Re: GENR SPA Primary endpoint and statistical threshold:
>>However, I find it odd that they don't mention the visual acuity standards or the statistical significance that the FDA is looking for when they agreed to the SPA.<<
GENR’s PR says the primary endpoint is visual acuity (VA) at one year (even though the duration of the trials is two years). This was also the case in the Macugen phase-3 trials.
The specific VA endpoint is almost certainly the same one used in the Macugen trials: avoidance of a loss of 3+ lines relative to baseline on the standard eye chart.
The statistical threshold specified in the SPA is presumably p<0.05 in each of the two phase-3 trials using the Hochberg correction to adjust for the fact that GENR is testing two doses (20mg and 40mg).
Applying the Hochberg correction means that each of the phase-3 trials will be considered statistically significant if: