Positive Results for Recorlev in Phase 3 Cushing's Syndrome Trial

Recorlev (levoketoconazole) is a cortisol synthesis inhibitor
Recorlev (levoketoconazole) is a cortisol synthesis inhibitor

Strongbridge Biopharma announced top-line results from the ongoing Phase 3 SONICS trial evaluating Recorlev (levoketoconazole), a cortisol synthesis inhibitor, for the treatment of endogenous Cushing's syndrome (CS). 

Results from this single-arm, open-label study found that 30% of patients achieved normalization of mean urinary free cortisol (UFC) after 6 months of maintenance treatment with levoketoconazole, without a dose increase (P<.25). The treatment was also associated with statistically significant and clinically meaningful improvements from baseline in fasting blood glucose, hemoglobin A1C, total cholesterol, low density lipoprotein (LDL)-cholesterol, body weight and body mass index (P<.0001 for each), all key secondary endpoints. A total of 12 patients (12.8%) discontinued the trial due to adverse events. Treatment-emergent adverse events included nausea (32%), headache (28%), peripheral edema (19%), hypertension (17%), and fatigue (16%), diarrhea (15%) and increased alanine aminotransferase (ALT; 15%) .

"The robust effect of Recorlev in normalizing or decreasing UFC levels was complemented by key secondary endpoint data showing significant improvements in multiple markers for cardiovascular risk,” said Maria Fleseriu, MD, FACE, professor of Neurological Surgery and Medicine, and director of the Oregon Health Sciences University Northwest Pituitary Center. “SONICS efficacy and safety results, including a low frequency (3.2%) of significant ALT elevations (more than 5 times above the upper limit of normal) without clinical sequelae and fully reversible, positions Recorlev, if approved, to play an important role in individualized medical therapy for Cushing's syndrome, including consideration as a first-line treatment.”  

Based on these findings, the Company plans on seeking accelerated approval of Recorlev with the Food and Drug Administration.

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