- Trials with a EudraCT protocol (52)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
52 result(s) found for: antiviral COVID-19.
Displaying page 2 of 3.
| EudraCT Number: 2022-002741-18 | Sponsor Protocol Number: GS-US-611-6273 | Start Date*: 2022-12-19 | |||||||||||
| Sponsor Name:Gilead Sciences, Inc. | |||||||||||||
| Full Title: A Phase 3, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of GS-5245 for the Treatment of COVID-19 in Participants With High-Risk for Disease Progression | |||||||||||||
| Medical condition: Coronavirus disease 2019 (COVID-19) in patients who have a high risk of developing serious or severe illness | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) HU (Completed) ES (Ongoing) BG (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-000842-32 | Sponsor Protocol Number: GS-US-540-5774 | Start Date*: 2020-03-18 | |||||||||||
| Sponsor Name:Gilead Sciences, Inc. | |||||||||||||
| Full Title: A Phase 3 Randomized Study to Evaluate the Safety and Antiviral Activity of Remdesivir (GS-5734™) in Participants with Moderate COVID-19 Compared to Standard of Care Treatment | |||||||||||||
| Medical condition: Coronavirus disease 2019 (COVID-19) | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) ES (Completed) FR (Completed) IT (Completed) NL (Completed) GB (Completed) SE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-003510-12 | Sponsor Protocol Number: GS-US-540-9012 | Start Date*: 2020-10-02 | |||||||||||
| Sponsor Name:Gilead Sciences, Inc | |||||||||||||
| Full Title: A Phase 3 Randomized, Double-Blind Placebo-Controlled Trial to Evaluate the Efficacy and Safety of Remdesivir (GS-5734™) Treatment of COVID-19 in an Outpatient Setting | |||||||||||||
| Medical condition: COVID-19 | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) GB (GB - no longer in EU/EEA) PT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-002106-68 | Sponsor Protocol Number: CTU/2020/354 | Start Date*: 2020-07-16 | |||||||||||
| Sponsor Name:University College London Comprehensive Clinical Trial Unit | |||||||||||||
| Full Title: Favipiravir, lopinavir/ritonavir or combination therapy: a randomised, double blind, 2x2 factorial placebo-controlled trial of early antiviral therapy in COVID-19 | |||||||||||||
| Medical condition: SARS-CoV-2 (Corona virus) infection | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-003475-18 | Sponsor Protocol Number: COV-AAT | Start Date*: 2020-10-21 |
| Sponsor Name:Ghent University Hospital | ||
| Full Title: The potential of oral Camostat in early COVID-19 disease in an ambulatory setting to reduce viral load and disease burden. | ||
| Medical condition: severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2021-005247-78 | Sponsor Protocol Number: OB003 | Start Date*: 2022-01-19 | |||||||||||
| Sponsor Name:Oxygen Biotech s.r.o. | |||||||||||||
| Full Title: A 2-Part, Open-label, Non-randomized (Part A) and Randomized, Double-blinded, Placebo-controlled (Part B) multicentric, international study with adaptive design to evaluate safety and tolerability ... | |||||||||||||
| Medical condition: COVID-19 patients suffering from moderate to severe pneumonia | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-002060-31 | Sponsor Protocol Number: WHOCOVID-19coreprotocol | Start Date*: 2020-06-22 |
| Sponsor Name:Masaryk University | ||
| Full Title: An international randomised trial of additional treatments for COVID-19 in hospitalised patients who are all receiving the local standard of care | ||
| Medical condition: COVID-19 | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: CZ (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-001363-85 | Sponsor Protocol Number: 60152610 | Start Date*: 2020-04-23 | ||||||||||||||||
| Sponsor Name:Odense University Hospital | ||||||||||||||||||
| Full Title: COVID-19 Prophylaxis with hydroxychloroquine, Vitamin D, and Zinc supplementation in Danish nursing home residents – a randomized controlled trial | ||||||||||||||||||
| Medical condition: Healthy volunteer (Prophylaxis for COVID-19) | ||||||||||||||||||
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| Population Age: Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DK (Prematurely Ended) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2020-001023-14 | Sponsor Protocol Number: SG016 | Start Date*: 2020-03-17 | |||||||||||
| Sponsor Name:Synairgen Research Limited | |||||||||||||
| Full Title: A randomised double-blind placebo-controlled trial to determine the safety and efficacy of inhaled SNG001 (IFNβ-1a for nebulisation) for the treatment of patients with confirmed SARS-CoV-2 infectio... | |||||||||||||
| Medical condition: COVID-19 | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-001541-39 | Sponsor Protocol Number: BEVACOR | Start Date*: 2020-04-24 | ||||||||||||||||
| Sponsor Name:Fundación para la Investigación Biomédica de Córdoba | ||||||||||||||||||
| Full Title: Pilot study of single-dose bevacizumab as a treatment for acute respiratory distress syndrome in patients with COVID-19 | ||||||||||||||||||
| Medical condition: Acute respiratory distress syndrome in patients with COVID-19 | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: ES (Prematurely Ended) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2021-001663-24 | Sponsor Protocol Number: INSIGHT012 | Start Date*: 2021-09-20 | |||||||||||
| Sponsor Name:Office of Sponsored Projects,University of Minnesota | |||||||||||||
| Full Title: An International Multicenter, Randomized, Double-Blind, Placebo-Controlled Trial of the Safety and Efficacy of Anti-Coronavirus Hyperimmune Intravenous Immunoglobulin for the Treatment of Adult Out... | |||||||||||||
| Medical condition: We are investigating Coronavirus disease 2019 (COVID-19) which is predominantly a respiratory disease caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GR (Trial now transitioned) DK (Trial now transitioned) ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-000841-15 | Sponsor Protocol Number: GS-US-540-5773 | Start Date*: 2020-03-18 | |||||||||||
| Sponsor Name:Gilead Sciences, Inc. | |||||||||||||
| Full Title: A Phase 3 Randomized Study to Evaluate the Safety and Antiviral Activity of Remdesivir (GS-5734™) in Participants with Severe COVID-19 | |||||||||||||
| Medical condition: Coronavirus disease 2019 (COVID-19) | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) ES (Completed) FR (Completed) IT (Completed) NL (Completed) GB (Completed) SE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-002166-13 | Sponsor Protocol Number: HUB-MdI-ICAT-COVID-201 | Start Date*: 2020-07-09 | |||||||||||||||||||||
| Sponsor Name:Dr. Ramón Lleonart Bellfill / Dr. Xavier Corbella Virós | |||||||||||||||||||||||
| Full Title: Randomized, open, multicenter phase II clinical trial, proof of concept, to evaluate efficacy and safety of Icatibant in hospitalized patients with SARS-COV-2 (COVID-19) without assisted ventilatio... | |||||||||||||||||||||||
| Medical condition: Pneumonia caused by COVID-19 | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2020-001614-38 | Sponsor Protocol Number: S63935 | Start Date*: 2020-04-22 | |||||||||||
| Sponsor Name:UZLeuven | |||||||||||||
| Full Title: Covid-19: A randomized, open-label, adaptive, proof-of- concept clinical trial of new antiviral drug candidates against SARS-CoV-2. | |||||||||||||
| Medical condition: COVID-19 | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-002869-34 | Sponsor Protocol Number: AT-03A-001 | Start Date*: 2020-08-11 | |||||||||||
| Sponsor Name:Atea Pharmaceuticals, Inc. | |||||||||||||
| Full Title: A Phase 2 Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Safety and Efficacy of AT-527 in Subjects with Moderate COVID-19 | |||||||||||||
| Medical condition: COVID-19 | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-003237-11 | Sponsor Protocol Number: TMP-2005-2020-36 | Start Date*: 2021-11-11 | ||||||||||||||||
| Sponsor Name:Fraunhofer Gesellschaft for its Institute for translationale Medicine and Pharmacology ITMP | ||||||||||||||||||
| Full Title: Effect of Bronchipret on antiviral immune response in patients with mild COVID-19 (BroVID) | ||||||||||||||||||
| Medical condition: Adult patients suffering from mild COVID-19 with cough and at least one other symptoms will be recruited for this study. | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2020-001467-82 | Sponsor Protocol Number: P020.051 | Start Date*: 2020-10-23 | ||||||||||||||||
| Sponsor Name:Leiden University Medical Center | ||||||||||||||||||
| Full Title: An Open-Label Study Evaluating Anti-Viral Effects of Voclosporin in SARS-CoV-2 Positive Kidney Transplant Recipients – the VOCOVID Study (COVID-19) | ||||||||||||||||||
| Medical condition: SARS-CoV-2 infection in Kidney Transplant Recipients | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: NL (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2020-004743-83 | Sponsor Protocol Number: SG018 | Start Date*: 2020-11-09 | |||||||||||
| Sponsor Name:Synairgen Research Limited | |||||||||||||
| Full Title: A randomised, double-blind, placebo-controlled, Phase III trial to determine the efficacy and safety of inhaled SNG001 for the treatment of patients hospitalised due to moderate COVID-19 | |||||||||||||
| Medical condition: COVID-19 | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) BE (Completed) PT (Completed) FR (Completed) NL (Completed) IT (Completed) DE (Completed) RO (Completed) ES (Ongoing) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-001390-76 | Sponsor Protocol Number: ESCAPE | Start Date*: 2020-04-27 | |||||||||||
| Sponsor Name:ISTITUTO NAZIONALE PER LE MALATTIE INFETTIVE "LAZZARO SPALLANZANI" | |||||||||||||
| Full Title: A phase 3, randomized, open-labeled, multi-center study comparing clinical efficacy and safety of intravenous sarilumab plus standard of care compared to standard of care, in the treatment of patie... | |||||||||||||
| Medical condition: Covid-19 coronavirus infection | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-001329-30 | Sponsor Protocol Number: 2020P000787 | Start Date*: 2020-04-09 |
| Sponsor Name:Massachussetts General Hospital | ||
| Full Title: Inhaled Nitric Oxide Gas Therapy in Mechanically Ventilated Patients with Severe Acute Respiratory Syndrome in COVID-19 | ||
| Medical condition: ARDS caused by COVID-19 infection | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Prematurely Ended) | ||
| Trial results: (No results available) | ||
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