- Trials with a EudraCT protocol (336)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
336 result(s) found for: Drug culture.
Displaying page 6 of 17.
EudraCT Number: 2016-005161-31 | Sponsor Protocol Number: AT-201 | Start Date*: 2017-07-04 | ||||||||||||||||
Sponsor Name:Allecra Therapeutics SAS | ||||||||||||||||||
Full Title: Randomized, Double-Blind, Multi-Center Study of Cefepime/AAI101 in Hospitalized Adults With Complicated Urinary Tract Infections, Including Acute Pyelonephritis | ||||||||||||||||||
Medical condition: Complicated urinary tract infections including acute pyelonephritis | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: HU (Completed) PL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2006-006215-68 | Sponsor Protocol Number: CMA-0631-PR-0010 | Start Date*: 2008-07-29 | ||||||||||||||||
Sponsor Name:Chiesi Farmaceutici S.p.A | ||||||||||||||||||
Full Title: A MULTICENTRE,MULTINATIONAL, OPEN-LABEL, RANDOMISED, PARALLEL GROUP CLINICAL TRIAL OF TOBRINEB®/ACTITOB®/ BRAMITOB® (TOBRAMYCIN SOLUTION FOR NEBULISATION, 300 MG TWICE DAILY IN 4 ML UNIT DOSE VIALS... | ||||||||||||||||||
Medical condition: cystic fibrosis and P. aeruginosa chronic infection | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: CZ (Completed) HU (Completed) ES (Completed) DE (Completed) FR (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-004868-35 | Sponsor Protocol Number: AT-301 | Start Date*: 2018-08-23 | ||||||||||||||||
Sponsor Name:Allecra Therapeutics SAS | ||||||||||||||||||
Full Title: A Phase 3, Randomized, Double-Blind, Multi-Center Study to Evaluate the Efficacy, Safety, and Tolerability of Cefepime- AAI101 Compared to Piperacillin/Tazobactam in the Treatment of Complicated Ur... | ||||||||||||||||||
Medical condition: Complicated urinary tract infections including acute pyelonephritis | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: LT (Completed) LV (Completed) ES (Completed) BG (Completed) SK (Completed) PL (Completed) HU (Completed) HR (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-003773-34 | Sponsor Protocol Number: IT001-303 | Start Date*: 2018-11-23 |
Sponsor Name:Iterum Therapeutics International Limited | ||
Full Title: A prospective Phase 3, double-blind, multicenter, randomized study of the efficacy and safety of sulopenem followed by sulopenem etzadroxil with probenecid versus ertapenem followed by ciprofloxaci... | ||
Medical condition: Complicated intra-abdominal infection | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: LV (Completed) HU (Completed) BG (Completed) CZ (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-004911-35 | Sponsor Protocol Number: MK-0991-043 | Start Date*: 2015-04-03 |
Sponsor Name:Merck & Co., Inc. | ||
Full Title: A Multicenter, Open-Label, Noncomparative Study to Evaluate the Safety, Tolerability, and Efficacy of Caspofungin Acetate in Children with Documented Candida or Aspergillus Infections | ||
Medical condition: Candida and Aspergillus infections | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2016-000371-24 | Sponsor Protocol Number: DOBO-01-16 | Start Date*: 2016-05-24 |
Sponsor Name:Laboratorios Ordesa | ||
Full Title: Multicenter pilot study for comparison of the efficacy of vaginal capsules with boric acid and L. gasseri and L. rhamnosus versus other vaginal drugs, in patients with bacterial or candida Vulvovag... | ||
Medical condition: Bacterial or candidiasic vulvovaginitis | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2007-004660-47 | Sponsor Protocol Number: BCX1812-203 | Start Date*: 2007-11-20 |
Sponsor Name:BioCryst Pharmaceuticals Inc | ||
Full Title: A Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Virologic Activity, Safety, and Pharmacodynamics of Intravenous Peramivir for the Treatment of Experimental Influenza | ||
Medical condition: Treatment of experimental influenza | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2013-005483-25 | Sponsor Protocol Number: SMT19969/C003 | Start Date*: 2014-10-08 | |||||||||||
Sponsor Name:Summit (Oxford) Limited | |||||||||||||
Full Title: A Phase II, Randomized, Open-Label, Active-Controlled Clinical Study to Investigate the Safety and Efficacy of SMT19969 (200 mg BID) for 10 days Compared with Fidaxomicin (200 mg BID) for 10 days f... | |||||||||||||
Medical condition: Clostridium difficile infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-001530-40 | Sponsor Protocol Number: HEC WST06 1276N/WST 2.24 | Start Date*: 2006-07-18 | |||||||||||
Sponsor Name:STEBA FRANCE | |||||||||||||
Full Title: Vascular targeted photodynamic therapy using WST09 for patients with untreated localised prostate cancer - Repeat procedure – Phase IIa, Single centre, open-label study. | |||||||||||||
Medical condition: Localised Prostate Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000396-26 | Sponsor Protocol Number: EA-US-205-0111 | Start Date*: 2015-02-02 |
Sponsor Name:Gilead Sciences, Inc. | ||
Full Title: Expanded Access Program for Aztreonam Lysine for Inhalation in Patients with Cystic Fibrosis and Pseudomonas aeruginosa Airway Infection Who Have Limited Treatment Options and are at Risk for Disea... | ||
Medical condition: Adult and paediatric cystic fibrosis (CF) patients with pulmonary Pseudomonas aeruginosa (PA) infection. | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2005-005239-80 | Sponsor Protocol Number: 10007 | Start Date*: 2005-12-23 |
Sponsor Name:University Hospitals Leicester, Leicester General Hospital | ||
Full Title: Prospective study to assess the emergence of drug resistance to oseltamivir following treatment of acute influenza A among children | ||
Medical condition: Influenza A | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-000164-17 | Sponsor Protocol Number: tobra nasal CF pilot | Start Date*: 2008-08-13 |
Sponsor Name:University of Jena | ||
Full Title: Nasale Inhalation von Tobramycin mit dem Pari Sinus-Vernebler bei Patienten mit Mukoviszidose und Pseudomonasnachweis im Nasen-Nasennebenhöhlenbereich. Nasal inhalation of tobramycin by the Pari ... | ||
Medical condition: subjects with cystic fibrosis and pseudomonas aeruginosa colonization in the upper airways | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2018-002949-11 | Sponsor Protocol Number: 601-0014 | Start Date*: 2019-08-05 | |||||||||||
Sponsor Name:Pulmatrix, Inc. | |||||||||||||
Full Title: A Randomized, Double-Blind, Multi-Center, Placebo-Controlled Phase 2 Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of Itraconazole Administered as a Dry Powder for Inhalation (PU... | |||||||||||||
Medical condition: Asthma with Allergic Bronchopulmonary Aspergillosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Prematurely Ended) GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-004677-14 | Sponsor Protocol Number: DIABOLO | Start Date*: 2018-03-09 |
Sponsor Name:Erasmus MC | ||
Full Title: Dose IndividualizAtion of Beta-lactam and fluOroquinoLone AntiBiotics in ICU patients: to TDM or not to TDM and the effects on Outcome (DIABOLO-study) | ||
Medical condition: ICU patients with infection | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2012-004620-38 | Sponsor Protocol Number: 242-12-233 | Start Date*: 2019-01-14 |
Sponsor Name:Otsuka Pharmaceutical Development & Commercialization, Inc. | ||
Full Title: Phase 2, Open-label, Multiple-dose Trial to Assess the Safety, Tolerability, Pharmacokinetics, and Efficacy of Delamanid (OPC 67683) in Pediatric Multidrug-resistant Tuberculosis Patients on Therap... | ||
Medical condition: Pediatric patients with multidrug-resistant tuberculosis (MDR-TB) who are receiving an optimized background regimen (OBR) of antituberculosis drugs | ||
Disease: | ||
Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2008-008314-40 | Sponsor Protocol Number: BAYq3939/12429 | Start Date*: 2009-06-22 | |||||||||||
Sponsor Name:Bayer HealthCare AG | |||||||||||||
Full Title: Randomized, double-blind, placebo-controlled, multicenter study to evaluate the safety and efficacy of inhaled ciprofloxacin compared to placebo in subjects with cystic fibrosis | |||||||||||||
Medical condition: Cystic fibrosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) SE (Completed) GB (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-002020-33 | Sponsor Protocol Number: OZBS32.18194 | Start Date*: 2019-12-10 | |||||||||||
Sponsor Name:Erasmus University Medical Center | |||||||||||||
Full Title: Pentoxifylline dose optimization in neonatal sepsis. | |||||||||||||
Medical condition: Neonatal late onset sepsis | |||||||||||||
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Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) PL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-003721-25 | Sponsor Protocol Number: High-shortRP | Start Date*: 2020-02-03 | |||||||||||
Sponsor Name:Region Östergötland | |||||||||||||
Full Title: Randomized prospective phase II clinical trial investigating pharmacokinetics and safety aspects of higher doses of rifampicin and pyrazinamide in an shortened tuberculosis treatment compared to st... | |||||||||||||
Medical condition: Tuberculosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000561-31 | Sponsor Protocol Number: PM1331 | Start Date*: 2015-06-15 | |||||||||||
Sponsor Name:Polichem S.A. | |||||||||||||
Full Title: A MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PARALLEL, VEHICLE-CONTROLLED STUDY TO EVALUATE THE EFFICACY AND SAFETY OF P-3058 10% NAIL SOLUTION IN THE TREATMENT OF ONYCHOMYCOSIS | |||||||||||||
Medical condition: Mild to moderate distal subungual Onychomycosis caused by Dermatophytes | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) LV (Completed) BG (Completed) SE (Completed) DE (Completed) SK (Completed) BE (Completed) PL (Completed) CZ (Completed) LT (Completed) GR (Completed) IS (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-003487-36 | Sponsor Protocol Number: 1 | Start Date*: 2015-12-23 | |||||||||||
Sponsor Name:The Newcastle upon Tyne Hospitals NHS Foundation Trust | |||||||||||||
Full Title: Alternatives to prophylactic antibiotics for the treatment of recurrent urinary tract infection in women | |||||||||||||
Medical condition: Recurrent urinary tract infection in women | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
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