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BevacizumabWiki

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Clinical Trial MeSH HPO Drug Gene SNP Protein Mutation


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D011014 Pneumonia NIH 0.08

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There is one clinical trial.

Clinical Trials


1 The Efficacy and Safety of Bevacizumab in Severe or Critical Patients With COVID-19--a Multicenter Randomized Controlled Clinical Trial

The novel coronavirus (SARS-CoV-2) is a new strain of coronavirus found in human in 2019, which causes epidemic worldwide. Novel coronavirus disease (COVID-19) causes acute lung injury (ALI) and acute respiratory distress syndrome (ARDS) in the severe and critically severe patients. Pulmonary edema is the key detrimental feature of ALI/ARDS. Autopsy of patients died from COVID-19 reported that, pulmonary mucus exudation was severe, more obvious than SARS infection. Pulmonary CT scanning and pathological findings also suggest that pulmonary edema caused by inflammatory exudation is a distinguished feature of COVID-19. However, specific pharmacotherapy is lacking.Vascular endothelial growth factor (VEGF) is known as the most potent inducing factors to increase vascular permeability. Bevacizumab is an anti VEGF recombinant humanized monoclonal antibody, which has been used in anti-tumor treatment for 16 years. Evidence suggest that Bevacizumab is a promising drug for severe and critical COVID-19 patients.

NCT04305106 COVID-19 Pneumonia Drug: Bevacizumab
MeSH:Pneumonia
HPO:Pneumonia

Primary Outcomes

Description: The time from randomization to an improvement of two points on a seven-category ordinal scale or live discharge from the hospital

Measure: The time from randomization to clinical improvement

Time: No more than 28 days


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