.6 percent of patients (n=252) which was superior to IPM/CS at 54.6 percent (n=119), a weighted difference of 18.58 percent (95 percent CI: 8.23, 28.92).

“We are very excited about the results of this trial. Unlike most studies, this cUTI study was designed to include patients that are more difficult to treat.  The data clearly demonstrate that cefiderocol will be an important option for serious Gram-negative infections,” said Dr. Tsutae Den Nagata, Chief Medical Officer.

Cefiderocol was well tolerated in the study, with 40 percent of patients experiencing an adverse event in the cefiderocol arm vs 50 percent of patients in the IPM/CS arm. Serious adverse events (SAEs) occurred in 14 patients (4.7 percent) who received cefiderocol and 12 patients (8.1 percent) who received IPM/CS. Shionogi plans to submit an NDA for cefiderocol to the FDA in 2017. The data from the APEKs-cUTI* clinical study are planned to be presented in early 2017.