Abstract

CEND-1 (iRGD), a bifunctional cyclic peptide, enhances delivery of co-administered anti-cancer agents by transforming the solid tumour microenvironment into a temporary drug conduit. The present study explored the pharmacokinetic (PK) properties of CEND-1, as well as its distribution, tumor selectivity and duration of action in preclinical tumor models.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call