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Column | Value |
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Trial registration number | NCT04358549 |
Full text link
Last imported at : Oct. 26, 2020, 11:31 p.m. Source : ClinicalTrials.gov |
|
First author
Last imported at : Oct. 26, 2020, 11:31 p.m. Source : ClinicalTrials.gov |
|
Contact
Last imported at : Oct. 26, 2020, 11:31 p.m. Source : ClinicalTrials.gov |
favipiravircontact.fphu@fujifilm.com |
Registration date
Last imported at : Oct. 26, 2020, 11:31 p.m. Source : ClinicalTrials.gov |
2020-04-24 |
Recruitment status
Last imported at : July 28, 2021, noon Source : ClinicalTrials.gov |
Completed |
Study design
Last imported at : Oct. 26, 2020, 11:31 p.m. Source : ClinicalTrials.gov |
RCT |
Allocation
Last imported at : Oct. 26, 2020, 11:31 p.m. Source : ClinicalTrials.gov |
Randomized |
Design
Last imported at : Oct. 26, 2020, 11:31 p.m. Source : ClinicalTrials.gov |
Parallel |
Masking
Last imported at : Oct. 26, 2020, 11:31 p.m. Source : ClinicalTrials.gov |
Open label |
Center
Last imported at : March 15, 2023, 4 a.m. Source : ClinicalTrials.gov |
multi-center |
Study aim
Last imported at : Oct. 26, 2020, 11:31 p.m. Source : ClinicalTrials.gov |
Treatment |
Inclusion criteria
Last imported at : March 30, 2022, 3 p.m. Source : ClinicalTrials.gov |
inclusion criteria: 1) adults (18 to 80 years old): within 72 hours of their hospitalization for infection with severe acute respiratory syndrome - corona virus - 2 (sars-cov-2), and, within 72 hours of the latest polymerase chain reaction (pcr) positive result and within 7 days of the 1st pcr positive result for sars-cov-2. (the latest pcr could be the only pcr result.), and, within 10 days of onset of any covid-19 symptoms. |
Exclusion criteria
Last imported at : Nov. 16, 2021, 6:30 p.m. Source : ClinicalTrials.gov |
subject has a concomitant bacterial respiratory infection unless cleared by the sponsor subject has a history of abnormalities of uric acid metabolism unless cleared by the sponsor. subject has a history of hypersensitivity to an anti-viral nucleoside analog drug targeting a viral rna polymerase subject is using adrenocorticosteroids (except topical or inhaled preparations or oral preparations equivalent to or less than 10 mg of oral prednisone) or immunosuppressive or immunomodulatory drugs (e.g., immunosuppressants, anticancer drugs, interleukins, interleukin antagonists or interleukin receptor blockers). dexamethasone 6 mg daily (po or iv) for 10 days is permitted. subject has a serious chronic disease (e.g., human immunodeficiency virus (hiv), cancer requiring chemotherapy within the preceding 6 months, moderate or severe hepatic insufficiency and/or unstable renal, cardiac, pulmonary, neurologic, vascular, or endocrinologic disease states requiring medication dose adjustments within the last 30 days). has previously received favipiravir within the past 30 days has renal insufficiency requiring hemodialysis or continuous ambulatory peritoneal dialysis (capd) or glomerular filtration rate of less than 20 ml/min. has liver impairment greater than child-pugh a. has a history of alcohol or drug abuse in the previous 6 months. has a psychiatric disease that is not well controlled where controlled is defined as: stable on a regimen for more than one year. has taken another investigational drug within the past 30 days. is on another antiviral or is participating in another clinical trial for the treatment of covid-19 subject is on a ventilator at the time of study entry is deemed by the investigator to be ineligible for any reason. |
Number of arms
Last imported at : Oct. 26, 2020, 11:31 p.m. Source : ClinicalTrials.gov |
2 |
Funding
Last imported at : Oct. 26, 2020, 11:31 p.m. Source : ClinicalTrials.gov |
Fujifilm Pharmaceuticals U.S.A., Inc. |
Inclusion age min
Last imported at : Oct. 26, 2020, 11:31 p.m. Source : ClinicalTrials.gov |
18 |
Inclusion age max
Last imported at : Oct. 26, 2020, 11:31 p.m. Source : ClinicalTrials.gov |
80 |
Countries
Last imported at : Oct. 26, 2020, 11:31 p.m. Source : ClinicalTrials.gov |
United States |
Type of patients
Last imported at : Oct. 26, 2020, 11:31 p.m. Source : ClinicalTrials.gov |
Moderate/severe disease at enrollment |
Severity scale
Last imported at : Oct. 26, 2020, 11:31 p.m. Source : ClinicalTrials.gov |
4: Moderate/severe disease at enrollment |
Total sample size
Last imported at : Oct. 26, 2020, 11:31 p.m. Source : ClinicalTrials.gov |
50 |
primary outcome
Last imported at : Oct. 26, 2020, 11:31 p.m. Source : ClinicalTrials.gov |
Time to viral clearance |
Notes
Last imported at : Oct. 26, 2020, 11:31 p.m. Source : ClinicalTrials.gov |
None |
Phase
Last imported at : Feb. 25, 2021, 7:58 p.m. Source : ClinicalTrials.gov |
Phase 2 |
Arms
Last imported at : March 30, 2022, 3 p.m. Source : ClinicalTrials.gov |
[{"arm_notes": "nan", "treatment_id": 504, "treatment_name": "Favipiravir", "treatment_type": "Antivirals", "pharmacological_treatment": "Pharmacological treatment"}, {"arm_notes": "nan", "treatment_id": 2188, "treatment_name": "Standard of care", "treatment_type": "Standard of care", "pharmacological_treatment": "Standard of care"}] |