- Trials with a EudraCT protocol (25)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
25 result(s) found for: shionogi.
Displaying page 1 of 2.
EudraCT Number: 2020-000696-20 | Sponsor Protocol Number: 1719T0834 | Start Date*: 2020-03-31 |
Sponsor Name:Shionogi & Co., Ltd. | ||
Full Title: A phase 3 randomized, double-blind, placebo-controlled study to confirm the efficacy of a single dose of baloxavir marboxil in the prevention of influenza virus infection | ||
Medical condition: Influenza | ||
Disease: | ||
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: 2021-001026-22 | Sponsor Protocol Number: 1813T0835 | Start Date*: 2021-03-05 |
Sponsor Name:Shionogi & Co., Ltd. | ||
Full Title: An Open-label Study to Assess the Safety, Tolerability, Pharmacokinetics, and Efficacy of Baloxavir Marboxil 2% Granules after Administration of a Single Dose to Otherwise Healthy Pediatric Patient... | ||
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: 2013-002949-11 | Sponsor Protocol Number: 1326V9235 | Start Date*: 2014-02-11 | |||||||||||
Sponsor Name:Shionogi Inc. | |||||||||||||
Full Title: A Randomized Double-blind, Placebo-controlled, Parallel-group, Multicenter, Phase 3 Study to Evaluate the Long-term Safety of Naldemedine for the Treatment of Opioid-induced Constipation in Subje... | |||||||||||||
Medical condition: Opioid-induced Constipation in Subjects with Non-malignant Chronic Pain Receiving Opioid Therapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) SE (Completed) BE (Completed) EE (Completed) PT (Completed) HU (Completed) AT (Completed) DK (Completed) ES (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-002283-27 | Sponsor Protocol Number: 1812VA323 | Start Date*: 2020-03-18 | |||||||||||
Sponsor Name:Shionogi B.V. | |||||||||||||
Full Title: A phase 2b, multicenter, randomized, double-blind, placebo-controlled, parallel-group, dose selection study of S-600918 in patients with refractory chronic cough | |||||||||||||
Medical condition: Refractory chronic cough | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) CZ (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004942-91 | Sponsor Protocol Number: 1423M0634 | Start Date*: 2015-06-17 | |||||||||||
Sponsor Name:Shionogi Ltd | |||||||||||||
Full Title: A Phase 3 Randomised, Double-blind, Placebo-controlled Study to Assess the Safety and Efficacy of S-888711 (Lusutrombopag) for the Treatment of Thrombocytopenia in Patients with Chronic Liver Disea... | |||||||||||||
Medical condition: Thrombocytopenia in patients with Chronic Liver Disease (CLD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) AT (Completed) HU (Completed) DE (Completed) BE (Completed) IT (Completed) ES (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-003577-25 | Sponsor Protocol Number: 1907V921F | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Shionogi B.V. | |||||||||||||
Full Title: A Phase 1/2, Multicentre, Open-label Study to Evaluate the Pharmacokinetics, Safety, and Tolerability of Naldemedine in Paediatric Patients Who Are Receiving or Who Are About to Receive Treatment w... | |||||||||||||
Medical condition: Opioid induced constipation | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) FR (Ongoing) HU (Ongoing) IT (Ongoing) NL (Ongoing) BE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-002948-91 | Sponsor Protocol Number: 1315V9232 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Shionogi Inc. | |||||||||||||
Full Title: A Randomized, Double-blind, Placebo-controlled, Parallel-group Study of Naldemedine in the Treatment of Opioid-induced Constipation in Subjects with Non-malignant Chronic Pain Receiving Opioid Therapy | |||||||||||||
Medical condition: Opioid-induced Constipation in Subjects with Non-malignant Chronic Pain Receiving Opioid Therapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) CZ (Completed) AT (Completed) ES (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-005014-12 | Sponsor Protocol Number: 1122P1811 | Start Date*: 2012-06-13 | |||||||||||
Sponsor Name:Shionogi & Co., Ltd. | |||||||||||||
Full Title: A Phase 1/2 Study to Evaluate the Safety, Tolerability, Immune Response, and Clinical Efficacy of Cancer Peptide Vaccine S-488210 in Patients with Unresectable Locoregionally Recurrent and/or Metas... | |||||||||||||
Medical condition: Head and Neck Squamous Cell Carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004223-46 | Sponsor Protocol Number: SL75.14 | Start Date*: 2015-09-16 | |||||||||||
Sponsor Name:Stallergenes | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled, multi-center study of the efficacy and safety of STG320 sublingual tablets of house dust mite (HDM) allergen extracts in adults and adolescents with ... | |||||||||||||
Medical condition: House dust mite allergic rhinitis | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) SK (Completed) DE (Completed) CZ (Completed) BG (Completed) PL (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-002241-11 | Sponsor Protocol Number: 1314V9231 | Start Date*: 2014-03-10 | |||||||||||
Sponsor Name:Shionogi Inc. | |||||||||||||
Full Title: A Randomized, Double-blind, Placebo-controlled, Parallel-group Study of Naldemedine in the Treatment of Opioid-induced Constipation in Subjects with Non-malignant Chronic Pain Receiving Opioid Therapy | |||||||||||||
Medical condition: Opioid-induced Constipation in Subjects with Non-malignant Chronic Pain Receiving Opioid Therapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) CZ (Completed) GB (Completed) ES (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002688-32 | Sponsor Protocol Number: 1602T0832 | Start Date*: 2017-11-07 | |||||||||||||||||||||
Sponsor Name:Shionogi Ltd. | |||||||||||||||||||||||
Full Title: A Phase 3, Multicenter, Randomized, Double-blind Study of a Single Dose of S-033188 Compared with Placebo or Oseltamivir 75 mg Twice Daily for 5 Days in Patients with Influenza at High Risk of Infl... | |||||||||||||||||||||||
Medical condition: Influenza | |||||||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Completed) LV (Completed) HU (Completed) GB (Completed) PL (Completed) BG (Completed) ES (Completed) BE (Completed) RO (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-004703-23 | Sponsor Protocol Number: 1424R2131 | Start Date*: 2017-02-09 | ||||||||||||||||||||||||||
Sponsor Name:Shionogi Ltd. | ||||||||||||||||||||||||||||
Full Title: A Multicenter, Randomized, Open-label Clinical Study of S-649266 or Best Available Therapy for the Treatment of Severe Infections Caused by Carbapenem-resistant Gram-negative Pathogens | ||||||||||||||||||||||||||||
Medical condition: Hospital acquired pneumonia (HAP)/ventilator associated pneumonia (VAP)/healthcare-associated pneumonia (HCAP) or bloodstream infections/sepsis (BSI/sepsis) caused by carbapenem-resistant Gram-nega... | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: ES (Completed) DE (Completed) GR (Completed) GB (Completed) HR (Completed) FR (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-005274-22 | Sponsor Protocol Number: 1408P1921 | Start Date*: 2014-07-30 | |||||||||||
Sponsor Name:Shionogi & Co., Ltd | |||||||||||||
Full Title: A multicenter, open-label, phase 2 study of S-588410 as maintenance monotherapy after first-line platinum-containing chemotherapy in patients with advanced and/or metastatic bladder cancer | |||||||||||||
Medical condition: Advanced and/or metastatic bladder cancer, which is under control according to first-line chemotherapy. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) BG (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-002120-32 | Sponsor Protocol Number: 1802R2135 | Start Date*: 2019-12-09 | |||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Shionogi B.V. | |||||||||||||||||||||||||||||||||||||||||||
Full Title: A Single Arm, Open-label Study to Assess the Safety, Tolerability, and Pharmacokinetics of Single and Multiple Doses of Cefiderocol in Hospitalized Paediatric Subjects 3 Months to < 18 Years of Age... | |||||||||||||||||||||||||||||||||||||||||||
Medical condition: Including but not limited to complicated urinary tract infection [cUTI], complicated intra-abdominal infection [cIAI], hospital-acquired pneumonia [HAP]/ventilator-acquired pneumonia [VAP], and sep... | |||||||||||||||||||||||||||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||
Trial protocol: HU (Completed) BE (Completed) LV (Completed) | |||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-000914-76 | Sponsor Protocol Number: 1409R2121 | Start Date*: 2014-11-24 | |||||||||||
Sponsor Name:Shionogi Inc. | |||||||||||||
Full Title: A Multicenter, Double-blind, Randomized, Clinical Study to Assess the Efficacy and Safety of Intravenous S-649266 in Complicated Urinary Tract Infections with or without Pyelonephritis or Acute Unc... | |||||||||||||
Medical condition: Complicated Urinary Tract Infections with or without Pyelonephritis or Acute Uncomplicated Pyelonephritis caused by Gram-negative Pathogens | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) HU (Completed) IT (Completed) ES (Completed) DE (Completed) PL (Completed) RO (Completed) HR (Completed) LV (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-003020-23 | Sponsor Protocol Number: 1615R2132 | Start Date*: 2017-11-23 | |||||||||||||||||||||
Sponsor Name:Shionogi B.V. | |||||||||||||||||||||||
Full Title: A Multicenter, Randomized, Double-blind, Parallelgroup, Clinical Study of S-649266 Compared with Meropenem for the Treatment of Hospital-acquired Bacterial Pneumonia, Ventilator-associated Bacteria... | |||||||||||||||||||||||
Medical condition: Hospital-acquired Bacterial Pneumonia, Ventilator-associated Bacterial Pneumonia, or Healthcare-associated Bacterial Pneumonia Caused by Gram-negative Pathogens. | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: CZ (Completed) GB (Completed) LV (Completed) HU (Completed) ES (Completed) BE (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-006787-11 | Sponsor Protocol Number: 0819D1522 | Start Date*: 2009-01-15 | |||||||||||
Sponsor Name:Shionogi & Co., Ltd. | |||||||||||||
Full Title: A randomized, double blind, placebo-controlled, 2-period cross over study to evaluate effects of S-555739 on prostaglandin D2 (PGD2) induced nasal airway resistance in healthy adult volunteers | |||||||||||||
Medical condition: Allergic rhinitis | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-000069-34 | Sponsor Protocol Number: PAMORA_2020_RAP | Start Date*: 2021-11-19 | |||||||||||
Sponsor Name:Mech-Sense, Aalborg University Hospital | |||||||||||||
Full Title: Effects of a peripherally acting μ-opioid receptor antagonist on recurrent acute pancreatitis: An investigator-initiated, randomized, placebo-controlled, double-blind clinical trial | |||||||||||||
Medical condition: Recurrent acute pancreatitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-017942-30 | Sponsor Protocol Number: 0914M0622 | Start Date*: 2010-06-15 | ||||||||||||||||
Sponsor Name:Shionogi USA, Inc. | ||||||||||||||||||
Full Title: An open-label safety study of S-888711 in adult subjects with relapsed persistent or chronic immune thrombocytopenia with or without prior splenectomy | ||||||||||||||||||
Medical condition: Relapsed persistent or chronic immune thrombocytopenia with or without prior splenectomy | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Ongoing) GB (Prematurely Ended) DE (Prematurely Ended) HU (Completed) IT (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002121-30 | Sponsor Protocol Number: 1704R2133 | Start Date*: 2020-04-17 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Shionogi B.V. | ||||||||||||||||||||||||||||||||||||||
Full Title: An Open-label Study with a Nonrandomized Single-dose Phase in Subjects with Suspected or Confirmed Aerobic Gram-negative Bacterial Infections followed by a Randomized, Multiple-dose, Active-control... | ||||||||||||||||||||||||||||||||||||||
Medical condition: Single dose: Pneumonia, cUTI, complicated intra-abdominal infections [cIAI], hospital acquired bacterial pneumonia [HABP]/ventilator-associated bacterial pneumonia [VABP], and sepsis or bloodstream... | ||||||||||||||||||||||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: LT (Ongoing) GR (Ongoing) CZ (Completed) | ||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
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