Prana Biotechnology raises U.S.$6 Million to fund trial of PBT2 in patients with Alzheimer's disease.

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Prana Biotechnology today announced it has entered into agreements to raise approximately A$7.77 million (US$6 million) from new institutional investors in Australia, existing institutional investors in the United States and a founding member of the Company.

As a result, the Company now has A$13.2 million (US$10.2 million) in cash to immediately commence its Phase IIa trial of PBT2 in Patients with early Alzheimer's disease, for which it has received full regulatory approval in Sweden.

The investment involves the purchase of 21.8 million ordinary shares (equivalent to 2.18 million ADRs) at a price of A$0.357 per ordinary share (approximately US$2.80 per ADR). In addition, the investors receive three-year warrants to purchase an additional 4.35 million ordinary shares (equivalent to 435,000 ADRs) at an exercise price of A$0.446 per ordinary share (approximately US$3.40 per ADR), which could raise an additional A$1.94 million (US$1.5 million) for the Company.

"We believe these commitments from new and existing investors reinforce the enthusiasm for PBT2 and its potential as an effective treatment for Alzheimer's disease," said Geoffrey Kempler, chairman and CEO. "The proceeds raised in this private offering will fully fund the upcoming Phase IIa clinical trial of PBT2 to its conclusion. We are optimistic that this trial will demonstrate the safety and tolerability, as well as the potency and efficacy of PBT2 for the treatment of Alzheimer's disease. We believe that our drug, unlike any currently available Alzheimer's drug, could offer a disease modifying therapy for patients, which is of enormous interest to major pharmaceutical companies."

Prana has received the regulatory and ethics approvals needed to start the Phase IIa study of patients with early Alzheimer's disease at seven Swedish sites. Screening of patients will commence next week. The Company plans to announce the results of the PBT2 Phase IIa trial in the fourth quarter of calendar year 2007.

Mr. Kempler concluded, "PBT2 is one of over 300 proprietary molecules that Prana has developed as candidates to treat a variety of neurodegenerative disorders. We plan to use the balance of the funds raised today for other activities over the next 12 months, designed to strengthen the evidence in support of our MPACs ("Metal Protein Attenuating Compounds") theory and development platform for our target diseases."

Comments

  1. JOHN CAMPBELL JOHN CAMPBELL United States says:

    Why can't Prana get clinical trial 3 started and PBT2 approved. Is the FDA the problem?.

The opinions expressed here are the views of the writer and do not necessarily reflect the views and opinions of News Medical.
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