Table 1.
Drotrecogin alfa (activated) clinical trials
Study | Study type/patients or treatments included | Number of patients included | Study period | Reference |
EVAA | Dose-finding phase II | 131 | 1997 to 1998 | [10] |
PROWESS | Phase III | 1,690 | 1998 to 2000 | [11] |
ENHANCE | Open-label | 2,378 | 2001 to 2003 | [12] |
ADDRESS | Low risk for death | 2,640 | 2002 to 2004 | [13] |
RESOLVE | Sepsis in children | 477 | 2002 to 2005 | [24] |
XPRESS | Heparin + DrotAA | 1,927 | 2003 to 2005 | [14] |
ADDRESS, Efficacy and Safety of Drotrecogin alfa [activated] in Adult Severe Sepsis Patients at Low Risk of Death; DrotAA, drotrecogin alfa (activated); ENHANCE, Extended Evaluation of Recombinant Human Activated Protein C, drotrecogin alfa (activated); EVAA, [dose finding study]; PROWESS, Recombinant Human Activated Protein C Worldwide Evaluation in Severe Sepsis; RESOLVE, REsearching severe Sepsis and Organ dysfunction in children: a gLobal perspective; XPRESS, Xigris and Prophylactic Heparin Evaluation in Severe Sepsis.