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A multi-centre, double-blind, parallel-group, randomized controlled study to investigate efficacy and safety of orally administered BI 425809 during a 12-week treatment period compared to placebo in patients with cognitive impairment due to

Project: Research

Project Details

StatusFinished
Effective start/end date08/6/1808/6/20

Funding

  • Boehringer Ingelheim Pharmaceutical: $14,064.00