- Completed Successful FDA Meeting for DCCR in Prader-Willi Syndrome
- Preparing to begin Phase III program by the end of the year
- Monetized Non-Strategic Assets Through Sale of NeoForce, Inc. Subsidiary
REDWOOD CITY, Calif., Aug. 11, 2017 (GLOBE NEWSWIRE) -- Soleno Therapeutics, Inc. (NASDAQ:SLNO), a clinical-stage biopharmaceutical company developing novel therapeutics for the treatment of rare diseases, today provided a corporate update and announced financial results for the three and six months ended June 30, 2017.
“Following our recent successful meeting with the FDA, we expect to initiate a Phase III clinical trial of DCCR in Prader-Willi Syndrome by the end of the year,” said Anish Bhatnagar, M.D., Chief Executive Officer of Soleno Therapeutics. “We are in the process of finalizing the design of a Phase III, randomized, double-blind placebo-controlled study that will treat approximately 100 patients. We remain excited about the potential of DCCR to safely and effectively treat this catastrophic disease. We also recently strengthened our balance sheet through the sale of one of our non-strategic subsidiaries, NeoForce.”
Recent Corporate Highlights
- Completion of FDA Meeting for Diazoxide Choline Controlled-Release (DCCR) in Prader-Willi Syndrome (PWS)
• Received positive guidance on key elements of Phase III program
• Company expects to initiate pivotal Phase III clinical trial by year-end 2017; will take approximately 9-12 months to complete
- Sold a non-strategic subsidiary, NeoForce, Inc., which manufactures and promotes a range of innovative pulmonary resuscitation solutions in the neonatal market, to Flexicare, Inc., a privately-held, leading UK-based manufacturer of airway management, anesthesia, and critical care medical devices
Second Quarter Ended June 30, 2017 Financial Results for Continuing Operations
As a result of the decision to sell NeoForce and either divest or partner the CoSense business, all revenue and expenses for these businesses have been excluded from continuing operations for all periods herein and reported as discontinued operations. All assets and liabilities of these businesses have been classified as assets held for sale on the balance sheet. All prior period information has been recast to conform to this presentation.
Research and development expenses in the second quarter of 2017 were $1.0 million, compared to $0.7 million for the same period in 2016. The increase was primarily due to an increase in DCCR clinical activities.
General and Administrative expenses in the second quarter of 2017 were $2.2 million, compared to $1.4 million for the same period in 2016. The increase was primarily due to the amortization from the acquisition of intangibles from the completed Essentialis merger in March 2017, and an increase in stock compensation expense.
Net loss from continuing operations for the second quarter of 2017 was $3.2 million, or $0.06 per share, compared to a net loss of $2.4 million, or $0.15 per share, for the second quarter in 2016.
Net loss from discontinued operations for the second quarter of 2017 was $0.7 million, or $0.01 per share, compared to a net loss of $1.1 million, or $0.07 per share, for the second quarter in 2016.
Net loss for the second quarter of 2017 was $4.0 million, or $0.07 per share, compared to a net loss of $3.5 million, or $0.22 per share, for the second quarter in 2016.
Six-Months Ended June 30, 2017 Financial Results for Continuing Operations
As a result of the decision to sell NeoForce, Inc. and either divest or partner the CoSense business, all revenue and expenses of these businesses have been excluded from continuing operations for all periods herein and reported as discontinued operations. All assets and liabilities of these businesses have been classified as assets held for sale on the balance sheet. All prior period information has been recast to conform to this presentation.
Research and development expenses in the six months ended June 30, 2017, were $1.5 million, compared to $1.6 million for the same period in 2016. The decrease was primarily due to a reduction in headcount.
General and Administrative expenses in the six months ended June 30, 2017, were $3.2 million, compared to $3.3 million for the same period in 2016. The decrease was primarily due to a decrease in legal fees and decreased headcount.
The change in fair value of warrants income for the six months ended June 30, 2017, was $0.1 million, which represents a decrease in the fair value of the Series A and Series C Warrants compared to the value of the warrants at December 31, 2016. The change in fair value of warrants income for the six months ended June 30, 2016, was $1.1 million, which represented an increase in the fair value of the Series A, Series B and Series C Warrants compared to the value of the warrants at December 31, 2015.
Net loss from continuing operations for the six months ended June 30, 2017, was $5.5 million, or $0.14 per share, compared to a net loss of $4.3 million, or $0.29 per share, for the same period in 2016.
Net loss from discontinued operations for the six months ended June 30, 2017, was $1.4 million, or $0.03 per share, compared to a net loss of $2.4 million, or $0.16 per share, for the same period in 2016.
Net loss for the six months ended June 30, 2017, was $6.9 million, or $0.17 per share, compared to a net loss of $6.7 million, or $0.45 per share, for the same period in 2016.
Cash and cash equivalents at June 30, 2017, totaled $7.5 million, compared to $2.7 million at December 31, 2016.
PWS is a rare and complex genetic neurobehavioral/metabolic disorder affecting appetite, growth, metabolism, cognitive function and behavior. The committee on genetics of the American Academy of Pediatrics states PWS affects both genders equally and occurs in people from all geographic regions: its estimated incidence is one in 15,000 to 25,000 live births. This disorder is typically characterized by hyperphagia, a chronic feeling of insatiable hunger, behavioral problems, cognitive disabilities, low muscle tone, short stature (when not treated with growth hormone), the accumulation of excess body fat, developmental delays, and incomplete sexual development. Hyperphagia, in the absence of effective limitations to access to food, can lead to morbid obesity. In a global survey conducted by the Foundation for Prader-Willi Research, 96.5% of respondents (parent and caregivers) rated hyperphagia, which is the unrelenting hunger that severely diminishes the quality of life for patients and their families, as the most important or a very important symptom to be relieved by a new medicine. There are currently no approved therapies to treat the hyperphagia/appetite, metabolic, cognitive function, or behavioral aspects of the disorder. DCCR has received Orphan Drug Designation from the US FDA for the treatment of PWS.
About Diazoxide Choline Controlled-Release Tablet
Diazoxide choline controlled-release tablet is a novel, proprietary controlled-release, crystalline salt formulation of diazoxide, which is administered once-daily. The parent molecule, diazoxide, as an oral suspension, has been used for decades in thousands of patients in a few rare diseases in neonates, children and/or adults, but not in PWS. Essentialis conceived of and established extensive patent protection on the therapeutic use of diazoxide and DCCR in patients with PWS. The DCCR development program is supported by positive data from two completed Phase II clinical studies and six completed Phase I clinical studies in various metabolic indications, as well as a pilot study in PWS patients. In the PWS pilot study, DCCR showed promise in addressing the hallmark symptoms of PWS, most notably hyperphagia.
About Soleno Therapeutics, Inc.
Soleno Therapeutics, Inc. is focused on the development and commercialization of novel therapeutics for the treatment of rare diseases. The company is currently advancing its lead candidate, DCCR, a once-daily oral tablet for the treatment of PWS, into a Phase III clinical development program at the end of 2017. Soleno, through its wholly-owned subsidiary, Capnia, Inc., continues to market Capnia’s innovative medical device, the CoSense® End-Tidal Carbon Monoxide (ETCO) monitor, which measures ETCO and is used by hospitals to detect hemolysis in newborns. It is expected that this product will be monetized and will not be a focus for the company in the long term.
For more information, please visit www.soleno.life.
This press release contains forward-looking statements that are subject to many risks and uncertainties. Forward-looking statements include statements regarding our intentions, beliefs, projections, outlook, analyses or current expectations concerning, among other things, our ability to initiate the Phase III clinical development program of DCCR in PWS by the end of 2017. We may use terms such as "believes," "estimates," "anticipates," "expects," "plans," "intends," "may," "could," "might," "will," "should," "approximately" or other words that convey uncertainty of future events or outcomes to identify these forward-looking statements. Although we believe that we have a reasonable basis for each forward-looking statement contained herein, we caution you that forward-looking statements are not guarantees of future performance and that our actual results of operations, financial condition and liquidity, and the development of the industry in which we operate may differ materially from the forward-looking statements contained in this presentation. As a result of these factors, we cannot assure you that the forward-looking statements in this presentation will prove to be accurate. Additional factors that could materially affect actual results can be found in Soleno’s Form 10-Q filed with the Securities and Exchange Commission on May 11, 2017, including under the caption titled "Risk Factors." Soleno expressly disclaims any intent or obligation to update these forward-looking statements, except as required by law.
|Soleno Therapeutics, Inc.|
|Condensed Consolidated Balance Sheets|
|(In thousands, except share amounts)|
|As of June 30,||As of December 31,|
|Cash & Cash Equivalents||$||7,547||$||2,726|
|Prepaid expenses and other current assets||246||247|
|Current assets held for sale||2,323||790|
|Total Current Assets||10,318||3,801|
|Property & Equipment, net||53||54|
|Other intangible assets, net||19,884||-|
|Long-term assets held for sale||-||1,584|
|Liabilities and stockholders' equity|
|Accrued compensation and other current liabilities||879||1,050|
|Current liabilities held for sale||214||246|
|Total Current Liabilities||2,122||1,707|
|Series A Warrant Liability||415||194|
|Series C Warrant Liability||24||86|
|Long-term liabilities held for sale||-||81|
|Total Long-Term Liabilities||1,571||423|
|Preferred Stock, $.001 par value, 10,000,000 shares authorized|
|Series B convertible preferred stock, 13,780 are designated at June|
|30, 2017 and December 31, 2016; 12,179 and 12,780 shares||-||-|
|issued and outstanding at June 30, 2017 and at December 31, 2016,|
|respectively. Liquidation value of zero|
|Common stock, $0.001 par value, 100,000,000 shares|
|authorized, 47,587,647 and 16,786,952 shares issued and|
|outstanding at June 30, 2017 and December 31, 2016, respectively||48||17|
|Total stockholders' equity||26,688||3,435|
|Total liabilities and stockholders' equity||$||30,381||$||5,565|
|Soleno Therapeutics, Inc.|
|Condensed Consolidated Statements of Operations|
|(In thousands, except share and per share amounts)|
|Three Months Ended||Six Months Ended|
|June 30,||June 30, |
|Cost of product revenue||42||51||42||69|
|Gross profit (loss)||(41||)||(49||)||(38||)||(67||)|
|Research and Development||974||658||1,506||1,623|
|Sales and Marketing||-||165||27||360|
|General and Administrative||2,195||1,423||3,214||3,273|
|Operating income (loss)||(3,210||)||(2,295||)||(4,785||)||(5,323||)|
|Interest and other income (expense)|
|Change in fair value of warrant liabilities (expense)||(32||)||(56||)||(101||)||1,095|
|Interest and other income (expense), net||(29||)||(72||)||(701||)||983|
|Net loss from continuing operations||(3,239||)||(2,367||)||(5,486||)||(4,340||)|
|Net loss from discontinued operations||(727||)||(1,146||)||(1,370||)||(2,362||)|
|Net income (loss) per common share from continuing|
|operations, basic and diluted||$||(0.06||)||$||(0.15||)||$||(0.14||)||$||(0.29||)|
|Net income (loss) per common share from discontinued|
|operations, basic and diluted||(0.01||)||(0.07||)||(0.03||)||(0.16||)|
|Net loss per common share, basic and diluted||$||(0.07||)||$||(0.22||)||$||(0.17||)||$||(0.45||)|
|Weighted-average common shares outstanding used|
|to calculate basic and diluted net loss|
|per common share||53,060,868||15,528,922||40,029,547||15,162,520|
Contact: Brian Ritchie LifeSci Advisors, LLC 212-915-2578