|D012127||Respiratory Distress Syndrome, Newborn NIH||0.08|
|D055371||Acute Lung Injury NIH||0.08|
|D012128||Respiratory Distress Syndrome, Adult NIH||0.07|
There is one clinical trial.
This is an adaptive Phase I-II trial of a vaccine consisting of autologous dendritic cells previously loaded ex vivo with SARS-CoV-2 spike protein, with or without GM-CSF, to prevent COVID-19 in adults.
Description: Confirm safety of AV-COVID-19 by adverse event monitoringMeasure: Confirm safety Time: 1 year
Description: Measurement of IgG in subject bloodMeasure: Suggestion of efficacy Time: 1 month
Description: Measurement of IgG in subject bloodMeasure: Optimal dose of SARS-CoV-2 antigen and GM-CSF Time: 1 months
Description: Measurement of IgG in subject bloodMeasure: Duration of detecting IgG against SARS-CoV-2 in blood after vaccination Time: 12 months
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