- Trials with a EudraCT protocol (1,653)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
1,653 result(s) found for: Viral Infection.
Displaying page 30 of 83.
| EudraCT Number: 2012-003535-27 | Sponsor Protocol Number: 1241.36 | Start Date*: 2012-10-17 | |||||||||||
| Sponsor Name:SCS Boehringer Ingelheim Comm.V | |||||||||||||
| Full Title: A phase III randomised, partially double-blind and placebo-controlled study of BI 207127 in combination with faldaprevir and ribavirin for chronic genotype 1 hepatitis C infection in an extended p... | |||||||||||||
| Medical condition: | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) DE (Completed) PT (Completed) GB (Completed) ES (Completed) GR (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-004531-22 | Sponsor Protocol Number: MBA 1/2005 | Start Date*: 2006-05-02 |
| Sponsor Name:Májbetegekért Alapítvány | ||
| Full Title: Efficacy and Safety of Continuing for a Total of 48 or Prolonging for a Total of 72 weeks of Combined Treatment of Patients Receiving Pegasys and Copegus who are Biochemical Responders but Virolo... | ||
| Medical condition: Chronic hepatitis C virus infection | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: HU (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-000926-79 | Sponsor Protocol Number: GS-US-380-4458 | Start Date*: 2018-08-07 | ||||||||||||||||
| Sponsor Name:Gilead Sciences, Inc. | ||||||||||||||||||
| Full Title: A Phase 3, Randomized, Double-Blind Study to Evaluate the Safety and Efficacy of Fixed Dose Combination of Bictegravir/Emtricitabine/Tenofovir Alafenamide versus Dolutegravir + Emtricitabine/Tenofo... | ||||||||||||||||||
| Medical condition: Human Immunodeficiency Virus (HIV-1) Infection Hepatitis B Virus | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: FR (Completed) ES (Restarted) GR (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2009-014313-27 | Sponsor Protocol Number: RAL-IC | Start Date*: 2009-11-11 | |||||||||||
| Sponsor Name:Fundació Lluita contra la SIDA | |||||||||||||
| Full Title: ESTUDIO PILOTO PARA COMPARAR LOS PARÁMETROS FARMACOCINÉTICOS EN PLASMA E INTRACELULARES DE RALTEGRAVIR ADMINISTRADO UNA VEZ AL DÍA EN PACIENTES ADULTOS INFECTADOS POR EL VIH. | |||||||||||||
| Medical condition: Infección VIH-1 | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-018709-12 | Sponsor Protocol Number: OSCAR | Start Date*: 2010-09-23 | |||||||||||
| Sponsor Name:FONDAZIONE CENTRO S. RAFFAELE DEL MONTE TABOR | |||||||||||||
| Full Title: Optimizing Susceptibility to CCR5 Antagonist Response | |||||||||||||
| Medical condition: HIV infection | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-005104-33 | Sponsor Protocol Number: ALS-8176-503 | Start Date*: 2014-02-14 | |||||||||||
| Sponsor Name:Janssen Research & Development, LLC | |||||||||||||
| Full Title: A Randomized, Double-blind, Placebo-controlled, 2-Part Study of Orally Administered ALS-008176 to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Single Ascending Dosing... | |||||||||||||
| Medical condition: Respiratory Syncytial Virus (RSV) Infection | |||||||||||||
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| Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) FR (Completed) RO (Ongoing) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-005579-16 | Sponsor Protocol Number: APV109141 | Start Date*: 2007-04-13 | |||||||||||
| Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
| Full Title: Study of Once-Daily Versus Twice-Daily Fosamprenavir plus Ritonavir, Administered with Abacavir/Lamivudine Once-Daily in Antiretroviral-Naïve HIV-1 Infected Adult Subjects. | |||||||||||||
| Medical condition: Treatment of HIV-1 infection. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) BE (Completed) GB (Completed) FR (Completed) ES (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-005287-21 | Sponsor Protocol Number: AI444-046 | Start Date*: 2012-02-09 | |||||||||||
| Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
| Full Title: A Long-Term Follow-up Study of Subjects Who Participated in a Clinical Trial in Which Asunaprevir (BMS-650032) and/or Daclatasvir (BMS-790052) Was Administered for the Treatment of Chronic Hepatiti... | |||||||||||||
| Medical condition: Chronic Hepatitis C | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) IE (Completed) SE (Completed) IT (Completed) GB (Completed) DK (Completed) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-000492-21 | Sponsor Protocol Number: 7678 | Start Date*: 2021-06-11 |
| Sponsor Name:Les Hôpitaux Universitaires de Strasbourg | ||
| Full Title: Multicenter randomized two arms study evaluating the efficacy of prophylactic Rituximab in adult EBV negative kidney transplant recipients on incidence of EBV primary infection and post-transplant ... | ||
| Medical condition: Kidney transplantation Epstein Barr virus | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2017-002563-18 | Sponsor Protocol Number: PC_RSV_003 | Start Date*: 2017-10-09 | |||||||||||
| Sponsor Name:Pulmocide Ltd | |||||||||||||
| Full Title: A single-blind, placebo controlled, randomised study to evaluate antiviral activity and safety and pharmacokinetics of inhaled PC786 against respiratory syncytial virus (RSV) in healthy adult subje... | |||||||||||||
| Medical condition: Human Respiratory Syncytial Virus (RSV) | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-023532-16 | Sponsor Protocol Number: TMC125IFD3002 | Start Date*: 2012-01-26 | |||||||||||
| Sponsor Name:Janssen R&D Ireland | |||||||||||||
| Full Title: An open-label study to evaluate the safety, tolerability and pharmacokinetics of etravirine (ETR) in combination with other antiretrovirals (ARVs) in antiretroviral treatment-experienced HIV-1 infe... | |||||||||||||
| Medical condition: HIV-1 infection | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: RO (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-003147-35 | Sponsor Protocol Number: M14-567 | Start Date*: 2014-12-16 | |||||||||||
| Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
| Full Title: A Randomized, Open-Label Study to Evaluate the Safety and Efficacy of the Co-Administration of Ombitasvir/ABT-450/Ritonavir (Ombitasvir/ABT-450/r) With Sofosbuvir (SOF) With or Without Ribavirin (R... | |||||||||||||
| Medical condition: Chronic Hepatitis C Virus (HCV) Infection | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-002012-33 | Sponsor Protocol Number: M15-461 | Start Date*: 2015-09-24 | |||||||||||
| Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
| Full Title: An Open-Label Study to Evaluate the Safety and Efficacy of Ombitasvir/Paritaprevir/Ritonavir With or Without Dasabuvir in Adults With Genotype 1a or Genotype 4 Chronic Hepatitis C Virus (HCV) Infec... | |||||||||||||
| Medical condition: Chronic Hepatitis C infection | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-015884-15 | Sponsor Protocol Number: IMPAACT-P1066 | Start Date*: 2011-06-30 | |||||||||||
| Sponsor Name:The National Institute of Allergy and Infectious Diseases (NIAID) and The Eunice Kennedy Shriver NICHD | |||||||||||||
| Full Title: A Phase I/II, Multicenter, Open-Label, Non comparative Study of the International Maternal, Pediatric, Adolescent AIDS Clinical Trials (IMPAACT) Group to Evaluate the Safety, Tolerability, Pharmac... | |||||||||||||
| Medical condition: HIV | |||||||||||||
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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: 2022-002268-53 | Sponsor Protocol Number: 219288 | Start Date*: 2022-12-09 | |||||||||||
| Sponsor Name:GlaxoSmithKline Research & Development Limited | |||||||||||||
| Full Title: Phase 3 Multicenter, Randomized, Double-Blind, Study to Assess the Efficacy and Safety of Treatment with Bepirovirsen in HBeAg-negative Nucleos(t)ide Analogue-treated Participants with Chronic Hepa... | |||||||||||||
| Medical condition: Chronic Hepatitis B infection | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) IT (Trial now transitioned) FR (Trial now transitioned) PL (Trial now transitioned) DE (Ongoing) GR (Trial now transitioned) HU (Trial now transitioned) BG (Trial now transitioned) RO (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-005139-22 | Sponsor Protocol Number: 202009 | Start Date*: 2022-12-09 | |||||||||||
| Sponsor Name:GlaxoSmithKline Research & Development Limited | |||||||||||||
| Full Title: Phase 3 Multicenter, Randomized, Double-Blind, Study to Assess the Efficacy and Safety of Treatment with Bepirovirsen in HBeAg-negative Nucleos(t)ide Analogue-treated Participants with Chronic Hepa... | |||||||||||||
| Medical condition: Chronic Hepatitis B infection | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) IT (Trial now transitioned) FR (Trial now transitioned) PL (Trial now transitioned) DE (Ongoing) GR (Trial now transitioned) HU (Trial now transitioned) BG (Trial now transitioned) RO (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-003003-54 | Sponsor Protocol Number: NP25138 | Start Date*: 2016-08-09 |
| Sponsor Name:F. Hoffmann-La Roche AG | ||
| Full Title: An Open-label, Prospective, Pharmacokinetic/Pharmacodynamic and Safety Evaluation of Intravenous Oseltamivir in the Treatment of Infants Less Than One Year of Age With Influenza Infection | ||
| Medical condition: Influenza | ||
| Disease: | ||
| Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | |
| Trial protocol: Outside EU/EEA | ||
| Trial results: View results | ||
| EudraCT Number: 2007-004720-20 | Sponsor Protocol Number: VX07-950-108 | Start Date*: 2008-07-03 | |||||||||||
| Sponsor Name:Vertex Pharmaceuticals Incorporated | |||||||||||||
| Full Title: A Phase 3 Study of 2 Dose Regimens of Telaprevir in Combination With Peginterferon Alfa-2a (Pegasys®) and Ribavirin (Copegus®) in Treatment-Naive Subjects with Genotype 1 Chronic Hepatitis C | |||||||||||||
| Medical condition: Chronic Hepatitis C, Genotype 1 | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) DE (Completed) FR (Completed) AT (Completed) ES (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-005055-14 | Sponsor Protocol Number: P7977-1231 | Start Date*: 2012-03-19 | |||||||||||
| Sponsor Name:Gilead Sciences Inc. | |||||||||||||
| Full Title: A Phase 3, Multicenter, Randomized, Active-Controlled Study to Investigate the Safety and Efficacy of PSI-7977 and Ribavirin for 12 Weeks Compared to Pegylated Interferon and Ribavirin for 24 Weeks... | |||||||||||||
| Medical condition: Chronic Genotype 2 or 3 HCV Infection | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) EE (Completed) IT (Completed) ES (Completed) NL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-000511-40 | Sponsor Protocol Number: ANRS_VRI04_(DALIA_2) | Start Date*: 2020-02-18 | |||||||||||
| Sponsor Name:Inserm-ANRS | |||||||||||||
| Full Title: Phase II, randomized, multicentric, clinical trial of a therapeutic vaccination, with ex vivo generated autologous Dentritic Cells pulsed with HIV lipopetides, combined or not with a TLR-3 agonist ... | |||||||||||||
| Medical condition: Human Immunodeficiency Virus (HIV) Infection | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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