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Effect of Intrapulmonary Recombinant Human Activated Protein C (APC) on Coagulation and Inflammation After Lipopolysaccharide (LPS)

A

Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

Status

Completed

Conditions

Lipopolysaccharides
Pneumonia

Treatments

Drug: Saline (NaCl 0.9%)
Drug: Drotrecogin alpha
Drug: Endotoxin
Procedure: Blood sampling
Procedure: Bronchoscopy

Study type

Interventional

Funder types

Other

Identifiers

NCT00943267
CEMM-APC-01
MEC 08/188

Details and patient eligibility

About

Recombinant human Activated Protein C (rhAPC) has been shown to reduce the mortality of patients with severe sepsis. The biological effects of APC are pleiotropic, and can be roughly divided in anticoagulant and cytoprotective effects. Lung infection and inflammation are associated with reduced bronchoalveolar levels of endogenous APC. Recent evidence derived from animal studies indicates that local administration of rAPC into the lungs exerts local anti-inflammatory and anticoagulant effects. In this study we propose to study the potential of locally administered APC, within a lung subsegment, to inhibit lipopolysaccharide (LPS) induced lung inflammation and coagulation in humans.

Enrollment

52 estimated patients

Sex

Male

Ages

18 to 35 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Male, 18-35 years of age
  • No clinically significant findings during physical examination and hematological and biochemical screening
  • Normal spirometry and ECG
  • Able to communicate well with the investigator and to comply with the requirements of the study
  • No medication
  • Written informed consent
  • No smoking

Exclusion criteria

  • Known diseases
  • A history of smoking within the last six months, or regular consumption of greater than three units of alcohol per day
  • Administration of any investigational drug within 30 days of study initiation
  • Donation of blood within 60 days, or loss of greater than 400 ml of blood within 12 weeks of study initiation
  • History of enhanced bleeding tendency
  • History of heparin-induced thrombocytopenia
  • History of serious drug-related reactions, including hypersensitivity

Trial design

52 participants in 2 patient groups, including a placebo group

Activated protein C
Experimental group
Treatment:
Drug: Endotoxin
Procedure: Blood sampling
Drug: Drotrecogin alpha
Procedure: Bronchoscopy
Saline
Placebo Comparator group
Treatment:
Drug: Endotoxin
Procedure: Blood sampling
Drug: Saline (NaCl 0.9%)
Procedure: Bronchoscopy

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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