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Update: Biovest Aims for BLA, not NDA (OTC:BVTI)

Source: http://feedproxy.google.com/~r/stockshaven/~3/i00pASdajCo/
Posted on Tuesday, September 22nd, 2009 | In Investing Lessons, Stocks to Watch
Contributed by: Michael Vlaicu (http://www.stockshaven.com) -

Biovest International, Inc.

(Public, OTC:BVTI)

Today, on 9/22/09, StocksHaven Investments had the opportunity of speaking to the Investor Relations representative at Biovest International Inc., Douglas W. Calder regarding the recent profile we conducted. A few minor erroneous details were present, and thus we are issuing a company verified update to clarify these issues.

The first problem at hand was that we mentioned it would be a new drug application, however, it is in fact a biologic license application or, for short BLA. So what is a BLA? A biologics license application is a submission that contains specific information on the manufacturing processes, chemistry, pharmacology, clinical pharmacology and the medical affects of the biologic product. If the information provided meets FDA requirements, the application is approved and a license is issued allowing the firm to market the product. Essentially, it is a formal application analogous to a New Drug Application, but for biotechnology-derived pharmaceuticals (for example, complex, large molecules). In other words, BLA is equivalent in some respects to an NDA, when it comes to therapeutics.

Moreover, they are in fact expecting to have a face-to-face meeting with the FDA with regards to BiovaxID sometime in Q1 of 2010, afterwhich depending on the outcome, a BLA submission could follow shortly thereafter. Currently, Biovest is preparing an informational package for the FDA in order to share data on BiovaxID, and a number of other items, such as the manufacturing facility in Miniapolis Minnesota, analysis ongoing with the clinical studies related to immune response, mechanisms of action involving b-cells, t-cells, or perhaps combination of both. Douglas went on to state that, data points the FDA wants to see include the possibility of other predictors that can indicate a more likely outcome of success for the patient. During the meeting, Biovest will also discuss the possibilities of an accelerated approval process for BiovaxID.

Communication with the FDA is ongoing, and Biovest is paying close attention to the draft guidance issued for companies seeking approval with cancer vaccines which are unique to patients, and as well the section for granting of accelerated approval process.

On an ending note, it is important to keep into consideration that the company is under Chapter 11, thus there always exists the unlikely scenario that the current common shares may be cancelled.

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Disclosure: Short term position in BVTI
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By reading StocksHaven Investments company profiles you agree to the disclaimer, and thereby will not hold Michael Vlaicu accountable for any transactions or decisions you make. It is up to you to do your own due diligence.

StocksHaven Investments is not paid, compensated or in any way incentivized to report news and developments about publicly traded companies, unless otherwise stated.

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About Michael Vlaicu (http://www.stockshaven.com)
A young and savvy, yet experienced and accomplished investments mogul since ‘01; Michael has amassed a fortune as a private self investor. Recently starting his own successful blog and turning it in to a self-proprietorship — StocksHaven Investments, a company offering advice to thousands of people worldwide and attracting contracts from various reputable sources. The financial news portal can be found at www.StocksHaven.com. Michael has reached Expert Stock Analyst status from a variety of accredited publications.

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