CLINICAL TRIALS PROFILE FOR TYGACIL
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All Clinical Trials for Tygacil
| Trial ID | Title | Status | Sponsor | Phase | Start Date | Summary |
|---|---|---|---|---|---|---|
| NCT00481962 ↗ | Health Economic Assessment of Tygacil® in the Treatment of Secondary Peritonitis in Intensive Care Units (ICUs) | Completed | Wyeth is now a wholly owned subsidiary of Pfizer | 2006-02-01 | The main goals of the study are: Assessment of Tygacil's cost-effectiveness; Process cost analysis from a hospital perspective (including length of stay, treatment costs, side effect management costs, costs of monitoring, costs of diagnostic procedures, cost of care (TISS 10 score etc.); Efficacy of Tygacil under usual care conditions (cure rate). | |
| NCT00488345 ↗ | Study Evaluating the Pharmacokinetics (PK), Safety, and Tolerability of Tigecycline in Patients 8 to 11 Years of Age | Completed | Wyeth is now a wholly owned subsidiary of Pfizer | Phase 2 | 2007-12-01 | To determine the pharmacokinetic profile and to evaluate the safety and tolerability of ascending multiple doses of tigecycline in patients aged 8 to 11 years with selected serious infections; complicated intra-abdominal infections (cIAI), complicated skin and skin structure infections (cSSSI), or community-acquired pneumonia (CAP). |
| NCT00488488 ↗ | A Pharmacovigilance Evaluation And Assessment Of The Prescribing Practice For Tygacil In Usual Health Care Setting | Completed | Pfizer | 2006-11-01 | To assess the efficacy and safety of Tygacil in the usual German hospital setting. The main goals are: to assess the efficacy of Tygacil under usual care conditions (cure rate); to assess the main side effects observed in daily medical practice (Safety of Tygacil); to determine whether patients are optimally dosed with Tygacil (according to the label) and the proportion of patients receiving a monotherapy versus combination therapy; to observe the potential resistance development against Tygacil in Germany; to determine which antibiotic agents are chosen for a combination therapy with Tygacil; to determine to which antibiotic substance non-responders to Tygacil are switched; to assess the duration of the intravenous therapy with Tygacil and to determine whether and which patients receive an oral antibiotic substance after the therapy with Tygacil; to collect information on profile, comorbidities and characteristics of patients treated with Tygacil. | |
| NCT00600600 ↗ | Tigecycline for Treatment of Rapidly Growing Mycobacteria | Completed | Wyeth is now a wholly owned subsidiary of Pfizer | Phase 2 | 2002-04-01 | To determine the safety, tolerance, and efficacy of Tigecycline when given daily to patients with rapidly growing mycobacterial disease (especially M.abscessus). |
| NCT00600600 ↗ | Tigecycline for Treatment of Rapidly Growing Mycobacteria | Completed | The University of Texas Health Science Center at Tyler | Phase 2 | 2002-04-01 | To determine the safety, tolerance, and efficacy of Tigecycline when given daily to patients with rapidly growing mycobacterial disease (especially M.abscessus). |
| NCT00683332 ↗ | Post-Marketing Study Of The Safety Of Tygacil (Tigecycline) | Completed | Pfizer | 2007-04-01 | The purpose of this study is to collect post-marketing information on the safety of Tygacil in Filipino patients. | |
| NCT00827541 ↗ | Post-Authorization Study Evaluating Safety Of Tigecycline | Completed | Pfizer | 2008-08-01 | This is a study to evaluate the safety of tigecycline in patients with complicated intra-abdominal infections (cIAI) and complicated skin and soft tissue infections (cSSTI) under real practice in the usual hospital setting and patients' conditions, in order to assess the "real incidence" of adverse events related with tigecycline in these patients. | |
| >Trial ID | >Title | >Status | >Sponsor | >Phase | >Start Date | >Summary |
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