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LactoferrinWiki

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Clinical Trial MeSH HPO Drug Gene SNP Protein Mutation


Correlated Drug Terms (2)


Name (Synonyms) Correlation
drug308 BVRS-GamVac Wiki 1.00
drug2950 placebo Wiki 0.27

Correlated MeSH Terms (2)


Name (Synonyms) Correlation
D013577 Syndrome NIH 0.11
D018352 Coronavirus Infections NIH 0.04

Correlated HPO Terms (0)


Name (Synonyms) Correlation

There is one clinical trial.

Clinical Trials


1 Efficacy and Safety of Lactoferrin as an Adjunct Therapeutic Agent for COVID-19

There is currently no clinically proven specific antiviral agent available for SARS-CoV-2 infection. Supportive treatment, including oxygen therapy, remains the most important management strategy. Since its discovery, lactoferrin and its related peptides are mainly considered to be important non-specific host defense molecules against a broad range of viruses including SARS-CoV, which is closely related to SARS-CoV-2 that causes COVID-19. Lactoferrin has been found to experimentally inhibit viral entry in murine coronavirus, and human coronaviruses hCOV-NL63 and pseudotyped SARS-CoV. Besides reducing viral entry, lactoferrin can also suppress virus replication after the viral entry. Another major aspect of lactoferrin bioactivity relates to its immunomodulatory and anti-inflammatory functions. Current thinking suggests that mortality from COVID-19 is not simply due to viral infection but is a result of a cytokine storm associated with hyper-inflammation leading to acute respiratory distress and subsequent mortality. A cytokine profile in severe COVID-19 cases is characterized by increases in cytokines and acute phase reactants and ferritin. In this regard, lactoferrin was demonstrated to reduce IL-6, TNF a, and downregulate ferritin in experimental settings simulating sepsis. In this study, we aim to study the potential application of lactoferrin against SARS-CoV-2 and propose the possibility of using different doses of supplemental lactoferrin as a potential adjunct treatment for COVID-19.

NCT04421534 COVID-19 Drug: Lactoferrin

Primary Outcomes

Description: time from randomization to improvement of two points on used scale or live discharge from the hospital, whichever came first.

Measure: Time to clinical improvement

Time: 28 days

Secondary Outcomes

Description: time from randomization to cure (2 SARS-COV-2 PCR samples negative with 48 hours apart)

Measure: Rate of virological cure

Time: 28 days


No related HPO nodes (Using clinical trials)