CovidResearchTrials by Shray Alag


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Imatinib MesylateWiki

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


Correlated Drug Terms (1)


Name (Synonyms) Correlation
drug2319 Standard of Care Wiki 0.20

Correlated MeSH Terms (1)


Name (Synonyms) Correlation
D011014 Pneumonia NIH 0.06

Correlated HPO Terms (1)


Name (Synonyms) Correlation
HP:0002090 Pneumonia HPO 0.06

There is one clinical trial.

Clinical Trials


1 Imatinib for the Treatment of SARS-COV-2 Induced Pneumonia: A Pilot Study

A randomized controlled pilot study on the safety & efficacy of imatinib for the treatment of patient with moderate to severe SARS-COV-2 induced pneumonia.

NCT04422678 COVID-19 Drug: Imatinib Mesylate Drug: Standard of Care
MeSH:Pneumonia
HPO:Pneumonia

Primary Outcomes

Description: Proportion of patients with COVID-19 pneumonia progressed to critical illness in need for invasive mechanical ventilation.

Measure: Primary endpoint: Disease Progression

Time: 30 Days

Secondary Outcomes

Description: Improvement of Hypoxic index( PaO2 / FiO2) calculated daily

Measure: Improvement in Hypoxic Index

Time: From inclusion to 30 days follow up

Description: Hospital Length of stay

Measure: Hospital Length of Stay

Time: From inclusion to 30 days follow up

Description: Days on mechanical ventilation for patients needing intubation & invasive mechanical ventilation

Measure: Days on invasive mechanical ventilation

Time: From inclusion to 30 days follow up

Description: Difference in the median levels of serum IL-6, serum ferritin, CRP at the end of the follow up period between all groups

Measure: Inflammatory Markers

Time: From inclusion to 30 days

Description: Rate of viral clearance as monitored by SARS-COV-2 PCR

Measure: Viral clearance

Time: From inclusion to 30 days

Description: Difference in the overall evaluation of pulmonary infiltrative (improving / deteriorating) as assessed by imaging (Chest X-ray or Non-contrast pulmonary CT)

Measure: Radiological assessment

Time: From inclusion to 30 days

Description: Rate of serious adverse events (SAEs)

Measure: Safety of Imatinib

Time: From inclusion to 60 days


Related HPO nodes (Using clinical trials)