Clinical trial

Study Evaluating the Pharmacokinetics of Tigecycline in Human Bone

NCT00376324 · Wyeth is now a wholly owned subsidiary of Pfizer, Industry · Completed

Key facts

NCT number NCT00376324
Title Study Evaluating the Pharmacokinetics of Tigecycline in Human Bone
Official title An Open-Label, Multiple-Dose Study of the Pharmacokinetics of Tigecycline in Human Bone
Lead sponsor Wyeth is now a wholly owned subsidiary of Pfizer, Industry
Status Completed
Phase Phase 1
Study type Interventional
Conditions Healthy Subjects
Intervention type Drug
Interventions Tigecycline
Enrollment 36
Start date Sep 1, 2006
Primary completion Oct 1, 2008
Completion Oct 1, 2008
First posted Sep 14, 2006
Last update posted Jul 10, 2009
Countries United States

At a glance

  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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