- Trials with a EudraCT protocol (288)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
288 result(s) found for: SARS coronavirus.
Displaying page 11 of 15.
| EudraCT Number: 2020-001528-32 | Sponsor Protocol Number: ARCO-Homestudy | Start Date*: 2020-05-14 | |||||||||||
| Sponsor Name:ISTITUTO NAZIONALE PER LE MALATTIE INFETTIVE "LAZZARO SPALLANZANI" | |||||||||||||
| Full Title: Adaptive Randomized trial for therapy of COrona virus disease 2019 at home with oral antivirals | |||||||||||||
| Medical condition: Coronavirus Covid 19 infection | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-001367-88 | Sponsor Protocol Number: 25032020 | Start Date*: 2020-04-14 | |||||||||||
| Sponsor Name:Department of Infectious diseases | |||||||||||||
| Full Title: Efficacy and safety of novel treatment options for adults with COVID-19 pneumonia. A double-blinded, randomized, multi-stage, 6-armed placebo-controlled trial in the framework of an adaptive trial ... | |||||||||||||
| Medical condition: COVID-19 | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-001265-36 | Sponsor Protocol Number: UCDCRC/20/01 | Start Date*: 2020-05-05 | |||||||||||
| Sponsor Name:University College Dublin | |||||||||||||
| Full Title: A multicentre, prospective, randomised trial comparing standard of care (SOC) alone, SOC plus hydroxychloroquine monotherapy or SOC plus a combination of hydroxychloroquine and azithromycin in the ... | |||||||||||||
| Medical condition: SARS-CoV-2 PCR-positive population | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-000492-36 | Sponsor Protocol Number: HOPECOVID-19 | Start Date*: 2021-05-31 | |||||||||||
| Sponsor Name:UCLouvain | |||||||||||||
| Full Title: Home and Outpatients Precocious Eradication of COVID-19 | |||||||||||||
| Medical condition: COVID-19 | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2022-000063-51 | Sponsor Protocol Number: mRNA-1273-P305 | Start Date*: 2024-01-01 |
| Sponsor Name:ModernaTX, Inc. | ||
| Full Title: A Phase 2/3, Randomized, Observer-blind, Active-controlled, Multicenter Study to Evaluate the Immunogenicity and Safety of Omicron Variant Vaccines in Comparison with mRNA-1273 (Prototype) Booster ... | ||
| Medical condition: SARS-CoV-2 | ||
| Disease: | ||
| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
| Trial protocol: Outside EU/EEA | ||
| Trial results: View results | ||
| EudraCT Number: 2021-000344-21 | Sponsor Protocol Number: MP1032-CT05 | Start Date*: 2021-07-21 | ||||||||||||||||||||||||||
| Sponsor Name:MetrioPharm AG | ||||||||||||||||||||||||||||
| Full Title: A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, MULTICENTER, PROOF-OF-CONCEPT, PHASE IIA STUDY OF MP1032 PLUS STANDARD OF CARE VS STANDARD OF CARE IN THE TREATMENT OF HOSPITALIZED PATIENTS WITH MOD... | ||||||||||||||||||||||||||||
| Medical condition: Moderate to severe coronavirus disease 2019 (COVID 19) | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: FR (Completed) HU (Completed) ES (Ongoing) BG (Completed) IT (Completed) RO (Ongoing) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
| EudraCT Number: 2020-006082-11 | Sponsor Protocol Number: ADG20-TRMT-001 | Start Date*: 2021-06-02 | |||||||||||
| Sponsor Name:Adagio Therapeutics Inc. | |||||||||||||
| Full Title: A Phase 2/3 Randomized, Double-Blind, Placebo-Controlled Trial to Evaluate the Efficacy and Safety of ADG20 in the Treatment of Ambulatory Participants with Mild or Moderate COVID-19 (STAMP) | |||||||||||||
| Medical condition: COVID-19 | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GR (Prematurely Ended) DE (Prematurely Ended) HU (Completed) BG (Prematurely Ended) PL (Prematurely Ended) RO (Ongoing) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-001782-37 | Sponsor Protocol Number: PО-COV-III-20 | Start Date*: 2020-11-07 | |||||||||||
| Sponsor Name:NPO Petrovax Pharm, LLC | |||||||||||||
| Full Title: A multi-centre, adaptive, randomized, double-blind, placebo-controlled comparative clinical trial of the safety and efficacy of 12 mg Polyoxidonium®, lyophilizate solution for injections (NPO Petro... | |||||||||||||
| Medical condition: | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2022-000618-32 | Sponsor Protocol Number: GNC-501 | Start Date*: 2022-09-29 | ||||||||||||||||
| Sponsor Name:GENEURO SA | ||||||||||||||||||
| Full Title: Temelimab as a Disease Modifying Therapy in Patients with Neurological, Neuropsychological, and Psychiatric (=Neuropsychiatric) Symptoms in Post-COVID-19 or Postacute Sequelae of COVID-19 (PASC) Sy... | ||||||||||||||||||
| Medical condition: Postacute Sequelae of COVID-19 (PASC) Syndrome | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: IT (Completed) ES (Ongoing) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2020-001696-32 | Sponsor Protocol Number: GC2004 | Start Date*: 2020-05-08 | ||||||||||||||||
| Sponsor Name:Instituto Grifols, S.A | ||||||||||||||||||
| Full Title: A Multicenter, Randomized, Open-label Parallel Group Pilot Study to Evaluate Safety and Efficacy of High Dose Intravenous Immune Globulin (IVIG) plus Standard Medical Treatment (SMT) versus SMT alo... | ||||||||||||||||||
| Medical condition: Patients with Mild to Moderate Coronavirus Disease (COVID-19) | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: ES (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2020-002011-21 | Sponsor Protocol Number: MARACOVID | Start Date*: 2020-06-02 |
| Sponsor Name:Fundación para la Investigación e Innovación Biomédica del Hospital Universitario Infanta Leonor y Sureste (FIIB) | ||
| Full Title: Bicentric, phase 2, randomized, open-label study to evaluate the efficacy and safety of maraviroc associated with standard treatment in hospitalized patients with pulmonary SARS-CoV-2 infection (CO... | ||
| Medical condition: COVID-19 Pneumonia | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-002895-38 | Sponsor Protocol Number: C4671005 | Start Date*: 2021-08-23 | |||||||||||
| Sponsor Name:Pfizer Inc. | |||||||||||||
| Full Title: AN INTERVENTIONAL EFFICACY AND SAFETY, PHASE 2/3, DOUBLE-BLIND, 2-ARM STUDY TO INVESTIGATE ORALLY ADMINISTERED PF-07321332/RITONAVIR COMPARED WITH PLACEBO IN NONHOSPITALIZED SYMPTOMATIC ADULT PARTI... | |||||||||||||
| Medical condition: Coronavirus Disease 2019 (COVID-19) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) CZ (Completed) HU (Completed) BG (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-001904-41 | Sponsor Protocol Number: GETAFIX-2020 | Start Date*: 2020-05-20 | |||||||||||
| Sponsor Name:NHS Greater Glasgow and Clyde [...] | |||||||||||||
| Full Title: Glasgow Early Treatment Arm FavIpiravir : A randomized controlled study of favipiravir as an early treatment arm in COVID-19 patients | |||||||||||||
| Medical condition: COVID-19 | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-001405-23 | Sponsor Protocol Number: Ruxo-Sim-20 | Start Date*: 2020-06-05 | |||||||||||
| Sponsor Name:Fundación de Investigación HM Hospitales | |||||||||||||
| Full Title: Randomized phase II clinical trial of ruxolitinib plus simvastatin in the prevention and treatment of respiratory failure of COVID-19.Ruxo-Sim-20 clinical trial. | |||||||||||||
| Medical condition: COVID19 | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-001203-16 | Sponsor Protocol Number: LIBERATE | Start Date*: 2020-05-06 | |||||||||||||||||||||
| Sponsor Name:Guy's and St Thomas' NHS Foundation Trust [...] | |||||||||||||||||||||||
| Full Title: Lipid ibuprofen versus standard of care for acute hypoxaemic respiratory failure due to COVID-19: a multicentre, randomised, controlled trial | |||||||||||||||||||||||
| Medical condition: COVID-19; respiratory failure; hypoxaemia. | |||||||||||||||||||||||
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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: 2020-001767-86 | Sponsor Protocol Number: COVIRL-002 | Start Date*: 2020-06-25 | |||||||||||
| Sponsor Name:University College Dublin | |||||||||||||
| Full Title: An open-label, multi-centre, randomised trial comparing different doses of single-dose tocilizumab in adults with severe, non-critical, PCR-confirmed COVID-19 infection with evidence of progressive... | |||||||||||||
| Medical condition: COVID-19 infection | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-001505-22 | Sponsor Protocol Number: BST-COVID-01 | Start Date*: 2020-04-23 | |||||||||||
| Sponsor Name:Banc de Sang i Teixits | |||||||||||||
| Full Title: Double-blind, randomized, parallel, placebo-controlled pilot clinical trial, nested in a prospective cohort observational study, for the evaluation of the efficacy and safetyof two doses of WJ-MSC ... | |||||||||||||
| Medical condition: Acute respiratory distress syndrome | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-002259-39 | Sponsor Protocol Number: TL-895-202 | Start Date*: 2020-09-23 | |||||||||||
| Sponsor Name:Telios Pharma, Inc. | |||||||||||||
| Full Title: A Phase 1/2, Double-Blind, Randomized, Placebo-Controlled Study of TL-895 with Standard Available Treatment versus Standard Available Treatment for the Treatment of COVID-19 in Patients with Cancer | |||||||||||||
| Medical condition: Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) in patients with cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: RO (Prematurely Ended) HU (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-000627-12 | Sponsor Protocol Number: CV43140 | Start Date*: 2021-06-01 | |||||||||||
| Sponsor Name:F. Hoffmann La Roche Ltd. | |||||||||||||
| Full Title: A MULTICENTER, OBSERVATIONAL, 6 MONTH FOLLOW-UP STUDY OF PATIENTS WITH COVID 19 PREVIOUSLY ENROLLED IN A RO7496998 (AT-527) STUDY | |||||||||||||
| Medical condition: Coronavirus disease 2019 (COVID-19) | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) PT (Prematurely Ended) DK (Completed) DE (Completed) IT (Prematurely Ended) RO (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-005332-27 | Sponsor Protocol Number: WA43811 | Start Date*: 2022-01-31 |
| Sponsor Name:F. Hoffmann-La Roche Ltd | ||
| Full Title: A PHASE Ib, SINGLE-ARM, OPEN-LABEL STUDY EVALUATING THE PHARMACOKINETICS, PHARMACODYNAMICS, AND SAFETY OF TOCILIZUMAB IN PEDIATRIC PATIENTS HOSPITALIZED WITH COVID-19 | ||
| Medical condition: Coronavirus disease 2019 (COVID-19) | ||
| Disease: | ||
| Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) IT (Prematurely Ended) GR (Completed) FR (Completed) DE (Completed) PL (Completed) | ||
| Trial results: View results | ||
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