Namenda neuropathic pain trial
Executive Summary
Forest will initiate a new Phase II trial of Namenda (memantine) for neuropathic pain, with a possible NDA submission by 2006. A previous Phase III study failed to show overall statistical significance in primary endpoint of nocturnal pain, although there was improvement in weekly assessments. Namenda was approved for treatment of moderate to severe Alzheimer's disease Oct. 16 (1"The Pink Sheet" Oct. 20, 2003, p. 3)...
You may also be interested in...
Forest Namenda Clears FDA; Alzheimer Drug Shipments To Begin In December
Forest is planning a slow roll-out of Namenda (memantine) after a faster-than-expected approval of the Alzheimer's agent
Boehringer Ingelheim Overtakes Bayer As Germany’s Biggest Pharma Company
The privately owned company is searching for a successor to Jardiance, while the outcome of US Inflation Reduction Act talks on price cuts to the blockbuster will be revealed in September.
Synthekine Joins Quest To Tame IL-2 In Cancer Therapies
First clinical data from Synthekine’s IL-2 candidate and that ofrivalsMedicennawere presented at the AACR, suggesting there’s life in the modality yet.