TEVA TO INITIATE THIRD PHASE III TRIAL OF ORAL LAQUINIMOD FOR THE TREATMENT OF RELAPSING REMITTING MULTIPLE SCLEROSIS
The clinical trial protocol has been granted a Special Protocol Assessment agreement by the Food and Drug Administration
…The third Phase III laquinimod trial CONCERTO will evaluate two doses of the investigational product (0.6mg and 1.2mg) in approximately 1,800 patients for up to 24 months. The primary outcome measure will be confirmed disability progression as measured by the Expanded Disability Status Scale (EDSS).
Laquinimod may not be dead but, in all likelihood, it will remain a day late and a dollar short.
“The efficient-market hypothesis may be the foremost piece of B.S. ever promulgated in any area of human knowledge!”