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Nventa Initiates HspE7 Phase 1 Cervical Dysplasia Trial
Date:9/10/2007

horts. Patients will be immunized every 28 days for a period of 8 weeks (3 administrations). Post-treatment evaluations will begin four weeks after the last of the three injections. Patients enrolled with high-grade CIN (CIN 2/3) disease will be eligible to undergo clinically appropriate treatment of the cervix at the twelfth week of the study.

Nventa will also collect immunological data from these patients that may provide an early indication of potential efficacy of the compound. To determine if HspE7 plus adjuvant elicit T-cell and B-cell specific HPV-E7 immune responses, all patients will be typed for class I and II human leukocyte antigen (HLA) subtypes, and will be evaluated for cytokine responses, anti-HspE7 antibodies and cellular (T-cell) immunology.

Conference Call:

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Nventa will hold a conference call on Thursday, September, 13, 2007, at 9:00 am Eastern Time (6:00 am Pacific Time) to allow securities analysts and shareholders the opportunity to hear Management discuss an update on the progress with HspE7 and other important milestones.

Live Participant Dial In Numbers:

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If you are in the U.S. or Canada call (Toll Free): 877 407-8031. If you

are International call: 201 689-8031.

Replay of Audio Portion:

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A replay of this call will be available at 12:00 noon Eastern Time from

September 13 through 11:59 pm Eastern Time on September 20, 2007. The

playback number (Toll Free): 877-660-6853 (North America) or 201 612-

7415 (International), Account Number: 286; Conference Identification

Number: 254756 (both required for playback).

Webcast:

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Nventa will also webcast its investor call on Thursday, September 13,

2007, at 9:00 am Eastern Time (6:00 am Pacific Time). The call is being

webcast by Vcall and can be accessed through Nventa's
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SOURCE Nventa Biopharmaceuticals Corporation
Copyright©2007 PR Newswire.
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