- Trials with a EudraCT protocol (87)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
87 result(s) found for: Community-acquired pneumonia.
Displaying page 1 of 5.
EudraCT Number: 2014-002867-13 | Sponsor Protocol Number: POP6135,HMR3647B/3005 | Start Date*: 2015-03-17 | |||||||||||
Sponsor Name:Sanofi-aventis | |||||||||||||
Full Title: Multinational, randomized, double blind, double dummy, pharmacokinetic study of telithromycin oral suspension (25 mg/kg once daily for 7-10 days), with secondary assessments of safety relative to a... | |||||||||||||
Medical condition: Community acquired pneumonia | |||||||||||||
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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: 2017-001406-15 | Sponsor Protocol Number: NACATB | Start Date*: 2018-07-19 | |||||||||||
Sponsor Name:Fundació Clínic per la Recerca Biomèdica | |||||||||||||
Full Title: Adequate duration of antibiotic treatment in community acquired pneumonia categorized by pneumonia severity index (PSI) | |||||||||||||
Medical condition: Community Acquired Pneumonia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005096-93 | Sponsor Protocol Number: 070864 | Start Date*: 2009-09-03 |
Sponsor Name:Jordi Carratalá | ||
Full Title: SIMVASTATINA EN LA NEUMONIA ADQUIRIDA EN LA COMUNIDAD QUE REQUIERE HOSPITALIZACION. ESTUDIO ALEATORIZADO, DOBLE-CIEGO, CONTROLADO CON PLACEBO (SIMVASTATIN IN COMMUNITY-ACQUIRED PNEUMONIA REQUIRIN... | ||
Medical condition: NEUMONIA ADQUIRIDA EN LA COMUNIDAD QUE REQUIERE HOSPITALIZACION (COMMUNITY-ACQUIRED PNEUMONIA REQUIRING HOSPITALIZATION) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2022-002390-28 | Sponsor Protocol Number: INSPIRE | Start Date*: 2022-10-10 | ||||||||||||||||
Sponsor Name:Hellenic Institute for the Study of Sepsis | ||||||||||||||||||
Full Title: IMMUNOTHERAPY NAVIGATED BY SERUM PRESEPSIN FOR INFECTIONS OF THE RESPIRATORY TRACT: THE INSPIRE DOUBLE-BLIND, RANDOMIZED, PHASE IIa EXPLORATORY TRIAL | ||||||||||||||||||
Medical condition: community-acquired pneumonia, hospital-acquired pneumonia | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GR (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006842-33 | Sponsor Protocol Number: MOX-06191 | Start Date*: 2007-11-23 | |||||||||||
Sponsor Name:Fundación para Investigación y Desarrollo en el Área Cardiovascular del Hospital Clínico San Carlos | |||||||||||||
Full Title: Estudio Piloto Comparativo de Eficacia, Tolerancia y Seguridad de Moxifloxacino VO frente a Levofloxacino en Terapia Secuencial en Adultos Inmunocompetentes con Neumonía Adquirida en la Comunidad. | |||||||||||||
Medical condition: Neumonía adquirida en la comunidad | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-003067-22 | Sponsor Protocol Number: PRISTINE | Start Date*: 2012-11-19 | |||||||||||
Sponsor Name:LUMC | |||||||||||||
Full Title: Pneumonia treated with rifampicine attenuates inflammation | |||||||||||||
Medical condition: Community acquired pneumonia CURB-65 class >1 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-001735-66 | Sponsor Protocol Number: NXL103/2001 | Start Date*: 2007-10-01 | |||||||||||
Sponsor Name:Novexel S. A. | |||||||||||||
Full Title: A double blind, multicentre, multinational, randomized, double dummy, three-arm parallel-group comparative study of the efficacy, safety and tolerance of oral NXL103 (500 mg twice daily) versus NXL... | |||||||||||||
Medical condition: Community-Acquired Pneumonia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: EE (Completed) DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004566-14 | Sponsor Protocol Number: SanteonCAP | Start Date*: 2012-01-09 |
Sponsor Name: | ||
Full Title: Santeon-CAP study Dexamethasone in community-acquired pneumonia. | ||
Medical condition: Patients with a community-acquired pneumonia who are admitted to the hospital. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2007-000599-18 | Sponsor Protocol Number: P903-09 | Start Date*: 2008-03-25 | |||||||||||
Sponsor Name:Cerexa, Inc. | |||||||||||||
Full Title: A Phase 3, Multicenter, Randomized, Double-blind, Comparative Study to Evaluate the Safety and Efficacy of Ceftaroline versus Ceftriaxone in the Treatment of Adult Subjects with Community-Acquired ... | |||||||||||||
Medical condition: Adult Subjects with Community-Acquired Pneumonia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Completed) DE (Completed) HU (Completed) AT (Completed) LV (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-002619-10 | Sponsor Protocol Number: OP-634-001 | Start Date*: 2004-11-10 | |||||||||||
Sponsor Name:Oscient Pharmaceuticals | |||||||||||||
Full Title: A Phase IIIb, Randomized, Double-Blind, Multicenter, Parallel Group Study to Assess the Efficacy and Safety of Oral Gemifloxacin 320 mg Once Daily for 5 Days Versus Oral Gemifloxacin 320 mg Once Da... | |||||||||||||
Medical condition: Mild to moderate community acquired bacterial pneumonia. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) LT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000598-41 | Sponsor Protocol Number: P903-08 A4 | Start Date*: 2007-11-22 | |||||||||||
Sponsor Name:Cerexa, Inc. | |||||||||||||
Full Title: "A Phase 3, Multicenter, Randomized, Double-blind, Comparative Study to Evaluate the Safety and Efficacy of Ceftaroline versus Ceftriaxone, with Adjunctive Clarithromycin, in the Treatment of Adult... | |||||||||||||
Medical condition: Adults Subjects with Community-Acquired Pneumonia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) ES (Completed) AT (Completed) LT (Completed) EE (Completed) SK (Completed) BG (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-003971-20 | Sponsor Protocol Number: CE01-300 | Start Date*: 2013-05-07 | |||||||||||
Sponsor Name:Cempra Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Randomized, Double-Blind, Multi-Center Study to Evaluate the Efficacy and Safety of Oral Solithromycin (CEM-101) Compared to Oral Moxifloxacin in the Treatment of Adult Patients with Community-Ac... | |||||||||||||
Medical condition: Community-Acquired Bacterial Pneumonia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) CZ (Completed) ES (Completed) PL (Completed) LV (Completed) EE (Completed) BG (Completed) RO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-001239-19 | Sponsor Protocol Number: PHRN14-PFD-CAPE_COD | Start Date*: 2015-08-14 | |||||||||||
Sponsor Name:CHRU de TOURS | |||||||||||||
Full Title: Effects of low-dose corticosteroids on survival of severe Community-Acquired Pneumonia | |||||||||||||
Medical condition: Severe community-acquired pneumonia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002027-15 | Sponsor Protocol Number: CIVI/2018/CR-01 | Start Date*: 2019-08-30 | |||||||||||
Sponsor Name:CHU DE NIMES | |||||||||||||
Full Title: | |||||||||||||
Medical condition: Community acquired pneumonia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-003854-28 | Sponsor Protocol Number: REP-FAR-006 | Start Date*: 2008-01-06 | |||||||||||
Sponsor Name:Replidyne, Inc. | |||||||||||||
Full Title: Prospective, Randomized, Double-Blind Trial to Evaluate the Efficacy and Safety of Faropenem Medoxomil 600 mg PO, BID for 10 Days Versus Clarithromycin in the Treatment of Community-Acquired P... | |||||||||||||
Medical condition: Community-acquired pneumonia. This disease can be defined as an acute lower respiratory tract infection not acquired in a hospital or a long-term care facility. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-022380-35 | Sponsor Protocol Number: 982 | Start Date*: 2011-06-10 | |||||||||||
Sponsor Name:Biotest AG | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled, multicenter, parallel-group, adaptive group-sequential phase II study, to determine the efficacy and safety of BT086 as an adjunctive treatment in ... | |||||||||||||
Medical condition: severe Community Acquired Pneumonia (sCAP) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Completed) GB (Completed) BE (Completed) | |||||||||||||
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: 2020-002986-32 | Sponsor Protocol Number: PTK0796-CABP-19302 | Start Date*: 2020-10-26 | |||||||||||
Sponsor Name:Paratek Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Phase 3b 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 ... | |||||||||||||
Medical condition: Community-Acquired Bacterial Pneumonia (CABP) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Completed) HR (Completed) HU (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-002110-35 | Sponsor Protocol Number: CL06-001 | Start Date*: 2006-08-24 | |||||||||||
Sponsor Name:Advanced Life Sciences | |||||||||||||
Full Title: A Double-Blinded, Randomized, Parallel group, Multi-Centre, Multi-National Comparative Study of the Safety and Efficacy of Cethromycin 300mg QD to Clarithromycin (KLACID®) 250mg BID for the treatme... | |||||||||||||
Medical condition: Community Acquired Pneumonia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) EE (Completed) DE (Completed) HU (Completed) | |||||||||||||
Trial results: (No results available) |
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 |
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