The (Laetrile) efficacy tests...clinically in humans..(by) the US NCI...were obviously conducted so that a negative result could be formulated. The limited number and types of human cancer cases selected...the omission of necessary additional measures ('e.g dietary'), the far too short observation periods, and the undefined chemical properties of the (Laetrile)... all contributed to devaluation of...conclusions.
You wouldn't believe how many FDA officials or relatives or acquaintances of FDA officials come to see me as patients in Hanover. You wouldn't believe this, or directors of the AMA, or ACA, or the presidents of orthodox cancer institutes. That's the fact
The oral (Laetrile) had been 'toxified' by adding cyano-urea in the NCI...(NCI's) Mayo (Clinic) dismissed well responding patients to discard them from statistical evaluation...This kind of fraud which I expressed...and which was openly published...has...not resulted in any denial.
