The Prurisol trial is delayed so that Dr Reddy's can mfr a batch using the new mfg method that requires less steps resulting in less cost to mfr.
Assume everything goes great in the trial and CTIX licenses the rights to Prurisol to Pfizer or next year we get bought out by Pfizer (one can always dream). Let's say they buy out CTIX and get rights to Kevetrin as well.
Being as large as they are, I would expect Pfizer to have their own mfg facilities. Anybody know if the majors do mfg all their own product or do they, in fact, contract out to such as Dr Reddy's?
If they have their own facilities, or don't do business with a certain contract mfr who happened to mfr the trials product (I don't even know who made the Kevetrin for the trials), thus deciding to make the product themselves, how do they go about getting their product authorized by the FDA? Do they have to go thru another trial with their product or does the contract mfr have to provide them with the specific steps in making the product so that the product coming out of Pfizer's plant conforms exactly to that which was made for the trials?
Nothing of major importance now, question just came to mind.
Hope we have a great Kentucky Derby, all jockeys and horses come thru unscathed, and everybody at the track has a wonderful day. I could really go for a mint julep or a mojito as I love mint. Wish they spent more time showing the wild hats worn by the female fans as they can get pretty outrageous.