- Trials with a EudraCT protocol (8)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (10)
8 result(s) found for: Streptococcus pyogenes.
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EudraCT Number: 2020-002219-24 | Sponsor Protocol Number: IMPET-001 | Start Date*: 2020-08-17 | |||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Basic Pharma Technologies | |||||||||||||||||||||||||||||||||||||||||||
Full Title: A Randomized, Double-Blind, Parallel Group, Equivalence, Multicenter Phase III Trial to Compare the Efficacy and Safety of Fusidic Acid Hydrophilic Cream 20 mg/g and Fucidin® Cream in the Treatment... | |||||||||||||||||||||||||||||||||||||||||||
Medical condition: Impetigo contagiosa | |||||||||||||||||||||||||||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||
Trial protocol: BE (Completed) CZ (Completed) | |||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-004631-39 | Sponsor Protocol Number: EFC6134,HMR3647B/3006 | Start Date*: 2015-03-17 | |||||||||||
Sponsor Name:Sanofi-aventis | |||||||||||||
Full Title: Multinational, randomized, double blind, comparative study to evaluate the efficacy and safety of telithromycin, 800 mg once daily for 5 days, versus penicillin V, 500 mg three times daily for 10 d... | |||||||||||||
Medical condition: Tonsillitis Pharyngitis | |||||||||||||
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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: 2014-004630-26 | Sponsor Protocol Number: EFC6133,HMR3647B/3004 | Start Date*: 2015-03-17 | |||||||||||
Sponsor Name:Sanofi-aventis | |||||||||||||
Full Title: Multinational, Randomized, Double-Blind, Double Dummy, Comparative Study to Evaluate the Efficacy and Safety of 5 Days Telithromycin 25mg/kg od Versus 10 Days Penicillin V 13.3 mg/kg Tid in Childre... | |||||||||||||
Medical condition: Tonsillitis Pharyngitis | |||||||||||||
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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: 2011-003402-25 | Sponsor Protocol Number: OCT-UKE-2011 | Start Date*: 2011-12-13 | |||||||||||
Sponsor Name:Schülke & Mayr GmbH | |||||||||||||
Full Title: Randomized, Double-blind, Single-center, Placebo-controlled Study to evaluate the Efficacy of octenisept® in Patients with Chronic Wounds. | |||||||||||||
Medical condition: Chronic leg ulcers | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002001-30 | Sponsor Protocol Number: IMUP | Start Date*: 2011-12-09 |
Sponsor Name:INFECTOPHARM Arzneimittel und Consilium GmbH | ||
Full Title: Multicenter, prospective, double-blind, two-armed phase III study for efficacy and safety of the topic impetigo therapy of two 2 % mupirocin ointments | ||
Medical condition: Impetigo | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-004002-15 | Sponsor Protocol Number: KETOP_L_03102 | Start Date*: 2014-12-19 | |||||||||||
Sponsor Name:Sanofi | |||||||||||||
Full Title: Local, Phase IV, Multicenter, Double-blind, Randomized, Parallel, With Two Treatment Arms, Placebo-controlled Study to Evaluate the Reduction of Inflammatory Symptoms in the Treatment of Bacterial ... | |||||||||||||
Medical condition: Pharyngotonsillitis | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-000886-42 | Sponsor Protocol Number: BV-2020/08 | Start Date*: 2022-09-06 | |||||||||||
Sponsor Name:OM Pharma SA | |||||||||||||
Full Title: A Randomised, Placebo-Controlled, 3-Arm, Double-Blind, Multicentre, Phase 4 Study to Assess the Efficacy of OM-85 (Broncho Vaxom) Short- and Long-Term Treatment vs. Placebo in the Prevention of Res... | |||||||||||||
Medical condition: Respiratory Tract Infections with Wheezing Lower Respiratory Illness | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Trial now transitioned) PL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-003179-33 | Sponsor Protocol Number: BV-2021/06 | Start Date*: 2021-11-29 | |||||||||||
Sponsor Name:OM Pharma SA | |||||||||||||
Full Title: A Randomised, Double-Blind, Placebo-controlled, 32-week, Phase IIa trial to investigate the efficacy of OM-85 versus matched placebo in reducing disease severity in children aged 3 to 24 months wit... | |||||||||||||
Medical condition: Atopic Dermatitis | |||||||||||||
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Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) NL (Prematurely Ended) PL (Prematurely Ended) FR (Prematurely Ended) | |||||||||||||
Trial results: View results |
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