CLINICAL TRIALS PROFILE FOR FINAFLOXACIN
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All Clinical Trials for finafloxacin
Trial ID | Title | Status | Sponsor | Phase | Start Date | Summary |
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NCT00483158 ↗ | First Time in Man Study of Finafloxacin Hydrochloride | Completed | MerLion Pharmaceuticals GmbH | Phase 1 | 2007-08-01 | The purpose of this study is to study the safety of single doses and multiple doses of Finafloxacin hydrochloride in healthy volunteers. The level of Finafloxacin hydrochloride will be measured in the subjects blood and urine. One part of the study will assess if Finafloxacin hydrochloride eradicates Helicobacter pylori, a stomach bacteria. Another part of the study will assess the activity of the drug in urine. |
NCT00722735 ↗ | Finafloxacin 300 mg Twice a Day (b.i.d.) Versus Ciprofloxacin 250 mg Twice a Day (b.i.d) in Patients With Lower Uncomplicated UTI (uUTI) | Completed | MerLion Pharmaceuticals GmbH | Phase 2 | 2008-10-01 | To compare the bacteriological eradication rates of Finafloxacin and Ciprofloxacin in female patients with uUTI. |
NCT00723502 ↗ | Efficacy and Safety Study of Finafloxacin Used in Helicobacter Pylori Infected Patients | Completed | MerLion Pharmaceuticals GmbH | Phase 2 | 2008-09-01 | The primary objective of this study is to compare the H. pylori eradication rates with Finafloxacin in combination with Amoxicillin or Esomeprazole. The secondary objective is to evaluate and compare the safety and tolerability of multiple oral doses of Finafloxacin plus Amoxicillin versus Finafloxacin plus Esomeprazole. |
>Trial ID | >Title | >Status | >Sponsor | >Phase | >Start Date | >Summary |
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