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Newsletter
October 12, 2001
Volume IV, Issue 88
Email : info@otcjournal.com
URL : http://www.otcjournal.com

To OTC Journal Members:
 

Astralis/Hercules Development (OTC BB: HDVG) Announces Negotiations With European Pharmaceutical Co.

News today from Astralis confirms our original suspicions that Astralis would be seeking major value added partners for both capital and technology expertise to help move the company forward.

The company announced it has entered into advanced negotiations with a European based Pharmaceutical company for a strategic investment. According to the press release "If successful in completing the transaction, Astralis anticipates a significant infusion of capital into the Company".

If you missed our original profile on this company, now would be a good time to review it. Click Here to be taken directly to the original profile. For individual investors in the microcap arena, this company is one of the most exciting situations we have ever seen, and we believe all risk oriented investors should own some stock in this company.

We have already covered most of the risk factors associated with investing in Hercules Development at this time. They include the following:

  • The merger has not been completed. The purchase of shares of Hercules is not Astralis yet. According to both parties, the transaction should close by the end of October. If it becomes derailed you stand to lose a substantial portion of your investment.
  • The editors of the OTC Journal do not have the technical expertise to evaluate the merits of this revolutionary new drug. We have not been to Caracas, Venezuela to interview treated patients or the Venezuelan FDA which has already approved the drug.
  • It is anticipated the FDA approval process could take five to six years.
  • As it stands today, the company does not have the anticipated required capital to take this drug through the FDA Approval Process.
An investment of both capital and technology from a major pharmaceutical company would go a long ways towards mitigating the risks associated with this company.

Pharmaceutical companies have the expertise to evaluate the technology. If a major pharmaceutical company were to make a significant investment, this would confirm the upside potential of this drug and mitigate risks associated with both the lack of capital and the need for technological help.

We advised investors to start with 25% to 50% of the risk capital they planned to set aside for this exciting company. Today's news release helps mitigate some of the risk associated with this investment, and therefore it would be appropriate to add to your current position on this news. However, the closing of a major financing with a pharmaceutical company would trigger our belief that you should be 100% invested.

Today the stock closed $.38 below our original entry price of $3.66. If you invested on the first day, today's price provides the opportunity to lower your average cost. If you don't own this stock yet, you should invest if you have any risk capital available. This company has exciting upside potential, and every risk oriented investor should participate. We expect the stock will trade at much higher levels if and when a final deal is announced with a Pharmaceutical company but there are no guarantees.

Here is the complete text of the press release for your review:
 

Friday October 12, 4:03 pm Eastern Time
Press Release
SOURCE: Hercules Development Group/Astralis

Hercules in Negotiations With European-Based Pharmaceutical Company For Strategic Investment

Pharmaceutical company specializing in drug delivery technologies to provide essential services in the development, testing and commercialization of Psoraxine

FLORHAM PARK, N.J.--(BUSINESS WIRE)--Oct. 12, 2001-- Hercules Development Group (OTC BB: HDVG - news) announced today that it is currently in negotiations with a European-based pharmaceutical company for the purposes of strategic investment in Astralis, the company with which it has executed a definitive merger agreement. If successful in completing the transaction, Astralis anticipates a significant infusion of capital into the Company. Astralis also contemplates engaging the strategic investor, a leader in the dermatological field in drug delivery technologies, for a number of services essential to the development, testing and commercialization of Psoraxine. 

Although there can be no assurances that the transaction will be consummated, Astralis CEO Mike Ajnsztajn stated: ``We are presently in advanced negotiations, and we are optimistic that a deal will be finalized in the near future.'' 

Psoraxine, the first drug to be developed by Astralis, has brought about clinical remission of Psoriasis during clinical trials conducted in Venezuela. The Company has treated 3,000 patients with Psoraxine to-date. Of these, 638 experienced complete remission and 1,000 have experienced between 70% and 90% remission. The primary end point was the reduction of the Psoriasis Area and Severity Index (PASI) before and after treatment with Psoraxine. Overall, 96% of patients have responded positively to Psoraxine, with few adverse effects, although these results were not independently verified. 

Psoriasis affects 7 million people in the United States alone, and conservative estimates indicate that up to 3% of the world population also suffer from this condition-as many as 180 million people. Psoriasis results due to an overproduction of skin by blood cells associated with the immune system. These blood cells become confused and act as though the skin was damaged, manufacturing skin cells at a much faster rate than is required by undamaged skin. This overproduction of skin can cause everything from itchy rash-like patches to painful pustules and massive inflammation. Most current treatments are sub-optimal and some systematic treatments can cause serious side effects. In fact, of the 7 million people living with Psoriasis in the US today, only 1.6 million choose treatment. 

Astralis is the developer of PSORAXINE, a drug that has brought about a clinical remission of the skin condition Psoriasis in patient trials. The Company has applied for patent protection for composition of matter, method of use, DNA sequence of peptides, and the new gene sequence that fuels Psoraxine. The company is in the process of submitting the IND for FDA approval to commence US clinical trials. 

--------------------------------------------------------------------------------
Contact: 

     for Hercules Development Group/Astralis
     The Investor Relations Group
     Peter Waal, 800/689-2966
 


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Disclaimer
The OTCjournal.com Newsletter is an independent electronic publication committed to providing our readers with factual information on selected  publicly traded companies. All companies are chosen on the basis of certain financial analysis and other pertinent criteria with a view toward  maximizing the upside potential for investors while minimizing the downside risk, whenever possible.  Moreover, as detailed below, this publication accepts compensation from certain of the companies which it features.  Likewise, this newsletter is owned by MarketByte, LLC. To the degrees enumerated herein,  this newsletter should not be regarded as an independent publication.

Click Here to view our compensation on every company we have ever covered, or visit the following web address:  http://www.otcjournal.com/disclaimer.html for our full profiles and http://www.otcjournal.com/trading-alerts/disclaimer.html for Trading Alerts. MarketByte LLC has been paid a fee of $100,000 in cash and 100,000 options exercisable at $2.50 by the Investor Relations Group for publishing information on Astralis LLC for a period of one year. Fifty thousand options are exercisable immediately, and fifty thousand become eligible on April 1, 2002. Please review our policy on selling shares found within our Mission Statement at our home page.

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