MGC yesterday received Ethics Committee approval for the Phase III Clinical Trial (‘the Trial’) of CimetrA™ on Patients Diagnosed with COVID-19 (SARS-CoV-2). CimetrA™ is designed with the scientific aim to target viral infections with inflammatory complications.
Having already been successfully evaluated on infected patients in a double-blind placebo-controlled, Phase II clinical trial. Although a significant initial worldwide supply agreement has already been signed for ArtemiC™ Rescue in its form of a food supplement, the product has now also undertaken a name change to CimetrA™, in recognition of the transfer of its status to an Investigational Medicinal Product (‘IMP’) ahead of the Trial’s commencement. Importantly in this respect, CimetrA™ encapsulates Graft Polymer Limited’s GraftBio™ SNEDDS technology (Self-Nano Emulsifying Drug Delivery System), as a unique platform to deliver higher concentrations of the natural active ingredients more effectively in to the cells, thereby improving their bioavailability.
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