CHARLOTTESVILLE, Va., Aug. 14, 2017 (GLOBE NEWSWIRE) -- Diffusion Pharmaceuticals Inc. (NASDAQ:DFFN) (“Diffusion” or “the Company”), a clinical-stage biotechnology company focused on the development of novel small molecule therapeutics for cancer and other hypoxia-related diseases, today reported financial results for the three months ended June 30, 2017 and provided a business update.
Highlights of the second quarter of 2017 and recent weeks include:
- Advanced trans sodium crocetinate (TSC) for the treatment of newly diagnosed inoperable glioblastoma multiforme (GBM) in preparation for a planned Phase 3 trial with the engagement of a contract research organization and the completion of a major TSC production run
- Appointed long-standing pharmaceutical executive Robert R. Ruffolo, Jr., Ph.D. to the Company’s board of directors
- Received $8.3 million from the second closing of a private placement of Series A convertible preferred stock
- Obtained stockholder approval for a potential offering of up to $20.0 million of Series B convertible preferred stock
David Kalergis, Chairman and Chief Executive Officer of Diffusion Pharmaceuticals, stated, “During the second quarter we made solid progress in advancing preparations for a planned Phase 3 trial of TSC in newly diagnosed inoperable GBM patients, and are on track to complete a protocol review in the third quarter of 2017. Assuming FDA sign-off on the final protocol design, we plan to begin enrolling patients into the study by the end of 2017.”
“We have engaged a premier contract research organization to conduct the Phase 3 study and entered into agreements with top-tier partners to manage the MRI imaging, clinical data management, drug supply and other functions related to the trial,” Mr. Kalergis added. “We completed a major production run of TSC and now have sufficient quantity of the drug to support the entire Phase 3 trial.”
Second Quarter Financial Results
Research and development expenses for the second quarter of 2017 were $1.2 million, compared with $1.4 million for the second quarter of 2016. This decrease was attributable to lower expenses related to animal toxicology studies, partially offset by an increase in API and drug manufacturing costs.
General and administrative expenses for the second quarter of 2017 were $1.8 million, compared with $2.3 million for the second quarter of 2016. The decrease was primarily attributable to lower professional fees, partially offset by an increase in salary and salary-related expenses.
The Company recorded a loss from operations of $3.0 million for the second quarter of 2017, compared with a loss from operations of $3.8 million for the second quarter of 2016. The narrowed operating loss reflects lower research and development expenses, as well as lower general and administrative expenses.
We recognized a non-cash gain of $23.4 million in the second quarter of 2017 related to the change in fair value of warrant liabilities, which was attributable to a decrease in the fair market value of our common stock during the period. This non-cash gain resulted in net income for the second quarter, which is not indicative of ongoing operations.
Net cash used in operating activities for the first half of 2017 was $6.2 million, compared with $7.5 million during the first half of 2016.
In April 2017 we received the remaining $8.3 million related to our Series A financing and as of June 30, 2017, the Company had cash and cash equivalents of $7.4 million and a certificate of deposit of $10.0 million.
At our annual meeting of stockholders on June 15, 2017, stockholders approved a potential offering of up to $20.0 million of shares of our Series B convertible preferred stock, $0.001 par value per share (“Series B Preferred Stock”), at a price of $2.10 per share, with each share of Series B Preferred Stock being initially convertible into one share of our common stock, subject to adjustment. For each share of Series B Preferred Stock purchased in the offering, the investor will receive a five-year warrant to purchase one share of common stock with an exercise price of $2.31. There is no assurance we will successfully close such an offering at such terms due to the current trading price of our common stock or for any other reason.
This press release is neither an offer to sell, nor a solicitation of an offer to buy, any securities and shall not constitute an offer, solicitation or sale in any jurisdiction in which such offer, solicitation or sale is unlawful. The Series B Preferred Stock and related warrants described herein have not been and will not be registered under the Securities Act, or any state securities laws, and unless so registered, may not be offered or sold in the United States except pursuant to an exemption from the registration requirements of the Securities Act, and applicable state securities laws.
About Diffusion Pharmaceuticals Inc.
Diffusion Pharmaceuticals Inc. is a clinical-stage biotechnology company focused on extending the life expectancy of cancer patients by improving the effectiveness of current standard-of-care (“SOC”) treatments including radiation therapy and chemotherapy. Diffusion is developing its lead product candidate, trans sodium crocetinate (TSC), for use in the many cancers where tumor hypoxia (oxygen deprivation) is known to diminish the effectiveness of SOC treatments. TSC targets the cancer's hypoxic micro-environment, re-oxygenating treatment-resistant tissue and making the cancer cells more vulnerable to the therapeutic effects of SOC treatments without the apparent addition of any serious side effects.
A Phase 2 clinical program was completed in the second quarter of 2015 and evaluated 59 patients with newly diagnosed glioblastoma multiforme (GBM), a type of brain cancer. This open-label, historically controlled study demonstrated a favorable safety and efficacy profile for TSC combined with SOC, including a 37% improvement in overall survival compared with the control group at two years. A particularly strong efficacy signal was seen in the subset of inoperable patients where survival of TSC-treated patients at two years was nearly four-fold higher compared with the controls. At an End-Of-Phase 2 Meeting, the U.S. Food and Drug Administration provided Diffusion with extensive guidance on the design for a Phase 3 trial of TSC in newly diagnosed GBM patients. Assuming FDA sign-off on the final protocol design focusing on inoperable patients, the study is planned to initiate by the end of 2017. Due to its novel mechanism of action, TSC has safely re-oxygenated a range of tumor types in our preclinical and clinical studies. Diffusion believes its therapeutic potential is not limited to specific tumors, thereby making it potentially useful to improve SOC treatments of other life-threatening cancers. Additional planned studies include Phase 2 trials in pancreatic cancer and brain metastases, with study initiation subject to receipt of additional funding or collaborative partnering. The Company also believes that TSC has potential application in other indications involving hypoxia, such as neurodegenerative diseases and emergency medicine.
To the extent any statements made in this news release deal with information that is not historical, these are forward-looking statements under the Private Securities Litigation Reform Act of 1995. Such statements include, but are not limited to, statements about the company's plans, objectives, expectations and intentions with respect to future operations and products, the potential of the company's technology and product candidates, the anticipated timing of future clinical trials and protocol review, and other statements that are not historical in nature, particularly those that utilize terminology such as "would," "will," "plans," "possibility," "potential," "future," "expects," "anticipates," "believes," "intends," "continue," "expects," other words of similar meaning, derivations of such words and the use of future dates. Forward-looking statements by their nature address matters that are, to different degrees, uncertain. Uncertainties and risks may cause the company's actual results to be materially different than those expressed in or implied by such forward-looking statements. Particular uncertainties and risks include: general business and economic conditions; the company's need for and ability to obtain additional financing, including pursuant to the proposed Series B Preferred Stock offering; and the difficulty of developing pharmaceutical products, obtaining regulatory and other approvals and achieving market acceptance, and the various risk factors (many of which are beyond Diffusion’s control) as described under the heading “Risk Factors” in Diffusion’s filings with the United States Securities and Exchange Commission. All forward-looking statements in this news release speak only as of the date of this news release and are based on management's current beliefs and expectations. Diffusion undertakes no obligation to update or revise any forward-looking statement, whether as a result of new information, future events or otherwise.
David Kalergis, CEO
Diffusion Pharmaceuticals Inc.
LHA Investor Relations
Kim Sutton Golodetz
(Tables to follow)
|Diffusion Pharmaceuticals Inc.|
|Condensed Consolidated Balance Sheets|
|Cash and cash equivalents||$||7,413,399||$||1,552,852|
|Certificate of deposit||10,000,000||—|
|Prepaid expenses, deposits and other current assets||287,893||50,844|
|Total current assets||17,701,292||1,603,696|
|Property and equipment, net||479,650||79,755|
|Liabilities, Convertible Preferred Stock and Stockholders’ Equity|
|Current portion of convertible debt||$||2,430,000||$||1,880,000|
|Accrued expenses and other current liabilities||1,232,696||874,264|
|Common stock warrant liability||24,757,670||—|
|Total current liabilities||29,459,368||4,438,422|
|Convertible debt, net of current portion||—||550,000|
|Deferred income taxes||3,279,363||3,279,363|
|Commitments and Contingencies|
|Convertible preferred stock, $0.001 par value:|
|Series A - 13,750,000 shares authorized, 12,376,329 and 10,449,338 shares issued and|
outstanding, respectively at June 30, 2017; No shares authorized, issued or outstanding
at December 31, 2016 (liquidation value of $21,107,663 at June 30, 2017)
|Total convertible preferred stock||—||—|
|Common stock, $0.001 par value:|
|1,000,000,000 shares authorized; 12,298,363 and 10,345,637 shares issued and|
outstanding at June 30, 2017 and December 31, 2016, respectively
|Additional paid-in capital||69,596,807||69,363,575|
|Total stockholders' equity||1,167,698||9,184,684|
|Total liabilities, convertible preferred stock and stockholders' equity||$||33,906,429||$||17,484,384|
|Diffusion Pharmaceuticals Inc.|
|Condensed Consolidated Statements of Operations|
|Three Months Ended|
|Six Months Ended|
|Research and development||$||1,179,544||$||1,444,906||$||2,187,115||$||3,797,713|
|General and administrative||1,795,886||2,349,227||3,349,025||6,211,711|
|Loss from operations||2,981,220||3,799,978||5,548,533||10,023,122|
|Other expense (income):|
|Interest expense, net||18,889||6,216||74,608||6,237|
|Change in fair value of warrant liability||(23,387,850||)||—||(10,468,176||)||—|
|Warrant related expenses||—||—||10,225,846||—|
|Other financing expenses||—||—||2,870,226||—|
|Net income (loss)||$||20,387,741||$||(3,806,194||)||$||(8,251,037||)||$||(10,029,359||)|
|Per share information:|
|Net income (loss) per share of common stock, basic||$||0.88||$||(0.37||)||$||(0.83||)||$||(0.99||)|
|Net income (loss) per share of common stock, diluted||$||(1.00||)||$||(0.37||)||$||(1.56||)||$||(0.99||)|
|Weighted average shares outstanding, basic||10,828,063||10,263,703||10,582,521||10,130,042|
|Weighted average shares outstanding, diluted||13,872,632||10,263,703||12,339,386||10,130,042|
|Diffusion Pharmaceuticals Inc.|
|Condensed Consolidated Statements of Cash Flows|
|Six Months Ended June 30,|
|Adjustments to reconcile net loss to net cash used in operating activities:|
|Loss on sale or disposal of assets||—||6,761|
|Stock-based compensation expense||681,449||731,633|
|Common stock issued for advisory services||—||1,409,363|
|Warrant related expense, change in fair value, and other financing expenses||2,627,896||—|
|Non-cash interest expense||85,309||4,754|
|Changes in operating assets and liabilities:|
|Prepaid expenses, deposits and other assets||(68,189||)||17,712|
|Accounts payable, accrued expenses and other liabilities||(1,249,735||)||356,124|
|Net cash used in operating activities||(6,161,914||)||(7,489,314||)|
|Cash flows (used in) provided by investing activities:|
|Purchases of property and equipment||(64,002||)||(2,331||)|
|Purchase of certificate of deposit||(10,000,000||)||—|
|Cash received in reverse merger transaction||—||8,500,602|
|Net cash (used in) provided by investing activities||(10,064,002||)||8,498,271|
|Cash flows provided by financing activities:|
|Proceeds from the sale of Series A convertible preferred stock and warrants, net||22,129,774||—|
|Payment of offering costs for Series B||(43,311||)||—|
|Net cash provided by financing activities||22,086,463||—|
|Net increase in cash and cash equivalents||5,860,547||1,008,957|
|Cash and cash equivalents at beginning of period||1,552,852||1,997,192|
|Cash and cash equivalents at end of period||$||7,413,399||$||3,006,149|
|Supplemental disclosure of non-cash investing and financing activities:|
|Purchases of property and equipment in accounts payable and accrued expenses||$||(348,286||)||$||—|
|Series B offering costs in accounts payable and accrued expenses||$||(50,103||)||$||—|
|Series A cumulative preferred dividends||$||(546,305||)||$||—|
|Conversion of accrued dividends related to convertible preferred stock||$||70,890||$||—|
|Conversion of convertible notes and related accrued interest into common stock||$||—||$||711,495|
|Consideration in connection with RestorGenex Corporation merger transaction||$||—||$||21,261,000|
Source:Diffusion Pharmaceuticals, Inc.