UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
FORM 8-K
CURRENT REPORT
Pursuant to Section 13 or 15(d)
of the Securities Exchange Act of 1934
Date of Report (date of earliest event reported): August 7, 2019
SOLENO THERAPEUTICS, INC.
(Exact name of registrant as specified in its charter)
| Delaware | 001-36593 | 77-0523891 | ||
| (State or other jurisdiction of incorporation) |
(Commission File No.) |
(IRS Employer Identification Number) |
1235 Radio Road, Suite 110
Redwood City, CA 94065
(Address of principal executive offices)
(650) 213-8444
(Registrant’s telephone number, including area code)
Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions:
| ☐ | Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425) |
| ☐ | Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12) |
| ☐ | Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b)) |
| ☐ | Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c)) |
Securities registered pursuant to Section 12(b) of the Act:
| Title of each class |
Trading symbols |
Name of each exchange on which registered | ||
| Common Stock, $0.001 par value | SLNO | NASDAQ | ||
| Common Stock, $0.001 per value, underlying the warrants | SLNOW | NASDAQ |
Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§ 230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§ 240.12b-2 of this chapter).
Emerging growth company ☒
If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. ☐
ITEM 2.02. Results of Operations and Financial Conditions
On August 7, 2019, Soleno Therapeutics, Inc. (the “Company”) issued a press release announcing its financial results for the second quarter and six months ended June 30, 2019. The full text of the press release is attached hereto as Exhibit 99.1 and is incorporated herein by reference.
This information is intended to be furnished under Item 2.02 and Item 9.01 of Form 8-K, “Results of Operations and Financial Condition” and shall not be deemed “filed” for purposes of Section 18 of the Securities Exchange Act of 1934, as amended (the “Exchange Act”), or otherwise subject to the liabilities of that Section, nor shall be deemed incorporated by reference in any filing under the Securities Act of 1933, as amended, or the Exchange Act, except as shall be expressly set forth by specific reference in such a filing.
ITEM 9.01 Financial Statements and Exhibits
(d) Exhibits
| Exhibit No. |
Description | |
| 99.1 | Press release issued by Soleno Therapeutics, Inc. dated August 7, 2019. | |
SIGNATURES
Pursuant to the requirements of the Securities Exchange Act of 1934, the Registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.
| SOLENO THERAPEUTICS, INC. | ||||||
| Date: August 7, 2019 | ||||||
| By: | /s/ Anish Bhatnagar | |||||
| Anish Bhatnagar | ||||||
| Chief Executive Officer | ||||||
Exhibit 99.1
Soleno Therapeutics Provides Corporate Update and Reports Second Quarter 2019
Financial Results
REDWOOD CITY, Calif., August 7, 2019 — Soleno Therapeutics, Inc. (“Soleno”) (NASDAQ: SLNO), a clinical-stage biopharmaceutical company developing novel therapeutics for the treatment of rare diseases, today provided a corporate update, and reported financial results for the second quarter and six months ended June 30, 2019.
“We are pleased with the progress in our ongoing Phase III clinical trial, DESTINY PWS, evaluating once-daily Diazoxide Choline Controlled-Release (DCCR) tablets for patients with Prader Willi Syndrome (PWS). We currently anticipate the availability of top-line data from DESTINY PWS in the first half of 2020,” said Anish Bhatnagar, M.D., Chief Executive Officer of Soleno Therapeutics. “Additionally, we are encouraged by the continued interest of families and investigators in keeping patients on DCCR, as 90% of those subjects completing the DESTINY PWS study have elected to continue in C602, our open-label safety extension study. Moreover, 90% of those patients enrolled in study C602 have continued to receive DCCR treatment.”
Recent Corporate Highlights
| • | Continued enrollment for Phase III DESTINY PWS study of DCCR |
| • | Approximately 50% of the targeted number of patients have been enrolled into the DESTINY PWS clinical study, and approximately 90% of them have either successfully completed or continue to be treated in the study |
| • | Approximately 90% of those completing the DESTINY PWS study have elected to continue in C602, Soleno’s open-label safety extension study, and approximately 90% of those enrolled have continued to receive DCCR treatment in study C602 |
| • | The duration of C602 has been increased from 9 to 12 months, and Soleno is in the process of initiating another open-label study for patients who complete the C602 study |
| • | No serious, unexpected adverse events related to DCCR have been reported in these studies to date |
| • | Approximately 20 sites in the U.S. and Europe are active and able to enroll patients |
| • | Enrollment in DESTINY PWS is expected to conclude around the end of 2019 |
| • | Top-line data are anticipated in the first half of 2020 |
| • | Entered into a collaboration with Casimir, a rare disease research organization that designs outcome measures capturing the real-world impact of treatment interventions on individual patients’ quality-of-life |
| • | Casimir will collaborate with Soleno on the development of DCCR for patients with PWS |
| • | Appointed Birgitte Volck, M.D., Ph.D., a veteran biopharmaceutical industry executive, to Board of Directors |
Financial Results
Soleno’s current research and development efforts are primarily focused on advancing its lead product candidate, DCCR tablets for the treatment of PWS, into late-stage clinical development.
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Second Quarter Ended June 30, 2019 Financial Results for Continuing Operations
Research and development expenses were $3.7 million for the quarter ended June 30, 2019, compared to $1.7 million in the same period of 2018. The increase was primarily due to increased activities related to the DCCR development program.
General and administrative expense was $1.7 million for the quarter ended June 30, 2019, generally consistent with the same period of 2018.
The change in the fair value of contingent consideration results from Soleno’s obligation to make cash payments to Essentialis stockholders upon the achievement of certain future commercial milestones associated with the sale of Essentialis’ product in accordance with the terms of the Essentialis merger agreement. The fair value of the liability for the contingent consideration payable by Soleno was initially established as approximately $2.6 million at the time of the merger in March 2017, and was estimated at approximately $5.1 million at December 31, 2017, at $5.5 million at March 31, 2018, $5.4 million at June 30, 2018, $5.7 million at September 30, 2018, $5.6 million at December 31, 2018, and $5.9 million at March 31, 2019. The fair value was estimated to be approximately $6.0 million at June 30, 2019, resulting in an increase in expense of approximately $0.4 million from the balance at December 31, 2018.
Total Other expense of $4.4 million and $3.2 million in 2019 and 2018, respectively, consisted primarily of the change in the fair value of the liability for warrants of approximately $4.3 million and $3.3 million in 2019 and 2018, respectively.
Net loss for the quarter ended June 30, 2019, was approximately $10.0 million, or ($0.31) per share, compared to a net loss of approximately $7.1 million, or ($0.35) per share, for the quarter ended June 30, 2018, which includes a Loss from Discontinued Operations of $0.4 million.
Six Months Ended June 30, 2019 Financial Results for Continuing Operations
Research and development expenses were $6.5 million for the six months ended June 30, 2019, compared to $2.9 million in the same period of 2018. The increase was primarily due to increased activities related to the DCCR development program.
General and administrative expense was $3.7 million for the six months ended June 30, 2019, generally consistent with the same period of 2018.
Total Other expense of $6.4 million and $3.0 million in 2019 and 2018, respectively, consisted primarily of the change in the fair value of the liability for warrants of approximately $6.2 million and $3.1 million in 2019 and 2018, respectively.
Net loss for the six months ended June 30, 2019, was approximately $17.0 million, or ($0.54) per share, compared to a net loss of approximately $10.9 million, or ($0.55) per share, for the six months ended June 30, 2018, which includes a Loss from Discontinued Operations of $0.9 million.
As of June 30, 2019, Soleno had cash and cash equivalents of approximately $15.5 million, as compared to $23.1 million at December 31, 2018.
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About PWS
The Prader-Willi Syndrome Association USA estimates that approximately one in 15,000 people in the US have PWS. The hallmark symptom of this disorder is hyperphagia, a chronic feeling of insatiable hunger that severely diminishes the quality of life for PWS patients and their families. Additional characteristics of PWS include 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 can lead to significant morbidities (e.g., stomach rupture, obesity, diabetes, cardiovascular disease) and mortality (e.g., choking, accidental death due to food seeking behavior). In a global survey conducted by the Foundation for Prader-Willi Research, 96.5% of respondents (parent and caregivers) rated hyperphagia 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. Diazoxide choline has received Orphan Drug Designation for the treatment of PWS in the U.S. and E.U.
About the DESTINY PWS Trial
DESTINY PWS is a randomized, double-blind, placebo-controlled study of once-daily oral administration of DCCR versus placebo in approximately 100 patients with a confirmed diagnosis of PWS. Patients who complete DESTINY PWS have the option to enroll into C602.
For further information about DESTINY PWS (NCT03440814), please visit: www.clinicaltrials.gov.
About Diazoxide Choline Controlled-Release (DCCR) Tablet
Diazoxide choline controlled-release tablet is a novel, proprietary extended-release, crystalline salt formulation of diazoxide, which is administered once-daily. The parent molecule, diazoxide, has been used for decades in thousands of patients in a few rare diseases in neonates, infants, children and adults, but has not been approved for use in PWS. Soleno 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 data from five completed Phase I clinical studies in healthy volunteers and three completed Phase II clinical studies, one of which was in PWS patients. In the PWS Phase II study, DCCR showed promise in addressing hyperphagia, the hallmark symptom of PWS, as well as several other symptoms such as aggressive/destructive behaviors, fat mass and abnormal lipid profiles.
About Soleno Therapeutics, Inc.
Soleno is focused on the development and commercialization of novel therapeutics for the treatment of rare diseases. The company’s lead candidate, DCCR, a once-daily oral tablet for the treatment of PWS, is currently being evaluated in a Phase III clinical development program.
For more information, please visit www.soleno.life.
Forward-Looking Statements
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 complete enrollment of the Phase III C601 study in PWS during 2019 and receive top-line data in the first half of 2020. 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
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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 press release will prove to be accurate. Additional factors that could materially affect actual results can be found in Soleno’s annual and quarterly reports filed with the Securities and Exchange Commission, 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.
Corporate Contact:
Brian Ritchie
LifeSci Advisors, LLC
212-915-2578
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Soleno Therapeutics, Inc.
Condensed Consolidated Balance Sheets
(In thousands except share and per share data)
| June 30, 2019 |
December 31, 2018 |
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| (Unaudited) | ||||||||
| Assets |
||||||||
| Current assets |
||||||||
| Cash and cash equivalents |
$ | 15,503 | $ | 23,099 | ||||
| Prepaid expenses and other current assets |
471 | 529 | ||||||
| Due from related party |
18 | 64 | ||||||
| Minority interest investment in former subsidiary |
623 | 978 | ||||||
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| Total current assets |
16,615 | 24,670 | ||||||
| Long-term assets |
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| Property and equipment, net |
22 | 12 | ||||||
| Intangible assets, net |
17,497 | 18,469 | ||||||
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| Total assets |
$ | 34,134 | $ | 43,151 | ||||
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| Liabilities and stockholders’ equity |
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| Current liabilities |
||||||||
| Accounts payable |
$ | 1,740 | $ | 934 | ||||
| Accrued compensation and other current liabilities |
1,115 | 943 | ||||||
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| Total current liabilities |
2,855 | 1,877 | ||||||
| Long-term liabilities |
||||||||
| Series A warrant liability |
51 | 49 | ||||||
| 2017 PIPE Warrant liability |
10,202 | 4,563 | ||||||
| 2018 PIPE Warrant liability |
1,145 | 600 | ||||||
| Contingent liability for Essentialis purchase price |
6,038 | 5,649 | ||||||
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| Total liabilities |
20,291 | 12,738 | ||||||
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| Commitments and contingencies (Note 6) |
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| Stockholders’ equity |
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| Preferred Stock, $.001 par value, 10,000,000 shares authorized: |
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| Series B convertible preferred stock, 13,780 shares designated at June 30, 2019 and December 31, 2018; zero shares issued and outstanding at June 30, 2019 and at December 31, 2018. Liquidation value of zero. |
— | — | ||||||
| Common stock, $0.001 par value, 100,000,000 shares authorized, 31,793,292 and 31,755,169 shares issued and outstanding at June 30, 2019 and December 31, 2018, respectively. |
32 | 32 | ||||||
| Additional paid-in-capital |
157,881 | 157,413 | ||||||
| Accumulated deficit |
(144,070 | ) | (127,032 | ) | ||||
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| Total stockholders’ equity |
13,843 | 30,413 | ||||||
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| Total liabilities and stockholders’ equity |
$ | 34,134 | $ | 43,151 | ||||
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Soleno Therapeutics, Inc.
Condensed Consolidated Statements of Operations
(unaudited)
(In thousands except share and per share data)
| Three Months Ended June 30, |
Six Months Ended June 30, |
|||||||||||||||
| 2019 | 2018 | 2019 | 2018 | |||||||||||||
| Operating expenses |
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| Research and development |
$ | 3,745 | $ | 1,714 | $ | 6,505 | $ | 2,894 | ||||||||
| General and administrative |
1,695 | 1,766 | 3,707 | 3,633 | ||||||||||||
| Change in fair value of contingent consideration |
183 | (67 | ) | 389 | 361 | |||||||||||
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| Total operating expenses |
5,623 | 3,413 | 10,601 | 6,888 | ||||||||||||
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| Operating loss |
(5,623 | ) | (3,413 | ) | (10,601 | ) | (6,888 | ) | ||||||||
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| Other income (expense) |
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| Cease-use income |
— | 3 | — | 6 | ||||||||||||
| Change in fair value of warrants liabilities |
(4,267 | ) | (3,255 | ) | (6,186 | ) | (3,092 | ) | ||||||||
| Loss from minority interest investment |
(165 | ) | — | (355 | ) | — | ||||||||||
| Interest income |
47 | 30 | 104 | 49 | ||||||||||||
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| Total other income (expense) |
(4,385 | ) | (3,222 | ) | (6,437 | ) | (3,037 | ) | ||||||||
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| Loss from continuing operations |
(10,008 | ) | (6,635 | ) | (17,038 | ) | (9,925 | ) | ||||||||
| Loss from discontinued operations |
— | (423 | ) | — | (937 | ) | ||||||||||
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| Net loss |
$ | (10,008 | ) | $ | (7,058 | ) | $ | (17,038 | ) | $ | (10,862 | ) | ||||
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| Loss per common share from continuing operations, basic and diluted |
$ | (0.31 | ) | $ | (0.33 | ) | $ | (0.54 | ) | $ | (0.50 | ) | ||||
| Loss per common share from discontinued operations, basic and diluted |
— | (0.02 | ) | — | (0.05 | ) | ||||||||||
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| Net loss per common share, basic and diluted |
$ | (0.31 | ) | $ | (0.35 | ) | $ | (0.54 | ) | $ | (0.55 | ) | ||||
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| Weighted-average common shares outstanding used to calculate basic and diluted net loss per common share |
31,776,951 | 20,345,437 | 31,766,593 | 19,940,126 | ||||||||||||
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