Table 1.
Phase | Intervention | Primaryoutcomes | Size | Duration | |
---|---|---|---|---|---|
Active immunisation | |||||
NCT00498602 | Phase II | ACC-001+QS21 vs ACC-001 vs placebo | Safety, tolerability | 228 | Nov, 2007, to March, 2012 |
NCT00411580 | Phase I | CAD106 | Safety, tolerability | 60 | June, 2005, to April, 2008 |
NCT00464334 | Phase I | V950 | Safety | 70 | April, 2007, to Sept, 2011 |
Passive immunisation | |||||
NCT00575055 | Phase III | Bapineuzumab | Cognitive, functional | 800 | Dec, 2007, to Dec, 2010 |
NCT00329082 | Phase II | LY2062430 | Safety, tolerability | 25 | May, 2006, to May, 2008 |
NCT00299988 | Phase II | Intravenous immunoglobulin | ADAS-cog,ADAS-CGIC | 24 | Start Feb, 2006; ongoing but recruitment complete |
NCT00455000 | Phase I | PF-04360365 | Safety, tolerability, pharmacokinetics | 36 | March, 2007, to June, 2008 |
NCT00531804 | Phase I | R1450 | Adverse events, laboratory measures, vital signs | 80 | Dec, 2006, to Jan, 2009 |
ADAS-cog/CGIC=Alzheimer’s disease assessment score cognitive scale/clinician’s global impression of change.