FDA Shows Greenlight For Clinical Trial Of Herbal Treatment Of Covid-19

The Food and Drugs Authority (FDA) and the National Medicine Regulatory Agency (NMRA) have given the approval for the School of Public Health at the Kwame Nkrumah University of Science and Technology (KNUST) to begin clinical trials for a potential treatment for Covid-19 in the country.

According to the FDA, the researchers submitted a clinical trial application back in September 2020 to assess the safety and efficacy of the herb.

The FDA in a statement noted that ‘The FDA, after detailed assessment of the application gave the requisite regulatory authorization for the conduct of the trial as per the mandate outlined under Part 8 (Sections 150 – 166) of the Public Health Act 2012 (Act 851), which gives the Authority the legal mandate to regulate clinical trials of drugs, herbal medicinal products, cosmetics or medical devices.

The trial will be conducted two sites,

It further noted that the approval comes on the back of results from laboratory studies conducted by the KNUST research team which points in the direction of possible clinical benefits.

The potential treatments, however, must be studied in laboratory animals first to determine potential toxicity before they can be tried in people.

Treatments having acceptable safety profiles and showing the most promise are then moved into clinical trials,” the statement said.

 

By: Edwin Abanga

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