- Trials with a EudraCT protocol (49)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (5)
49 result(s) found for: Skin and skin structure infection.
Displaying page 1 of 3.
EudraCT Number: 2007-001774-88 | Sponsor Protocol Number: TAR-ORI-SD001 | Start Date*: 2007-11-15 | |||||||||||
Sponsor Name:Targanta Therapeutics Corporation | |||||||||||||
Full Title: Nuvocid™ (oritavancin) at Single or Infrequent Doses for the Treatment of Complicated Skin and Skin Structure Infections (SIMPLIFI) | |||||||||||||
Medical condition: Complicated skin and skin structure infections (cSSSI). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-000419-15 | Sponsor Protocol Number: DUR001-303 | Start Date*: 2014-07-28 | |||||||||||
Sponsor Name:Durata Therapeutics International B.V. | |||||||||||||
Full Title: A Phase 3b, Double-Blind, Multicenter, Randomized Study to Compare the Efficacy and Safety of Single Dose Dalbavancin to a Two Dose Regimen of Dalbavancin for the Treatment of Acute Bacterial Skin ... | |||||||||||||
Medical condition: Acute Bacterial Skin and Skin Structure Infections | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LV (Completed) EE (Completed) HU (Completed) BG (Completed) HR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-002910-12 | Sponsor Protocol Number: 0017 | Start Date*: 2005-06-17 | |||||||||||
Sponsor Name:Theravance Inc. | |||||||||||||
Full Title: A Phase 3, Randomized, Double-Blind, Multinational Trial of Intravenous Telavancin Versus Vancomycin for Treatment of Complicated Gram-Positive Skin and Skin Structure Infections with a focus on Pa... | |||||||||||||
Medical condition: Complicated Gram-Positive Skin and Skin Structure Infections With a Focus on Patients With Infections Due to Methicillin-Resistant Staphylococcus aureus. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003374-10 | Sponsor Protocol Number: TOC106489 | Start Date*: 2007-08-03 |
Sponsor Name:GlaxoSmithKline Research & Development Ltd | ||
Full Title: An Open-Label, Non-Comparative Study to Assess the Pharmacokinetics, Safety and Efficacy of Topical Retapamulin (SB-275833) Ointment, 1%, Twice Daily for Five Days in the Treatment of Uncomplicated... | ||
Medical condition: Uncomplicated skin and skin structure infections | ||
Disease: | ||
Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: DE (Completed) NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-021424-94 | Sponsor Protocol Number: TMC-ORI-10-01 | Start Date*: 2012-03-16 | |||||||||||||||||||||||||||||||
Sponsor Name:The Medicines Company | |||||||||||||||||||||||||||||||||
Full Title: A Multicenter, Double-Blind, Randomized Study to Evaluate the Efficacy and Safety of Single-Dose IV Oritavancin versus IV Vancomycin for the Treatment of Patients with Acute Bacterial Skin and Skin... | |||||||||||||||||||||||||||||||||
Medical condition: Treatment of Patients with acute bacterial skin and skin structure infections | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: GB (Completed) DE (Completed) PL (Prematurely Ended) ES (Prematurely Ended) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-001936-11 | Sponsor Protocol Number: 3074K4-3339-WW | Start Date*: 2009-03-20 | |||||||||||||||||||||||||||||||
Sponsor Name:Wyeth Pharmaceuticals Inc. | |||||||||||||||||||||||||||||||||
Full Title: A Phase 3, Multicenter, Randomized, Double-blind Study to Evaluate the Safety and Efficacy of Tigecycline Versus Clindamycin for the Treatment of Complicated Skin and Skin Structure Infections, Inc... | |||||||||||||||||||||||||||||||||
Medical condition: Complicated skin and skin structure infection (cSSSI) with or without methicillin-resistant Staphylococcus aureus (MRSA) | |||||||||||||||||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: HU (Completed) BE (Completed) GB (Completed) Outside EU/EEA | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-002914-12 | Sponsor Protocol Number: 0018 | Start Date*: 2005-04-13 | |||||||||||
Sponsor Name:Theravance Inc. | |||||||||||||
Full Title: A phase 3, Randomized, Double-Blind, Multinational Trial of Intravenous Televancin Versus Vancomycin for Treatment of Complicated Gram-positive Skin and Skin Structure Infections with a focus on Pa... | |||||||||||||
Medical condition: Complicated Gram-Positive Skin and Skin Structure Infections With a Focus on Patients With Infections Due to Methicillin-Resistant Staphylococcus aureus. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Completed) GB (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-001599-18 | Sponsor Protocol Number: BAY 12-8039/11974 | Start Date*: 2006-11-03 | |||||||||||
Sponsor Name:Bayer HealthCare AG | |||||||||||||
Full Title: A prospective, randomized, double dummy, double blind, multinational, multicenter trial comparing the safety and efficacy of sequential (intravenous/oral) moxifloxacin 400 mg once daily to intraven... | |||||||||||||
Medical condition: complicated skin and skin structure Infections | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) LT (Completed) BE (Completed) LV (Completed) FR (Completed) GR (Completed) IE (Completed) HU (Completed) ES (Completed) NL (Prematurely Ended) AT (Completed) IT (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005283-47 | Sponsor Protocol Number: P903-07 | Start Date*: 2006-12-29 | |||||||||||
Sponsor Name:Cerexa, Inc. | |||||||||||||
Full Title: A Phase 3, Multicenter, Randomized, Double-Blind, Comparative Study to Evaluate the Safety and Efficacy of Ceftaroline Versus Vancomycin plus Aztreonam in Adult Subjects with Complicated Skin and ... | |||||||||||||
Medical condition: Complicated Skin and Skin Structure Infections (cSSSI) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) GB (Completed) DE (Completed) LV (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003644-23 | Sponsor Protocol Number: PTK0796-ABSI-1108 | Start Date*: 2015-07-02 | |||||||||||
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 Linezolid IV/PO for Treating Adult Subjects with Acute Bacterial Skin and Skin Str... | |||||||||||||
Medical condition: Acute Bacterial Skin and Skin Structure Infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LV (Completed) HU (Completed) ES (Completed) PL (Completed) GR (Completed) HR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-002239-29 | Sponsor Protocol Number: WI18274 | Start Date*: 2006-03-06 |
Sponsor Name:F. Hoffmann - La Roche AG | ||
Full Title: A phase II prospective, open label, randomized, active-controlled, parallel group, multi-center ‘proof of concept’ trial in adult patients with complicated skin and skin structure infections requir... | ||
Medical condition: Treatment of adult patients with complicated skin and skin structure infections requiring hospitalization. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: LT (Completed) EE (Completed) DE (Completed) LV (Completed) HU (Completed) GR (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-003884-20 | Sponsor Protocol Number: MK-1986-018 | Start Date*: 2017-06-05 | |||||||||||
Sponsor Name:Merck Sharp & Dohme LLC | |||||||||||||
Full Title: A Phase III Randomized, Active-comparator-Controlled Clinical Trial to Study the Safety and Efficacy of MK-1986 (Tedizolid Phosphate) and Comparator, in Subjects 3 Months to <12 Years of Age with A... | |||||||||||||
Medical condition: Acute Bacterial Skin and Skin Structure Infections (ABSSSI) | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA DE (Completed) PL (Completed) BG (Completed) LT (Completed) LV (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-001276-56 | Sponsor Protocol Number: AIDA | Start Date*: 2014-07-11 |
Sponsor Name:North Bristol NHS - Southmead Hospital | ||
Full Title: A prospective, open label, randomised controlled clinical trial, with pharmacokinetic-pharmacodynamic validation, to compare antimicrobial treatment with oral minocycline plus rifampicin to treatme... | ||
Medical condition: Complicated Skin and Skin Structure infections caused by Methicillin Resistant Staphylococcus Aureus | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: IT (Completed) GR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-005332-25 | Sponsor Protocol Number: P903-06 | Start Date*: 2007-03-16 | |||||||||||
Sponsor Name:Cerexa, Inc. | |||||||||||||
Full Title: A Phase 3, Multicenter, Randomized, Double-Blind, Comparative Study to Evaluate the Safety and Efficacy of Ceftaroline Versus Vancomycin plus Aztreonam in Adult Subjects with Complicated Skin and ... | |||||||||||||
Medical condition: Complicated Skin and Skin Structure Infections (cSSSI) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-001767-71 | Sponsor Protocol Number: RX-3341-302 | Start Date*: 2013-06-20 | |||||||||||
Sponsor Name:Melinta Therapeutics, Inc | |||||||||||||
Full Title: A PHASE 3, MULTICENTER, RANDOMIZED, DOUBLE BLIND, ACTIVE CONTROLLED STUDY TO EVALUATE THE EFFICACY AND SAFETY OF DELAFLOXACIN COMPARED WITH VANCOMYCIN + AZTREONAM IN PATIENTS WITH ACUTE BACTERIAL S... | |||||||||||||
Medical condition: ACUTE BACTERIAL SKIN AND SKIN STRUCTURE INFECTIONS | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) LV (Completed) ES (Completed) BG (Completed) HR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022168-11 | Sponsor Protocol Number: TR-701-112 | Start Date*: 2011-03-08 | |||||||||||
Sponsor Name:Trius Therapeutics, Inc. | |||||||||||||
Full Title: A Phase 3 Randomized, Double-Blind, Multicenter Study Comparing the Efficacy and Safety of 6-Day Oral TR-701 Free Acid and 10-Day Oral Linezolid for the Treatment of Acute Bacterial Skin and Skin... | |||||||||||||
Medical condition: Acute Bacterial Skin and Skin Structure Infections | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) CZ (Completed) LV (Completed) HU (Completed) SK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-021720-10 | Sponsor Protocol Number: TMC-ORI-10-02 | Start Date*: 2012-03-16 | |||||||||||||||||||||||||||||||
Sponsor Name:The Medicines Company | |||||||||||||||||||||||||||||||||
Full Title: A Multicenter, Double-Blind, Randomized Study to Evaluate the Efficacy and Safety of Single-Dose IV Oritavancin versus IV Vancomycin for the Treatment of Patients with Acute Bacterial Skin and Skin... | |||||||||||||||||||||||||||||||||
Medical condition: Treatment of Patients with acute bacterial skin and skin structure infections | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: GB (Completed) DE (Completed) ES (Prematurely Ended) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-003812-22 | Sponsor Protocol Number: P903-23 | Start Date*: 2011-10-31 | |||||||||||
Sponsor Name:Cerexa, Inc. (subsidary of Forest Laboratories) | |||||||||||||
Full Title: A Multicenter, Randomized, Observer-Blinded, Active-Controlled Study to Evaluate the Safety, Tolerability, Efficacy, and Pharmacokinetics of Ceftaroline Versus Comparator in Pediatric Subjects With... | |||||||||||||
Medical condition: Acute Bacterial Skin and Skin Structure Infections | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA LT (Completed) LV (Completed) ES (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-002669-45 | Sponsor Protocol Number: ICL-23-ABSSSI1 | Start Date*: 2016-02-18 | |||||||||||
Sponsor Name:Motif BioSciences Inc. | |||||||||||||
Full Title: A Phase 3, randomized, double-blind, multicenter study to evaluate the safety and efficacy of intravenous iclaprim versus vancomycin in the treatment of acute bacterial skin and skin structure infe... | |||||||||||||
Medical condition: Acute bacterial skin and skin structure infections (ABSSSIs) suspected or confirmed to be due to Gram-positive pathogens. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LV (Completed) DE (Completed) BG (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004983-39 | Sponsor Protocol Number: RX-3341-303 | Start Date*: 2015-01-26 | |||||||||||
Sponsor Name:Melinta Therapeutics, Inc | |||||||||||||
Full Title: A PHASE 3, MULTICENTER, RANDOMIZED, DOUBLE-BLIND, ACTIVE-CONTROLLED STUDY TO EVALUATE THE EFFICACY AND SAFETY OF IV AND ORAL DELAFLOXACIN COMPARED WITH VANCOMYCIN + AZTREONAM IN PATIENTS WITH ACUTE... | |||||||||||||
Medical condition: ACUTE BACTERIAL SKIN AND SKIN STRUCTURE INFECTIONS | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) EE (Completed) LV (Completed) SK (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
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