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Tifacogin for the Treatment of Patients with Severe Community-Acquired Pneumonia - Article


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Pneumonia


Clinical Trial: Tifacogin for the Treatment of Patients with Severe Community-Acquired Pneumonia

This study is currently recruiting patients.

Sponsored by: Chiron Corporation
Information provided by: Chiron Corporation

Purpose

The purpose of this study is to determine whether tifacogin is effective and safe in the treatment of patients with severe community-acquired pneumonia.

Condition Treatment or Intervention Phase
Pneumonia
 Drug: Tifacogin
Phase III

MedlinePlus related topics:  Pneumonia

Study Type: Interventional
Study Design: Treatment

Official Title: Tifacogin (recombinant tissue factor pathway inhibitor) for the Treatment of Patients with Severe Community-Acquired Pneumonia

Eligibility

Genders Eligible for Study:  Both

Criteria

Inclusion Criteria:

  • Diagnosis of community-acquired pneumonia supported by additional clincal, radiological, and microbiological evidence
  • Pneumonia of sufficient severity to require ICU admission and management

Exclusion Criteria:

  • Pregnancy
  • Weight over 150 kg
  • Patients at increased risk of bleeding
  • Treatment with drotrecogin alfa or anticipated need for drotrecogin alfa
  • Treatment with heparin or anticipated need for heparin

Location and Contact Information

Kathy Haenftling      510-923-3170    kathy_haenftling@chiron.com

Alabama
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Louisiana
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Maine
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Maryland
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Missouri
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Washington
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Australia, Australian Capital Territory
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Australia, Western Australia
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Belgium
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Belgium, Jette
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Brazil, BA
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Brazil, CE
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Brazil, RJ
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Brazil, RS
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Brazil, SC
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Brazil, Sao Paulo
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Canada, Alberta
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Canada, British Columbia
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Canada, Manitoba
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Canada, Ontario
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Canada, Quebec
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Chile
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France
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Germany
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New Zealand
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New Zealand, Auckland
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Peru
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South Africa
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Spain
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Spain, Barcelona
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United Kingdom
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More Information

Study ID Numbers:  TFP008
Record last reviewed:  February 2005
Last Updated:  February 23, 2005
Record first received:  June 4, 2004
ClinicalTrials.gov Identifier:  NCT00084071
Health Authority: United States: Food and Drug Administration
ClinicalTrials.gov processed this record on 2005-04-08


Source: ClinicalTrials.gov
Cache Date: April 9, 2005


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