A Safety and Efficacy Study of Intravenous E5564 in Patients With Severe Sepsis

Completed · Phase 2

Conditions studied: Sepsis, Shock, Septic, Sepsis Syndrome, Septicemia, Infection

In brief

Sepsis is a serious condition where there is inflammation and damage to body tissue, usually caused by an infection. This infection can lead to decreased function of vital body organs and in some cases may lead to permanent health problems or death. Much of the injury is due to endotoxin, a harmful substance produced by certain types of bacteria. An endotoxin antagonist is designed to block the effects of endotoxin. This study is designed to study the safety and efficacy when treating patients with severe sepsis.

Key facts

Study ID

NCT00046072

Run by

Eisai Inc.

People needed

300

Starts

2001-10-01

Expected to finish

2005-04-01

Last updated by the study team

2005-12-12

Who can join

Age: 18 and older, up to 85. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Presently admitted, or about to be transferred, to the ICU.
• Women of Child-bearing potential must have a negative serum (or urine) hCG assay within 24 hours prior to drug administration.
• Any Race.
• Severe Sepsis [newly developed respiratory failure, refractory shock, renal dysfunction, hepatic dysfunction, or metabolic acidosis and at least three signs of SIRS (systematic inflammatory response syndrome)].
• Objective signs of infection likely to be caused by a bacterial or fungal pathogen.
• Patients must receive study medication within 8 to 12 hours of recognition of the initial sepsis-related organ failure.
• APACHE Predicted risk of mortality score between 20% and 80%.
• An intent by physicians and family to aggressively treat the patient for the 28 day study period.

You may not qualify if…

• Cardiogenic or hypovolemic shock.
• Acute third degree burns involving >20% of body surface.
• Recipients of non-autologous organ transplants within the past year.
• Pregnancy.
• Chronic vegetative state.
• Uncontrolled serious hemorrhage (.2 units of blood/platelets in the previous 24 hours). Patients may be considered for enrollment if bleeding has stopped and patients are still otherwise qualified.
• Unwilling or unable to be fully evaluated for all follow-up visits.
• Patients who are classified as "Do not resusitate" or "Do not treat."
• Patients who develop severe sepsis <36 hours post trauma or post-surgery. Patients may be considered for enrollment >36 hours post-trauma or post-surgery, if they meet other inclusion criteria.
• Patients with a predicted risk of mortality score of <20% or >80% after recognition of qualifying organ failure.
• Patients with a predicted risk of mortality of <51% for whom Xigris® use is planned.

Where it is running

• Study site — Mobile, Alabama, United States
• Study site — San Diego, California, United States
• Study site — Santa Barbara, California, United States
• Study site — Jacksonville, Florida, United States
• Study site — Miami, Florida, United States
• Study site — Pensacola, Florida, United States
• Study site — Columbus, Georgia, United States
• Study site — Elk Grove, Illinois, United States
• Study site — Kansas City, Kansas, United States
• Study site — Boston, Massachusetts, United States
• Study site — Springfield, Massachusetts, United States
• Study site — Buffalo, New York, United States
• Study site — Manhasset, New York, United States
• Study site — Oklahoma City, Oklahoma, United States
• Study site — Dallas, Texas, United States
• Study site — Galveston, Texas, United States
• Study site — San Antonio, Texas, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.