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.
Full Title of Study: “An Open-Label, Randomized, Multicenter, Two-Arms Efficacy and Safety Study of 14 Days Treatment With Finafloxacin 400 mg b.i.d. Plus Amoxicillin 1000 mg b.i.d.Versus Finafloxacin 400 mg b.i.d. Plus Esomeprazole 40 mg b.i.d. in Patients With Helicobacter Pylori Infection”
- Study Type: Interventional
- Study Design
- Allocation: Randomized
- Intervention Model: Parallel Assignment
- Primary Purpose: Treatment
- Masking: None (Open Label)
- Study Primary Completion Date: April 2009
- Drug: Finafloxacin + Amoxicillin
- Finafloxacin, tablets, 400 mg b.i.d. (8 X 50 mg tablets), oral administration; Amoxicillin, tablet 1000 mg b.i.d. (1 X 1000 mg tablet), oral administration
- Drug: Finafloxacin + Esomeprazole
- Finafloxacin, tablets, 400 mg b.i.d. (8 X 50 mg tablets), oral administration; Esomeprazole, tablet, 40 mg b.i.d. (1 X 40 mg tablet), oral administration
Arms, Groups and Cohorts
- Experimental: 1
- Experimental: 2
Clinical Trial Outcome Measures
- Eradication of Helicobacter pylori
- Time Frame: 14 days
Participating in This Clinical Trial
1. Male or female patients of 18 to 70 years old, with dyspepsia or dyspeptic symptoms.
2. The patient must understand the nature of the study and must provide written informed consent.
3. Each patient must be able to communicate with study personnel.
4. Gastroscopic confirmation of H. pylori infection by Rapid Urease Test.
5. Positive Urea Breath Test.
6. Absence of blood in stools.
1. Gastroscopic confirmation of gastric ulcers.
2. History of Zollinger-Ellison syndrome.
3. Gastroesophageal Reflux Disease (GERD).
4. Subtotal gastrectomy or vagotomy in medical history.
5. Pyloric stenosis.
6. Previous H. pylori eradication therapy.
7. Patients likely to need to take one of the following medication within two weeks prior to and during the study period:
- any other antibiotic than the study medication;
- any other proton-pump inhibitor than the study medication;
- NSAIDs including aspirin and glucocorticoids;
8. Patients taking antacids and/or H2-blockers during the study period.
9. Patients taking bismuth compound within four weeks prior to and during the study period.
10. Patients with psychiatric, neurological, or behavioral disorders that may interfere with the conduct or interpretation of the study.
11. Patients with severe concomitant disease of the cardiovascular, pulmonic, hepatic, renal, hematological, lymphatic, metabolic, and endocrine system.
12. Clinically significant serious unstable physical illness: treated, controlled and thus stable hypertension is not considered an exclusion criterion.
13. Patients with known uncontrolled hypertension or symptomatic hypotension.
14. Patients who are immunocompromised.
15. Patients with malignant disease of any kind except Basalioma.
16. Patients showing clinically significant abnormal vital signs.
17. Patients with clinically significant abnormal ECG findings.
18. Clinically significant abnormal laboratory data at Screening, or any abnormal laboratory value that could interfere with the assessment of safety.
19. Exposure to any investigational drug within 30 days prior Screening.
20. Known hypersensitivity or contraindication to the use of fluoroquinolones.
21. Prior participation in Finafloxacin study.
22. Pregnant or nursing woman, or woman of childbearing potential who is not using an effective contraceptive method during the study, e.g. oral (stable doses for at least three months prior to Screening) or injectable (stable doses for at least two months prior to Screening) contraceptives, implantation of levonorgestrel system and intrauterine devices (for at least two months prior Screening), barrier methods (combination of diaphragm and spermicide or condom and spermicide).
23. Current diagnosis or known history of substance abuse.
24. Site personnel and their immediate families, defined as their spouse, parent, child, grandparent, or grandchild.
25. Reasonable likelihood for non-compliance with the protocol or any other reason that, in the investigator's opinion, prohibits the inclusion of the patient into the study.
Gender Eligibility: All
Minimum Age: 18 Years
Maximum Age: 70 Years
Are Healthy Volunteers Accepted: No
- Lead Sponsor
- MerLion Pharmaceuticals GmbH
- Provider of Information About this Clinical Study
- Prof. Dr. P. Malfertheiner, Director, Hospiltal for Gastroenterology and Hepatology
- Overall Official(s)
- Peter Malfertheiner, MD, Director, Principal Investigator, Not affiliated
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