- Trials with a EudraCT protocol (180)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (39)
180 result(s) found for: Herpes.
Displaying page 3 of 9.
EudraCT Number: 2017-001220-22 | Sponsor Protocol Number: 204487 | Start Date*: 2018-03-22 | |||||||||||
Sponsor Name:GlaxoSmithKline Biologicals | |||||||||||||
Full Title: A Phase IIIB, randomized, open-label, multicenter clinical trial to assess the immunogenicity and safety of GSK Biologicals’ Herpes Zoster vaccine GSK1437173A when co-administered with Prevenar13 i... | |||||||||||||
Medical condition: Healthy volunteers (Prevention of Herpes Zoster (HZ) and related complications in adults ≥50 years of age (YOA)) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) EE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003239-31 | Sponsor Protocol Number: HOVIR_700 | Start Date*: 2014-03-14 |
Sponsor Name:HOV GmbH | ||
Full Title: A randomised, placebo-controlled, single-centre, double-blind study to evaluate the efficacy, safety and tolerability of topically applied piroxicam gel in patients with recurrent herpes labialis | ||
Medical condition: Recurrent Herpes labialis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Temporarily Halted) | ||
Trial results: (No results available) |
EudraCT Number: 2012-003438-18 | Sponsor Protocol Number: 116428 | Start Date*: 2013-01-08 | |||||||||||
Sponsor Name:GlaxoSmithKline Biologicals | |||||||||||||
Full Title: A Phase III, randomised, observer-blind, placebo-controlled, multicentre study to assess the safety and immunogenicity of GSK Biologicals’ Herpes Zoster HZ/su candidate vaccine when administered in... | |||||||||||||
Medical condition: Vaccination against HZ in adults with haematologic malignancies. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) BE (Completed) FI (Completed) ES (Completed) IT (Completed) CZ (Completed) GB (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-017809-11 | Sponsor Protocol Number: 112673 | Start Date*: 2010-09-27 | |||||||||||
Sponsor Name:GlaxoSmithKline Biologicals | |||||||||||||
Full Title: A phase I/IIa randomized, observer-blind, placebo-controlled, multicenter study to evaluate the safety and immunogenicity of the GSK Biologicals’ herpes zoster vaccine, gE/AS01B in comparison to pl... | |||||||||||||
Medical condition: Vaccination against herpes zoster (HZ) in adult HIV-infected subjects. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-001778-17 | Sponsor Protocol Number: 201190 | Start Date*: 2016-03-17 | |||||||||||
Sponsor Name:GlaxoSmithKline Biologicals | |||||||||||||
Full Title: A phase IIIb, open-label, multi-country, multi-centre, long-term follow-up study (ZOE-LTFU) of studies 110390 and 113077 (ZOSTER-006/022) to assess the prophylactic efficacy, safety, and immunogeni... | |||||||||||||
Medical condition: Vaccination against HZ and its related complications in adults older than 50 years (at the time of primary vaccination). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) EE (Completed) CZ (Completed) GB (GB - no longer in EU/EEA) DE (Completed) ES (Ongoing) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-005059-18 | Sponsor Protocol Number: 116886 | Start Date*: 2013-05-24 | |||||||||||
Sponsor Name:GlaxoSmithKline S.A. | |||||||||||||
Full Title: A Phase III, randomised, observer-blind, placebo-controlled, multicentre clinical study to assess the immunogenicity and safety of GSK Biologicals? HZ/su candidate vaccine when administered intramu... | |||||||||||||
Medical condition: Herpes Zoster (HZ) and its related complications | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) CZ (Completed) BE (Completed) FI (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-004400-30 | Sponsor Protocol Number: 204926 | Start Date*: 2016-02-24 | ||||||||||||||||||||||||||
Sponsor Name:GlaxoSmithKline Biologicals | ||||||||||||||||||||||||||||
Full Title: A phase IIIB, open, long term extension study to evaluate the persistence of immune responses and the safety of GSK Biologicals’ Herpes Zoster subunit (HZ/su) vaccine 1437173A, at Months 108 and 12... | ||||||||||||||||||||||||||||
Medical condition: Herpes Zoster (HZ) | ||||||||||||||||||||||||||||
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Population Age: Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: SE (Completed) DE (Completed) CZ (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-000577-22 | Sponsor Protocol Number: AKF-UMCN11.05 | Start Date*: 2012-07-17 | |||||||||||
Sponsor Name:Radboud University Nijmegen Medical Centre | |||||||||||||
Full Title: Palatability testing of a new paediatric formulation of valacyclovir for the prophylaxis and treatment of VZV and HSV infections in children – VALID 0 | |||||||||||||
Medical condition: Herpes virus infections, especially Herpes Simplex, Varicella Zoster and Cytomegalovirus | |||||||||||||
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Population Age: Children, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-001085-15 | Sponsor Protocol Number: LLB-2018-01 | Start Date*: 2019-11-06 | |||||||||||||||||||||
Sponsor Name:LABO’LIFE Belgium sprl | |||||||||||||||||||||||
Full Title: Randomized, placebo-controlled, double-blind study to evaluate the efficacy of 2LHERP® in patients with recurrent orofacial herpes infections. | |||||||||||||||||||||||
Medical condition: Patients presenting recurrent orofacial herpes infections (6 or more episodes within the 12-months’ period prior to their study entry). | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: BE (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-005825-75 | Sponsor Protocol Number: 105909 MeMuRu-OKA 047 | Start Date*: 2006-03-20 | |||||||||||
Sponsor Name:GLAXO SMITHKLINE | |||||||||||||
Full Title: A phase II, open, randomised, comparative study to evaluate the immunogenicity and safety of GlaxoSmithKline s GSK Biologicals measles-mumps-rubella-varicella candidate vaccine MeMuRu-OKA and ... | |||||||||||||
Medical condition: Active immunisation against mumps, measles, rubella and varicella | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-002669-19 | Sponsor Protocol Number: X04-VAR-402 | Start Date*: 2004-12-23 | |||||||||||
Sponsor Name:AVENTIS PASTEUR MSD S.P.A. | |||||||||||||
Full Title: A double-blind, randomised, controlled, multi-centre safety study of a refrigerator-stable formulation of VARIVAX® in healthy 12 to 15 month-old infants. | |||||||||||||
Medical condition: Active immunisation against varicella | |||||||||||||
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Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-004443-40 | Sponsor Protocol Number: CFAM810B2305 | Start Date*: 2016-04-12 |
Sponsor Name:Novartis Pharmaceuticals | ||
Full Title: A Multicenter, Open-label, Single-arm Study to Evaluate the Safety and Pharmacokinetics of Famciclovir Single 1500 mg Dose in Adolescents With Recurrent Herpes Labialis | ||
Medical condition: Herpes Labialis | ||
Disease: | ||
Population Age: Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2005-001705-26 | Sponsor Protocol Number: CYD-GER-0401 | Start Date*: 2005-09-21 |
Sponsor Name:Spirig Pharma AG | ||
Full Title: Efficacy and safety of topically applied cyclodextrin gel (Spirig Pharma) in the treatment of recurrent genital herpes simplex virus infections: a randomised, double-blind, placebo-controlled, mult... | ||
Medical condition: Genito-anal herpes simplex infections | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
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: 2005-005863-26 | Sponsor Protocol Number: TAK-583/EC201 | Start Date*: 2006-09-22 | |||||||||||
Sponsor Name:Takeda Global Research & Development Centre (Europe) Ltd | |||||||||||||
Full Title: A Phase II, double blind, placebo controlled, dose-ranging study in patients with post herpetic neuralgia (PHN) to evaluate the efficacy, safety, tolerability and pharmacokinetics of four doses of ... | |||||||||||||
Medical condition: Postherpetic neuralgia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) NL (Completed) DE (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-002828-42 | Sponsor Protocol Number: 609-07 | Start Date*: 2006-11-01 |
Sponsor Name:Medivir AB | ||
Full Title: An open label, multi-centre, phase III, subject initiated safety study of ME-609 in treatment of recurrent herpes simplex labialis in adolescents. | ||
Medical condition: Herpes simplex labialis | ||
Disease: | ||
Population Age: Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2015-004441-17 | Sponsor Protocol Number: CFAM810B2303 | Start Date*: 2016-04-12 |
Sponsor Name:Novartis Pharmaceuticals | ||
Full Title: A Multicenter, Open-label, Single-arm, Two-step Study to Evaluate the Safety and Single-dose Pharmacokinetics of Famciclovir and Multiple-dose Safety After Administration of Famciclovir Oral Pediat... | ||
Medical condition: Herpes Simplex | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2006-005788-24 | Sponsor Protocol Number: BA2005/21/02 | Start Date*: 2007-02-15 |
Sponsor Name:Bioalliance Pharma | ||
Full Title: A Randomised, Double-Blind, Single dose, One-Day Early Administration, Multicentre Study comparing the Efficacy and Safety of Acyclovir Lauriad 50 mg muco-adhesive buccal tablet to matching Placebo... | ||
Medical condition: Herpes labialis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Completed) DE (Completed) FR (Completed) GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-006065-14 | Sponsor Protocol Number: 105908 | Start Date*: 2006-04-04 |
Sponsor Name:GlaxoSmithKline Biologicals | ||
Full Title: A phase II, open, randomised, comparative study to evaluate the immunogenicity and safety of GlaxoSmithKline's (GSK) Biologicals' measles-mumps-rubella-varicella candidate vaccine (MeMuRu-OKA) and ... | ||
Medical condition: Healthy male and female children between 15 months and 6 years of age who previously received an MMR vaccine will receive one dose of MMR + V or MMRV. A second dose of varicella vaccine will be giv... | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: DE (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-001332-22 | Sponsor Protocol Number: RG_12-201 | Start Date*: 2013-06-20 | |||||||||||
Sponsor Name:University of Birmingham | |||||||||||||
Full Title: PEPtalk 2: Pilot of a randomised controlled trial to compare VZIG and aciclovir as post-exposure prophylaxis against chickenpox in children with cancer | |||||||||||||
Medical condition: Exposure to Varicella by children who have cancer. | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
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