- Trials with a EudraCT protocol (44)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (3)
44 result(s) found for: Oseltamivir.
Displaying page 1 of 3.
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: 2009-018200-17 | Sponsor Protocol Number: UHLHM0002 | Start Date*: 2010-02-01 |
Sponsor Name:University Hospitals of Leicester NHS Trust | ||
Full Title: Plasma Levels of Oseltamivir in critically ill, suspected or confirmed H1N1 infected patients on Extra Corporeal membrane Oxygenation (ECMO)support. | ||
Medical condition: Treatment of confirmed or suspected H1N1 (swine flu) infection in critically ill patients supported on ECMO | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-003004-31 | Sponsor Protocol Number: NP25139 | 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 (Tamiflu) in the Treatment of Children 1 to 12 Years of Age With Influenza Infection | ||
Medical condition: Influenza | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2016-001008-49 | Sponsor Protocol Number: NV22155 | Start Date*: 2016-09-30 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche AG | |||||||||||||
Full Title: A randomized, multicenter trial of oseltamivir doses of 75 mg for 5 or 10 days versus 150 mg for 5 or 10 days in influenza patients with pandemic (H1N1) 2009 | |||||||||||||
Medical condition: Influenza | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-005239-80 | Sponsor Protocol Number: 10007 | Start Date*: 2005-12-23 |
Sponsor Name:University Hospitals Leicester, Leicester General Hospital | ||
Full Title: Prospective study to assess the emergence of drug resistance to oseltamivir following treatment of acute influenza A among children | ||
Medical condition: Influenza A | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-001044-18 | Sponsor Protocol Number: ML22789 | Start Date*: 2016-10-03 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche AG | |||||||||||||
Full Title: A phase IIIb, openlabel, comparative, randomized study on resistance of Influenza A/H1N1 2009 virus to treatment with Oseltamivir at standard dose versus double dose | |||||||||||||
Medical condition: Influenza A/H1N1 | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-005037-11 | Sponsor Protocol Number: WP21272 | Start Date*: 2008-01-02 |
Sponsor Name:F.Hoffmann-La Roche Ltd | ||
Full Title: An open-label, randomized 2-period crossover study to investigate the pharmacodynamics, pharmacokinetics, safety and tolerability of warfarin in combination with oseltamivir in volunteers stabilize... | ||
Medical condition: Drug interaction study to investigate the the PD, PK, safety and tolerability of warfarin in combination with oseltamivir in volunteers stabilized on warfarin therapy. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-014365-12 | Sponsor Protocol Number: WP22849 | Start Date*: 2010-01-26 | |||||||||||
Sponsor Name:F.Hoffmann-La Roche Ltd. | |||||||||||||
Full Title: Evaluación prospectiva en régimen abierto de la farmacocinética, la farmacodinamia y la seguridad de oseltamivir (Tamiflu®) en el tratamiento de lactantes de menos de 12 meses con infección gripal ... | |||||||||||||
Medical condition: Tratamiento de la gripe. Treatment of influenza. | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) FR (Completed) DE (Completed) GB (Completed) BE (Completed) NL (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002633-11 | Sponsor Protocol Number: NV25719 | Start Date*: 2013-01-24 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd. | |||||||||||||
Full Title: An open label, randomised, adaptive, multicenter, pharmacokinetic/pharmacodynamic, phase Ib, study of oseltamivir (Tamiflu®) in the treatment of influenza in immunocompromised children, between 0-1... | |||||||||||||
Medical condition: Treatment of influenza in immunocompromised paedriatric patients. | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) DE (Completed) FI (Completed) IT (Completed) PL (Completed) BE (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-004543-11 | Sponsor Protocol Number: 2008-517 | Start Date*: 2008-10-03 | |||||||||||
Sponsor Name:HOSPICES CIVILS DE LYON | |||||||||||||
Full Title: COMBINA. Efficacité et tolérance des bithérapies oseltamivir + zanamivir ou oseltamivir + amantadine en comparaison avec la monothérapie oseltamivir dans le traitement de la grippe saisonnière A | |||||||||||||
Medical condition: Grippe de type A confirmée | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001805-21 | Sponsor Protocol Number: RA486120 | Start Date*: 2020-05-15 |
Sponsor Name:University Hospital Coventry & Warwickshire | ||
Full Title: Prospective, Randomized, Parallel-Group, Open-Label Study to Evaluate the Efficacy and Safety of IMU-838, in Combination with Oseltamivir, in Adults with Coronavirus Disease COVID-19 | ||
Medical condition: Sars-Cov-2 | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2010-019372-72 | Sponsor Protocol Number: MV22970 | Start Date*: 2010-04-16 | |||||||||||
Sponsor Name:Pharmahungary Group | |||||||||||||
Full Title: An Observational Study on the Pharmacokinetics of Oseltamivir in the Treatment of Influenza during Lactation. | |||||||||||||
Medical condition: Lactating women who present with clinical symptoms indicative of influenza will be recruited to receive immediate treatment with oseltamivir at a standard dose of 75 mg twice daily. These subjects ... | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: HU (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-000461-43 | Sponsor Protocol Number: GV29216 | Start Date*: 2014-12-22 | |||||||||||||||||||||
Sponsor Name:Genentech Inc. | |||||||||||||||||||||||
Full Title: A PHASE 2 RANDOMIZED, DOUBLE-BLIND TRIAL OF MHAA4549A, A MONOCLONAL ANTIBODY IN COMBINATION WITH OSELTAMIVIR VERSUS OSELTAMIVIR FOR TREATMENT OF SEVERE INFLUENZA A INFECTION | |||||||||||||||||||||||
Medical condition: Treatment of Influenza | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: IT (Prematurely Ended) GB (Completed) HU (Completed) DE (Completed) CZ (Prematurely Ended) ES (Completed) BE (Completed) NL (Completed) BG (Prematurely Ended) PL (Completed) FR (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-020083-38 | Sponsor Protocol Number: NV25118 | Start Date*: 2010-10-12 | ||||||||||||||||||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | ||||||||||||||||||||||||||||
Full Title: A Multicenter, Study of the Safety of Oseltamivir Administered Intravenously for the Treatment of Influenza in Patients Aged ≥13 Years | ||||||||||||||||||||||||||||
Medical condition: Treatment of Influenza [seasonal or pandemic (H1N1) 2009] | ||||||||||||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: HU (Completed) DE (Completed) LT (Prematurely Ended) DK (Prematurely Ended) FR (Ongoing) IT (Prematurely Ended) ES (Prematurely Ended) PL (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2022-002377-28 | Sponsor Protocol Number: APHP210090 | Start Date*: 2022-10-17 | |||||||||||
Sponsor Name:Assistance Publique – Hôpitaux de Paris (AP-HP) | |||||||||||||
Full Title: Prognostic impact of early oseltamivir carboxylate underdosing in patients admitted to the ICU with severe influenza: a multicenter prospective cohort study | |||||||||||||
Medical condition: Adult patients admitted to the ICU for management of severe influenza infection requiring orotracheal intubation for invasive mechanical ventilation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-004009-15 | Sponsor Protocol Number: VIS410-203 | Start Date*: 2017-07-03 | |||||||||||
Sponsor Name:Visterra, Inc. | |||||||||||||
Full Title: Phase 2b, Multicenter, Randomized, Double-blind, Controlled Study to Evaluate the Efficacy and Safety of Intravenous VIS410 in Addition to Oseltamivir (Tamiflu®) Compared With Oseltamivir Alone in ... | |||||||||||||
Medical condition: Influenza A infection in hospitalized patients who need supplemental oxygen | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) BG (Completed) EE (Completed) LV (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-002473-47 | Sponsor Protocol Number: NV20235 | Start Date*: 2007-01-25 | |||||||||||
Sponsor Name:F.Hoffmann-La Roche Ltd. | |||||||||||||
Full Title: A double blind, randomized, placebo controlled, multi-center trial of oseltamivir for the seasonal prophylaxis of influenza in immunocompromised patients | |||||||||||||
Medical condition: Seasonal prophylaxis of influenza in immonucompromised subjects | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) DE (Completed) LT (Completed) FR (Completed) CZ (Completed) BE (Completed) EE (Completed) IT (Completed) PL (Ongoing) GB (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-001610-38 | Sponsor Protocol Number: JAGG2020-1 | Start Date*: 2020-09-16 | |||||||||||
Sponsor Name:Slagelse Sygehus | |||||||||||||
Full Title: Irbesartan and Oseltamivir treatment of COVID-19 infection. | |||||||||||||
Medical condition: The combined treatment in this trial will be used to treat patients with Covid-19 infection in order to prevent the patients need for further treatment in a hospital. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-003002-17 | Sponsor Protocol Number: 63623872FLZ2002 | Start Date*: 2015-11-17 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: A Phase 2, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Pharmacokinetics, Safety, and Antiviral Activity of JNJ-63623872 in Combination With Oseltamivir in Adult and Elderly H... | |||||||||||||
Medical condition: Influenza A virus infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) BE (Completed) DE (Completed) NL (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002512-40 | Sponsor Protocol Number: 201023 | Start Date*: 2016-12-05 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
Full Title: A Phase II, global, randomized study to evaluate the efficacy and safety of Danirixin (GSK1325756) co-administered with a standard-of-care antiviral (oseltamivir), in the treatment of adults hospit... | |||||||||||||
Medical condition: Hospitalized influenza | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) ES (Completed) NL (Prematurely Ended) FR (Completed) | |||||||||||||
Trial results: View results |
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