- Trials with a EudraCT protocol (180)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
180 result(s) found for: Herpes.
Displaying page 2 of 9.
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: 2020-000926-24 | Sponsor Protocol Number: HTX101-03L | Start Date*: 2020-08-17 | ||||||||||||||||
Sponsor Name:Heidelberg ImmunoTherapeutics | ||||||||||||||||||
Full Title: A Randomised, Double-Blind Phase II Trial of Topical HDIT101 versus Placebo in Patients with Chronic Recurrent HSV-1 Infection and Orolabial Lesion | ||||||||||||||||||
Medical condition: Chronic Herpes Simplex Virus-1 Infection | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) AT (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-000344-26 | Sponsor Protocol Number: V211-012-00 | Start Date*: 2007-06-04 | |||||||||||
Sponsor Name:Merck & Co., Inc. | |||||||||||||
Full Title: A Phase III Double-Blind, Randomized Multicenter Study to Evaluate the Safety, Tolerability and Immunogenicity of ZOSTAVAX administered comcomitantly versus Non-concomitantly with PNEUMOVAX 23 in s... | |||||||||||||
Medical condition: herpes zoster, pneumococcal infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) IT (Completed) GB (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-012458-19 | Sponsor Protocol Number: ZTV03C | Start Date*: 2009-10-15 | |||||||||||
Sponsor Name:Sanofi Pasteur MSD S.N.C. | |||||||||||||
Full Title: An open-label, randomised, comparative, multicentre study of the immunogenicity and safety of ZOSTAVAX® when administered by intramuscular route or subcutaneous route to subjects ≥50 years of age | |||||||||||||
Medical condition: Not applicable as Prevention of herpes zoster ("zoster" or shingles) and herpes zoster-related post-herpetic neuralgia (PHN). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-000965-30 | Sponsor Protocol Number: 204486 | Start Date*: 2016-02-09 | |||||||||||
Sponsor Name:GlaxoSmithKline Biologicals | |||||||||||||
Full Title: A Phase IIIB, non-randomized, open-label, multi-country, multi-centric cross-vaccination study to evaluate the safety of GSK Biologicals' Herpes Zoster subunit (HZ/su) vaccine when administered int... | |||||||||||||
Medical condition: Herpes Zoster | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) EE (Completed) CZ (Completed) GB (Completed) DE (Completed) ES (Completed) FR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-004835-19 | Sponsor Protocol Number: 38RC16.015 | Start Date*: 2017-07-20 | |||||||||||
Sponsor Name:University Hospital Grenoble | |||||||||||||
Full Title: Dexamethasone in Herpes Simplex Virus Encephalitis Open label Randomized Controlled Trial with an Observer-blinded evaluation at 6 months | |||||||||||||
Medical condition: HSV encephalitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-014268-20 | Sponsor Protocol Number: VZV01 | Start Date*: 2009-12-24 | |||||||||||||||||||||
Sponsor Name:Erasmus MC | |||||||||||||||||||||||
Full Title: VZV vaccination to prevent herpes zoster after transplantation | |||||||||||||||||||||||
Medical condition: Herpes Zoster | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000373-76 | Sponsor Protocol Number: 117177 | Start Date*: 2014-01-16 | |||||||||||
Sponsor Name:GlaxoSmithKline Biologicals | |||||||||||||
Full Title: A phase III, randomized, double blind multicenter study, to evaluate consistency, immunogenicity, safety and reactogenicity of 3 lots of GSK Biologicals’ herpes zoster HZ/su candidate vaccine when ... | |||||||||||||
Medical condition: Herpes Zoster (HZ) and its related complications. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-002387-86 | Sponsor Protocol Number: 218S18VC | Start Date*: 2020-01-08 | |||||||||||
Sponsor Name:Pascoe pharmazeutische Präparate GmbH | |||||||||||||
Full Title: A DOUBLE-BLIND, PLACEBO-CONTROLLED, 4-ARM PILOT STUDY ON THE USE OF PASCORBIN® AS ADD-ON THERAPY IN PATIENTS WITH ACUTE HERPES ZOSTER | |||||||||||||
Medical condition: Acute herpes zoster infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-003035-52 | Sponsor Protocol Number: V211-011-00 | Start Date*: 2005-10-06 | |||||||||||
Sponsor Name:Merck & Co. Inc. | |||||||||||||
Full Title: A Double-Blind, Randomized, Multicenter Study to Evaluate the Safety, Tolerability, and Immunogenicity of ZOSTAVAX™ Administered Concomitantly Versus Nonconcomitantly with Influenza Virus Vaccine (... | |||||||||||||
Medical condition: Herpes Zoster | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000138-20 | Sponsor Protocol Number: 115523 | Start Date*: 2012-06-07 | |||||||||||
Sponsor Name:GlaxoSmithKline Biologicals | |||||||||||||
Full Title: A phase III, randomised, observer-blind, placebo-controlled, multicentre, clinical trial to assess the prophylactic efficacy, safety, and immunogenicity of GSK Biologicals’ herpes zoster gE/AS01B c... | |||||||||||||
Medical condition: Vaccination against herpes zoster (HZ) in adult autologous HCT recipients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) ES (Completed) DE (Completed) FI (Completed) EE (Completed) IT (Completed) CZ (Completed) GB (Completed) FR (Completed) NL (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-004456-11 | Sponsor Protocol Number: 116697 | Start Date*: 2012-12-11 | |||||||||||
Sponsor Name:GlaxoSmithKline Biologicals | |||||||||||||
Full Title: A phase III, randomised, open-label, multicentre, clinical trial to assess the safety and immunogenicity of GSK Biologicals’ HZ/su vaccine when administered intramuscularly according to a 0,2-month... | |||||||||||||
Medical condition: Vaccination against HZ and its related complications in adults older than 50 years | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: EE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-001451-30 | Sponsor Protocol Number: UMCN-AKF12.07 | Start Date*: 2019-06-17 | |||||||||||
Sponsor Name:Radboud university medical center | |||||||||||||
Full Title: Pharmacokinetics of a new paediatric formulation of valacyclovir used for prophylaxis and treatment of VZV and HSV infections in children, phase II (VALID II) | |||||||||||||
Medical condition: Herpes virus infections, especially Herpes Simplex and Varicella Zoster. | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002966-11 | Sponsor Protocol Number: 116427 | Start Date*: 2013-02-22 | ||||||||||||||||
Sponsor Name:GlaxoSmithKline | ||||||||||||||||||
Full Title: A phase II/III, randomised, observer-blind, placebo-controlled, multicentre, clinical trial to assess the immunogenicity and safety of GSK Biologicals? herpes zoster HZ/su candidate vaccine when ad... | ||||||||||||||||||
Medical condition: Herpes Zoster and related complications | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Completed) GB (Completed) CZ (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-005671-14 | Sponsor Protocol Number: 116760 | Start Date*: 2013-09-30 | ||||||||||||||||
Sponsor Name:GlaxoSmithKline Biologicals | ||||||||||||||||||
Full Title: A phase III, randomised, open-label, multicentre clinical trial to assess the safety and immunogenicity of GSK Biologicals’ HZ/su candidate vaccine when administered subcutaneously as compared to i... | ||||||||||||||||||
Medical condition: Healthy volunteers (Prevention of Herpes Zoster [HZ] and related complications in adults ≥50 years of age [YOA] and immunocompromised adults ≥18 YOA) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-000372-15 | Sponsor Protocol Number: 117036 | Start Date*: 2013-10-02 | ||||||||||||||||
Sponsor Name:GlaxoSmithKline Biologicals | ||||||||||||||||||
Full Title: A phase III, randomized, open-label, multicentre clinical trial to assess the immunogenicity and safety of GSK Biologicals’ Herpes Zoster vaccine GSK1437173A when co-administered with GSK Biologica... | ||||||||||||||||||
Medical condition: Healthy volunteers (Prevention of Herpes Zoster [HZ] and related complications in adults ≥ 50 years of age [YOA ] and immunocompromised adults ≥ 18 YOA.) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-005314-19 | Sponsor Protocol Number: 116889 | Start Date*: 2014-01-30 | ||||||||||||||||
Sponsor Name:GlaxoSmithKline Biologicals | ||||||||||||||||||
Full Title: A phase III, randomized, open-label, multicenter clinical trial to assess the immunogenicity and safety of GSK Biologicals’ Herpes Zoster vaccine GSK1437173A when co-administered with Pneumovax 23 ... | ||||||||||||||||||
Medical condition: Healthy volunteers (Prevention of Herpes Zoster [HZ] and related complications in adults ≥ 50 years of age [YOA ] and immunocompromised adults ≥ 18 YOA.) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: EE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-000367-42 | Sponsor Protocol Number: 110390 | Start Date*: 2010-07-12 |
Sponsor Name:GlaxoSmithKline SA | ||
Full Title: Ensayo clínico de vacunación fase III, aleatorizado, observador-ciego, controlado con placebo, multicéntrico para evaluar la eficacia profiláctica, seguridad e inmunogenicidad de la vacuna gE/AS01B... | ||
Medical condition: Inmunización primaria frente a herpes zoster (HZ) en sujetos igual o mayores de 50 años de edad. La población del estudio está formada por hombres y mujeres no inmunocomprometidos con un intervalo ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Prematurely Ended) FI (Prematurely Ended) FR (Prematurely Ended) DE (Prematurely Ended) GB (Prematurely Ended) SE (Prematurely Ended) EE (Prematurely Ended) IT (Completed) CZ (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2009-015791-94 | Sponsor Protocol Number: 113077 | Start Date*: 2010-07-12 |
Sponsor Name:GlaxoSmithKline SA | ||
Full Title: Ensayo clínico de vacunación fase III, aleatorizado, observador-ciego, controlado con placebo, multicéntrico para evaluar la eficacia profiláctica, seguridad e inmunogenicidad de la vacuna gE/AS01B... | ||
Medical condition: Inmunización primaria frente a Herpes Zoster (HZ) en sujetos igual o mayores de 70 años de edad. La población del estudio está formada por hombres y mujeres en un rango de edad de 70 a 79 años e ig... | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: ES (Prematurely Ended) FI (Prematurely Ended) DE (Prematurely Ended) GB (Prematurely Ended) SE (Prematurely Ended) EE (Prematurely Ended) FR (Completed) IT (Prematurely Ended) CZ (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2009-010971-26 | Sponsor Protocol Number: 2-BOPH | Start Date*: 2009-10-05 | |||||||||||
Sponsor Name:Menarini Ricerche S.p.A. | |||||||||||||
Full Title: A Phase II trial comparing Brivudin 0.1% ophthalmic solution with Aciclovir 3 % ophthalmic ointment in the treatment of patients with herpetic dendritic keratitis | |||||||||||||
Medical condition: Herpetic dendritic keratitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) ES (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
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