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ADAPT trial update: NSAIDs in AD

 

The Alzheimer’s Disease Anti-Inflammatory Prevention Trial (ADAPT) was launched a decade ago to determine if an NSAID (naproxen 220 mg BID or celecoxib 200 mg BID) could delay the onset of AD (ADAPT Research Group et al. Alzheimers Dement 2009; 5: 93-104; free full text at www.ncbi.nlm.nih.gov/pmc/articles/PMC2866447/pdf/nihms185404.pdf). The trial was suspended in 2004 following the finding from the Adenoma Prevention with Celecoxib (APC) trial of an increased cardiovascular risk with celecoxib (Solomon et al. N Engl J Med 2005; 352: 1071-1080; free full text at www.nejm.org/doi/full/10.1056/NEJMoa050405).

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Indeed, data from ADAPT subsequently suggested an increased cardiovascular and cerebrovascular risk with celecoxib and naproxen (ADAPT Research Group. PLoS Clin Trials 2006; 1: e33; free full text at www.ncbi.nlm.nih.gov/pmc/articles/PMC1851724/pdf/pctr.0010033.pdf).

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Emerging MS therapies: update on injectable drugs

 

REPORT FROM THE 25TH CONGRESS OF THE EUROPEAN COMMITTEE FOR TREATMENT AND RESEARCH IN MULTIPLE SCLEROSIS (ECTRIMS) – AMSTERDAM, THE NETHERLANDS, OCTOBER 19-22, 2011 – Late-breaking sessions at ECTRIMS 2011 presented phase III data for two novel MS therapies administered by injection/infusion.

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CONFIRM – Second phase III trial results for BG-12

 

REPORT FROM THE 25TH CONGRESS OF THE EUROPEAN COMMITTEE FOR TREATMENT AND RESEARCH IN MULTIPLE SCLEROSIS (ECTRIMS) – AMSTERDAM, THE NETHERLANDS, OCTOBER 19-22, 2011 – Just days after ECTRIMS, top-line  results from the second of two phase III trials of BG-12 were announced in a press release (www.biogenidec.com/PRESS_RELEASE_DETAILS.aspx?ID=5981&ReqId=1621631) and in a webcast to investors (www.biogenidec.com/investors.aspx?ID=5494).

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No benefit with simvastatin add-on therapy in MS

 

The most recent results from the SIMCOMBIN trial of combined beta-interferon and simvastatin, an HMG CoA reductase inhibitor, indicate that there is no beneficial effect with add-on therapy (Sorensen et al. Lancet Neurol 2011; 10: 691-701).

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