The effect of EA-230 on the immuneresponse

Phase 1

• Conditions: Systemic inflammatory respons (SIRS) and associated acute kidney injury (AKI); Therapeutic area: Body processes [G] - Immune system processes [G12]

• Registration Number: EUCTR2014-002481-78-NL
• Lead Sponsor: Exponential Biotherapies Inc

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2014-09-30
• Last Update Posted: 30 November 2020

Recruitment & Eligibility

• Status: ot Recruiting
• Sex: Male
• Target Recruitment: 60

Inclusion Criteria

1.Written informed consent to participate in this trial prior to any study-mandated procedure.
2.Subjects aged 18 to 35 years inclusive, for part 2 only male subjects will be included.
3.Subjects and their partners have to agree to use a reliable way of contraception from study entry until 3 months after study drug administration.
4.BMI between 18 and 30 kg/m², with a lower limit of body weight of 50 kg
5.Healthy as determined by medical history, physical examination, vital signs, 12 lead electrocardiogram, and clinical laboratory parameters
6.Negative results for hard drug use from urine drug screen at screening
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range 60
F.1.3 Elderly (>=65 years) no
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

1.Unwillingness to abstain from any medication, recreational drugs or anti-oxidant vitamin supplements during the course of the study and within 7 days prior to study Day 1.
2.Unwillingness to abstain from nicotine, or alcohol or within 1 day prior to study Day 1
3.Previous participation in a trial where LPS was administered
4.Surgery or trauma with significant blood loss or blood donation within 3 months prior to studyDay 1
5.History, signs or symptoms of cardiovascular disease, in particular:
•History of frequent vaso-vagal collapse or of orthostatic hypotension
•Resting pulse rate =45 or =100 beats / min
•Hypertension (RR systolic >160 or RR diastolic >90)
•Hypotension (RR systolic <100 or RR diastolic <50)
•conduction abnormalities on the ECG consisting of a 1st degree atrioventricular block or a complex bundle branch block
6.Renal impairment: plasma creatinine >120 µmol/L
7.Liver function tests (alkaline phosphatase, AST, ALT and/or ?-GT) above 2x the upper limit of normal

Study & Design

• Study Type: Interventional clinical trial of medicinal product
• Study Design: Not specified