InvestorsHub Logo

concordia

08/22/17 10:12 AM

#74086 RE: rudygerner #74084

We all feel that the suggested changes we received from the FDA should not take long to make
February 13, 2017

6 months later no updates.

JimboPMCB

08/22/17 2:03 PM

#74103 RE: rudygerner #74084

All a Hoax. The technology has a good marketing story.

rudygerner

08/22/17 9:46 PM

#74121 RE: rudygerner #74084

Partnership and IND coming 4Q17: https://www.facebook.com/austrianova/photos/a.806632359368640.1073741832.747212361977307/1616942508337617/?type=3&theater

Next step is to file the IND: http://ir.pharmacytebiotech.com/press-releases/detail/133/pharmacyte-biotech-moves-closer-to-filing-ind-with-naming

"Other highly positive news provided by Mr. Waggoner concerning the pre-IND meeting with the FDA included:

- agreement with the FDA that PharmaCyte is on the “right track” in its development program;

-agreement with the FDA on the cell line that will be used in the clinical trial;

-agreement with the FDA on the patient population to be studied in the clinical trial;

-agreement with the FDA on the secondary endpoints of the clinical trial, except that PFS will be added to the list of secondary endpoints if the trial becomes a pivotal trial;

-agreement with the FDA on the number of patients needed to comprise an adequate safety database for a Biologics Licensing Application for CypCaps™;

-agreement that the FDA believes CypCaps™ is a drug/device combination product;

-agreement with the FDA that it will assist PharmaCyte in its development program;


-agreement with the FDA that the next step for PharmaCyte is to submit an IND.

IND coming 4Q17.