- Trials with a EudraCT protocol (91)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
		
	   		
	   		    
                    
                   	
                   	    91 result(s) found for: Tazobactam.
                    
                
			
   			
		
		Displaying page 1 of 5.
	
	
	| EudraCT Number: 2016-000398-19 | Sponsor Protocol Number: AGO/2016/002 | Start Date*: 2016-03-08 | 
| Sponsor Name:Ghent University | ||
| Full Title: Pilot study: pharmacokinetics of beta-lactam antibiotics, piperacillin-tazobactam, ceftazidim and meropenem in blood and sputum of cystic fibrosis patients. | ||
| Medical condition: Cystic fibrosis | ||
| Disease: | ||
| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
| Trial protocol: BE (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2008-005131-15 | Sponsor Protocol Number: 2008/0828 | Start Date*: 2008-12-19 | |||||||||||
| Sponsor Name:CHRU de Lille | |||||||||||||
| Full Title: ETUDE DE LA PHARMACOCINETIQUE DE L’ASSOCIATION PIPERACILLINE – TAZOBACTAM EN UTILISATION INTRA-VEINEUSE CONTINUE CHEZ L’ENFANT NEUTROPENIQUE FEBRILE . | |||||||||||||
| Medical condition: febrile episodes in neutropenic patients | |||||||||||||
| 
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-003374-40 | Sponsor Protocol Number: 1-2016 | Start Date*: 2016-11-29 | 
| Sponsor Name:University of Tartu | ||
| Full Title: The effects of augmented renal clearance on the pharmacokinetic/pharmacodynamic profile of piperacillin/tazobactam in children and young adults with malignant or non-malignant haematological or onc... | ||
| Medical condition: The state of renal hyperfiltration during infection in children and young adults with malignant or non-malignant haematological or oncological diagnosis | ||
| Disease: | ||
| Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
| Trial protocol: EE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2015-002644-14 | Sponsor Protocol Number: | Start Date*: 2015-09-15 | |||||||||||
| Sponsor Name:Alder Hey Children's NHS Foundation Trust | |||||||||||||
| Full Title: POPPET Study - Pharmacokinetics of continuous administration of Piperacillin/Tazobactam to children using an elastomeric pump | |||||||||||||
| Medical condition: Febrile Neutropenia | |||||||||||||
| 
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-003485-24 | Sponsor Protocol Number: CXA-PEDS-13-08 | Start Date*: 2014-09-25 | ||||||||||||||||
| Sponsor Name:Cubist Pharmaceuticals LLC, a subsidiary of Merck & Co., Inc. | ||||||||||||||||||
| Full Title: A Phase 1, Non-comparative, Open-label Study to Characterize the Pharmacokinetics of a Single Intravenous Dose of Ceftolozane/tazobactam in Pediatric Patients Receiving Standard of Care Antibiotic ... | ||||||||||||||||||
| Medical condition: This study is designed to assess the PK, safety, and tolerability of a single intravenous dose of ceftolozane/tazobactam in pediatric patients. | ||||||||||||||||||
| 
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| Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
| Trial protocol: Outside EU/EEA | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2010-021369-66 | Sponsor Protocol Number: UMM062010FS | Start Date*: 2010-11-16 | 
| Sponsor Name:Department of Pharmacy Universitaetsmedizin Mainz | ||
| Full Title: Investigation of pharmacokinetics of Ciprofloxacin and Piperacillin/Tazobactam in Patients receiving continuous renal replacement therapy | ||
| Medical condition: Sepsis and acute renal failure (ARF) are two pathological entities that commonly co-exist in patients admitted to intensive care. Antibiotic dosing in septic patients with ARF can be complicated a... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2018-000059-42 | Sponsor Protocol Number: 31/17/0334 | Start Date*: 2018-07-25 | |||||||||||
| Sponsor Name:CHU DE TOULOUSE | |||||||||||||
| Full Title: Comparison of short infusion versus prolonged infusion of ceftolozane-tazobactam among patients with ventilator associated-pneumonia to Pseudomonas aeruginosa in intensive care units | |||||||||||||
| Medical condition: Ventilator associated-pneumonia to Pseudomonas aeruginosa in intensive care units | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-004704-19 | Sponsor Protocol Number: MK-7625A-036 | Start Date*: 2019-08-28 | |||||||||||
| Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co.,Inc | |||||||||||||
| Full Title: A Phase 1, open-label, non-comparative, multicenter clinical study to evaluate the safety, tolerability, and pharmacokinetics of ceftolozane/tazobactam (MK-7625A) in pediatric participants with nos... | |||||||||||||
| Medical condition: Nosocomial pneumonia | |||||||||||||
| 
 | |||||||||||||
| Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Trial now transitioned) EE (Trial now transitioned) Outside EU/EEA GR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-021050-20 | Sponsor Protocol Number: AGO/2010/003 | Start Date*: 2010-08-25 | 
| Sponsor Name:Ghent University Hospital | ||
| Full Title: Assessment of the optimal dosing of piperacillin-tazobactam in intensive care unit patients: extended versus continuous infusion | ||
| Medical condition: Patients admitted on the intensive care unit (surgical and medical surgery) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2016-002388-33 | Sponsor Protocol Number: ZKSJ0086 | Start Date*: 2016-09-05 | 
| Sponsor Name:Friedrich-Schiller-University Jena | ||
| Full Title: Therapeutic drug monitoring (TDM) for personalized antibiotic treatment with piperacillin-tazobactam (PipTaz) in patients with febrile neutropenia after myelo-suppressive cytostatic chemotherapy | ||
| Medical condition: Patients with febrile neutropenia after myelo-suppressive chemotherapy treated with piperacillin/tazobactam | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2015-001809-14 | Sponsor Protocol Number: E2015-PK-HD-PTAZ-MERO-CTAZ | Start Date*: 2015-06-24 | ||||||||||||||||
| Sponsor Name:Hopital Erasme | ||||||||||||||||||
| Full Title: Beta-Lactams (ceftazidime, piperacilline-tazobactam, meropenem) dosing scheme validation in septic hemodialysed patient | ||||||||||||||||||
| Medical condition: sepsis in patient undergoing dialysis for renal insufficiency | ||||||||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: BE (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2019-000955-16 | Sponsor Protocol Number: PIPLEVOLUNG | Start Date*: 2020-01-28 | 
| Sponsor Name:Medical University of Vienna | ||
| Full Title: Pulmonary pharmacokinetics of piperacillin/tazobactam and levofloxacin in patients with chronic obstructive pulmonary disease or cystic fibrosis: Comparison of epithelial lining fluid, in-vivo micr... | ||
| Medical condition: Pneumonia | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2011-004470-28 | Sponsor Protocol Number: 2011RM010 | Start Date*: 2011-10-18 | |||||||||||
| Sponsor Name:University Hospital of South Manchester | |||||||||||||
| Full Title: Plasma and intrapulmonary population pharmacokinetics of piperacillin/tazobactam in critically ill patients | |||||||||||||
| Medical condition: Critical illness, ventilator associated pneumonia | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2022-002636-31 | Sponsor Protocol Number: APHP211034 | Start Date*: 2022-09-15 | 
| Sponsor Name:Assistance Publique Hôpitaux de Paris/DRCI | ||
| Full Title: Piperacillin-tazobactam and temocillin as carbapenem-alternatives for the treatment of severe infections due to extended-spectrum beta-lactamase–producing Gram-negative Enterobacteriaceae in the in... | ||
| Medical condition: severe infections due to extended-spectrum beta-lactamase–producing Gram-negative Enterobacteriaceae | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2012-002862-11 | Sponsor Protocol Number: CXA-NP-11-04 | Start Date*: 2015-07-27 | |||||||||||
| Sponsor Name:Cubist Pharmaceuticals GmbH | |||||||||||||
| Full Title: A Prospective, Randomized, Double-Blind, Multicenter, Phase 3 Study to Assess the Safety and Efficacy of Intravenous Ceftolozane/tazobactam Compared With Meropenem in Adult Patients with Ventilated... | |||||||||||||
| Medical condition: Ventilated Nosocomial Pneumonia | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) EE (Completed) DE (Completed) BE (Completed) LV (Completed) CZ (Completed) HU (Completed) SK (Completed) AT (Completed) GR (Completed) PT (Completed) HR (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-000246-34 | Sponsor Protocol Number: 7655A-014 | Start Date*: 2015-09-28 | 
| Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | ||
| Full Title: A Phase III, Randomized, Double-Blind, Active Comparator-Controlled Clinical Trial to Study the Safety, Tolerability, and Efficacy of Imipenem/Cilastatin/Relebactam (MK-7655A) Versus Piperacillin/T... | ||
| Medical condition: Treatment for hospital-acquired/ventilator-associated bacterial pneumonia (HABP/VABP). | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) EE (Completed) LV (Completed) BG (Completed) PT (Completed) LT (Completed) FR (Completed) ES (Completed) HR (Completed) CZ (Completed) IT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2018-002278-33 | Sponsor Protocol Number: PK_AB_NICU | Start Date*: 2018-09-27 | 
| Sponsor Name:Department of Clinical Pharmacology/Medical University of Vienna | ||
| Full Title: Pharmacokinetics of antibiotics in cerebrospinal fluid of children with external ventricular drain | ||
| Medical condition: We will obtain pharmacokinetic data of cefuroxime, vancomycin, gentamicin, ampicillin, linezolid, piperacillin/tazobactam and cefazolin in cerebrospinal fluid and plasma of children with external v... | ||
| Disease: | ||
| Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | |
| Trial protocol: AT (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-003496-36 | Sponsor Protocol Number: 69HCL17_0843 | Start Date*: 2019-11-06 | ||||||||||||||||
| Sponsor Name:Hospices Civils de Lyon | ||||||||||||||||||
| Full Title: Dosage optimization of piperacillin/tazobactam in ICU patients based on therapeutic drug monitoring of amikacin - OPTIMA | ||||||||||||||||||
| Medical condition: sepsis or septic shock | ||||||||||||||||||
| 
 | ||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: FR (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2010-024606-34 | Sponsor Protocol Number: 2010-PI-0521 | Start Date*: 2011-04-11 | |||||||||||
| Sponsor Name:Mª Victoria Gil Navarro | |||||||||||||
| Full Title: Eficacia y seguridad de Piperacilina/Tazobactam administrada en perfusión continua versus infusión intermitente en pacientes con infección complicada o nosocomial con sospecha o aislamiento de Pseu... | |||||||||||||
| Medical condition: infecciones complicadas o de origen nosocomial con sospecha o aislamiento de Pseudomonas aeruginosa | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-004820-41 | Sponsor Protocol Number: MK-7625A-035 | Start Date*: 2017-08-23 | |||||||||||
| Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||
| Full Title: A Phase 2, Randomized, Active Comparator-Controlled, Multicenter, Double-Blind Clinical Trial to Study the Safety and Efficacy of Ceftolozane/Tazobactam (MK-7625A) Plus Metronidazole Versus Meropen... | |||||||||||||
| Medical condition: Complicated intra-abdominal infection (cIAI) | |||||||||||||
| 
 | |||||||||||||
| Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: LT (Completed) ES (Completed) HU (Completed) Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
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