Phase III result is the biggie, the link below is the interview with Dr Nadya Lisovoder on the phase II clinical study of 50 patients with moderate COVID-19 symptoms, definitely worth a read.
plenty more of news to come this month, AMC to get regulatory approval, phase 3 interim results, just be patient cause Mgc is definitely heading in the right direction
· MGC Pharma has been granted government approval to import its phytomedicine CimetrA™ into India as a final step towards obtaining Emergency Use Authorisation for the treatment of patients with COVID-19.
· Emergency Use Authorisation is the registration process for medicines approved for the treatment of COVID-19 around the world.
· Emergency Use Authorisation would enable MGC Pharma to market and sell CimetrA™ as an approved medicine for the treatment of COVID-19 in India, and potentially in other territories under international Mutual Recognition protocols for medicines.
· Medopharm Private Ltd (Medopharm), one of the leading manufacturers and exporters of pharmaceutical products in India, is managing the Emergency Use Authorisation process for CimetrA™ in India on MGC Pharma's behalf.
· Medopharm has been appointed importer for CimetrA™ in India once the Emergency Use Authorisation has been granted
· CimetrA™ is currently undergoing Phase III trial for the treatment of COVID-19 l in Israel
MGC Pharma has been granted government approval to import its phytomedicine CimetrA™ into India as a final step towards obtaining Emergency Use Authorisation for the treatment of patients with COVID-19.