t the end of year, the trial at Dana-Farber should be nearly complete with Maximum Tolerated Dose (MTD) established, a safety profile compiled and, probably most importantly, clinical data collected on Kevetrin's effect on p53 via the p21 biomarker. If it hits p53, I would suspect that leading drug manufacturers are going to amplify their efforts to test Kevetrin on a great many indications. Cellceutix taking its anti-cancer drug to Dana-Farber is underscored by a critical benefit that most investors don't consider because of the cancer center's tumor mapping program. Ultimately, the mapping technology should help define which types of cancer Kevetrin may prove most efficacious, delineating a pathway to specific indications similar to catalytic situation with Pharmacyclic's ibrutinib.
CTIX
Se esperan resultados para Fase I de KEVETRIN a finales de año....