- Trials with a EudraCT protocol (4)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
4 result(s) found for: Meningococcemia.
Displaying page 1 of 1.
| EudraCT Number: 2014-003504-79 | Sponsor Protocol Number: V59P13 | Start Date*: 2014-10-24 | ||||||||||||||||||||||||||||||||||||
| Sponsor Name:Novartis Vaccines & Diagnostics, Inc. | ||||||||||||||||||||||||||||||||||||||
| Full Title: A Phase 3, Randomized, Observer-blind, Controlled, Multi-Center Study to Evaluate the Lot to Lot Consistency of Investigational Meningococcal ACWY Conjugate Vaccine when One Dose is Administered t... | ||||||||||||||||||||||||||||||||||||||
| Medical condition: Novartis Meningococcal ACWY conjugate vaccine is intended for prevention of meningitis and septicemia caused by Neisseria meningitidis serogroups A, C, W and Y. | ||||||||||||||||||||||||||||||||||||||
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| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
| Trial protocol: Outside EU/EEA | ||||||||||||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2017-004609-42 | Sponsor Protocol Number: OVG2017/08 | Start Date*: 2018-02-21 | ||||||||||||||||
| Sponsor Name:Clinical Trials and Research Governance (CTRG), University of Oxford | ||||||||||||||||||
| Full Title: Evaluating the effect of immunisation with group B meningococcal vaccines on meningococcal carriage | ||||||||||||||||||
| Medical condition: Oropharyngeal meningococcal carriage. Meningococci have the potential to cause invasive meningococcal disease. This study investigates the ability of Meningococcal B vaccines to reduce the carriage... | ||||||||||||||||||
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| Population Age: Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2013-001549-15 | Sponsor Protocol Number: C0921004 | Start Date*: 2013-09-19 | ||||||||||||||||||||||||||||||||||||
| Sponsor Name:Pfizer Inc (235 East 42nd Street, New York, New York 10017) | ||||||||||||||||||||||||||||||||||||||
| Full Title: The long-term antibody persistence of MenACWY-TT vaccine (PF-06866681) versus Meningitec® or Mencevax® ACWY in healthy adolescents and adults and a booster dose of MenACWY-TT administered 10 years ... | ||||||||||||||||||||||||||||||||||||||
| Medical condition: Meningococcal disease | ||||||||||||||||||||||||||||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
| Trial protocol: FI (Completed) | ||||||||||||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2012-002251-42 | Sponsor Protocol Number: 3-001 | Start Date*: 2012-11-05 | |||||||||||
| Sponsor Name: Asahi Kasei Pharma America Corporation | |||||||||||||
| Full Title: A RANDOMIZED, DOUBLE BLIND, PLACEBO–CONTROLLED, PHASE 3 STUDY TO ASSESS THE SAFETY AND EFFICACY OF ART-123 IN SUBJECTS WITH SEVERE SEPSIS AND COAGULOPATHY | |||||||||||||
| Medical condition: severe sepsis and coagulopathy | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) NL (Completed) HU (Completed) FI (Completed) CZ (Completed) ES (Completed) BG (Prematurely Ended) GB (Completed) DE (Completed) GR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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Query did not match any studies.