A Study in Sepsis Patients With Renal Failure

Phase 2

Terminated

• Conditions: Sepsis; Bacterial Infections and Mycoses
• Interventions: Drug: BIAP; Drug: Placebo

• Registration Number: NCT00511186
• Lead Sponsor: AM-Pharma

Brief Summary

The purpose of this study is to investigate the safety and tolerability of AP in sepsis patients with renal failure and to investigate the effect of AP on inflammatory and clinical parameters in sepsis patients with renal failure.

Detailed Description

RATIONALE FOR THE STUDY

A previous clinical study conducted in centers in The Netherlands and Belgium have shown a substantial clinical benefit of AP treatment in patients with sepsis and associated acute renal failure (see Introduction above). The latter results require confirmation in a prospective study, as the current subject of this Protocol.

Choice of Drugs

The proposed study medication (AP) is identical to the study medication used in the previous clinical study in sepsis patients with single or multiple end-organ failure. Since there is no current proven treatment for these patients, the controls (as in previous studies) is placebo.

Choice of patient population

The aim is to enroll a maximum of 26 patients positive for sepsis with an APACHE score of ≥20 and ≤28 (determined within 24 hours of entry), and who will be analyzed on an intention to treat (ITT) basis.

Study Timeline

• Study First Submitted: 2007-08-02
• Study First Submitted QC: 2007-08-02
• Study First Posted: 2007-08-03
• Study Start: 2008-05
• Primary Completion: 2009-12
• Study Completion: 2009-12
• Status Verified: 2012-03
• Last Update Submitted: 2012-03-30
• Last Update Posted: 2012-04-02

Recruitment & Eligibility

• Status: TERMINATED
• Sex: All
• Target Recruitment: 36

Inclusion Criteria

• Patients between the age of 18 and 80 years.

• Proven or suspected infection.

• Two out of four SIRS criteria of systemic inflammation, existing for less than 24 hours after admission in the intensive care unit, as follows:

  • Core temperature higher then 38 degree Celsius or lower then 36 degree Celsius.
  • Heart rate above 90 beats/min (unless the patient has a medical condition known to increase heart rate or is receiving treatment that would prevent tachycardia).
  • Respiratory rate above 20 breaths/min, a PaCO2 lower then 32mmHg or the use of mechanical ventilation for an acute respiratory process.
  • White-cell count above 12,000/mm3 or below 4,000/mm3 or a differential count showing >10 percent immature neutrophils.

• Acute renal failure, defined as

  • Rise in serum creatinine level to ≥150μmol/L within the previous 48 hours, in the absence of primary underlying renal disease OR
  • Minimally a stage 1 Kidney Injury according to AKIN creatinine criteria: Increase in serum creatinine ≥26.2µmol/L (0.3mg/dL) or increase to ≥150% (≥1.5 -fold) from baseline in the previous 48 hours in the absence of primary underlying renal disease and where baseline creatinine is less than 150 µmol/L) OR
  • Minimally a stage 1 Kidney Injury according to AKIN Urine Output criteria: Urine Output of ≤ 0.5mg/kg/h for ≥6h and following adequate fluid resuscitation when applicable, in the absence of underlying primary renal disease and where baseline creatinine is less than 150µmol/L)

• Written informed consent obtained prior to any study intervention.

Exclusion Criteria

• Pregnant women or nursing mothers and fecund females who are not on effective contraception (chemical: pill; or mechanical: IUD)
• Patients already on dialysis (RTT) at entry
• Known HIV (sero-positive) patients
• Patients receiving immunosuppressant therapy or on chronic high doses of steroids equivalent to prednisone 1mg/Kg/day
• Patients expected to have rapidly fatal disease within 24 hours
• Known confirmed gram-positive sepsis
• Known confirmed fungal sepsis
• Acute pancreatitis with no established source of infection
• Patients not expected to survive for 28 days due to other medical conditions such as end-stage neoplasm or other diseases
• Participation in another investigational study within 90 days prior to start of the study which might interfere with this study
• Any previous administration of active study medication.
• Known allergy for dairy (bovine) products including cow milk.
• Sepsis without renal failure as defined in the Entry Criteria.
• History of chronic renal failure or history of persistent creatinine level equal or greater than 150umol/L prior to entry for reasons other than the current sepsis condition".

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Bovine Intestinal AP	BIAP	Bovine Intestinal Alkaline Phosphatase (BIAP) Intravenous administration of 10" bolus (67,5U/kg) and 48h continuous infusion (132,5U/kg)
2	Placebo	Placebo Intravenous administration of 10" bolus and 48h continuous infusion

Primary Outcome Measures

Name	Time	Method
Haematology, biochemistry, and microbiological evaluation. Adverse event monitoring.	28 Days

Secondary Outcome Measures

Name	Time	Method
To investigate the effect of AP on inflammatory parameters in sepsis patients with renal failure.	28 Days
To investigate the effect of AP on clinical variables in sepsis patients with renal failure.	28 Days
To investigate the effect of AP on renal function markers in sepsis patients with renal failure.	28 Days

Trial Locations

Locations (9)

ULB Hopital Erasme; 🇧🇪 Brussels, Belgium

Jeroen Bosch Ziekenhuis lokatie GZG; 🇳🇱 's-Hertogenbosch, Netherlands

Canisius Wilhelmina Ziekenhuis; 🇳🇱 Nijmegen, Netherlands

VU University Medical Center; 🇳🇱 Amsterdam, Netherlands

University Medical Center Antwerp (UZA); 🇧🇪 Antwerp, Belgium

Universitair Ziekenhuis Brussel; 🇧🇪 Brussels, Belgium

Cliniques Universitaires Saint Luc-UCL; 🇧🇪 Brussels, Belgium

UMC Nijmegen University Medical Center St Radboud; 🇳🇱 Nijmegen, Gelderland, Netherlands

Isala Clinics; 🇳🇱 Zwolle, Overijssel, Netherlands