Alzheimer's disease Latrepirdine attracted renewed interest in 2009 after being shown in small preclinical trials to have positive effects on persons suffering from
Alzheimer's disease. Animal studies showing potential beneficial effects on Alzheimer's disease models were shown in Russian research in 2000. Preliminary results from human trials have also been promising. In an initial six-month phase II trial, results have shown significant improvement over placebo at 12 months. Latrepirdine showed promising results in a phase III-equivalent, double-blind trial in Russia with mild–moderate stage patients. In April 2009, Pfizer and Medivation initiated a phase III trial (CONCERT study) aiming for FDA approval. In March 2010, Pfizer announced that this clinical trial failed to show any benefit for the treatment of Alzheimer's disease patients. In July 2009, Pfizer and Medivation announced that "latrepirdine" was to be the proposed
international nonproprietary name for latrepirdine for the treatment of Alzheimer's. In March 2010, the results of a clinical trial phase III were released; the investigational Alzheimer's disease drug dimebon failed in the pivotal CONNECTION trial of patients with mild-to-moderate disease. Pfizer had paid $225 million after bidding against several pharmaceutical companies to purchase the rights to Dimebon. With CONCERT, the remaining Pfizer and Medivation Phase III trial for latrepirdine in Alzheimer's disease failed in 2012, effectively ending the development in this indication. Latrepirdine thus failed to alter the existing
pharmacologic management of Alzheimer's disease.
Huntington's disease In April 2011, latrepirdine failed in a phase III clinical trial of patients affected with Huntington's disease. The trial was sponsored by Medivation Inc. and
Pfizer. == Pharmacology ==