Adverse Event reporting information can be found in footer
Request a Meeting
Adapted from Boccon-Gibod L, et al. 2012
*In a long-term extension of a Phase 3 trial. Delay defined as time taken for 25% of patients considered to be at high-risk (with a baseline PSA ≥ 20 ng/ml) to experience PSA failure or death (TTP 25%).
TTP25% was significantly longer with FIRMAGON® than leuprorelin (514 vs. 303 days, p=0.001).
**As calculated using the Weibull estimate.
† The primary endpoint of the trial was suppression of testosterone to ≤ 0.5 ng/ml at all monthly measurements from day 28 to day 364
*High risk defined as patients with baseline PSA ≥20 ng/ml.1,2