Wednesday, July 30, 2014 7:20:15 AM
1) nanoviricides, armed with virus targeting ligands, can attach and destroy a particular virus among a multitude of viruses (as defined in virus/therapeutic drug pipeline)
2) nanoviricides, armed with several virus strains targeting ligands, can attach to and destroy a multitude of virus strains
The cGMP Pilot Plant is operational and scientists are racing to get it validated. We are also racing (stockpiling) to start the full tox study (GLP) of the FluCide candidate.
The Company has already successfully scaled up the synthesis to multi-gram scale, sufficient for animal testing, and can easily scale the processes to make kilogram quantities for widespread application in human patients if they are found to be effective and safe. PR May 2014
We have now begun production of the large quantities of the anti-influenza ligand needed for the GLP safety/toxicology study. We intend to begin the GLP Safety/Toxicology study as soon as feasible. PR Monday, May 19th, 2014
The Company has undertaken the production of certain quantities of its FluCide anti-influenza drug for use in detailed pre-IND Safety/ "Tox Package" studies at its current facilities in West Haven. This process is expected to take some time due to the limitations of scale at the current facility. The Company is making progress in making this material in the required quantities. PR Wednesday, June 25th, 2014
Flu Season in Australia is NOT going to wait for us to start, we burn approximately 2M a quarter, therefore if we are racing (no pressure?), progressing in making material in the required quantities, is for one ultimate reason/goal, to file the sponsor applications for human clinical trials internationally, and also an Investigational New Drug application (IND) in the USA. Full Tox study (GLP) 2014 otherwise, why would we be racing?
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