- Trials with a EudraCT protocol (6)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
6 result(s) found for: Salmonella enterica.
Displaying page 1 of 1.
EudraCT Number: 2011-000381-35 | Sponsor Protocol Number: OVG 2011/02 | Start Date*: 2011-09-26 | ||||||||||||||||
Sponsor Name:University of Oxford | ||||||||||||||||||
Full Title: Understanding typhoid disease after vaccination: a single centre, randomised, double-blind, placebo-controlled study to evaluate M01ZH09 in a healthy adult challenge model, using Ty21a vaccine as a... | ||||||||||||||||||
Medical condition: Active immunisation for the prevention of typhoid infection in healthy adults. | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-001448-31 | Sponsor Protocol Number: H01_04E1TP | Start Date*: 2011-09-12 | |||||||||||
Sponsor Name:Novartis Vaccines Institute for Global Health (NVGH) | |||||||||||||
Full Title: A Phase 2, open-label, single-center, extension study to evaluate the booster response induced by Vi-CRM197 after priming with either Vi-CRM197 or Typherix administered in adult subjects in H01_04T... | |||||||||||||
Medical condition: Prophylaxis for Salmonella enterica serovar Typhi (S. Typhi) disease | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-002978-36 | Sponsor Protocol Number: OVG2014/08 | Start Date*: 2015-01-26 | |||||||||||
Sponsor Name:The University of Oxford | |||||||||||||
Full Title: Vaccines Against Salmonella Typhi: a phase IIb, single centre, observer-blind, randomised controlled trial to assess the immunogenicity and protective efficacy of Vi conjugated (Vi-TCV) and unconju... | |||||||||||||
Medical condition: Salmonella enterica serovar Typhi infection | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-003653-26 | Sponsor Protocol Number: OVG2011/07 | Start Date*: 2011-12-08 | |||||||||||
Sponsor Name:Clinical Trials and Research Governance | |||||||||||||
Full Title: A phase II, single-centre, randomised, single-blind, study to evaluate Vi-CRM197 against historical unvaccinated controls in a healthy adult challenge model, with a Vi-PS vaccine control arm. | |||||||||||||
Medical condition: Prophylaxis for Salmonella enterica serovar Typhi (S. Typhi) disease | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-021874-12 | Sponsor Protocol Number: H01_04TP | Start Date*: 2010-09-13 |
Sponsor Name:Novartis Vaccines Institute for Global Health (NVGH) | ||
Full Title: A Phase 2, Randomized, Observer–blind, Controlled, Single Center Study to Evaluate the Safety and Immunogenicity of Three Formulations of the NVGH Glycoconjugate Vaccine against S. Typhi in Adult S... | ||
Medical condition: Salmonella enterica serovar Typhi (S. Typhi) disease | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-005293-70 | Sponsor Protocol Number: MS04.03 | Start Date*: 2006-06-19 |
Sponsor Name:Emergent Product Development UK Ltd | ||
Full Title: A double blind, placebo controlled study to evaluate the safety and immunogenicity of escalating doses of 108 CFU, 109 CFU and 1010 CFU of M04NM11 in patients who have chronic Hepatitis B infection. | ||
Medical condition: Chronic hepatitis B virus infection | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
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• Outside EU/EEA: Date study was submitted in EudraCT
