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

Eisai

Status and phase

Completed

Phase 2

Conditions

Sepsis Syndrome

Infection

Shock, Septic

Septicemia

Sepsis

Treatments

Drug: E5564

Study type

Interventional

Funder types

Industry

Identifiers

NCT00046072

E5564-A001-201

Details and patient eligibility

About

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.

Sex

All

Ages

18 to 85 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

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.

Exclusion criteria

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.