- Trials with a EudraCT protocol (33)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
33 result(s) found for: Viral encephalitis.
Displaying page 1 of 2.
EudraCT Number: 2013-004366-34 | Sponsor Protocol Number: 311_FU2013 | Start Date*: 2013-12-13 |
Sponsor Name:Medizinische Universität Wien | ||
Full Title: Neutralizing Antibody Titers 6 Years after the Third Dose of Inactivated Japanese Encephalitis Vaccine and Projected Duration of Protection | ||
Medical condition: Study population: adult volunteers who received a booster dose of JE-VC in prestudy IC51-311, no specific medical condition is investigated, only antibody check. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2009-015595-10 | Sponsor Protocol Number: IC51-322 | Start Date*: 2010-03-23 | |||||||||||||||||||||||||||||||
Sponsor Name:Intercell AG | |||||||||||||||||||||||||||||||||
Full Title: IMMUNOGENICITY AND SAFETY OF THE JAPANESE ENCEPHALITIS VACCINE IC51 (IXIARO®, JESPECT®) IN A PEDIATRIC POPULATION IN NON‐ENDEMIC COUNTRIES. UNCONTROLLED, OPEN‐LABEL PHASE 3 STUDY | |||||||||||||||||||||||||||||||||
Medical condition: Japanese Encephalitis (JE) | |||||||||||||||||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: DE (Completed) SE (Completed) DK (Prematurely Ended) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-022265-10 | Sponsor Protocol Number: IC51-325 | Start Date*: 2011-12-28 | |||||||||||||||||||||||||||||||
Sponsor Name:Intercell AG | |||||||||||||||||||||||||||||||||
Full Title: LONG TERM IMMUNITY AND SAFETY WITH OR WITHOUT A BOOSTER DOSE FOLLOWING PRIMARY VACCINATION WITH THE JAPANESE ENCEPHALITIS VACCINE IC51 (IXIARO®) IN A PEDIATRIC POPULATION IN A JEV-ENDEMIC COUNTRY. ... | |||||||||||||||||||||||||||||||||
Medical condition: Japanese Encephalitis (JE) | |||||||||||||||||||||||||||||||||
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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: 2009-015588-15 | Sponsor Protocol Number: IC51-323 | Start Date*: 2011-12-28 | |||||||||||||||||||||||||||||||
Sponsor Name:Intercell AG | |||||||||||||||||||||||||||||||||
Full Title: SAFETY AND IMMUNOGENICITY OF THE JAPANESE ENCEPHALITIS VACCINE IC51 (IXIARO®) IN A PEDIATRIC POPULATION. OPEN LABEL, RANDOMIZED, ACTIVE CONTROLLED, PHASE 3 STUDY | |||||||||||||||||||||||||||||||||
Medical condition: Japanese Encephalitis (JE) | |||||||||||||||||||||||||||||||||
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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: 2010-022266-27 | Sponsor Protocol Number: IC51-324 | Start Date*: 2010-12-13 | |||||||||||||||||||||||||||||||
Sponsor Name:Valneva Austria GmbH | |||||||||||||||||||||||||||||||||
Full Title: Long term immunity and safety following vaccination with the Japanese Encephalitis vaccine IC51 (IXIARO®, JESPECT®) in a pediatric population in non-endemic countries. Uncontrolled, Phase 3 Follow-... | |||||||||||||||||||||||||||||||||
Medical condition: JE can be fatal or lead to long-term disability. Vaccination should therefore be considered for people who are at risk of exposure to JEV by travelling to endemic regions. The study within which no... | |||||||||||||||||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: DE (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-018630-52 | Sponsor Protocol Number: IC51-315 | Start Date*: 2010-05-27 | |||||||||||||||||||||||||||||||
Sponsor Name:Intercell AG | |||||||||||||||||||||||||||||||||
Full Title: AN OPEN-LABEL, UNCONTROLLED PHASE 4 STUDY TO ASSESS THE SAFETY AND IMMUNOGENICITY OF THE JAPANESE ENCEPHALITIS (JE) VACCINE IXIARO® (IC51) IN AN ELDERLY POPULATION | |||||||||||||||||||||||||||||||||
Medical condition: IXIARO® is used to protect adults against Japanese encephalitis (JE). JE can be fatal or lead to long-term disability. Vaccination with Ixiaro should be considered for people who are at risk of exp... | |||||||||||||||||||||||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: DE (Completed) AT (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-004634-24 | Sponsor Protocol Number: IC51-314 | Start Date*: 2008-09-18 | |||||||||||
Sponsor Name:Intercell AG | |||||||||||||
Full Title: IMMUNOGENICITY OF A COMMERCIAL BATCH OF THE JAPANESE ENCEPHALITIS VACCINE IC51 UP TO TWENTY-FOUR MONTHS POST FILLING, OPEN-LABEL, MULTICENTER, PHASE 3 STUDY | |||||||||||||
Medical condition: Japanese Encephalitis (JE) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-005173-23 | Sponsor Protocol Number: V49_23 | Start Date*: 2012-03-08 | |||||||||||||||||||||
Sponsor Name:Novartis Vaccines and Diagnostics GmbH | |||||||||||||||||||||||
Full Title: A Phase III, Multicenter, Observer-blind, Safety and Immunogenicity Study of Rabies Vaccine and Japanese Encephalitis Vaccine Administered Concomitantly and/or Separately According to 1 of 2 Differ... | |||||||||||||||||||||||
Medical condition: Safety and Immunogenicity of Rabies Vaccine and Japanese Encephalitis Vaccine administered concomitantly and/or separately according to 1 of 2 different pre-exposure prophylaxis schedules to health... | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: AT (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-001348-31 | Sponsor Protocol Number: 2011-001348-31 | Start Date*: 2011-05-31 | |||||||||||
Sponsor Name:Mälarsjukhuset | |||||||||||||
Full Title: Can the dosage of vaccine against TBE is optimized by means of changes in dosing interval for those over 50 years | |||||||||||||
Medical condition: Tick-borne Encephalitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-004892-36 | Sponsor Protocol Number: SLE subcuvia 04 Sep 2006 | Start Date*: 2007-03-15 | |||||||||||
Sponsor Name:Department of Rheumatology,University hospital,Lund | |||||||||||||
Full Title: An open randomized and comparative study on the efficacy and safety of additional treatment of subcutaneous immunoglobulin (Subcuvia) during cessation of Prednisolon in patients with active systemi... | |||||||||||||
Medical condition: Systemic Lupus Erythematosus (SLE) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000440-27 | Sponsor Protocol Number: 690701 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Baxter AG | |||||||||||||
Full Title: OPEN-LABEL PHASE IV STUDY TO INVESTIGATE THE SEROPERSISTENCE OF TICK-BORNE ENCEPHALITIS (TBE) VIRUS ANTIBODIES AFTER THE FIRST BOOSTER AND THE RESPONSE TO A SECOND BOOSTER VACCINATION WITH FSME-IMM... | |||||||||||||
Medical condition: In this Study the Seropersistence of Tick Borne Encephalitis (TBE) Virus Antibodies after the First Booster and the Response to a Second Booster Vaccination with FSME-IMMUN 0.5ml in Adults will be ... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-020097-42 | Sponsor Protocol Number: 701001 | Start Date*: 2010-08-03 | |||||||||||
Sponsor Name:Baxter Innovations GmbH | |||||||||||||
Full Title: Open Phase IV Clinical Study to Evaluate the Immunogenicity and Safety of a Rapid Immunization Schedule with FSME-IMMUN 0.25ml JUNIOR in Healthy Children aged 1 to below 15 Years | |||||||||||||
Medical condition: Evaluation of Immunogenicity of a TBE (Tick Borne Encephalitis) Vaccine in previously unvaccinated children aged 1 to below 15 years | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000810-35 | Sponsor Protocol Number: TBE-Ped-Accel-01 | Start Date*: 2007-04-19 | |||||||||||
Sponsor Name:BIOVOMED | |||||||||||||
Full Title: Open Phase IV Clinical Study to Evaluate the Immunogenicity and Safety of a Rapid Immunization Schedule with FSME-IMMUN 0.25 ml JUNIOR in Healthy Children aged 3 - 15 Years | |||||||||||||
Medical condition: Prevention of Tick-born encephalitis (TBE). The rapid immunization schedule recommended in the current SPC for FSME-IMMUN 0.5 ml (Day 0, Day 14) has been used in Austria for 20 years. FSME-IMMUN 0.... | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-001676-21 | Sponsor Protocol Number: V48P7E1 | Start Date*: 2006-08-14 | |||||||||||
Sponsor Name:Novartis Vaccines and Diagnostics GmbH & Co. KG | |||||||||||||
Full Title: A phase IV, open-label, single-center study in adolescents and adults: Evaluation of immunogenicity and safety of the first booster immunization with Chiron’s TBE vaccine for adults in participants... | |||||||||||||
Medical condition: TBE prophylaxis | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-004457-40 | Sponsor Protocol Number: SL0023 | Start Date*: 2016-09-19 | |||||||||||
Sponsor Name:UCB Biopharma SPRL | |||||||||||||
Full Title: A MULTI-CENTER, RANDOMIZED, DOUBLE BLIND, PLACEBO-CONTROLLED, PARALLEL GROUP, DOSE RANGING STUDY FOLLOWED BY AN OBSERVATIONAL PERIOD TO EVALUATE THE EFFICACY AND SAFETY OF DAPIROLIZUMAB PEGOL IN SU... | |||||||||||||
Medical condition: SUBJECTS WITH MODERATELY TO SEVERELY ACTIVE SYSTEMIC LUPUS ERYTHEMATOSUS | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) RO (Completed) HU (Completed) BG (Completed) ES (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-002691-10 | Sponsor Protocol Number: 700801 | Start Date*: 2008-08-28 | |||||||||||
Sponsor Name:Baxter Innovations GmbH | |||||||||||||
Full Title: Single-Blind, randomized, Phase III B Study in children aged 1-11 years to investigate the immunogenicity, safety and interchangeability of two tick-borne encephalitis (TBE) vaccines administered a... | |||||||||||||
Medical condition: assess the immunogenicity, safety and interchangeability of two tick-borne encephalitis (TBE) vaccines in children aged 1-11 years | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-009324-36 | Sponsor Protocol Number: B9371021_(Formerly_Baxter_700802) | Start Date*: 2009-03-04 | |||||||||||
Sponsor Name:Pfizer Inc., 235 East 42nd Street, New York, NY 10017 | |||||||||||||
Full Title: OPEN-LABEL PHASE IV STUDY TO INVESTIGATE THE SEROPERSISTENCE OF TICK-BORNE ENCEPHALITIS (TBE) VIRUS ANTIBODIES AFTER THE FIRST BOOSTER AND THE RESPONSE TO A SECOND BOOSTER VACCINATION WITH FSME-IMM... | |||||||||||||
Medical condition: Active (prophylactic) immunization against TBE The main purpose of this study is to assess the seropersistence of TBE virus antibodies in children, adolescents and young adults who received the fi... | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) DE (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-000100-14 | Sponsor Protocol Number: IC51- 302 | Start Date*: 2005-09-08 |
Sponsor Name:Intercell AG | ||
Full Title: Safety and tolerability of the Japanese encephalitis vaccine IC51 (JE-PIV). Double blind, randomized, placebo controlled phase 3 study | ||
Medical condition: Japanese encephalitis (JE) is the most common viral encephalitis, with over 50,000 cases reported annually. It is a considerable public health problem for many Asian countries (WHO 1997). Close to ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) AT (Completed) GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-003201-81 | Sponsor Protocol Number: GFVT01026904 (GACHE) | Start Date*: 2006-12-20 |
Sponsor Name:Universitätsklinikum Heidelberg | ||
Full Title: GACHE: German trial of Acyclovir and Corticosteroids in Herpes-simplex-virus-Encephalitis. A multicenter, multinational, randomized, double-blind, placebo-controlled German, Austrian and Dutch trial. | ||
Medical condition: Herpes simplex virus type-1 (HSV-1) is the most frequent cause of fatal sporadic encephalitis in humans. Herpes simplex encephalitis (HSE) was one of the first viral infections to be successfully t... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-002474-36 | Sponsor Protocol Number: IC51-301 | Start Date*: 2005-04-20 |
Sponsor Name:Intercell AG | ||
Full Title: Observer blinded, randomized Phase III study to investigate the non-inferiority of IC51 (JE-PIV) vs. JE-VAX as vaccines for japanese encephalitis in healthy volunteers | ||
Medical condition: Japanese encephalitis (JE) is the most common viral encephalitis, with over 50,000 cases reported annually. It is a considerable public health problem for many Asian countries (WHO 1997). Close to ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
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