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- OGX-427 is designed to reduce production of Hsp27, a protein that is
over-produced in response to many cancer treatments including hormone
ablation therapy, chemotherapy and radiation therapy. OGX-427 is in a
Phase 1 clinical trial for the treatment of solid tumors including
prostate, non-small cell lung, breast, ovarian, and bladder cancers.
The company anticipates that the single-agent aspect of this trial
will be completed in the second half of 2008, and Phase 2 clinical
development will begin in 2009. Like OGX-011, this product candidate
has potential as a treatment in a broad number of cancers;
- SN2310 is a novel prodrug of SN-38, which is a potent anti-cancer
drug belonging to the class of topoisomerase I inhibitors. It is
currently in a Phase 1 trial and progress is being made to determine
its safety and pharmacokinetic profile, in addition to the maximum
tolerated dose. SN2310 is designed to enhance the delivery and
exposure of SN-38 to the tumor by providing greater prodrug
conversion and a longer half-life than achieved with irinotecan; and
- OGX-225 aims to reduce the production of both Insulin-Like Growth
Factor Binding Protein -2 and Insulin-Like Growth Factor Binding
Protein -5 with a single product to enhance treatment sensitivity and
delay tumor progression. IGFBP-2 and IGFBP-5 are both hormones that
make an alternate hormone, IGF-1, available to the tumor that
facilitates continued tumor growth. Employing OGX-225 as a single
product to simultaneously inhibit the production of both IGFBP-2 and
IGFBP-5 has the potential to delay disease progression in cancers
dependent upon IGF-1 for tumor growth. OGX-225 is in pre-clinical
development and has completed pre-clinical pharmacology.
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| SOURCE OncoGenex Technologies Inc. Copyright©2008 PR Newswire. All rights reserved |