- Trials with a EudraCT protocol (22)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
22 result(s) found for: moxifloxacin hydrochloride.
Displaying page 1 of 2.
| EudraCT Number: 2010-018628-14 | Sponsor Protocol Number: DRUG10_MOXI | Start Date*: 2010-03-11 |
| Sponsor Name:University Ghent | ||
| Full Title: Pharmacokinetic evaluation of moxifloxacin administered intravenously and orally in healthy volunteers who have had a gastric bypass. | ||
| Medical condition: Healthy volunteers who have had a gastric bypass at least 6 months ago | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2010-021574-11 | Sponsor Protocol Number: 32729463CAP2001 | Start Date*: 2011-01-24 | |||||||||||
| Sponsor Name:Furiex Pharmaceuticals, Inc | |||||||||||||
| Full Title: A Randomized, Controlled, Double-Blind, Multicenter, Phase 2 Study of the Safety/Tolerability and Efficacy of JNJ-32729463 Compared With Moxifloxacin for the Treatment of Subjects Requiring Hospita... | |||||||||||||
| Medical condition: Community-Acquired Bacterial Pneumonia (CABP) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) HU (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-022150-16 | Sponsor Protocol Number: Moxifloxacin Sepsis PEG | Start Date*: 2011-01-27 |
| Sponsor Name:Medizinische Universität Wien, Univ.Klinik f.klinische Pharmakologie | ||
| Full Title: Determination of Moxifloxacin concentrations in interstitial space fluid of muscle and subcutis in septic patients including a pilot phase | ||
| Medical condition: To evaluate feasibility of Moxifloxacin determination in septic patients | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2009-017319-13 | Sponsor Protocol Number: C-09-033 | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:Alcon Research Ltd. | |||||||||||||
| Full Title: Safety and Efficacy Evaluation of Topical Moxidex Otic Solution in the Treatment of Acute Otitis Media with Otorrhea in Tympanostomy Tubes | |||||||||||||
| Medical condition: Acute otitis media with otorrhea in tympanostomy tubes | |||||||||||||
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Ongoing) BE (Completed) FI (Prematurely Ended) DK (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-003453-13 | Sponsor Protocol Number: CE01-301 | Start Date*: 2014-06-18 | |||||||||||
| Sponsor Name:Cempra Pharmaceuticals, Inc. | |||||||||||||
| Full Title: A Randomized, Double-Blind, Multi-Center Study to Evaluate the Efficacy and Safety of Intravenous to Oral Solithromycin (CEM-101) Compared to Intravenous to Oral Moxifloxacin in the Treatment of Ad... | |||||||||||||
| Medical condition: Community-Acquired Bacterial Pneumonia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) BG (Completed) LV (Completed) DE (Completed) ES (Completed) RO (Completed) SK (Completed) NL (Completed) SI (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-000640-26 | Sponsor Protocol Number: C-05-36 | Start Date*: 2018-04-05 | |||||||||||
| Sponsor Name:Alcon Research Ltd | |||||||||||||
| Full Title: Safety and Efficacy Evaluation of Topical Moxidex Otic Solution Compared to Moxifloxacin Solution in the Treatment of Acute Otitis Media with Otorrhea through Tympanostomy Tubes (AOMT) | |||||||||||||
| Medical condition: acute otitis media | |||||||||||||
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-000643-37 | Sponsor Protocol Number: C-09-033 | Start Date*: 2018-04-05 | |||||||||||
| Sponsor Name:Alcon Research Ltd | |||||||||||||
| Full Title: Safety and Efficacy Evaluation of Topical Moxidex Otic Solution in the Treatment of Acute Otitis Media with Otorrhea in Tympanostomy Tubes | |||||||||||||
| Medical condition: Acute Otitis Media | |||||||||||||
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-004851-37 | Sponsor Protocol Number: RTDATAUC | Start Date*: 2007-12-28 | |||||||||||
| Sponsor Name:Freistaat Bayern, vertreten durch die Universität Regensburg, Klinikum | |||||||||||||
| Full Title: Doppelblinde, randomisierte, prospektive multizentrische klinische Studie zur Definition der optimalen antibiotischen Therapiedauer bei Patienten mit unkomplizierter akuter Cholangitis: Moxifloxaci... | |||||||||||||
| Medical condition: Acute uncomplicated cholangitis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-015578-37 | Sponsor Protocol Number: BAY12-8039/11643 | Start Date*: 2010-05-10 | |||||||||||
| Sponsor Name:Bayer HealthCare AG | |||||||||||||
| Full Title: A randomized, double-blind, multicenter trial to evaluate the safety and efficacy of sequential (intravenous, oral) moxifloxacin versus comparator in pediatric subjects with complicated intraabdomi... | |||||||||||||
| Medical condition: Complicated intra-abdominal infections (cIAI) | |||||||||||||
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) ES (Prematurely Ended) LV (Completed) LT (Completed) CZ (Completed) BE (Prematurely Ended) HU (Completed) BG (Completed) GR (Completed) Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-000641-39 | Sponsor Protocol Number: C-05-37 | Start Date*: 2018-04-05 | |||||||||||
| Sponsor Name:Alcon Research Ltd | |||||||||||||
| Full Title: Safety and Efficacy Evaluation of Topical Moxidex Otic Solution in the Treatment of Acute Otitis Externa (AOE) | |||||||||||||
| Medical condition: Acute Otitis externa | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-002729-39 | Sponsor Protocol Number: C-07-40 | Start Date*: 2017-11-07 | |||||||||||
| Sponsor Name:Alcon Research Ltd | |||||||||||||
| Full Title: An Evaluation of the Safety and Efficacy of Moxifloxacin AF Ophthalmic Solution 0.5% for the Treatment of Bacterial Conjunctivitis in the USA | |||||||||||||
| Medical condition: Bacterial conjunctivitis | |||||||||||||
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-002730-23 | Sponsor Protocol Number: C-04-38 | Start Date*: 2017-11-07 | |||||||||||
| Sponsor Name:Alcon Research Ltd | |||||||||||||
| Full Title: An Evaluation of the Safety and Efficacy of Moxifloxacin AF Ophthalmic Solution 0.5% for the Treatment of Bacterial Conjunctivitis in the USA | |||||||||||||
| Medical condition: Bacterial conjunctivitis | |||||||||||||
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-003026-14 | Sponsor Protocol Number: ML-3341-306 | Start Date*: 2016-02-04 | |||||||||||
| Sponsor Name:Melinta Therapeutics, Inc. | |||||||||||||
| Full Title: A PHASE 3, MULTICENTER, RANDOMIZED, DOUBLE-BLIND, COMPARATOR-CONTROLLED STUDY TO EVALUATE THE SAFETY AND EFFICACY OF INTRAVENOUS TO ORAL DELAFLOXACIN IN ADULT SUBJECTS WITH COMMUNITY-ACQUIRED BACTE... | |||||||||||||
| Medical condition: Community-Acquired Bacterial Pneumonia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) ES (Completed) LV (Completed) BG (Completed) DE (Completed) SI (Completed) PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-004071-13 | Sponsor Protocol Number: PTK0796-CABP-1200 | Start Date*: 2015-05-20 | |||||||||||
| Sponsor Name:Paratek Pharma LLC | |||||||||||||
| Full Title: A Phase 3 Randomized, Double-Blind, Multi-Center Study to Compare the Safety and Efficacy of Omadacycline IV/PO to Moxifloxacin IV/PO for Treating Adult Subjects with Community-Acquired Bacterial P... | |||||||||||||
| Medical condition: Community-Acquired Bacterial Pneumonia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SK (Completed) HU (Completed) CZ (Completed) LV (Completed) DE (Completed) ES (Completed) BE (Completed) PL (Prematurely Ended) GR (Completed) HR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-002501-11 | Sponsor Protocol Number: BIO-CAP_2015 | Start Date*: 2016-04-01 | |||||||||||
| Sponsor Name:Nordsjællands Hospital | |||||||||||||
| Full Title: Biomarker guided antibiotic treatment in Community-Acquired Pneumoni (BIO-CAP) | |||||||||||||
| Medical condition: community acquired pneumonia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-005169-63 | Sponsor Protocol Number: NAB-BC-3781-3101 | Start Date*: 2016-01-12 | |||||||||||
| Sponsor Name:Nabriva Therapeutics AG | |||||||||||||
| Full Title: A Phase 3, Randomized, Double-Blind, Double-Dummy Study to Compare the Efficacy and Safety of Lefamulin (BC 3781) Versus Moxifloxacin (With or Without Adjunctive Linezolid) in Adults With Community... | |||||||||||||
| Medical condition: Community-Acquired Bacterial Pneumonia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Completed) HU (Completed) LV (Completed) PL (Completed) BG (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-010810-31 | Sponsor Protocol Number: AEPOC-ATB | Start Date*: 2010-02-24 |
| Sponsor Name:Fundació Clínic per a la Recerca Biomèdica | ||
| Full Title: UTILIDAD DEL TRATAMIENTO ANTIBIÓTICO EN LAS AGUDIZACIONES DE LA ENFERMEDAD PULMONAR OBSTRUCTIVA CRONICA (EPOC) SIN PURULENCIA EN EL ESPUTO: ENSAYO CLINICO, ALEATORIZADO, CONTROLADO Y DOBLE CIEGO DE... | ||
| Medical condition: agudización EPOC | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2019-000404-15 | Sponsor Protocol Number: 34666 | Start Date*: 2019-04-29 | |||||||||||
| Sponsor Name:Thomas Benfield | |||||||||||||
| Full Title: Shortened Antibiotic Treatment in Community-Acquired Pneumonia: A Nationwide Danish Randomized Controlled Trial | |||||||||||||
| Medical condition: Community-acquired pneumonia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-001024-34 | Sponsor Protocol Number: OraPAT-IE-GAMES | Start Date*: 2021-12-15 | |||||||||||
| Sponsor Name:Fundació Clínic per a la Recerca Biomèdica | |||||||||||||
| Full Title: Oral antimicrobial treatment vs. outpatient parenteral for infective endocarditis. | |||||||||||||
| Medical condition: infective endocarditis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-001246-26 | Sponsor Protocol Number: W-4873-201 | Start Date*: 2016-10-07 | |||||||||||
| Sponsor Name:Wockhardt Bio AG | |||||||||||||
| Full Title: A Phase II, Randomized, Double-Blind, Multicenter, Comparative Study to Determine the Safety, Tolerability, Pharmacokinetics and Efficacy of Oral Nafithromycin Versus Oral Moxifloxacin in the Treat... | |||||||||||||
| Medical condition: Community-Acquired Bacterial Pneumonia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: LV (Completed) BG (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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