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Nventa Provides Corporate Update and Advancement Plans for HspE7, Hsp 6/11 and Poly-ICR
Date:10/8/2008

ical studies as planned and that such studies will support the use of HspE7 as a treatment for CIN 1 and CIN 2/3; that we will complete the second protocol for the CIN 1 indication; that Poly-IRC will be useful as a broad immune stimulatory agent and vaccine adjuvant; that we will be able to advance Poly-ICR to generate revenue and for internal development; that Poly-ICR will provide us with near-term revenue opportunity; that Poly-ICR will be useful in the treatment of GW and actinic keratosis; that we will complete development activities and file an IND application in connection with Poly-ICR; that we will finalize manufacturing and formulation protocols and file an IND in connection with Hsp 6/11; that we will be able to execute our corporate restructuring as planned; that we will be able to expand corporate development efforts as planned and that such efforts will produce the desired results; that results from future clinical trials will be consistent with our expectations; that we will raise enough capital (through partnering or otherwise), on reasonable terms and in a timely manner; that we will retain our key personnel; that we will obtain the necessary regulatory approvals related to HspE7, Hsp 6/11 and Poly-ICR in a timely manner; that sufficient HspE7, Hsp 6/11 and Poly-ICR will be available to conduct our planned clinical trials; that we will obtain timely approval from additional Investigational Review Boards; that the results from additional preclinical and clinical work, if any, will be consistent with the results we have already obtained; and that a sufficient number of patients will be available to conduct our planned trials, and that sufficient data will be generated in such trials.

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 u
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SOURCE Nventa Corporation
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