|D045169||Severe Acute Respiratory Syndrome NIH||0.04|
|D018352||Coronavirus Infections NIH||0.04|
There is one clinical trial.
Maraviroc, a C-C Chemokine Receptor 5 (CCR5) antagonist, is well-tolerated without significant side effects in its current use in patients with HIV. CCR5 antagonism prior to the 'second wave' of inflammatory mediator expression in SARS-CoV-2 may reverse lymphoid depletion and may alter cell trafficking of inflammatory cells, both increasing viral control capacity and dampening damage to lung tissue, respectively. This study seeks to establish whether one week of treatment with Maraviroc, used at its approved dosage for HIV, is safe and tolerable in patients with SARS-CoV-2.
Description: Rate of subjects who complete the 7-day course of Maraviroc without discontinuation for serious adverse event or death.Measure: Rate of Completion Time: 7 days
Description: Percent of patients at Day 7 from enrollment achieving reduction of two points on a seven-category ordinal scale (defined below). Ordinal scale: 1, not hospitalized with resumption of normal activities; 2, not hospitalized, but unable to resume normal activities OR hospitalized pending disposition, not requiring COVID-related care; 3, hospitalized, not requiring supplemental oxygen; 4, hospitalized, requiring supplemental oxygen; 5, hospitalized, requiring nasal high-flow oxygen therapy, noninvasive mechanical ventilation, or both; 6, hospitalized, requiring ECMO, invasive mechanical ventilation, or both; and, 7, death.Measure: Clinical improvement at Day 7 Time: 7 days
Description: Measurement of Chi3l1 before, during and at completion of therapy.Measure: Change in Chitinase 3-like 1(Chi3l1) (ng/mL) Time: 7 days
Description: Measurement of IL-6 before, during and at completion of therapy.Measure: Change in Interleukin-6 (IL-6) (pg/mL) Time: 7 Days
Description: Measurement of CCL5 before, during and at completion of therapy.Measure: Change in CCL5 (RANTES) (ng/mL) Time: 7 Days
Description: 7-, 14- and 28-day all-cause-mortalityMeasure: Mortality Time: 28 days
Description: Time to improvement to Score of 2 or less (Days)Measure: Time to Discharge Time: 28 days
Data processed on December 13, 2020.
An HTML report was created for each of the unique drugs, MeSH, and HPO terms associated with COVID-19 clinical trials. Each report contains a list of either the drug, the MeSH terms, or the HPO terms. All of the terms in a category are displayed on the left-hand side of the report to enable easy navigation, and the reports contain a list of correlated drugs, MeSH, and HPO terms. Further, all reports contain the details of the clinical trials in which the term is referenced. Every clinical trial report shows the mapped HPO and MeSH terms, which are also hyperlinked. Related HPO terms, with their associated genes, protein mutations, and SNPs are also referenced in the report.Drug Reports MeSH Reports HPO Reports