Myovant Sciences Announces 97% Response Rate in Positive Phase 3 HERO Study of Once-Daily, Oral Relugolix in Men with Advanced Prostate Cancer
[caption id="attachment_9277" align="aligncenter" width="747"] Press Release[/caption]
- Primary efficacy endpoint met with 96.7% of men achieving sustained testosterone suppression to castrate levels (< 50 ng/dL) through 48 weeks
- Achieved all six key secondary endpoints, including superiority to leuprolide acetate on rapid suppression of testosterone and prostate-specific antigen (PSA), all with p-values < 0.0001
- New Drug Application (NDA) submission expected in the second quarter of 2020
- Conference call and webcast to be held today at?8:30 a.m. EST?/?5:30 a.m. PST