- Trials with a EudraCT protocol (34)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
34 result(s) found for: Endemic Disease.
Displaying page 1 of 2.
EudraCT Number: 2012-002645-38 | Sponsor Protocol Number: BIOMARCHA | Start Date*: 2012-09-04 |
Sponsor Name:CRESIB-Barcelona Centre for International Health Research | ||
Full Title: Evolution of serologic biomarkers and diastolic function and segmentary contractility determined by echocardiography after treatment in Chagas diseases | ||
Medical condition: The study will be held in 63 patients with chronic Chagas Disease and 63 healthy people | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2019-004403-12 | Sponsor Protocol Number: APHP190871 | Start Date*: 2020-10-26 |
Sponsor Name:ASSISTANCE PUBLIQUE DES HOPITAUX DE PARIS | ||
Full Title: Phase II multicenter study of talimogene laherparepvec in classic or endemic Kaposi sarcoma Kapvec Study | ||
Medical condition: The study will provide an overview of efficacy and safety of talimogene laherparepvec in classic and endemic KS | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: FR (Ongoing) | ||
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: 2021-006172-16 | Sponsor Protocol Number: CoVVacBoost | Start Date*: 2021-11-26 | |||||||||||
Sponsor Name:Medical University of Graz | |||||||||||||
Full Title: Detection and Characterization of Anti-SARS-CoV-2 Salivary Antibodies after COVID-19 Booster Vaccines – The CoVVacBoost Study | |||||||||||||
Medical condition: Covid (Coronavirus disease)- 19 immunisation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-023156-89 | Sponsor Protocol Number: V212-011 | Start Date*: 2011-02-24 | |||||||||||
Sponsor Name:Merck Sharp & Dohme Corp. a subsidiary of Merck & Co., Inc | |||||||||||||
Full Title: Ensayo clínico en fase III, aleatorizado y controlado con placebo para estudiar la seguridad y la eficacia de V212 en pacientes adultos con tumor sólido o neoplasia hematológica. A Phase III Rando... | |||||||||||||
Medical condition: Incidence of Herpes Zoster in adults with solid tumor or hematologic malignancy Incidencia de Herpes Zoster en pacientes adultos con tumor sólido o neoplasia hematológica. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) DE (Completed) CZ (Completed) GB (Completed) SK (Completed) AT (Completed) BE (Completed) EE (Completed) LT (Completed) GR (Completed) BG (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-000979-27 | Sponsor Protocol Number: V102_16 | Start Date*: 2015-05-07 |
Sponsor Name:Novartis Vaccines and Diagnostics | ||
Full Title: A Phase 2b, Randomized, Controlled, Observer-Blind, Multi-Center Study Assessing the Effectiveness, Immunogenicity and Safety of Novartis Meningococcal ABCWY Vaccine Administered to Healthy Adolesc... | ||
Medical condition: Prophylaxis against invasive disease strains of N. meningitidis serogroup B. | ||
Disease: | ||
Population Age: Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2010-020150-34 | Sponsor Protocol Number: V212-001-01 | Start Date*: 2010-10-28 | |||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||
Full Title: A Phase III, Double-Blind, Randomized, Placebo-Controlled, Multicenter Clinical Trial to Study the Safety, Tolerability, Efficacy, and Immunogenicity of V212 in Recipients of Autologous Hematopoiet... | |||||||||||||
Medical condition: Incidence of Herpes Zoster in recipients of Autologous HCTs | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) NL (Completed) ES (Completed) SE (Completed) CZ (Completed) GB (Completed) LT (Completed) IT (Completed) BE (Completed) PT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002313-11 | Sponsor Protocol Number: V212-009-00 | Start Date*: 2012-01-20 | |||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||
Full Title: A Phase II Randomized, Placebo-Controlled Clinical Trial to Study the Safety and Immunogenicity of V212 in Adult Patients with Autoimmune Disease | |||||||||||||
Medical condition: Prevention of herpes zoster in adults with autoimmune disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) BE (Completed) EE (Completed) DK (Completed) ES (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-001030-29 | Sponsor Protocol Number: V212-014 | Start Date*: 2014-05-27 |
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | ||
Full Title: A Phase III, Double-blind, Lot-to-Lot Consistency Clinical Trial to Evaluate the Safety, Tolerability and Immunogenicity of V212 in Healthy Adults | ||
Medical condition: Prevention of herpes zoster in adults with autoimmune disease | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (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: 2015-001030-16 | Sponsor Protocol Number: V102_16E1 | Start Date*: 2016-04-28 |
Sponsor Name:Novartis Vaccines and Diagnostics Inc. | ||
Full Title: A Phase 2b, Controlled, Observer-Blind, Multi-Center Study Assessing the Effectiveness, Immunogenicity and Safety of the 3rd Dose of Novartis Meningococcal ABCWY Vaccine Administered to Healthy Ado... | ||
Medical condition: Novartis Meningococcal ABCWY conjugate vaccine is intended for prevention of meningitis and septicemia caused by Neisseria meningitidis serogroups A, B, C, W and Y. | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2007-000744-28 | Sponsor Protocol Number: X06-Z-305 | Start Date*: 2007-09-21 |
Sponsor Name:Sanofi Pasteur MSD S.N.C. | ||
Full Title: An open-label, randomised, comparative, multi-centre study of the immunogenicity and safety of a 1-dose regimen and different 2-dose regimens of a Zoster vaccine (Live), ZOSTAVAX ®, in subjects ≥ 7... | ||
Medical condition: Herpes zoster [shingles] and post-herpetic neuralgia | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) FI (Completed) NL (Completed) ES (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-004020-20 | Sponsor Protocol Number: V211-022 | Start Date*: 2007-12-10 | |||||||||||
Sponsor Name:Merck & Co., Inc. | |||||||||||||
Full Title: A Phase III Clinical Trial to Evaluate the Efficacy, Immunogenicity, Safety and Tolerability of ZOSTAVAX™ in Subjects 50 to 59 Years of Age | |||||||||||||
Medical condition: Herpes Zoster | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FI (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003651-20 | Sponsor Protocol Number: V211-017 | Start Date*: 2007-06-04 | |||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||
Full Title: A Phase III Clinical Trial to Evaluate the Safety, Tolerability, and Immunogenicity of Zoster Vaccine Live (Oka/Merck) in Patients on Chronic/Maintenance Corticosteroids | |||||||||||||
Medical condition: Zoster Vaccine | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FR (Completed) BE (Completed) GB (Completed) | |||||||||||||
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: 2020-004501-30 | Sponsor Protocol Number: V181-003 | Start Date*: 2022-06-14 | |||||||||||
Sponsor Name:Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc. | |||||||||||||
Full Title: A Phase 2, Randomized, Double-Blind, Multicenter Study to Evaluate the Safety and Immunogenicity of Three Different Potency Levels of V181 (Dengue Quadrivalent Vaccine rDENVΔ30 [live, attenuated]) ... | |||||||||||||
Medical condition: Prevention of dengue disease in toddlers, children, and adults in endemic areas, as well as travelers to endemic areas | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) FI (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001666-15 | Sponsor Protocol Number: 205416 | Start Date*: 2020-08-14 |
Sponsor Name:GlaxoSmithKline Biologicals | ||
Full Title: A phase III, randomized, controlled, observer-blind study to demonstrate effectiveness, immunogenicity and safety of GSK's meningococcal Group B and combined ABCWY vaccines when administered to hea... | ||
Medical condition: Healthy volunteers (Active immunization against invasive disease caused by N. meningitidis serogroups A, B, C, W and Y) | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: FI (Completed) CZ (Completed) EE (Completed) Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2018-003640-23 | Sponsor Protocol Number: IRRB/05/18 | Start Date*: 2019-05-29 | |||||||||||||||||||||
Sponsor Name:ISTITUTO MEDITERRANEO PER I TRAPIANTI E TERAPIE AD ALTA SPECIALIZZAZIONE - ISMETT | |||||||||||||||||||||||
Full Title: USE OF HEPATITIS C+ DONORS FOR SOLID ORGAN TRANSPLANTATION IN A GEOGRAPHICAL AREA WITH HCV+ ENDEMIC INFECTION AND WITH A LOW-RATE CADAVERIC ORGAN DONOR AVAILABILITY. A PHASE II OPEN, MONOCENTRIC CL... | |||||||||||||||||||||||
Medical condition: USE OF POSITIVE DONORS FOR INFECTION OF THE HEPATITIS VIRUS FOR THE TRANSPLANTATION OF SOLID ORGANS IN AN ENDEMIC AREA FOR HEPATITIS C WITH LOW RATE OF DONATIONS FROM CADAVERS: OPEN PHASE II CLINI... | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001024-21 | Sponsor Protocol Number: nc5317 | Start Date*: 2018-02-23 | ||||||||||||||||
Sponsor Name:A.O.U. Università degli Studi della Campania "Luigi Vanvitelli" | ||||||||||||||||||
Full Title: innovative model for the eradication of HCV in a population at high risk of irregular immigrants and low-income refugees | ||||||||||||||||||
Medical condition: Chronic HCV hepatitis, all fibrosis | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-005427-20 | Sponsor Protocol Number: C4601003 | Start Date*: 2022-07-13 | |||||||||||
Sponsor Name:Pfizer Inc. | |||||||||||||
Full Title: A PHASE 3, MULTICENTER, PLACEBO-CONTROLLED, RANDOMIZED, OBSERVER-BLINDED TRIAL TO EVALUATE THE EFFICACY, SAFETY, TOLERABILITY, IMMUNOGENICITY, AND LOT CONSISTENCY OF A 6 VALENT OspA-BASED LYME DISE... | |||||||||||||
Medical condition: Prevention of Lyme disease caused by Borrelia species in individuals ≥5 years of age by active immunization | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) SE (Ongoing) EE (Prematurely Ended) FI (Ongoing) NL (Ongoing) PL (Ongoing) | |||||||||||||
Trial results: (No results available) |
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