Delaware
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8731
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26-2593535
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(State or other jurisdiction of
incorporation or organization)
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(Primary Standard Industrial
Classification Code Number)
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(I.R.S. Employer
Identification Number)
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Large accelerated filer
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Accelerated filer
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Non-accelerated filer
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¨ (Do not check if a smaller reporting company)
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Smaller reporting company
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Title of Each Class of
Securities to be Registered
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Proposed
Maximum
Aggregate
Offering Price(1)(2)
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Amount of
Registration Fee (5)
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Units consisting of:
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$ | 15,000,000 | $ | 2,046.00 | ||||
(i) Series C 8% Convertible Preferred Stock, $0.0001 par value per share
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— | — | ||||||
(ii) Warrants to purchase common stock
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— | (3) | — | |||||
Common Stock issuable upon conversion of the Series C 8% Convertible Preferred Stock and exercise of warrants(3)
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— | (4) | — |
(1)
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Estimated solely for the purpose of calculating the registration fee pursuant to Rule 457(o) under the Securities Act of 1933, as amended (the “Securities Act”).
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(2)
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Pursuant to Rule 416, this registration statement shall be deemed to cover the additional securities (i) to be offered or issued in connection with any provision of any securities purported to be registered hereby to be offered pursuant to terms that provide for a change in the amount of securities being offered or issued to prevent dilution resulting from stock splits, stock dividends or similar transactions and (ii) of the same class as the securities covered by this registration statement issued or issuable prior to completion of the distribution of the securities covered by this registration statement as a result of a split of, or a stock dividend on, the registered securities.
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(3)
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No additional consideration is payable pursuant to Rule 457(g) under the Securities Act.
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(4)
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No additional consideration is payable pursuant to Rule 457(i) under the Securities Act.
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(5) | Previously paid |
Per Unit
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Total
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Public offering price
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$ | [●] | $ | [●] | ||||
Placement Agent fees(1)
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$ | [●] | $ | [●] | ||||
Proceeds, before expenses, to us
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$ | [●] | $ | [●] |
(1)
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In addition, we have agreed to issue to the Placement Agent warrants to purchase a number of shares of common stock equal to 2% of the aggregate number of shares of common stock issuable upon conversion of the Series C 8% Convertible Preferred Stock sold in this offering and to reimburse the expenses of the Placement Agent as described in the Plan of Distribution herein.
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About this Prospectus
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1 | |||
Special Note Regarding Forward-Looking Statements
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1 | |||
Prospectus Summary
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2 | |||
Risk Factors
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8 | |||
Use of Proceeds
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10 | |||
Dilution
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11 | |||
Description of Capital Stock
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12 | |||
Description of Securities We Are Offering
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18 | |||
Plan of Distribution
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19 | |||
Legal Matters
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20 | |||
Experts
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20 | |||
Disclosure of Commission Position on Indemnification for Securities Act Liabilities
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20 | |||
Where You Can Find More Information
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21 | |||
Documents Incorporated by Reference
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21 |
Prospectus Summary
This summary is not complete and does not contain all of the information you should consider before investing in the securities offered by this prospectus. You should read this summary together with the entire prospectus, including our financial statements, the notes to those financial statements, and the other documents identified under the headings “Where You Can Find More Information” and “Documents Incorporated by Reference” in this prospectus before making an investment decision. See the Risk Factors section of this prospectus on page 8 for a discussion of the risks involved in investing in our securities.
Oxygen Biotherapeutics, Inc.
Company Overview
We are engaged in the business of developing biotechnology products with a focus on oxygen delivery to specific target tissues. We are currently developing Oxycyte®, a systemic perfluorocarbon, or PFC, product we believe is a safe and effective oxygen carrier for use in situations of acute ischemia. In addition, we have developed a family of perfluorocarbon-based oxygen carriers for use in personal care, topical wound healing, and other topical indications. While Oxycyte has been successful in two clinical trials and is currently being evaluated in a Phase II-b clinical trial for the treatment of traumatic brain injury, or TBI, we also plan to focus on developing our most advanced topical products: Dermacyte® and Wundecyte™, as we believe these products have a significant opportunity for near-term commercialization.
Oxycyte
Our Oxycyte oxygen carrier product is a PFC-based oil in water emulsion, which is provided to the patient intravenously. The physical-chemical properties of PFCs enable our product to concentrate oxygen from the lungs and transport it through the body releasing it along the way. Over a period of days Oxycyte is gradually exhaled through the lungs during the normal process of respiration. Oxycyte requires no cross matching, so it is immediately available and compatible with all patients’ blood types. Oxycyte has an extended shelf life compared to blood and is provided as a sterile emulsion ready for intravenous administration. Because it contains no biological components, there is reduced risk of transmission of blood-borne viruses from human blood products. Further, since Oxycyte is based on readily available inert compounds, we believe it can be manufactured on a cost-effective basis in amounts sufficient to meet demand.
We received approval of our Investigational New Drug application, or IND, for severe TBI filed with the U.S. Food and Drug Administration, or FDA, and began Phase I clinical studies in October 2003, which were completed in December 2003. We submitted a report on the results to the FDA along with a Phase II protocol in 2004. Phase II-A clinical studies began in the fourth quarter 2004, and were completed in 2006. A further Phase II study protocol was filed with the FDA in the spring of 2008, but remained on clinical hold by the FDA due to safety concerns raised by the regulatory agency. In March 2011, we received confirmation of a $2.07 million, two-year cost reimbursement award from the U.S. Army to conduct safety related studies for Oxycyte. PFC emulsions, as a therapeutic class, are known to interact with the reticuloendothelial system as part of the clearance mechanism, as well as affect the number of circulating platelets. The studies supported by this grant will examine the effects of Oxycyte on the immune system, platelet function and distribution, as well as the safety and efficacy of platelet transfusion, which can be necessary for patients with TBI and related polytrauma. Additional studies under this grant will be conducted to evaluate the pharmacokinetics of PFCs in relevant species. We believe the results of these studies will support the safety profile of Oxycyte PFC emulsion and adequately address the FDA’s safety concerns. The aforementioned comprehensive preclinical program is under way, and we have sought FDA input and guidance with the aim of ensuring that the data collected will answer the questions regulators raise. We expect to commit a substantial portion of our financial and business resources over the next three years to testing Oxycyte and advancing this product to regulatory approval for use in one or more medical applications.
Despite the FDA’s postponement of Oxycyte trials in the United States, we are authorized to continue our TBI clinical studies abroad. After receiving the FDA clinical hold, we filed a revised protocol as a dose-escalation study with the regulatory authorities in Switzerland and Israel. The relevant Swiss regulatory body approved the protocol in August 2009, and the Israel Ministry of Health approved the protocol in September 2009. The new study began in October 2009. In March 2010, we determined that it is feasible to simplify the trial design and also reduce the number of patients to be enrolled. In May 2010, we entered into a relationship with a contract research organization, or CRO, to assist us with plans to expand our study, possibly into India, and to initiate five to 10 new sites for our Phase IIb clinical trial. At that time, we believed study objectives as well as safety and efficacy endpoints would remain unchanged, and we believed the study could be concluded faster and more economically with these optimizations. The first of three cohorts has been completed and we were authorized by the Swiss and Israeli regulatory authorities to initiate the second cohort. Despite their authorization, we stopped enrollment in order to reevaluate the protocol’s patient enrollment parameters, secure our cGMP supply of Oxycyte, review our contractor and clinical sites, and examine the possibility of opening clinical sites in other countries. At this time, we have secured our cGMP supply of Oxycyte. We are in the process of reviewing our CRO agreement and existing clinical sites. Our objective is to resume enrollment in the second cohort during the first quarter of fiscal year 2014. Upon completion of the Phase II trials, a Phase III trial will need to be implemented. In that instance, we would seek a partner to either conduct the Phase III trials, or collaborate with us to conduct the trials.
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Should Oxycyte successfully progress in clinical testing and if it appears regulatory approval for one or more medical uses is likely, either in the United States or in another country, we intend to evaluate our options for commercializing the product. These options include licensing Oxycyte to a third party for manufacture and distribution, manufacturing Oxycyte ourselves for distribution through third party distributors, manufacturing and selling the product ourselves, or establishing some other form of strategic relationship for making and distributing Oxycyte with a participant in the pharmaceutical industry. We are currently investigating and evaluating all options.
Dermacyte
The Dermacyte line of topical cosmetic products contains our patented PFC technology and other known cosmetic ingredients to promote the appearance of skin health and other desirable cosmetic benefits. Dermacyte is designed to provide a moist and oxygen-rich environment for the skin when it is applied topically, even in small amounts. Dermacyte Concentrate has been formulated as a cosmetic in our lab and Dermacyte Eye Complex was created by a contract formulator, with the patent held by Oxygen Biotherapeutics. Both formulas have passed required safety and toxicity tests in the United States, and we have filed a Cosmetic Product Ingredient Statement, or CPIS with the FDA. The market for oxygen-carrying cosmetics includes anti-aging, anti-wrinkle, skin abrasions and minor skin defects.
In September 2009, we started production of our first commercial product under our topical cosmetic line, Dermacyte Concentrate. We produced and sold a limited pre-production batch in November 2009 as a market acceptance test. The product was sold in packs of 8 doses of 0.4ml. Based on the test market results we identified specific market opportunities for this product and reformulated Dermacyte Concentrate for better product stability. Marketing and shipments of the new Dermacyte Concentrate formulation began in April 2010. We worked with a contract formulator in California to develop the Dermacyte Eye Complex which contains PFC technology as well as other ingredients beneficial to the healthy appearance of the skin around the eyes.
Since June 2010 we had marketed and sold these products through www.DermacyteUS.com (previously www.buydermacyte.com) and to dermatologists, plastic surgeons and medical spas with a combination of in-house sales, independent sales agents and exclusive distributors. We had hired a sales director based in North Carolina, and had added sales people in South Florida and California. From October 2011 through February 2012, we evaluated that sales strategy. The outcome was that we adjusted our growth strategy to focus exclusively on the North Carolina and South Florida markets while we focused on developing new, improved packaging for the existing commercial products, as well as reformulating the products, and expanding the line to include more skin care products.
On February 5, 2013, we entered into a License and Supply Agreement, or the Dermacyte Agreement with the Cosmetics Division of Valor SA, or Valor, with respect to Dermacyte. The Dermacyte Agreement grants Valor the exclusive right to sell, import, export, distribute, package, label and otherwise commercialize Dermacyte worldwide for a five year term. Valor is also authorized to sublicense the license granted under the Dermacyte Agreement provided that such sublicenses are consistent with the terms of the Dermacyte Agreement. The Dermacyte Agreement will become effective upon our receipt from Valor of 75% of the estimated costs to complete certain product formulation and safety studies requested by Valor. As of June 26, 2013, Valor has not requested any additional formulation development or safety studies.
Under the Dermacyte Agreement, Valor will purchase bulk Dermacyte from us for 125% of our actual manufacturing cost, and must pay us an annual, non-refundable license fee of $140,000, payable on a quarterly basis, with the first year’s payment creditable against Dermacyte purchased by Valor in the first 12 months following the effective date of the Dermacyte Agreement. Valor must also pay us royalties of 5% of net sales of Dermacyte once Valor’s aggregate net sales of Dermacyte equals or exceeds $10,000,000.
Dermatology
We intend to develop additional clinical research protocols and conduct proof-of-concept studies for topical indications, such as the treatment of acne, rosacea, pruritis, psoriasis, and dermatitis. In January 2012 we initiated our first proof-of-concept study in India to assess the potential of our topical gel to reduce the itch (pruritis) associated with histamine-mediated allergic skin reactions. In May 2012, we revealed results of this study which showed that our topical gel elicited a larger reduction in Visual Analogue Scale scores following a standard histamine skin prick compared to placebo. The sample size of this study prevented a demonstration of statistical significance so further research is necessary to evaluate its effectiveness. We believe that we will need the support of partners in this sector to commercialize these dermatologic product candidates. We can provide no assurance that the topical indications we have under development will prove their claims and be successful commercial products.
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Wundecyte
Wundecyte is a novel gel developed under a contract agreement with a lab in Virginia that is designed to be used as a wound-healing gel. In July 2009, we filed a 510K medical device application for Wundecyte with the FDA. Several oxygen-producing and oxygen-carrying devices were cited as predicate devices. The FDA response was that the application likely would be classified as a combination device. The drug component of the combination device will require extensive preclinical and clinical studies to be conducted prior to potential commercialization of the product.
We have also developed a prototype for an oxygen-generating bandage that can be combined with Wundecyte gel. Wundecyte gel and the oxygen-generating bandage both entered preclinical testing in our first quarter of fiscal 2011. The studies were designed to measure factors such as time to wound closure and reduction in scar tissue formation as compared to a control group. Results showed an apparent increase in epithelial thickness versus the control. The treatment did not cause adverse effects and the models tolerated the treatment well. Our current product development plan is for Wundecyte to emerge into more complex wound-healing indications, also in combination with oxygen-producing technologies based on hydrogen peroxide. In December 2010 we signed a binding letter of intent with Sarasota Medical Products, Inc., or SMP, of Sarasota, Florida to determine the feasibility of pursuing a joint research and development venture for treating chronic ischemic wounds. The venture was to be based on combining Wundecyte with SMP’s topical medical devices. No significant development activities have resulted from this agreement as of April 30, 2013.
Recent Developments
As of July 11, 2013, we believe that our existing cash and cash equivalents will be sufficient to fund our projected operating requirements through July 31, 2013. We will need substantial additional capital in the future in order to complete the development and commercialization of Oxycyte and to fund the development and commercialization of our future product candidates. Until we can generate a sufficient amount of product revenue, if ever, we expect to finance future cash needs through public or private equity offerings, debt financings or corporate collaboration and licensing arrangements. Such funding, if needed, may not be available on favorable terms, if at all. In the event we are unable to obtain additional capital, we may delay or reduce the scope of our current research and development programs and other expenses.
While our common stock is currently listed on the NASDAQ Capital Market, or NASDAQ, we are not currently in compliance with NASDAQ’s continued listing standards. Continued listing of a security on NASDAQ is conditioned upon compliance with various continued listing standards, which require, among other things, that for 30 consecutive trading days (i) the closing minimum bid price for our listed securities not be lower than $1.00 per share and (ii) our market capitalization not be lower than $35 million. The closing bid price for our shares fell below $1.00 per share on August 21, 2012 and our market capitalization has been less than $35 million since August 8, 2012. As a result, NASDAQ notified us by letter dated March 20, 2013 of the Staff’s decision to delist our securities from NASDAQ. In addition, NASDAQ notified us by letter dated April 4, 2013 that our failure to maintain market capitalization not lower than $35 million serves as an additional basis to delist our securities from The NASDAQ Capital Market. We appealed NASDAQ’s determination by requesting a hearing before a NASDAQ Listing Qualifications Panel, or the Panel, to seek continued listing pending our return to compliance.
On May 15, 2013, we received notice from the Panel that the Panel has determined to grant our request for continued listing on The NASDAQ Capital Market pursuant to an extension through June 3, 2013 to evidence compliance with the minimum $1.00 bid price requirement, as set forth in NASDAQ Listing Rule 5550(a), and through July 31, 2013 to evidence compliance with the alternate minimum $2.5 million stockholders’ equity requirement, as set forth in NASDAQ Listing Rule 5550(b), for continued listing on The NASDAQ Capital Market. As of June 3, 2013, we have regained compliance with the minimum $1.00 bid price requirement, due in part to our 1-for-20 reverse stock split effective on May 13, 2013. We are working to timely evidence compliance with the additional terms of the Panel’s decision; however, there can be no assurance that we will be able to do so. See “Risk Factors” beginning on page 8 for additional information
Corporate Information
Our principal executive offices are located at ONE Copley Parkway, Suite 490, Morrisville, North Carolina 27560, and our telephone number is (919) 855-2100. Our Internet address is http://www.oxybiomed.com. The information on our website is not incorporated by reference into this prospectus, and you should not consider it part of this prospectus.
Our Company was originally formed as a New Jersey corporation in 1967 under the name Rudmer, David & Associates, Inc., and subsequently changed its name to Synthetic Blood International, Inc. Effective June 30, 2008, we changed the domiciliary state of the corporation to Delaware and changed the company name to Oxygen Biotherapeutics, Inc.
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Issuer
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Oxygen Biotherapeutics, Inc.
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Securities being offered by us
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6,000 units, with each unit consisting of (1) one share of Series C 8% Convertible Preferred Stock and (2) one warrant exercisable for [—] shares of our common stock. Units will not be issued or certificated. The shares of Series C 8% Convertible Preferred Stock and the warrants are immediately separable and will be issued separately.
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Offering Price
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$1,000 per unit
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Description of Series C 8% Convertible Preferred Stock
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Each unit includes one share of Series C 8% Convertible Preferred Stock. Series C 8% Convertible Preferred Stock has a liquidation preference. See “Description of Capital Stock – Series C 8% Convertible Preferred Stock” beginning on page 16.
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Conversion Price of Series C 8% Convertible Preferred Stock
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$[●]
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Shares of common stock underlying the shares of Series C 8% Convertible Preferred Stock included in units
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Based on an assumed conversion price of $2.24, which was 75% of the last reported sale price for our common stock on July 15, 2013, 2,678,572 shares.
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Subject to certain ownership limitations, the Series C 8% Convertible Preferred Stock is convertible at any time at the option of the holder into shares of our common stock at a conversion ratio determined by dividing the stated value of the Series C 8% Convertible Preferred Stock (or $1,000) by a conversion price of $[—] per share. The conversion price is subject to adjustment in the case of stock splits, stock dividends, combinations of shares and similar recapitalization transactions.
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Dividends and Make-Whole Payment
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Until the third anniversary of the date of issuance of the Series C 8% Convertible Preferred Stock, each holder of the Series C 8% Convertible Preferred Stock is entitled to receive dividends at the rate of 8% per annum of the stated value for each share of Series C 8% Convertible Preferred Stock held by such holder payable quarterly on January 1, April 1, July 1 and October 1, beginning on the first such date after the original issue date, and on each dividend payment date. We can elect to pay the dividends in cash or in duly authorized, validly issued, fully paid and non-assessable shares of common stock, or a combination thereof. If we pay the dividends in shares of common stock, the shares used to pay the dividends will be valued at 90% of the average volume weighted average price for the 20 consecutive trading days ending on the trading day immediately prior to the applicable dividend payment date. From and after the third anniversary of the date of issuance of the Series C 8% Convertible Preferred Stock, each holder of Series C 8% Convertible Preferred Stock will be entitled to receive dividends equal, on an as-if-converted to common stock basis, to and in the same form as dividends actually paid on shares of common stock when, as, and if such dividends are paid on shares of common stock. We have never paid dividends on our common stock and we do not intend to do so for the foreseeable future.
In the event a holder converts his, her or its Series C 8% Convertible Preferred Stock prior to the third anniversary of the date of issuance of the Series C 8% Convertible Preferred Stock, we must also pay to the holder in cash, or at our option in common stock valued as described above, or a combination of cash and shares of common stock, with respect to the Series C 8% Convertible Stock so converted, an amount equal to $240 per $1,000 of the stated value of the Series C 8% Convertible Preferred Stock, less the amount of any dividends paid in cash or in common stock on such Series C 8% Convertible Preferred Stock on or before the date of conversion.
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Conversion Rights
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Subject to certain ownership limitations, the Series C 8% Convertible Preferred Stock is convertible at any time at the option of the holder into shares of our common stock at a conversion ratio determined by dividing the stated value of the Series C 8% Convertible Preferred Stock (or $1,000) by a conversion price of $[—] per share. The conversion price is subject to adjustment in the case of stock splits, stock dividends, combinations of shares and similar recapitalization transactions.
Until such time that for at least 25 trading days during any 30 consecutive trading days, the volume weighted average price of our common stock exceeds 250% of the initial conversion price, if we sell or grant any option to purchase or sell any common stock or common stock equivalents entitling any person to acquire shares of common stock at an effective price per share that is lower than the then conversion price, or the Base Conversion Price, then the conversion price shall be reduced to equal the Base Conversion Price
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Covenants |
As long as any shares of Series C 8% Convertible Preferred Stock are outstanding, we may not, without the affirmative vote of the holders of 50.1% or more of the then outstanding shares of the Series C 8% Convertible Preferred Stock, (1) alter or change adversely the powers, preferences or rights given to the Series C 8% Convertible Preferred Stock or alter or amend the certificate of designation, (2) authorize or create any class of stock ranking as to dividends, redemption or distribution of assets upon liquidation senior to, or otherwise pari passu with, the Series C 8% Convertible Preferred Stock, (3) amend our certificate of incorporation or other charter documents in any manner that adversely affects any rights of the holders of Series C 8% Convertible Preferred Stock, (4) increase the number of authorized shares of Series C 8% Convertible Preferred Stock, or (5) enter into any agreement with respect to any of the foregoing.
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Liquidation Preference
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Upon any liquidation, dissolution or winding up of the Company after payment or provision for payment of debts and other liabilities of the Company, but before any distribution or payment is made to the holders of any junior securities, the holders of Series C 8% Convertible Preferred Stock shall be entitled to be paid out of the assets of the Company available for distribution to its stockholders an amount equal to $1,000 per share, after which any remaining assets of the Company shall be distributed among the holders of the other class or series of stock in accordance with the Company’s Certificate of Incorporation.
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Description of Warrants
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Each unit includes a warrant to purchase [—] shares of common stock. Warrants will entitle the holder to purchase shares of common stock for an exercise price equal to $[—] per share. The warrants will be exercisable beginning [—] and expire on the sixth anniversary of the initial exercise date. See “Description of Securities We Are Offering – Warrants” beginning on page 18.
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Warrant Anti-Dilution Adjustments
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The exercise price and the number of shares issuable upon exercise of the warrants is subject to appropriate adjustment in the event of recapitalization events, stock dividends, stock splits, stock combinations, reclassifications, reorganizations or similar events affecting our common stock, and also upon any distributions of assets, including cash, stock or other property to our stockholders.
In addition, the warrants will be subject to anti-dilution provisions until such time that for 25 trading days during any 30 consecutive trading days period, the volume weighted average price of the Company’s common stock exceeds $[●] and the daily dollar trading volume exceeds $350,000 per trading day.
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Fundamental Transactions
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In the event we consummate a merger or consolidation with or into another person or other reorganization event in which our common shares are converted or exchange for securities, cash or other property, or we sell, lease, license, assign, transfer, convey or otherwise dispose of all or substantially all of our assets or we or another person acquire 50% or more of our outstanding common shares, then following such event, the holders of the Series C 8% Convertible Preferred Stock and warrants will be entitled to receive upon conversion or exercise, as applicable, the same kind and amount of securities, cash or property which the holders would have received had they converted or exercised, as applicable, such securities immediately prior to such fundamental transaction.
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Shares of common stock outstanding before this offering
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2,124,440 shares
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Common stock to be outstanding after this offering, including shares of common stock underlying shares of Series C 8% Convertible Preferred Stock included in units
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[●] shares
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Use of proceeds
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Assuming all units are sold, we estimate that the net proceeds to us from this offering will be approximately $[—] million. We intend to use the net proceeds received from the sale of the securities for furthering our clinical trials and efforts to obtain regulatory approval for Oxycyte, developing our other product candidates, supporting manufacturing Oxycyte, distribution for Dermacyte, research and development and general corporate purposes. See “Use of Proceeds.”
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Limitations on Beneficial Ownership
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Subject to limited exceptions, the Company will not permit the conversion of the Series C 8% Convertible Preferred Stock or exercise of the warrants of any holder, if after such conversion or exercise such holder would beneficially own more than 4.99% of the shares of common stock then outstanding.
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Risk factors
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Investing in our securities involves a high degree of risk. See the “Risk Factors” section of this prospectus on page 8 and in the documents we incorporate by reference in this prospectus for a discussion of factors you should consider carefully before deciding to invest in our securities.
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● | 757,749 shares of common stock issuable upon the exercise of outstanding warrants with a weighted average exercise price of $11.26 per share; |
● | 128,192 shares of common stock issuable upon the exercise of outstanding Series B-2 preferred stock with a weighted average exercise price of $3.37 per share; |
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11,365 shares of common stock issuable upon the exercise of outstanding options with a weighted average exercise price of $57.07 per share and 13,975 shares of common stock issuable upon the vesting of outstanding restricted stock grants;
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270,068 shares of common stock reserved for future grants and awards under our equity incentive plans; and
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● | 108,648 shares of common stock issuable upon the conversion of outstanding convertible notes with a weighted average conversion price of $45.10. |
● | [●] shares of common stock issuable upon exercise of warrants to be issued in connection with this offering. |
Public offering price per unit
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2.24
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Net Tangible book value per share as of April 30, 2013
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(1.40)
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Increase per share attributable to the offering
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1.97
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Adjusted net tangible book value per share as of April 30, 2013 after giving effect to this offering
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0.57
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Dilution per share to new investors
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1.67
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108,648 shares of common stock issuable upon the conversion of outstanding convertible notes with a weighted average conversion price of $45.10.
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759,410 shares of common stock issuable upon the exercise of outstanding warrants with a weighted average exercise price of $11.00 per share;
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11,336 shares of common stock issuable upon the exercise of outstanding options with a weighted average exercise price of $57.00 per share and 1,917 shares of common stock issuable upon the vesting of outstanding restricted stock grants;
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282,726 shares of common stock reserved for future grants and awards under our equity incentive plans;
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197,400 shares of common stock issuable upon the exercise of outstanding Series B-1 and Series B-2 preferred stock with a weighted average exercise price of $5.00 per share.
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senior to our common stock, and, except as described below, to each other class of capital stock established after the original issue date of the Series A Convertible Preferred Stock, or the Issue Date, (which we will refer to collectively as “Junior Stock”);
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●
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equally with any class of capital stock established after the Issue Date, issued after the express written consent of the holders of a majority of the aggregate outstanding shares of Series A Convertible Preferred Stock, the terms of which expressly provide that the right of the holders thereof, either as to the payment of dividends or as to distributions in the event of our voluntary or involuntary liquidation, dissolution or winding up, (i) are not given preference over the rights of the holders of the Series A Convertible Preferred Stock and (ii) rank on an equality with the rights of the holders of the Series A Convertible Preferred Stock (which we will refer to collectively as “Parity Stock”); and
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●
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junior to each class of capital stock established after the Issue Date, issued after the express written consent of the holders of a majority of the aggregate outstanding shares of Series A Convertible Preferred Stock, the terms of which expressly provide that the rights of the holders thereof either as to the payment of dividends or as to distributions in the event of our voluntary or involuntary liquidation, dissolution or winding up are given preference over the right of the holders of the Series A Convertible Preferred Stock (which we will refer to collectively as “Senior Stock”).
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increase or decrease the aggregate number of authorized shares of Series B-1 Convertible Preferred Stock;
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increase or decrease the par value of the shares of Series B-1 Convertible Preferred Stock; or
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alter or change the powers, preferences, or special rights of the shares of Series B-1 Convertible Preferred Stock so as to affect them adversely.
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increase or decrease the aggregate number of authorized shares of Series C 8% Convertible Preferred Stock;
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increase or decrease the par value of the shares of Series C 8% Convertible Preferred Stock; or
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alter or change the powers, preferences, or special rights of the shares of Series C 8% Convertible Preferred Stock so as to affect them adversely.
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(i)
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by operation of law or by reason of our reorganization;
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(ii)
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to any FINRA member firm participating in the offering and the officers and partners thereof, if all securities so transferred remain subject to the lock-up restriction described above for the remainder of the time period;
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(iii)
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if the aggregate amount of our securities held by the Placement Agent or related person does not exceed 1% of the securities being offered;
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(iv)
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that is beneficially owned on a pro-rata basis by all equity owners of an investment fund, provided that no participating member manages or otherwise directs investments by the fund, and participating members in the aggregate do not own more than 10% of the equity in the fund; or
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(v)
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the exercise or conversion of any security, if all securities received remain subject to the lock-up restriction set forth above for the remainder of the time period.
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Per unit placement agent’s fees
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$ |
80
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Maximum offering total
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$ | 480.000 |
●
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may not engage in any stabilization activity in connection with our securities; and
|
●
|
may not bid for or purchase any of our securities or attempt to induce any person to purchase any of our securities, other than as permitted under the Exchange Act, until it has completed its participation in the distribution.
|
●
|
Our Annual Report on Form 10-K for the fiscal year ended April 30, 2013, filed with the SEC on June 26, 2013; and
|
●
|
Our Current Reports on Form 8-K filed with the SEC on May 1, 2013, May 15, 2013, May 16, 2013 and June 27, 2013.
|
ITEM 13.
|
OTHER EXPENSES OF ISSUANCE AND DISTRIBUTION
|
SEC registration fee
|
$ | 2,046 | |
Accounting fees and expenses
|
25,000 | ||
Legal fees and expenses
|
75,000 | ||
Printing expenses
|
10,000 | ||
Miscellaneous
|
7,954 | ||
Total
|
$ | 120,000 |
ITEM 14.
|
INDEMNIFICATION OF DIRECTORS AND OFFICERS
|
ITEM 15.
|
RECENT SALES OF UNREGISTERED SECURITIES
|
Date(s)
|
Number of Securities Issued
|
Purchaser
|
Consideration
|
2/3/2010 – 4/11/2011
|
1,755
|
Employees
|
Employee compensation
|
4/26/2010 – 11/15/2011
|
153,684 (1)
|
Vatea Fund
|
$9,000,000
|
4/26/2010 – 11/15/2011
|
30,737 (2)
|
Melixia SA
|
Consultant compensation
|
5/13/2013 | 20,839 (3) |
IRTH Communications
|
Consultant compensation
|
Date(s)
|
Number of Securities Issued
|
Purchaser
|
Consideration
|
6/29/2011
|
(4)
|
Empery Asset Master, LTD (6)
|
$300,000
|
7/1/2011
|
(5)
|
OXBT Fund (6)
|
$4,600,000
|
2/27/2013
|
(7)
|
Various
|
$500,000
|
Date(s)
|
Number of Securities Issued
|
Purchaser
|
Consideration
|
2/3/2010 – 10/14/2010
|
128
|
Various
|
Conversion of 2008 Convertible Notes
|
2/29/2012
|
4,368
|
Richard Rendon (8)
|
$114,448
|
10/2/2011 – 6/28/2013
|
32,843 (9)
|
Various
|
Convertible note interest
|
|
(1)
|
Issued pursuant to terms of the Securities Purchase Agreement with Vatea Fund.
|
|
(2)
|
In connection with the three closings with Vatea Fund between April 26, 2010 and November 15, 2011, we issued 30,737 shares of Common Stock to Melixia for their services provided as facilitating agent pursuant to the terms of the Securities Purchase Agreement with Vatea Fund.
|
|
(3)
|
Issued 20,839 shares of restricted common stock for investor and public relations services provided pursuant to the terms of the service agreement.
|
|
(4)
|
Notes or the 2011 Notes, and Warrants issued pursuant to terms of the Convertible Note and Warrant Purchase Agreement with Empery Asset Master, LTD that provided for the issuance of a note with a principal amount of approximately $300,000 convertible into Common Stock at a conversion price of $45.10 per share of Common Stock and Warrants to purchase an aggregate of 6,652 shares of Common Stock.
|
|
(5)
|
2011 Notes and Warrants issued pursuant to terms of the Convertible Note and Warrant Purchase Agreement with OXBT Fund that provided for the issuance of a note with a principal amount of approximately $4,600,000 convertible into Common Stock at a conversion price of $45.10 per share of Common Stock and Warrants to purchase an aggregate of 101,996 shares of Common Stock.
|
|
(6)
|
In connection with these closings, we paid a placement fee of $276,000 to FGP Capital.
|
|
(7)
|
Preferred Stock and Warrants issued pursuant to terms of the Securities Purchase Agreement with certain institutional investors that provided for the issuance of 500 shares of Series B-2 convertible preferred stock with a stated value of $500,000 convertible into Common Stock at a conversion price of $5.00 per share of Common Stock and Warrants to purchase an aggregate of 630,000 shares of Common Stock.
|
|
(8)
|
Issued upon exercise of warrants to purchase Common Stock issued pursuant to the terms of the 2008 Convertible Note and Warrant Purchase Agreement.
|
|
(9)
|
Issued as payment for quarterly interest due to the holders of the 2011 Notes.
|
ITEM 16.
|
EXHIBITS
|
ITEM 17.
|
UNDERTAKINGS
|
(a)
|
The undersigned registrant hereby undertakes:
|
1)
|
To file, during any period in which offers or sales are being made, a post-effective amendment to this registration statement:
|
i.
|
to include any prospectus required by section 10(a)(3) of the Securities Act of 1933;
|
ii.
|
to reflect in the prospectus any facts or events arising after the effective date of the registration statement (or the most recent post-effective amendment thereof) which, individually or in the aggregate, represent a fundamental change in the information set forth in the registration statement. Notwithstanding the foregoing, any increase or decrease in volume of securities offered (if the total dollar value of securities offered would not exceed that which was registered) and any deviation from the low or high end of the estimated maximum offering range may be reflected in the form of prospectus filed with the Commission pursuant to Rule 424(b) if, in the aggregate, the changes in volume and price represent no more than a 20% change in the maximum aggregate offering price set forth in the “Calculation of Registration Fee” table in the effective registration statement; and
|
iii.
|
to include any material information with respect to the plan of distribution not previously disclosed in the registration statement or any material change to such information in the registration statement.
|
2)
|
That, for the purpose of determining any liability under the Securities Act of 1933, each such post-effective amendment shall be deemed to be a new registration statement relating to the securities offered therein, and the offering of such securities at that time shall be deemed to be the initial bona fide offering thereof.
|
3)
|
To remove from registration by means of a post-effective amendment any of the securities being registered which remain unsold at the termination of the offering.
|
4)
|
That, for the purpose of determining liability under the Securities Act of 1933 to any purchaser:
|
i.
|
if the registrant is relying on Rule 430B: (A) each prospectus filed by the registrant pursuant to Rule 424(b)(3) shall be deemed to be part of the registration statement as of the date the filed prospectus was deemed part of and included in the registration statement; and (B) each prospectus required to be filed pursuant to Rule 424(b)(2), (b)(5), or (b)(7) as part of a registration statement in reliance on Rule 430B relating to an offering made pursuant to Rule 415(a)(1)(i), (vii), or (x) for the purpose of providing the information required by section 10(a) of the Securities Act of 1933 shall be deemed to be part of and included in the registration statement as of the earlier of the date such form of prospectus is first used after effectiveness or the date of the first contract of sale of securities in the offering described in the prospectus. As provided in Rule 430B, for liability purposes of the issuer and any person that is at that date an underwriter, such date shall be deemed to be a new effective date of the registration statement relating to the securities in the registration statement to which that prospectus relates, and the offering of such securities at that time shall be deemed to be the initial bona fide offering thereof. Provided, however, that no statement made in a registration statement or prospectus that is part of the registration statement or made in a document incorporated or deemed incorporated by reference into the registration statement or prospectus that is part of the registration statement will, as to a purchaser with a time of contract of sale prior to such effective date, supersede or modify any statement that was made in the registration statement or prospectus that was part of the registration statement or made in any such document immediately prior to such effective date; or
|
ii.
|
if the registrant is subject to Rule 430C, each prospectus filed pursuant to Rule 424(b) as part of a registration statement relating to an offering, other than registration statements relying on Rule 430B or other than prospectuses filed in reliance on Rule 430A, shall be deemed to be part of and included in the registration statement as of the date it is first used after effectiveness. Provided, however, that no statement made in a registration statement or prospectus that is part of the registration statement or made in a document incorporated or deemed incorporated by reference into the registration statement or prospectus that is part of the registration statement will, as to a purchaser with a time of contract of sale prior to such first use, supersede or modify any statement that was made in the registration statement or prospectus that was part of the registration statement or made in any such document immediately prior to such date of first use.
|
5)
|
That, for the purpose of determining liability under the Securities Act of 1933 to any purchaser in the initial distribution of the securities: the undersigned registrant undertakes that in a primary offering of securities of the undersigned registrant pursuant to this registration statement, regardless of the underwriting method used to sell the securities to the purchaser, if the securities are offered or sold to such purchaser by means of any of the following communications, the undersigned registrant will be a seller to the purchaser and will be considered to offer or sell such securities to such purchaser: (i) any preliminary prospectus or prospectus of the undersigned registrant relating to the offering required to be filed pursuant to Rule 424; (ii) any free writing prospectus relating to the offering prepared by or on behalf of the undersigned registrant or used or referred to by the undersigned registrant; (iii) the portion of any other free writing prospectus relating to the offering containing material information about the undersigned registrant or its securities provided by or on behalf of the undersigned registrant; and (iv) any other communication that is an offer in the offering made by the undersigned registrant to the purchaser.
|
(b)
|
Insofar as indemnification for liabilities arising under the Securities Act of 1933 may be permitted to directors, officers and controlling persons of the registrant pursuant to the foregoing provisions, or otherwise, the registrant has been advised that in the opinion of the Securities and Exchange Commission such indemnification is against public policy as expressed in the Act and is, therefore, unenforceable. In the event that a claim for indemnification against such liabilities (other than the payment by the registrant of expenses incurred or paid by a director, officer or controlling person of the registrant in the successful defense of any action, suit or proceeding) is asserted by such director, officer or controlling person in connection with the securities being registered, the registrant will, unless in the opinion of its counsel the matter has been settled by controlling precedent, submit to a court of appropriate jurisdiction the question whether such indemnification by it is against public policy as expressed in the Act and will be governed by the final adjudication of such issue.
|
(c)
|
The undersigned registrant hereby undertakes that:
|
1)
|
For purposes of determining any liability under the Securities Act of 1933, the information omitted from the form of prospectus filed as part of this registration statement in reliance upon Rule 430A and contained in a form of prospectus filed by the registrant pursuant to Rule 424(b)(1) or (4) or 497(h) under the Securities Act shall be deemed to be part of this registration statement as of the time it was declared effective.
|
OXYGEN BIOTHERAPEUTICS, INC.
|
|||
By:
|
/s/ Michael B. Jebsen | ||
Michael B. Jebsen | |||
President, Interim Chief Executive Officer and Chief Financial Officer | |||
Signature
|
|
Title
|
Date
|
|
*
|
|
July 16, 2013
|
||
Michael B. Jebsen | President, Interim Chief Executive Officer and Chief Financial Officer
(Principal Executive Officer, Principal Financial Officer and Principal Accounting Officer)
|
|||
*
|
|
July 16, 2013
|
||
Ronald Blanck, D.O. | Chairman and Director | |||
*
|
|
July 16, 2013
|
||
Gregory Pepin | Director | |||
*
|
|
July 16, 2013
|
||
William Chatfield | Director | |||
*
|
|
|
July 16, 2013
|
|
Anthony DiTonno | Director | |||
*
|
|
July 16, 2013
|
||
Chris Rallis | Director |
By:
|
/s/ Michael B. Jebsen | |
Michael B. Jebsen
|
||
President, Interim Chief Executive Officer
and Chief Financial Officer |
||
Exhibit No.
|
|
Exhibits Required by Item 601 of Regulation S-K
|
2.1
|
|
Agreement and Plan of Merger dated April 28, 2008 (1)
|
3.1
|
|
Certificate of Incorporation (1)
|
3.2
|
Certificate of Amendment of the Certificate of Incorporation (14)
|
|
3.3 |
Certificate of Amendment of the Certificate of Incorporation (30)
|
|
3.4 |
Certificate of Designations of Series A Convertible Preferred Stock (28)
|
|
3.5
|
Certificate of Designations of Series B-1 Convertible Preferred Stock**
|
|
3.6
|
Certificate of Designations of Series B-2 Convertible Preferred Stock **
|
|
3.7 |
Form of Certificate of Designations of Series C 8% Convertible Preferred Stock*
|
|
3.8
|
|
Amended and Restated Bylaws (22)
|
4.1
|
|
Specimen Stock Certificate (19)
|
5.1 |
Opinion of Smith, Anderson, Blount, Dorsett, Mitchell & Jernigan, L.L.P. *
|
|
10.1
|
|
Agreement with Leland C. Clark, Jr., Ph.D. dated November 20, 1992 with amendments, Assignment of Intellectual Property/ Employment (2)
|
10.2
|
|
Agreement between the Registrant and Keith R. Watson, Ph.D. Assignment of Invention (2)
|
10.3
|
|
Children’s Hospital Research Foundation License Agreement dated February 28, 2001 (2)
|
10.4
|
Exclusive License Agreement with Virginia Commonwealth University dated May 22, 2008 (9)
|
|
10.5
|
Amendment no. 1 to the Exclusive License Agreement with Virginia Commonwealth University Intellectual Property Foundation (10)
|
|
10.6
|
Amendment no. 2 to the Exclusive License Agreement with Virginia Commonwealth University Intellectual Property Foundation (10)
|
|
10.7
|
Agreement with Hospira to manufacture Oxycyte (8)
|
10.8
|
Termination Agreement between the Company and Hospira, dated August 30, 2011 (23)
|
|
10.9
|
Exclusive Supply Agreement with Exfluor dated November 12, 2009 (10)
|
|
10.10
|
Master Agreement with Dermacyte Switzerland (18)
|
|
10.11
|
Amendment no. 1 to Master Agreement with Dermacyte Switzerland (18)
|
|
10.12
|
|
Form of Option issued to Executive Officers and Directors (2)
|
10.13
|
|
Form of Option issued to Employees (2)
|
10.14
|
|
Restricted Stock Award Agreement (22)
|
10.15
|
|
Form of Warrant issued to Unsecured Note Holders 2006-2007 (3)
|
10.16
|
|
Form of Convertible Note – 2008 (4)
|
10.17
|
|
Form of Warrant issued to Convertible Note Holders (4)
|
10.18
|
|
Form of Purchase Agreement – US Purchase (without exhibits, which are included as exhibits 10.16 and 10.17, above) (4)
|
10.19
|
|
Form of Purchase Agreement – Non-US Purchase (without exhibits, which are included as exhibits 10.16 and 10.17, above) (4)
|
10.20
|
|
Form of Purchase Agreement – US Note Exchange (without exhibits, which are included as exhibits 10.16 and 10.17, above) (4)
|
10.21
|
|
Form of Purchase Agreement – Non-US Note Exchange (without exhibits, which are included as exhibits 10.16 and 10.17, above) (4)
|
10.22
|
|
Form of Warrant issued to Financing Consultants (5)
|
10.23
|
|
1999 Amended Stock Plan (amended 2008) (5)
|
10.24
|
|
Employment Agreement with Chris J. Stern dated February 1, 2009 (12)
|
10.25
|
Amended and Restated Employment Agreement with Chris J. Stern dated May 13, 2011 (20)
|
|
10.26
|
|
Business Consultant Agreement with Institute for Efficient Management, Inc., as amended March 26, 2008 (5)
|
10.27
|
|
Engagement and Consulting Agreement with Bruce Spiess (5)
|
10.28
|
|
Engagement and Consulting Agreement with Gerald L. Klein (5)
|
10.29
|
Employment Agreement with Gerald L. Klein dated May 13, 2011 (20)
|
|
10.30
|
|
Business Consultant Agreement with Edward Sitnik (8)
|
10.31
|
|
Business Consultant Agreement with J. Melville Engle (8)
|
10.32
|
|
Employment Agreement with Richard Kiral, restated February 1, 2009 (8)
|
10.33
|
Resignation of Employment and Consulting Agreement with Richard Kiral (20)
|
|
10.34
|
Employment Agreement with Michael B. Jebsen dated December 1, 2010 (16)
|
|
10.35
|
Amended and Restated Employment Agreement with Michael B. Jebsen dated May 19, 2011 (20)
|
|
10.36
|
Form of Indemnification Agreement (20)
|
|
10.37
|
|
Description of Non-Employee Director Compensation (25)
|
10.38
|
|
Securities Purchase Agreement (including exhibits) between Oxygen Biotherapeutics and Vatea Fund, Segregated Portfolio dated June 8, 2009 (6)
|
10.39
|
|
Amendment no. 1 to the Securities Purchase Agreement between Oxygen Biotherapeutics and Vatea Fund, Segregated Portfolio (11)
|
10.40
|
|
Amendment no. 2 to the Securities Purchase Agreement between Oxygen Biotherapeutics and Vatea Fund, Segregated Portfolio (12)
|
10.41
|
|
Amendment no. 3 to the Securities Purchase Agreement between Oxygen Biotherapeutics and Vatea Fund, Segregated Portfolio (23)
|
10.42
|
Form of Exchange Agreement dated July 20, 2009 (7)
|
|
10.43
|
Waiver—Convertible Note (10)
|
|
10.44
|
Amendment—Common Stock Purchase Warrant (10)
|
|
10.45
|
Form of Warrant for May 2010 offering (13)
|
|
10.46
|
Form of Subscription Agreement for May 2010 offering (13)
|
|
10.47
|
Warrant issued to Blaise Group International, Inc. (14)
|
10.48
|
Note Purchase Agreement between Oxygen Biotherapeutics and JP SPC 1 Vatea, Segregated Portfolio (15)
|
|
10.49
|
Form of Promissory Note under Note Purchase Agreement between Oxygen Biotherapeutics and JP SPC 1 Vatea, Segregated Portfolio (15)
|
|
10.50
|
First Amendment to Note Purchase Agreement between Oxygen Biotherapeutics and JP SPC 1 Vatea, Segregated Portfolio (17)
|
|
10.51
|
Lease Agreement for North Carolina corporate office (18)
|
|
10.52
|
Standard Industrial Lease relating to OBI’s California facility (12)
|
|
10.53
|
Task Order between the Company and NextPharma, dated November 15, 2011 (23)
|
|
10.54
|
Form of Convertible Note for July 2011 offering (included in exhibit 10.56)
|
|
10.55
|
Form of Warrant for July 2011 offering (included in exhibit 10.56)
|
|
10.56
|
Form of Convertible Note and Warrant Purchase Agreement for July 2011 offering (21)
|
|
10.57
|
Placement Agency Agreement, dated December 8, 2011, between Oxygen Biotherapeutics, Inc. and William Blair & Company, L.L.C., as placement agent (24)
|
|
10.58
|
Form of Warrant for December 2011 offering (24)
|
|
10.59
|
Form of Securities Purchase Agreement for December 2011 offering (24)
|
|
10.60
|
Form of Amendment Agreement for December 2011 offering (26)
|
|
10.61
|
Form of Lock-up Agreement for December 2011 offering (24)
|
|
10.62
|
Form of Amendment Agreement for December 2011 offering (27)
|
|
10.63
|
Fluoromed Supply Agreement(28)
|
|
10.64
|
Form of Warrant for February 2013 offering (29)
|
|
10.65
|
Placement Agency Agreement, dated February 22, 2013, between Oxygen Biotherapeutics, Inc. and Ladenburg Thalmann & Co. Inc., as placement agent (29)
|
|
10.66
|
Form of Securities Purchase Agreement for February 2013 offering (29)
|
|
10.67
|
Form of Registration Rights Agreement for February 2013 offering (29)
|
10.68
|
Form of Warrant Exchange Agreement, dated February 21, 2013, between Oxygen Biotherapeutics, Inc. and certain institutional investors party to the Securities Purchase Agreement for December 2011 Offering (29)
|
|
10.69 |
License and Supply Agreement dated February 5, 2013, between Oxygen Biotherapeutics, Inc. and Valor SA (31)
|
|
10.70 |
Settlement Agreement, dated March 14, 2013, among Oxygen Biotherapeutics, Inc., Tenor Opportunity Master Fund Ltd., Aria Opportunity Fund, Ltd., and Parsoon Opportunity Fund, Ltd. (31)
|
|
Form of Warrant*
|
||
Form of Placement Agency Agreement with Ladenburg Thalmann & Co. Inc., as placement agent *
|
||
Form of Securities Purchase Agreement*
|
||
23.1
|
Consent of Independent Registered Accounting Firm*
|
|
23.2
|
Consent of Smith, Anderson, Blount, Dorsett, Mitchell & Jernigan, L.L.P. (included in Exhibit 5.1) *
|
|
24.1
|
Power of Attorney **
|
(1)
|
These documents were filed as exhibits to the current report on Form 8-K filed by Oxygen Biotherapeutics with the SEC on June 30, 2008, and are incorporated herein by this reference.
|
(2)
|
These documents were filed as exhibits to the annual report on Form 10-K filed by Oxygen Biotherapeutics with the SEC on August 13, 2004, and are incorporated herein by this reference.
|
(3)
|
These documents were filed as exhibits to the current report on Form 8-K filed by Oxygen Biotherapeutics with the SEC on September 6, 2006, and are incorporated herein by this reference.
|
(4)
|
These documents were filed as exhibits to the quarterly report on Form 10-Q filed by Oxygen Biotherapeutics with the SEC on March 21, 2008, and are incorporated herein by this reference.
|
(5)
|
These documents were filed as exhibits to the annual report on Form 10-K filed by Oxygen Biotherapeutics with the SEC on August 13, 2008, and are incorporated herein by this reference.
|
(6)
|
This document was filed as an exhibit to the current report on Form 8-K filed by Oxygen Biotherapeutics with the SEC on June 8, 2009, and is incorporated herein by this reference.
|
(7)
|
This document was filed as an exhibit to the current report on Form 8-K filed by Oxygen Biotherapeutics with the SEC on July 21, 2009, and is incorporated herein by this reference.
|
(8)
|
These documents were filed as exhibits to the annual report on Form 10-K filed by Oxygen Biotherapeutics with the SEC on August 12, 2009, and are incorporated herein by this reference.
|
(9)
|
This document was filed as an exhibit to the quarterly report on Form 10-Q filed by Oxygen Biotherapeutics with the SEC on September 22, 2008, and is incorporated herein by this reference.
|
(10)
|
These documents were filed as exhibits to the quarterly report on Form 10-Q filed by Oxygen Biotherapeutics with the SEC on March 19, 2010, and are incorporated herein by this reference.
|
(11)
|
This document was filed as an exhibit to the current report on Form 8-K filed by Oxygen Biotherapeutics with the SEC on September 2, 2009, and is incorporated herein by this reference.
|
(12)
|
These documents were filed as exhibits to the current report on Form 8-K filed by Oxygen Biotherapeutics with the SEC on April 28, 2010, and are incorporated herein by this reference.
|
(13)
|
These documents were filed as exhibits to the current report on Form 8-K filed by Oxygen Biotherapeutics with the SEC on May 4, 2010, and are incorporated herein by this reference.
|
(14)
|
These documents were filed as exhibits to the current report on Form 8-K filed by Oxygen Biotherapeutics with the SEC on November 13, 2009, and are incorporated herein by reference.
|
(15)
|
These documents were filed as exhibits to the current report on Form 8-K filed by Oxygen Biotherapeutics with the SEC on October 13, 2010, and are incorporated herein by this reference.
|
(16)
|
These documents were filed as exhibits to the quarterly report on Form 10-Q filed by Oxygen Biotherapeutics with the SEC on December 9, 2010, and are incorporated herein by this reference.
|
(17)
|
This document was filed as an exhibit to the current report on Form 8-K filed by Oxygen Biotherapeutics with the SEC on December 30, 2010, and is incorporated herein by this reference.
|
(18)
|
These documents were filed as exhibits to the quarterly report on Form 10-Q filed by Oxygen Biotherapeutics with the SEC on March 21, 2011, and are incorporated herein by this reference.
|
(19)
|
These documents were filed as exhibits to the annual report on Form 10-K filed by Oxygen Biotherapeutics with the SEC on July 23, 2010, and are incorporated herein by this reference.
|
(20)
|
This document was filed as an exhibit to the annual report on Form 10-K filed by Oxygen Biotherapeutics with the SEC on July 15, 2011, and is incorporated herein by this reference.
|
(21)
|
This document was filed as an exhibit to the current report on Form 8-K/A filed by Oxygen Biotherapeutics with the SEC on July 1, 2011, and is incorporated herein by this reference.
|
(22)
|
This document was filed as an exhibit to the quarterly report on Form 10-Q filed by Oxygen Biotherapeutics with the SEC on December 15, 2011, and is incorporated herein by this reference.
|
(23)
|
These documents were filed as exhibits to the current report on Form 8-K filed by Oxygen Biotherapeutics with the SEC on November 16, 2011, and are incorporated herein by this reference.
|
(24)
|
These documents were filed as exhibits to the current report on Form 8-K filed by Oxygen Biotherapeutics with the SEC on December 9, 2011, and are incorporated herein by this reference.
|
(25)
|
This document was filed as an exhibit to the quarterly report on Form 10-Q filed by Oxygen Biotherapeutics with the SEC on March 15, 2012, and is incorporated herein by this reference.
|
(26)
|
This document was filed as an exhibit to the current report on Form 8-K filed by Oxygen Biotherapeutics with the SEC on June 15, 2012, and is incorporated herein by this reference.
|
(27)
|
This document was filed as an exhibit to the current report on Form 8-K filed by Oxygen Biotherapeutics with the SEC on June 15, 2012, and is incorporated herein by reference.
|
(28)
|
These documents were filed as exhibits to the annual report on Form 10-K filed by Oxygen Biotherapeutics with the SEC on July 25, 2012, and are incorporated herein by this reference.
|
(29)
|
These documents were filed as exhibits to the current report on Form 8-K filed by Oxygen Biotherapeutics with the SEC on February 25, 2013, and are incorporated herein by this reference.
|
(30) |
This document was filed as an exhibit to the current report on Form 8-K filed by Oxygen Biotherapeutics with the SEC on May 15, 2013, and is incorporated herein by this reference.
|
(31) |
These documents were filed as exhibits to the annual report on Form 10-K filed by Oxygen Biotherapeutics with the SEC on June 26, 2013, and are incorporated herein by this reference.
|
*
|
Filed herewith.
|
__________________________________________
Name:
Title:
|
__________________________________________
Name:
Title:
|
Date to Effect Conversion: _____________________________________________
|
|
Number of shares of Preferred Stock owned prior to Conversion: _______________
|
|
Number of shares of Preferred Stock to be Converted: ________________________
|
|
Stated Value of shares of Preferred Stock to be Converted: ____________________
|
|
Number of shares of Common Stock to be Issued: ___________________________
|
|
Applicable Conversion Price:____________________________________________
|
|
Number of shares of Preferred Stock subsequent to Conversion: ________________
|
|
DWAC Instructions:
Broker no: _________
Account no: ___________
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[NAME OF HOLDER]
By:___________________________________
Name:
Title:
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OFFICES
2300 Wells Fargo Capitol Center
Raleigh, North Carolina 27601
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July 16, 2013
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MAILING ADDRESS
P.O. Box 2611
Raleigh, North Carolina
27602-2611
TELEPHONE: (919) 821-1220
FACSIMILE: (919) 821-6800
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1.
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The Preferred Shares will be duly authorized, and when issued and delivered against payment of the purchase price therefore in accordance with the terms of the Securities Purchase Agreement and upon either (a) the countersigning of the certificates representing the Preferred Shares by a duly authorized signatory of the registrar for the Preferred Shares, or (b) the book entry of the Preferred Shares by the transfer agent for the Preferred Shares, such Preferred Shares will be validly issued, fully paid, and non-assessable.
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2.
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The Conversion Shares have been duly authorized, and when issued and delivered upon conversion of the Preferred Shares in accordance with the terms of the Certificate of Designation and upon either (a) the countersigning of the certificates representing the Conversion Shares by a duly authorized signatory of the registrar for the Common Stock or (b) the book entry of the Conversion Shares by the transfer agent for the Common Stock, such Conversion Shares will be validly issued, fully paid, and non-assessable.
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3.
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The Warrants have been duly authorized, and when executed and delivered by the Company in accordance with the terms of the Securities Purchase Agreement, such Warrants will constitute valid and binding obligations of the Company, enforceable against the Company in accordance with their terms.
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4.
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The Warrant Shares have been duly authorized, and when issued and delivered against payment of the exercise price therefore in accordance with the terms of the Warrants and upon either (a) the countersigning of the certificates representing the Warrant Shares by a duly authorized signatory of the registrar for the Common Stock or (b) the book entry of the Warrant Shares by the transfer agent for the Common Stock, such Warrant Shares will be validly issued, fully paid, and non-assessable.
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(a)
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This opinion is subject to the effect of applicable bankruptcy, insolvency, reorganization, fraudulent conveyance, moratorium, and similar laws affecting the enforcement of creditors’ rights generally.
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(b)
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This opinion is subject to the effect of general principals of equity (regardless of whether considered in a proceeding in equity or at law), which may, among other things, deny rights of specific performance.
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(A) = the VWAP on the Trading Day immediately preceding the date on which Holder elects to exercise this Warrant by means of a “cashless exercise,” as set forth in the applicable Notice of Exercise;
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(B) = the Exercise Price of this Warrant, as adjusted hereunder; and
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(X) = the number of Warrant Shares that would be issuable upon exercise of this Warrant in accordance with the terms of this Warrant if such exercise were by means of a cash exercise rather than a cashless exercise.
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OXYGEN BIOTHERAPEUTICS, INC. | |||
By:
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Name: | |||
Title: |
Dated: ______________, _______ | ||
Holder’s Signature: | _____________________________ | |
Holder’s Address: | _____________________________ | |
_____________________________ |
Very truly yours,
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OXYGEN BIOTHERAPEUTICS, INC.,
a Delaware corporation
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By: | |||
Name: Michael Jebsen
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Title: Interim Chief Executive Officer and Chief Financial Officer
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LADENBURG THALMANN & CO. INC.
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By: | ||
Name:
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Title:
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i.
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by operation of law or by reason of reorganization of the Company;
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ii.
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to any FINRA member firm participating in the offering and the officers or partners thereof, if all securities so transferred remain subject to the lock-up restriction in this Section 4(a) for the remainder of the time period;
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iii.
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if the aggregate amount of securities of the Company held by the Holder or related person do not exceed 1% of the securities being offered;
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iv.
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that is beneficially owned on a pro-rata basis by all equity owners of an investment fund, provided that no participating member manages or otherwise directs investments by the fund, and participating members in the aggregate do not own more than 10% of the equity in the fund; or
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v.
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the exercise or conversion of any security, if all securities received remain subject to the lock-up restriction in this Section 4(a) for the remainder of the time period.
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OXYGEN BIOTHERAPEUTICS, INC.
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By: | |||
Name | |||
Title |
OXYGEN BIOTHERAPEUTICS, INC.
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Address for Notice:
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By:__________________________________________
Name:
Title:
With a copy to (which shall not constitute notice):
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Fax:
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