Statistical Analysis Plan (SAP): A randomised, double-dummy, triple-blind, active placebo-controlled, parallel groups trial of LSD microdosing in patients with major depressive disorder (LSDDEP2)
The SAP specifies that analyses will assess the efficacy and safety of LSD (MB-22001) versus active placebo (caffeine), covering primary, secondary, and safety endpoints. No results are reported.
Abstract
The analyses described in this SAP will assess the efficacy and safety of LSD (MB-22001) in comparison with active placebo (caffeine). The analysis described cover those for the primary, secondary and safety endpoints described in the Protocol.