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Nventa Presents Findings on Proprietary Toll-like Receptor 3 (TLR3) Agonist, Poly-ICR, at World Vaccine Congress
Date:10/8/2008

ir our ability to advance Poly-ICR; that Poly-ICR will be found safe and effective; that we will be able to incorporate Poly-ICR into future internal product candidates; that it will be possible to develop Poly-ICR for topical application for the treatment of GW and actinic keratosis; that Poly-ICR will evolve into a revenue generating opportunity for Nventa in the near future; that we will be able to engage third party manufacturers who will successfully manufacture Poly-ICR on reasonable terms and in a timely manner; that our manufacturing processes will be validated for use in producing cGMP materials; and that we will retain key personnel.

In the event that any of these assumptions prove to be incorrect, or in the event that we are impacted by any of the risks identified above, we may not be able to continue in our business as planned.

For a complete discussion of the assumptions, risks and uncertainties related to our business, you are encouraged to review our filings with Canadian securities regulatory authorities, including our 2007 Annual Information Form filed on SEDAR at http://www.sedar.com.

All forward-looking statements and information made herein are based on our current expectations as of the date hereof and we disclaim any intention or obligation to revise or update such forward-looking statements and information to reflect subsequent events or circumstances, except as required by law.


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