- Trials with a EudraCT protocol (8)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (46)
8 result(s) found for: IRES.
Displaying page 1 of 1.
EudraCT Number: 2019-000690-22 | Sponsor Protocol Number: VAC52150EBL2002 | Start Date*: 2019-04-25 | |||||||||||
Sponsor Name:Janssen Vaccines & Prevention B.V. | |||||||||||||
Full Title: A Randomized, Observer-blind, Placebo-controlled, Phase 2 Study to Evaluate the Safety, Tolerability and Immunogenicity of Different Prime-boost Regimens of the Candidate Prophylactic Vaccines for ... | |||||||||||||
Medical condition: Prevention of Ebola virus disease | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-000596-27 | Sponsor Protocol Number: VAC52150EBL2001 | Start Date*: 2015-05-18 | |||||||||||
Sponsor Name:Janssen Vaccines & Prevention BV | |||||||||||||
Full Title: A Randomized, Observer-Blind, Placebo-Controlled, Phase 2 Study to Evaluate the Safety, Tolerability and Immunogenicity of Three Prime-Boost Regimens of the Candidate Prophylactic Vaccines for Ebol... | |||||||||||||
Medical condition: Ebola | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-004620-38 | Sponsor Protocol Number: 242-12-233 | Start Date*: 2019-01-14 |
Sponsor Name:Otsuka Pharmaceutical Development & Commercialization, Inc. | ||
Full Title: Phase 2, Open-label, Multiple-dose Trial to Assess the Safety, Tolerability, Pharmacokinetics, and Efficacy of Delamanid (OPC 67683) in Pediatric Multidrug-resistant Tuberculosis Patients on Therap... | ||
Medical condition: Pediatric patients with multidrug-resistant tuberculosis (MDR-TB) who are receiving an optimized background regimen (OBR) of antituberculosis drugs | ||
Disease: | ||
Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2008-005292-10 | Sponsor Protocol Number: ERRADVIH-02 | Start Date*: 2008-12-09 | |||||||||||
Sponsor Name:Fundación para la Investigación Biomédica Hospital Ramón y Cajal | |||||||||||||
Full Title: ESTUDIO PILOTO DEL EFECTO DE UN INHIBIDOR DE LA INTEGRASA SOBRE LA LATENCIA Y EL RESERVORIO DEL VIH-1 EN PACIENTES QUE RECIBEN TRATAMIENTO ANTIRRETROVIRAL DE GRAN ACTIVIDAD | |||||||||||||
Medical condition: Infección por el virus de la inmunodeficiencia humana (VIH) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-008432-82 | Sponsor Protocol Number: CP-MGA031-02 | Start Date*: 2009-07-01 | |||||||||||
Sponsor Name:MacroGenics, Inc. | |||||||||||||
Full Title: A Multicenter, Multinational Extension of Study CP-MGA031-01 to Evaluate the Long-Term Efficacy and Safety of Teplizumab (MGA031), a Humanized, FcR Non-Binding, Anti-CD3 Monoclonal Antibody, in Chi... | |||||||||||||
Medical condition: Recent-onset type 1 diabetes mellitus | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Prematurely Ended) ES (Prematurely Ended) SE (Prematurely Ended) LV (Prematurely Ended) EE (Prematurely Ended) DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-005107-26 | Sponsor Protocol Number: 242-07-208 | Start Date*: 2009-04-08 | |||||||||||
Sponsor Name:Otsuka Pharmaceutical Development and Commercialization, Inc. | |||||||||||||
Full Title: A Phase 2, Multi-center, Uncontrolled, Open-label Trial to Evaluate Safety, tolerability, and Efficacy of Orally Administered OPC-67683 as 100 mg BID with optional titration to 200 mg BID for up t... | |||||||||||||
Medical condition: Pulmonary Multidrug-resistant Tuberculosis (MDR TB) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: LV (Completed) EE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-000691-42 | Sponsor Protocol Number: VAC52150EBL3001 | Start Date*: 2019-04-25 | |||||||||||
Sponsor Name:Janssen Vaccines & Prevention B.V. | |||||||||||||
Full Title: A Staged Phase 3 Study, Including a Double-Blinded Controlled Stage to Evaluate the Safety and Immunogenicity of Ad26.ZEBOV and MVA-BN-Filo as Candidate Prophylactic Vaccines for Ebola | |||||||||||||
Medical condition: Prevention of Ebola virus disease | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-003995-21 | Sponsor Protocol Number: ERRADVIH-01 | Start Date*: 2007-12-03 | |||||||||||
Sponsor Name:Fundación para la Investigación Biomédica del Hospital Universitario Ramón y Cajal | |||||||||||||
Full Title: Estudio piloto del efecto de un antagonista de co-receptores CCR5 sobre la latencia y el reservorio del VIH-1 en pacientes que reciben tratamiento antirretroviral de gran actividad | |||||||||||||
Medical condition: VIH | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
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