CovidResearchTrials by Shray Alag


CovidResearchTrials Covid 19 Research using Clinical Trials (Home Page)


INC424 / RuxolitinibWiki

Developed by Shray Alag
Clinical Trial MeSH HPO Drug Gene SNP Protein Mutation


Correlated Drug Terms (1)


Name (Synonyms) Correlation
drug1608 Nitric Oxide-Releasing Drug Wiki 1.00

Correlated MeSH Terms (4)


Name (Synonyms) Correlation
D003141 Communicable Diseases NIH 0.09
D007239 Infection NIH 0.06
D045169 Severe Acute Respiratory Syndrome NIH 0.05
D018352 Coronavirus Infections NIH 0.04

Correlated HPO Terms (0)


Name (Synonyms) Correlation

There is one clinical trial.

Clinical Trials


1 Safety and Efficacy Study of Ruxolitinib in the Treatment of Severe Acute Respiratory Syndrome Due to SARS-COV-2

The treatment of COVID-19 severe acute respiratory syndrome with ruxolitinib 5 mg orally every 12 hours during 14 days would stop the disproportionate inflammatory response, causing a reduction in the proportion of patients who show a progression and worsening of the severe acute respiratory syndrome.

NCT04414098 COVID-19 Drug: INC424 / Ruxolitinib

Primary Outcomes

Description: Measuring the proportion of patients with clinical worsening (defined by a requirement of FIO2 >50% and/or mechanical respiratory assistance)

Measure: Evaluate the efficacy of ruxolitinib in the treatment of COVID-19 severe acute respiratory syndrome

Time: during 14 days after the commencement of treatment

Secondary Outcomes

Measure: Evaluate the median duration of hospitalization.

Time: after 45 days of commencement of treatment.

Description: Evaluation at the beginning (baseline), middle and end of the treatment with ruxolitinib of PCR, LDH, ESD, Ferritin and IL-6 (if available).

Measure: Evaluate the evolution of systemic inflammation parameters.

Time: after 45 days of commencement of treatment.

Measure: Evaluate COVID-19 mortality rate

Time: after 45 days of treatment.

Measure: Evaluate the proportion of the requirement of mechanical ventilation.

Time: with a total follow-up of 45 days

Measure: Evaluate ruxolitinib adverse reactions

Time: with a total follow-up of 45 days.

Measure: Evaluate the proportion of secondary infections during the treatment with ruxolitinib

Time: after 45 days of commencement of treatment.


No related HPO nodes (Using clinical trials)