Snatched this off of reddit/cydy: (is there going
Post# of 148261
Nadar Says Macleods to Submit for EUA and Compassionate Use Authorization Immediately with India's CDSCO (their FDA)
Summary of Todays Proactive video on youtuve:
Macleods reached out to Cytodyn
Cytodyn and Macleods closed a deal in 10 days (they had a WhatsApp group text!)
Macleods will take Cytodyn's Leronlimab data and submit to CDSCO for EUA and Compassionate Use Authorization Immediately
Cytodyn is requesting the EUA (through Macleods) concurrently while they begin a patient trial in India:
the CDSCO granted this for Tocilizumab while they ran a 30 patient trial
Cytodyn is doing the above (request an EUA while conducting a trial) with every country that is in covid trouble
Dr Kelly feels for the first time they have a supportive Board of Directors...
Best financial position they've ever been in
We have a global distribution network
We have the crucial regulatory piece
Not only are physicians embracing Leronlimab, but international pharmaceutical companies are embracing Cytodyn
Companies in the Philippines, Brazil, India, the U.K. and now Europe, are looking at our data, our safety, our manufacturing and they're understanding the pipeline of opportunities ahead of us...
Leronlimab works at the CCR5 receptor, so it won't be affected by any mutations in the spike protein.
As more covid variants continue to emerge this will put us in a unique position
Macleod can not distribute LL to all hospitals in India, but all over the world (140 different countries)
Nader and Kelly both feel they now have a perfect team in place
They are working to start a HIV Prep trial in Brazil