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Study Comparing Tigecycline to Imipenem/Cilastatin in Complicated Intra-Abdominal Infections in Hospitalized Subjects
This study has been completed.
Sponsored by: Wyeth
Information provided by: Wyeth
ClinicalTrials.gov Identifier: NCT00081744
  Purpose

Purpose: To provide a mechanism for the emergency use of tigecycline in the appropriate clinical situations.


Condition Intervention Phase
Gram-Positive Bacterial Infections
Cross Infection
Drug: Tigecycline
Phase III

MedlinePlus related topics: Bacterial Infections
Drug Information available for: Tigecycline Cilastatin Cilastatin sodium Imipenem
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Randomized, Double-Blind, Safety/Efficacy Study
Official Title: A Multicenter, Double-Blind, Randomized Comparison Study Of the Efficacy and Safety of Tigecycline to Imipenem/ Cilastatin to Treat Complicated Intra-Abdominal Infections in Hospitalized Subjects
  Eligibility

Ages Eligible for Study:   8 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Male or female subjects, ≥ 8 years of age and a weight of ≥ 35 kilograms
  • Subjects with selected culture-positive infections caused by a multiple antibiotic-resistant pathogen presumed to be susceptible to tigecycline
  • Subjects who have failed or are intolerant of other available appropriate antibiotic therapies or whose pathogens are resistant to other available antibiotics

Exclusion Criteria:

  • Subjects who are moribund with an expected survival of less than 2 weeks.
  • Subjects who have been designated as “Do Not Resuscitate”, unless it is anticipated within a reasonable degree of medical certainty that they can achieve benefit from potentially curative antibiotic therapy
  • Known or suspected hypersensitivity to tigecycline, tetracyclines, or other compounds related to this class of antibacterial agents
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00081744

Sponsors and Collaborators
Wyeth
Investigators
Study Director: Medical Monitor, MD Wyeth
  More Information

Publications of Results:
Study ID Numbers: 3074A1-301
Study First Received: April 19, 2004
Last Updated: May 17, 2006
ClinicalTrials.gov Identifier: NCT00081744  
Health Authority: United States: Food and Drug Administration

Keywords provided by Wyeth:
Bacterial Infections

Study placed in the following topic categories:
Bacterial Infections
Gram-Positive Bacterial Infections
Tigecycline
Cilastatin
Cross Infection
Imipenem

Additional relevant MeSH terms:
Anti-Infective Agents
Anti-Bacterial Agents
Communicable Diseases
Therapeutic Uses
Infection
Pharmacologic Actions

ClinicalTrials.gov processed this record on January 16, 2009