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old man river

09/02/13 11:25 AM

#40121 RE: HighYieldInvestments #40120

The OTC Markets is not a regulatory body.

Updating the financials and reporting them to the OTC will not stop the ongoing SEC investigation.

There are critical issues to be resolved before the SEC would be inclined to let BGMO continue. Some have reported the problems being:

- the failure to hold annual meetings
- the failure over time to report financial results according to GAAP
- the issuance of press releases announcing fundings that never close without any clarification by the Company why it did not happen
- the issuance of press releases announcing investment activities that never close without any clarification by the Company why it did not happen
- the massive share dilution without any notice to of approval of the shareholders
- the payment of massive commissions to HH and SP without shareholder approval.

There are also some commercial issues which would raise ethical questions outside of the normal SEC investigation. These would include:

- negotiating to purchase a controlling interest in a company without having the cash in the bank to complete the transaction
- even after negotiating in good faith, BGMO fails to honour even amended timings and amounts provided in share purchase agreements
- stating that BGMO will do one thing yet renegs on it days afterwards.

The core question to ask boils down to this...

Given the history of BGMO and its insiders, even if the HBSC money is real and audited statements are delivered, how can the SEC protect the investing public from past events repeating themselves?

My opinion is that they would likely err on the side of caution to protect investors. This would also send signals out to would be pump and dump artists that the Commission is watching.

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HighYieldInvestments

09/02/13 6:38 PM

#40130 RE: HighYieldInvestments #40120

VistaGen is a biotechnology company applying human pluripotent stem cell technology for drug rescue, predictive toxicology and drug metabolism screening. VistaGen's drug rescue activities combine its human pluripotent stem cell technology platform, Human Clinical Trials in a Test Tube(TM), with modern medicinal chemistry to generate novel, safer chemical variants (Drug Rescue Variants) of once-promising small molecule drug candidates. These are drug candidates discontinued by pharmaceutical companies, the U.S. National Institutes of Health (NIH) or university laboratories, after substantial investment in discovery and development, due to heart or liver toxicity or metabolism issues. VistaGen uses its pluripotent stem cell technology to generate early indications, or predictions, of how humans will ultimately respond to new drug candidates before they are ever tested in humans, bringing human biology to the front end of the drug development process.

VistaGen's small molecule prodrug candidate, AV-101, has completed Phase 1 development for treatment of neuropathic pain. Neuropathic pain, a serious and chronic condition causing pain after an injury or disease of the peripheral or central nervous system, affects millions of people worldwide.

Visit VistaGen at http://www.VistaGen.com, follow VistaGen at http://www.twitter.com/VistaGen or view VistaGen's Facebook page at http://www.facebook.com/VistaGen.