# Tenax Therapeutics, Inc.: Form 10-Q for the period ended Jul 31, 2014

- Company: [Tenax Therapeutics, Inc.](/companies/tenx.md) (CIK 34956)
- Form: 10-Q
- Filed: 2014-09-15
- Accepted by EDGAR: Sep 15, 2014, 16:45 ET
- Period: 2014-07-31
- Accession: 0001354488-14-004652
- Inline XBRL: yes
- Main document: https://www.sec.gov/Archives/edgar/data/34956/000135448814004652/oxbt_10q.htm
- All documents and exhibits: https://www.sec.gov/Archives/edgar/data/34956/000135448814004652/

## Figures reported in this filing

Standardized XBRL line items for the period ended 2014-07-31.

| Line item | Period | Value | XBRL concept |
| --- | --- | ---: | --- |
| Revenue | 3 months, 2014-05-01 to 2014-07-31 | $0 | us-gaap:Revenues |
| Cost of revenue | 3 months, 2014-05-01 to 2014-07-31 | $0 | us-gaap:CostOfGoodsSold |
| Gross profit | 3 months, 2014-05-01 to 2014-07-31 | $0 | us-gaap:GrossProfit |
| Research and development | 3 months, 2014-05-01 to 2014-07-31 | $966.5k | us-gaap:ResearchAndDevelopmentExpense |
| Selling, general and administrative | 3 months, 2014-05-01 to 2014-07-31 | $1.4m | us-gaap:SellingGeneralAndAdministrativeExpense |
| Operating income | 3 months, 2014-05-01 to 2014-07-31 | −$2.4m | us-gaap:OperatingIncomeLoss |
| Interest expense | 3 months, 2014-05-01 to 2014-07-31 | $46.3k | us-gaap:InterestExpense |
| Net income | 3 months, 2014-05-01 to 2014-07-31 | −$2.2m | us-gaap:NetIncomeLoss |
| Diluted EPS | 3 months, 2014-05-01 to 2014-07-31 | −$0.08 | us-gaap:EarningsPerShareDiluted |
| Basic EPS | 3 months, 2014-05-01 to 2014-07-31 | −$0.08 | us-gaap:EarningsPerShareBasic |
| Diluted shares (weighted) | 3 months, 2014-05-01 to 2014-07-31 | 27,661,499 shares | us-gaap:WeightedAverageNumberOfDilutedSharesOutstanding |
| Operating cash flow | 3 months, 2014-05-01 to 2014-07-31 | −$2.0m | us-gaap:NetCashProvidedByUsedInOperatingActivities |
| Capital expenditure | 3 months, 2014-05-01 to 2014-07-31 | $35.6m | us-gaap:PaymentsToAcquirePropertyPlantAndEquipment |
| Cash and equivalents | at 2014-07-31 | $22.0m | us-gaap:CashAndCashEquivalentsAtCarryingValue |
| Current assets | at 2014-07-31 | $26.7m | us-gaap:AssetsCurrent |
| Total assets | at 2014-07-31 | $91.4m | us-gaap:Assets |
| Current liabilities | at 2014-07-31 | $1.9m | us-gaap:LiabilitiesCurrent |
| Total liabilities | at 2014-07-31 | $9.9m | us-gaap:Liabilities |
| Shareholders' equity | at 2014-07-31 | $81.5m | us-gaap:StockholdersEquity |

## Management's discussion and analysis

As filed, 27,819 characters.

*This Quarterly Report on Form 10-Q contains forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended, or the Securities Act, and Section 21E of the Securities Exchange Act of 1934, as amended, or the Exchange Act, which are subject to the “safe harbor” created by those sections. Forward-looking statements are based on our management’s beliefs and assumptions and on information currently available to them. In some cases you can identify forward-looking statements by words such as “may,” “will,” “should,” “could,” “would,” “expects,” “plans,” “anticipates,” “believes,” “estimates,” “projects,” “predicts,” “potential” and similar expressions intended to identify forward-looking statements. Examples of these statements include, but are not limited to, statements regarding: the implications of interim or final results of our clinical trials, the progress of our research programs, including clinical testing, the extent to which our issued and pending patents may protect our products and technology, our ability to identify new product candidates, the potential of such product candidates to lead to the development of commercial products, our anticipated timing for initiation or completion of our clinical trials for any of our product candidates, our future operating expenses, our future losses, our future expenditures for research and development, and the sufficiency of our cash resources. Our actual results could differ materially from those anticipated in these forward-looking statements for many reasons, including the risks faced by us and described in Part II, Item 1A of this Quarterly Report on Form 10-Q, Part I, Item 1A of our Annual Report on Form 10-K, and our other filings with the Securities and Exchange Commission, or SEC. You should not place undue reliance on these forward-looking statements, which apply only as of the date of this Quarterly Report on Form 10-Q. You should read this Quarterly Report on Form 10-Q completely and with the understanding that our actual future results may be materially different from those we expect. Except as required by law, we assume no obligation to update these forward-looking statements, whether as a result of new information, future events or otherwise.*

*The following discussion and analysis should be read in conjunction with the unaudited consolidated financial statements and notes thereto included in Part I, Item 1 of this Quarterly Report on Form 10-Q and with the audited consolidated financial statements and related notes thereto included as part of our Annual Report on Form 10-K for the year ended April 30, 2014.*

*All references in this Quarterly Report to “Oxygen Biotherapeutics”, “we”, “our” and “us” means Oxygen Biotherapeutics, Inc.*

### Overview

### Strategy

We are a specialty pharmaceutical company focused on developing and commercializing drugs for critical care patients. Our principal business objective is to acquire, or discover, develop, and commercialize novel therapeutic products for disease indications that represent significant areas of clinical need and commercial opportunity. Our lead product is levosimendan, which was acquired in an asset purchase agreement with Phyxius Pharma, Inc., or Phyxius. Levosimendan is a calcium sensitizer developed for intravenous use in hospitalized patients with acutely decompensated heart failure. The treatment is currently approved in more than 50 countries for this indication. The United States Food and Drug Administration, or FDA, has granted Fast Track status for levosimendan for the reduction of morbidity and mortality in cardiac surgery patients at risk for developing Low Cardiac Output Syndrome or LCOS. In addition, the FDA has agreed to the Phase III protocol design under Special Protocol Assessment (SPA), and provided guidance that a single successful trial will be sufficient to support approval of levosimendan in this indication.

We had been developing Oxycyte®, a systemic perfluorocarbon, or PFC, product we believe is a safe and effective oxygen carrier for use in situations of acute ischemia. However, on September 11, 2014, the Company’s BOD determined to stop the current Phase II-b trial for the treatment of traumatic brain injury, or TBI, and consider strategic alternatives for the program moving forward. The company will review the data generated on the patients enrolled in the trial to date. There are no assurances about the availability, on favorable terms or at all, of strategic alternatives for the continued development of the Oxycyte program.

Our current strategy is to:

- Efficiently conduct clinical development to establish clinical proof of concept with our lead product candidates;
- Efficiently explore new high-potential therapeutic applications, leveraging third-party research collaborations and our results from related areas;
- Efficiently explore new high-potential therapeutic applications, leveraging third-party research collaborations and our results from related areas;
- Continue to expand our intellectual property portfolio; and
- Enter into licensing or product co-development arrangements in certain areas, while out-licensing opportunities in non-core areas.

We believe that this strategy will allow us to develop a portfolio of high quality product development opportunities, expand our clinical development and commercialization capabilities, and enhance our ability to generate value from our proprietary technologies

### First Quarter 2015 Highlights

The following summarizes certain key financial measures for the three months ended July 31, 2014:

- Cash and cash equivalents were $21.9 million at July 31, 2014.
- Warrants to purchase 209,230 shares of common stock were exercised for net proceeds of $543,998.
- Our loss from operations was $2.2 million for the first quarter of 2015 compared to $2.2 million for the three months ended July 31, 2013.
- Net cash used in operating activities was $2.0 million and $1.6 million for the three months ended July 31, 2014 and 2013, respectively.

Consistent with our strategy, during the three months ended July 31, 2014, we (i) activated the first of the planned 50 sites to enroll patients in our phase III LCOS clinical trial, and (ii) reached an agreement with Imperial College London to provide supplemental funding to support the accelerated enrollment and completion of the ongoing LeoPARDS Trial (Levosimendan for the Prevention of Acute oRgan Dysfunction in Sepsis).

### Opportunities and Trends

We initiated the Phase III trial for levosimendan and activated the initial sites in the first quarter ended July 31, 2014. Duke University’s Duke Clinical Research Institute or DCRI is conducting the Phase III trial. DCRI is the world’s largest academic clinical research organization, with substantial experience in conducting cardiac surgery trials. The DCRI is serving as the coordinating center and Drs. John H. Alexander and Rajendra Mehta as lead investigators for this trial.

The Phase III trial is being conducted in approximately 50 major cardiac surgery centers in North America. The trial is enrolling patients undergoing coronary artery bypass graphs, or CABG and/or mitral valve surgery who are at risk for developing LCOS. The trial is a double blind, randomized, placebo controlled study enrolling 760 patients. It is expected that enrollment will begin in the second quarter of 2015, and will take approximately 18 months to complete.

As we focus on the development of our existing products and product candidates, we also continue to position ourselves to execute upon licensing and other partnering opportunities. In order to do so, we will need to continue to maintain our strategic direction, manage and deploy our available cash efficiently and strengthen our collaborative research development and partner relationships.

During fiscal year 2015 we are focused on the following four key initiatives:

- Conducting well-designed studies early in the clinical development process to establish a robust foundation for subsequent development, partnership and expansion into complementary areas;
- Working with collaborators and partners to accelerate product development, reduce our development costs, and broaden our commercialization capabilities;
- Gaining regulatory approval for the continued development and commercialization of our products in the United States; and
- Developing new intellectual property to enable us to file patent applications that cover new applications of our existing technologies and product candidates.

### Critical Accounting Policies and Significant Judgments and Estimates

There have been no significant changes in critical accounting policies during the three months ended July 31, 2014, as compared to the critical accounting policies described in “*Item 7—Management’s Discussion and Analysis of Financial Condition and Results of Operations—Critical Accounting Policies and Significant Judgments and Estimates”* in our Annual Report on Form 10-K for the fiscal year ended April 30, 2014.

### Financial Overview

### Results of Operations- Comparison of the Three Months Ended July 31, 2014 and 2013

### Revenue

#### Product Revenue and Gross Profit

In the prior year, we generated revenue through the sale of Dermacyte® through distribution agreements, on-line retailers and direct sales to physician and medical spa facilities. We no longer sell the product through on-line retailers and direct sales, and under the terms of the license agreement for the development and commercialization of Dermacyte, we do not anticipate earning any significant royalty revenue from this product for the remainder of the current fiscal year. Product revenue and percentage changes for the three months ended July 31, 2014 and 2013 are as follows:

|  | Three months ended July 31, 2014 | 2013 | Increase/ (Decrease) | % Increase/ (Decrease) |  |
| --- | ---: | ---: | ---: | ---: | --- |
| Product revenue | $- | $35,394 | $(35,394) | (100 | ) % |
| Cost of sales | - | 27,510 | (27,510) | (100 | ) % |
| Gross profit | $- | $7,884 | $(7,884) | (100 | ) % |

#### Government Grant Revenue

We earn revenues, or Grant Revenue, through a cost-reimbursement grant sponsored by the United States Army, or the Grant. Grant Revenue is recognized as milestones under the Grant program are achieved. Grant Revenue is earned through reimbursements for the direct costs of labor, travel, and supplies, as well as the pass-through costs of subcontracts with third-party contract research organizations, or CROs. Product revenue and percentage changes for the three months ended July 31, 2014 and 2013 are as follows.

|  | Three months ended July 31, 2014 | 2013 | Increase/ (Decrease) | % Increase/ (Decrease) |  |
| --- | ---: | ---: | ---: | ---: | --- |
| Government grant revenue | $- | $157,920 | $(157,920) | (100 | ) % |

The decrease in revenue earned under the Grant is due to our completion of the majority of the studies under the Grant in the prior year.

### General and Administrative Expenses

General and administrative expenses consist primarily of compensation for executive, finance, legal and administrative personnel, including stock-based compensation. Other general and administrative expenses include facility costs not otherwise included in research and development expenses, legal and accounting services, other professional services, and consulting fees. General and administrative expenses and percentage changes for the three months ended July 31, 2014 and 2013, respectively, are as follows:

|  | Three months ended July 31, 2014 | 2013 | Increase/ (Decrease) | % Increase/ (Decrease) |
| --- | ---: | ---: | ---: | ---: |
| Legal and professional fees | $693,098 | $491,018 | $202,080 | 41% |
| Personnel costs | 562,202 | 347,205 | 214,997 | 62% |
| Other costs | 124,698 | 78,969 | 45,729 | 58% |
| Facilities | 39,966 | 36,819 | 3,147 | 9% |
| Depreciation and amortization | 29,895 | 28,408 | 1,487 | 5% |

#### Legal and professional fees:

Legal and professional fees increased approximately $202,000 for the three months ended July 31, 2014 compared to the same period in the prior year. This increase was primarily due to an increase in the current period of approximately $185,000 for fees associated with outsourced corporate communications and an increase of approximately $100,000 in fees paid to our Board of Directors, partially offset by a reduction in legal fees of approximately $35,000 and recruiting fees of approximately $65,000 compared to the same period in the prior year.

#### Personnel costs:

Personnel costs increased approximately $215,000 for the three months ended July 31, 2014 compared to the same period in the prior year. The increase was due primarily to increases in headcount including the Chief Executive Officer and two additional executive management positions.

#### Other costs:

Other costs include costs incurred for banking fees, travel, supplies, insurance and other miscellaneous charges. The approximately $46,000 increase in other costs was due primarily to an approximately $22,000 increase in banking fees, an approximately $15,000 increase in travel expenses, and an approximately $13,000 increase in insurance costs, compared to the same period in the prior year.

#### Facilities:

Facilities include costs paid for rent and utilities at our corporate headquarters in North Carolina. The approximately $3,000 increase during the three months ended July 31, 2014 compared to the same period in the prior year was the result of an increase in the pass-through costs for maintenance and utility charges.

#### Depreciation and Amortization:

Depreciation and amortization costs remained relatively consistent for the three months ended July 31, 2014 and 2013.

### Research and Development Expenses

Research and development expenses include, but are not limited to, (i) expenses incurred under agreements with CROs and investigative sites, which conduct our clinical trials and a substantial portion of our pre-clinical studies; (ii) the cost of manufacturing and supplying clinical trial materials; (iii) payments to contract service organizations, as well as consultants; (iv) employee-related expenses, which include salaries and benefits; and (v) facilities, depreciation and other allocated expenses, which include direct and allocated expenses for rent and maintenance of facilities and equipment, depreciation of leasehold improvements, equipment, laboratory and other supplies. All research and development expenses are expensed as incurred. Research and development expenses and percentage changes for the three months ended July 31, 2014 and 2013, respectively, are as follows:

|  | Three months ended July 31, 2014 | 2013 | Increase/ (Decrease) | % Increase/ (Decrease) |
| --- | ---: | ---: | ---: | ---: |
| Clinical and preclinical development | $778,015 | $495,115 | $282,900 | 57% |
| Personnel costs | 158,561 | 212,895 | (54,334) | (26 ) % |
| Other costs | 14,709 | 7,721 | 6,988 | 91% |
| Depreciation | 8,591 | 8,892 | (301) | (3 ) % |
| Consulting | 4,233 | 45,343 | (41,110) | (91 ) % |
| Facilities | 2,405 | 2,927 | (522) | (18 ) % |

#### Clinical and preclinical development:

The increase of approximately $283,000 in clinical and preclinical development costs for the three months ended July 31, 2014 compared to the same period in the prior year was primarily due to an increase of approximately $527,000 in costs associated with the Phase III trials for levosimendan, partially offset by a decrease of approximately $151,000 in costs associated with the Phase II-b trials for Oxycyte and a decrease of approximately $95,000 in costs incurred for preclinical safety studies and quality assurance for Oxycyte.

#### Personnel costs:

Personnel costs decreased approximately $54,000 for the three months ended July 31, 2014 compared to the same period in the prior year primarily due to the termination of the Chief Medical Officer position in the prior year.

#### Other costs:

Other costs increased approximately $7,000 for the three months ended July 31, 2014 compared to the same period in the prior year primarily due to repairs and maintenance costs for manufacturing equipment.

#### Depreciation:

Depreciation expense remained relatively consistent for the three months ended July 31, 2014 and 2013.

#### Consulting fees:

Consulting fees decreased approximately $41,000 for the three months ended July 31, 2014 compared to the same period in the prior year primarily due to a reduction in fees incurred to plan and prepare for regulatory submissions, clinical trial expansions and other clinical support activities associated with clinical development of Oxycyte.

#### Facilities:

Facilities expense remained relatively consistent for the three months ended July 31, 2014 and 2013.

Conducting a significant amount of research and development is central to our business model. Product candidates in later-stage clinical development generally have higher development costs than those in earlier stages of development, primarily due to the significantly increased size and duration of clinical trials. We plan to incur substantial research and development expenses for the foreseeable future in order to complete development of our most advanced product candidate, levosimendan, and to continue with the development of other potential product candidates.

The process of conducting preclinical studies and clinical trials necessary to obtain approval from the FDA is costly and time consuming. The probability of success for each product candidate and clinical trial may be affected by a variety of factors, including, among other things, the quality of the product candidate’s early clinical data, investment in the program, competition, manufacturing capabilities and commercial viability. As a result of the uncertainties discussed above, uncertainty associated with clinical trial enrollment and risks inherent in the development process, we are unable to determine the duration and completion costs of current or future clinical stages of our product candidates or when, or to what extent, we will generate revenues from the commercialization and sale of any of our product candidates. Development timelines, probability of success and development costs vary widely. We are currently focused on developing our most advanced product candidate, levosimendan; however, we will need substantial additional capital in the future in order to complete the development and potential commercialization of levosimendan, and to continue with the development of other potential product candidates.

### Interest expense

Interest expense includes the interest payments due under our convertible debt, amortization of debt issuance costs and accretion of discounts recorded against our convertible notes, and noncash amortization of premiums paid on our marketable securities. Interest expense and percentage changes for the three months ended July 31, 2014 and 2013, respectively, are as follows:

|  | Three months ended July 31, 2014 | 2013 | Increase/ (Decrease) | % Increase/ (Decrease) |  |
| --- | ---: | ---: | ---: | ---: | --- |
| Interest expense | $46,260 | $655,803 | $(609,543) | (93 | ) % |

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During the three months ended July 31, 2014, interest expense decreased approximately $610,000 compared to the same period in the prior year. The decrease was due primarily to the reduction in the principal balance of our convertible notes in the prior year. All of our convertible notes matured in the current period.

### Other income and expense

Other income and expense includes non-operating income and expense items not otherwise recorded in our consolidated statement of operations. These items include, but are not limited to, revenue earned under sublease agreements for our California facility, changes in the fair value of financial assets and liabilities, interest income earned and fixed asset disposals. Other income for the three months ended July 31, 2014 and 2013, respectively, is as follows:

|  | Three months ended July 31, 2014 | 2013 | (Increase)/ Decrease |
| --- | ---: | ---: | ---: |
| Other income, net | $(291,221) | $(141) | $(291,080) |

Other income increase increased approximately $291,000 for the three months ended July 31, 2014 compared to the same period in the prior year primarily due to change in fair value of our Series C warrant liability in the current period.

### Liquidity, Capital Resources and Plan of Operation

We have incurred losses since our inception and as of July 31, 2014 we had an accumulated deficit of $139 million. We will continue to incur losses until we generate sufficient revenue to offset our expenses, and we anticipate that we will continue to incur net losses for at least the next several years. We expect to incur increased expenses related to our development and potential commercialization of levosimendan and other product candidates and, as a result, we will need to generate significant net product sales, royalty and other revenues to achieve profitability.

### Liquidity

We have financed our operations since September 1990 through the issuance of debt and equity securities and loans from stockholders. We had $26,655,937 and $58,966,033 of total current assets and working capital of $24,760,513 and $56,394,986 as of July 31, 2014 and April 30, 2014, respectively. Based on our working capital and the value of our investments in marketable securities at July 31, 2014, we believe we have sufficient capital to fund our operations through our fiscal year ending April 30, 2017.

We are in the preclinical and clinical trial stages in the development of our product candidates. We are currently conducting a Phase III clinical trial for levosimendan and we have been conducting a Phase II-b clinical trial for the use of Oxycyte in the treatment of severe traumatic brain injury. We expect our primary focus will be on funding the Phase III clinical trials for levosimendan, since this product is the furthest along in the regulatory review process. Our ability to continue to pursue testing and development of our products beyond our fiscal year 2017 depends on obtaining license income or outside financial resources. There is no assurance that we will obtain any license agreement or outside financing or that we will otherwise succeed in obtaining the necessary resources.

### Cash Flows

The following table shows a summary of our cash flows for the three months ended July 31, 2014 and 2013:

|  | Three months ended July 31, 2014 | 2013 |
| --- | ---: | ---: |
| Net cash used in operating activities | $(1,982,377) | $(1,563,142) |
| Net cash used in investing activities | (34,576,954) | (33,156) |
| Net cash provided by financing activities | 196,437 | 4,885,811 |

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*Net cash used in operating activities.* Net cash used in operating activities was approximately $2.0 million for the three months ended July 31, 2014 compared to net cash used in operating activities of $1.6 million for the three months ended July 31, 2013. The increase in cash used for operating activities was due primarily to an increase in our costs incurred for the Phase III clinical trial for levosimendan and compensation costs incurred as a result of three additional management positions.

*Net cash used in investing activities.* Net cash used in investing activities was $34.6 million for the three months ended July 31, 2014 compared to net cash used in investing activities of $33,000 for the three months ended July 31, 2013. The increase in cash used in investing activities was primarily due the purchase of marketable securities in the current period.

*Net cash provided by financing activities.* Net cash provided by financing activities was $196,000 for the three months ended July 31, 2014 compared to net cash provided by financing activities of $4.9 million for the three months ended July 31, 2013. The increase of net cash provided by financing activities was due primarily to net proceeds of $4.9 million received from the issuance of Series C 8% Convertible Preferred Stock in the prior year.

### Operating Capital and Capital Expenditure Requirements

Our future capital requirements will depend on many factors that include, but are not limited to the following:

- the initiation, progress, timing and completion of clinical trials for our product candidates and potential product candidates;
- the outcome, timing and cost of regulatory approvals and the regulatory approval process;
- delays that may be caused by changing regulatory requirements;
- the number of product candidates that we pursue;
- the costs involved in filing and prosecuting patent applications and enforcing and defending patent claims;
- the timing and terms of future in-licensing and out-licensing transactions;
- the cost and timing of establishing sales, marketing, manufacturing and distribution capabilities;
- the cost of procuring clinical and commercial supplies of our product candidates;
- the extent to which we acquire or invest in businesses, products or technologies; and
- the possible costs of litigation.

We believe that our existing cash and cash equivalents, along with our investment in marketable securities, will be sufficient to fund our projected operating requirements through our fiscal year ending April 30, 2017. We will need substantial additional capital in the future in order to complete the development and commercialization of levosimendan 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.

To the extent that we raise additional funds by issuing equity securities, our stockholders may experience additional significant dilution, and debt financing, if available, may involve restrictive covenants. To the extent that we raise additional funds through collaboration and licensing arrangements, it may be necessary to relinquish some rights to our technologies or our product candidates or grant licenses on terms that may not be favorable to us. We may seek to access the public or private capital markets whenever conditions are favorable, even if we do not have an immediate need for additional capital.

### Recent Accounting Pronouncements

In June 2014, the Financial Accounting Standards Board (“FASB”) issued ASU 2014-12 – *Compensation – Stock Compensation: Accounting for Share-Based Payments When the Terms of an Award Provide That a Performance Target Could be Achieved after the Requisite Service Period*, which provides explicit guidance for the accounting treatment for these types of awards. The ASU requires that a performance target that affects vesting and that could be achieved after the requisite service period be treated as a performance condition. As such, the performance target should not be reflected in estimating the grant-date fair value of the award. This update is effective for annual periods and interim periods within those annual periods beginning after December 15, 2014. Early adoption is permitted. We do not expect the adoption of this ASU will have a material impact on its consolidated financial statements.

### Off-Balance Sheet Arrangements

Since our inception, we have not engaged in any off-balance sheet arrangements, including the use of structured finance, special purpose entities or variable interest entities.

## Market risk

As filed, 2,770 characters.

### Interest Rate Risk

We are subject to interest rate risk on our investment portfolio.

We invest in marketable securities in accordance with our investment policy. The primary objectives of our investment policy are to preserve capital, maintain proper liquidity to meet operating needs and maximize yields. Our investment policy specifies credit quality standards for our investments and limits the amount of credit exposure to any single issue, issuer or type of investment. We place our excess cash with high credit quality financial institutions, commercial companies, and government agencies in order to limit the amount of credit exposure. Some of the securities we invest in may have market risk. This means that a change in prevailing interest rates may cause the principal amount of the investment to fluctuate.

Our investment exposure to market risk for changes in interest rates relates to the increase or decrease in the amount of interest income we can earn on our portfolio, changes in the market value due to changes in interest rates and other market factors as well as the increase or decrease in any realized gains and losses. Our investment portfolio includes only marketable securities and instruments with active secondary or resale markets to help ensure portfolio liquidity. A hypothetical 100 basis point drop in interest rates along the entire interest rate yield curve would not significantly affect the fair value of our interest sensitive financial instruments. We generally have the ability to hold our fixed-income investments to maturity and therefore do not expect that our operating results, financial position or cash flows will be materially impacted due to a sudden change in interest rates. However, our future investment income may fall short of expectations due to changes in interest rates, or we may suffer losses in principal if forced to sell securities which have declined in market value due to changes in interest rates or other factors, such as changes in credit risk related to the securities’ issuers. To minimize this risk, we schedule our investments to have maturities that coincide with our expected cash flow needs, thus avoiding the need to redeem an investment prior to its maturity date. Accordingly, we do not believe that we have material exposure to interest rate risk arising from our investments. Generally, our investments are not collateralized. We have not realized any significant losses from our investments.

We do not use interest rate derivative instruments to manage exposure to interest rate changes. We ensure the safety and preservation of invested principal funds by limiting default risk, market risk and reinvestment risk. We reduce default risk by investing in investment grade securities.

## Controls and procedures

As filed, 1,768 characters.

### Evaluation of Disclosure Controls and Procedures

As required by paragraph (b) of Rules 13a-15 and 15d-15 promulgated under the Exchange Act, our management, including our Chief Executive Officer and Chief Financial Officer, conducted an evaluation as of the end of the period covered by this report, of the effectiveness of our disclosure controls and procedures as defined in Exchange Act Rule 13a-15(e) and 15d-15(e). Based on that evaluation, our Chief Executive Officer and Chief Financial Officer concluded that our disclosure controls and procedures were effective as of July 31, 2014, the end of the period covered by this report in that they provide reasonable assurance that the information we are required to disclose in the reports we file or submit under the Exchange Act is recorded, processed, summarized and reported within the time periods required by the SEC and is accumulated and communicated to our management, including the Chief Executive Officer and Chief Financial Officer, as appropriate to allow timely decisions regarding required disclosure.

### Changes in Internal Control over Financial Reporting

There were no significant changes in our internal control over financial reporting during our most recently completed fiscal quarter that has materially affected, or is reasonably likely to materially affect, our internal control over financial reporting. We routinely review our internal controls over financial reporting and from time to time make changes intended to enhance the effectiveness of our internal control over financial reporting. We will continue to evaluate the effectiveness of our disclosure controls and procedures and internal controls over financial reporting on an ongoing basis and will take action as appropriate.

## Risk factors

As filed, 1,760 characters.

We are supplementing the risk factors disclosed in our Annual Report on Form 10-K for the year ended April 30, 2014 with the risk factor below.

***Orion may have the right to terminate our license for the levosimendan product, and, if the license is terminated, our business would be materially harmed.***

The License grants Life Newco an exclusive, sublicenseable right to develop and commercialize pharmaceutical products containing levosimendan, 2.5 mg/ml concentrate for solution for infusion / 5ml vial in the United States and Canada. The License provided that if we did not enroll a randomized patient in a human clinical trial using the levosimendan product by July 31, 2014, Orion would have the right to immediately terminate the License. While we did not commence the trial by that date, on September 9, 2014, Orion notified us in writing that it does not intend to terminate the License so long as the trial is commenced on or before October 31, 2014. While we have commenced our clinical trial process, activated trial sites, and expect the enrollment of the first patient at any time, it is possible that the first patient will not be enrolled by October 31, 2014. In the event that we are not able to commence the trial by October 31, 2014, we intend to seek a waiver or amendment to this condition in the License. There can be no assurance that we will obtain such a waiver or amendment, if needed, before October 31, 2014, or at all, which could potentially result in Orion’s termination of the License. If Orion terminates the License, we would not be able to develop or commercialize the levosimendan product. The loss of our license with Orion with respect to the levosimendan product would have a material adverse effect on our business.

Filed Sep 15, 2014.
Source: SEC EDGAR, the filing index for accession 0001354488-14-004652. Last ingested by Listed: Oct 27, 2026, 17:29 ET. No prices; not investment advice.