2 results
Approved WMORecruitment stopped
To determine the safety and efficacy of Dimebon in patients with mild to moderate Huntington Disease
Approved WMORecruitment stopped
To evaluate the long-term safety and tolerability of Dimebon in AD patients who have successfully completed 26 weeks of blinded treatment in the CONNECTION Study (DIM14) (hereafter referred to as *CONNECTION*).