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The agent represents a nano-particle conjugate that consists of a drug delivery molecule, namely a cyclodextrin-based polymer (CDP) (Cyclosert) and an anti-cancer compound (camptothecin). It was developed by Dr. Mark Davis and associates at Insert Therapeutics, hence the IT label. Its novel delivery mode allows the agent and thus the toxic anti-cancer component to be preferentially accumulated in cancer tissue. In turn, toxic side effect are expected to be reduced.
Additional recommended knowledge
Camptothecin (CPT), an alkaloid extract from plants such as Camptotheca acuminata, exhibits anti-cancer activity possibly due, at least in part, by the inhibition of DNA topoisomerase I resulting in cell death. CPT is linked covalently through a glycine link to CDP which in turn consists of beta-cyclodextrin and polyethylene-glycol (PEG). The compound is water soluble. After intravenous injection, CPT is slowly released as the linkage is hydrolysed. The size of the compound facilitates its extravasation in the more leaky vessels of a cancer and the anticancer drug is retained in the abnormal tissue. As such the chemotherapeutic effect is enhanced in tumor tissue.
Phase I study
The Phase I clinical trial is conducted at the City of Hope Cancer Center. Patients who were entered had refractory and resistant solid tumor cancer of various types (pancreatic cancer, ovarian cancer, non small cell lung cancer). The initial study recruited 36 patients and lasted from May 2006 and is estimated to last to January 2008. Treatment consists of injections on day 1, 8, and 15 followed by 1 week rest.
|This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "IT-101". A list of authors is available in Wikipedia.|