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): May 6, 2020

 

STRONGBRIDGE BIOPHARMA plc

(Exact name of registrant as specified in its charter)

 

 

 

Registrant’s telephone number, including area code: (610) 254-9200

 

 

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 (see General Instruction A.2. below):

 

☐  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))

 

 

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 Condition.

 

On May 6, 2020, Strongbridge Biopharma plc (the “Company”) issued a press release reporting first quarter financial results and providing a corporate update. A copy of the press release is attached to this Current Report on Form 8-K as Exhibit 99.1.

 

The information contained in Item 2.02 of this Current Report on Form 8-K and Exhibit 99.1 is being furnished to the Commission and shall not be deemed “filed” for the purpose of Section 18 of the Securities Exchange Act of 1934, as amended (the “Exchange Act”), or otherwise subject to the liabilities of that section. The information in Exhibit 99.1 shall not be incorporated by reference into any registration statement or other document pursuant to the Securities Act of 1933, as amended (the “Securities Act”), except as expressly set forth by specific reference in such filing. The information set forth herein will not be deemed an admission as to the materiality of any information required to be disclosed solely to satisfy the requirements of Regulation FD.

 

Item 7.01Regulation FD Disclosure.

 

The response to Item 2.02 is incorporated herein by reference to this Item 7.01.

 

Item 9.01Financial Statements and Exhibits.

 

(d)   Exhibits

 

 

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.

 

 

 

 

Exhibit 99.1

 

 

 

Strongbridge Biopharma plc Reports First Quarter 2020 Financial Results and Provides Corporate Update

 

~ Phase 3 LOGICS Study of RECORLEV® (levoketoconazole) Reaches 41 of 42 Targeted Study Participants Completing the Randomized Withdrawal Phase; One Additional Patient Currently in the Randomized Withdrawal Phase and One Other Patient Scheduled to be Randomized Imminently ~

 

~ LOGICS Enrollment to Close on or Before May 14, 2020; Company Expects to Report Top-Line LOGICS Results During the Third Quarter of 2020 ~

 

~ Reports KEVEYIS® (dichlorphenamide) First Quarter 2020 Revenue of $6.7 Million, a 54 Percent Increase Compared to $4.3 Million During First Quarter of 2019 ~

 

~ Adjusts its Full-Year KEVEYIS Revenue Guidance Range for 2020 to $22 Million to $26 Million Due to Uncertainties Surrounding the Duration and Potential Business Impact of the COVID-19 Global Pandemic ~

 

~ Reiterates Guidance that the Company Has Sufficient Cash On-Hand to Fund Operations Through the Third Quarter of 2021 ~

 

~ Strongbridge to Host Conference Call Today at 8:30 am ET  ~

 

Dublin, Ireland and Trevose, Pa., May 6, 2020 – Strongbridge Biopharma plc, (Nasdaq: SBBP), a global commercial-stage biopharmaceutical company focused on the development and commercialization of therapies for rare diseases with significant unmet needs, today reported financial results for the first quarter of 2020 and provided a corporate update.   

 

“As an organization, our collective thoughts are with the individuals and their loved ones directly impacted by the COVID-19 global pandemic, as well as the healthcare professionals and first responders who are bravely serving on the frontlines. We would also like to thank all of those in the scientific and medical communities working toward developing COVID-19 vaccines and treatments for their efforts in responding to this global health emergency. As the situation evolves, our primary focus will remain on the health and safety of our employees and the patient and physician communities that we serve,” said John H. Johnson, executive chairman of Strongbridge Biopharma. “I would like to thank our global clinical development, medical affairs, quality and regulatory teams for their hard work on the Phase 3 LOGICS study. We are very pleased with the high study participant completion rate in the LOGICS trial and look forward to closing enrollment – an important milestone that brings us closer to the possibility of bringing this next-generation treatment to people with

endogenous Cushing’s syndrome. I am delighted by the progress our extended team has made in keeping the trial on track during these unprecedented and challenging times.”

 

Johnson added, “We had an excellent start to the year with KEVEYIS, with that momentum continuing through April – our highest month of revenue ever for the product. These strong revenue results can be attributed to a combination of improved discontinuation rates and a steady flow of new patient starts. However, during the past six to eight weeks since COVID-19 stay-at-home orders were implemented nationally, we have been experiencing a reduction in new patient starts, which we believe can be attributed to limitations in our field team’s ability to meet in-person with prescribers, a reduction in patient visits with doctors, and patient reluctance to try new medicines. Therefore, we have decided to adjust our KEVEYIS revenue guidance. Despite the potential KEVEYIS revenue reduction, we remain confident that off-setting expense savings will allow us to sustain our ability to fund operations through the third quarter of 2021.”

 

“We are especially pleased with the progress made in the LOGICS trial during this difficult time. LOGICS has 41 of 42 targeted completers, with one more participant in the randomized withdrawal phase and one participant scheduled to be randomized. We anticipate reporting top-line results from the LOGICS study during the third quarter of 2020. Our ability to reach these milestones during the COVID-19 pandemic is in large part due to innovative measures that we have undertaken in partnership with our global clinical trial sites. Measures such as home health visits, special transportation arrangements, telemedicine, direct-to-patient drug supply delivery, and regulatory authority-sanctioned protocol and monitoring flexibility are proving to be instrumental in facilitating timely completion of the study,” said Fredric Cohen, M.D., chief medical officer of Strongbridge Biopharma. “On behalf of Strongbridge, we would like to thank all of the stakeholders who have been integral to our RECORLEV clinical development program – our employees, the Phase 3 LOGICS and OPTICS study participants and research staff, our contract research organizations, and our vendor partners – for working together during this global crisis to mitigate potential disruption or delays to our research efforts.”

 

Corporate & Financial Highlights

 

Rare Endocrine Franchise: RECORLEV® (levoketoconazole)

 

Rare Neuromuscular Franchise: KEVEYIS® (dichlorphenamide)

 

Corporate

 

First Quarter 2020 Financial Results 

The Company net revenue from sales of KEVEYIS increased $2.3 million or 54 percent from $4.3 million for the three months ended March 31, 2019 to $6.7 million. The Company recorded cost of goods sold of $1.0 million for the three months ended March 31, 2020, compared to cost of goods sold of $0.8 million for the same period in 2019. Our gross margins were 85 percent for three months ended March 31, 2020, compared to gross margins of 81 percent for the same period in 2019.

 

Selling, general and administrative expenses were $10.4 million for the three months ended March 31, 2020, compared to $12.1 million for the same period in 2019. The decrease during the current period was due to reduction of third-party expenses and personnel costs.

Research and development expenses were $7.6 million for the three months ended March 31, 2020, compared to $6.6 million for the same period in 2019. The increase during the 2020 period was primarily due to expenses related to the RECORLEV LOGICS clinical trial and other RECORLEV development activities.

 

For the three months ended March 31, 2020, basic net loss attributable to ordinary shareholders on a GAAP basis was ($12.7 million), or ($0.23) per share, compared to a basic net loss attributable to ordinary shareholders of ($18.4) million, or ($0.34) per share, for the same period in 2019. Net loss for the three months ended March 31, 2020 was lower than the same period in 2019 primarily due to increase in KEVEYIS revenue of $2.3 million. In addition, selling, general, and administrative expenses during the three months ended March 31, 2020 were lower compared to the same period in 2019, due to lower third-party costs in the current period and reduced personnel costs. We also had an unrealized gain of $0.6 million on the fair value of warrants recorded in 2020, compared to an unrealized loss of $1.8 million in 2019.

 

For the three months ended March 31, 2020, non-GAAP basic net loss attributable to ordinary shareholders was ($10.3 million), or ($0.19) per share, compared to a non-GAAP basic net loss attributable to ordinary shareholders of ($13.0 million), or ($0.25) per share, for the same period in 2019. The decrease in non-GAAP net loss during the three months ended March 31, 2020 was primarily due to an increase in KEVEYIS revenue of $2.3 million. In addition, selling, general, and administrative expenses during the three months ended March 31, 2020 were lower compared to the same period in 2019, due to lower third-party costs in the current period and reduced personnel costs.

 

 

STRONGBRIDGE BIOPHARMA plc

Select Consolidated Balance Sheet Information (unaudited)

(in thousands, except share and per share data)

 

 

STRONGBRIDGE BIOPHARMA plc

Consolidated Statements of Operations and Comprehensive Loss (unaudited)

(in thousands, except share and per share data)

 

 

STRONGBRIDGE BIOPHARMA plc

Reconciliation of Non-GAAP Financial Measures (unaudited)

(in thousands, except share and per share data)

 

 

 

 

 

 

 

Conference Call Details

Strongbridge will host a conference call on Wednesday, May 6 at 8:30 a.m. ET. To access the live call, dial 844-285-7153 (domestic) or 478-219-0180 (international) with conference ID 5286566. The conference call will also be audio webcast from the Company’s website at www.strongbridgebio.com under the “Investor/Webcasts and Presentations” section. A replay of the call will be made available for one week following the conference call. To hear a replay of the call, dial 855-859-2056 (domestic) or 404-537-3406 (international) with conference ID 5286566.

 

About Strongbridge Biopharma

Strongbridge Biopharma is a global commercial-stage biopharmaceutical company focused on the development and commercialization of therapies for rare diseases with significant unmet needs. Strongbridge’s rare endocrine franchise includes RECORLEV® (levoketoconazole), a cortisol synthesis inhibitor currently being studied in Phase 3 clinical studies for the treatment of endogenous Cushing’s syndrome, and veldoreotide extended release, a pre-clinical next-generation somatostatin analog being investigated for the treatment of acromegaly and potential additional applications in other conditions amenable to somatostatin receptor activation. Both RECORLEV and veldoreotide have received orphan drug designation from the FDA and the European Medicines Agency. The Company’s rare neuromuscular franchise includes KEVEYIS® (dichlorphenamide), the first and only FDA-approved treatment for hyperkalemic, hypokalemic, and related variants of primary periodic paralysis. KEVEYIS has orphan drug exclusivity in the United States.

 

About KEVEYIS

KEVEYIS® (dichlorphenamide) is indicated for the treatment of primary hyperkalemic periodic paralysis, primary hypokalemic periodic paralysis, and related variants. In clinical studies, the most common side effects of KEVEYIS were a numbness or tingling, difficulty thinking and paying attention, changes in taste, and confusion. These are not all of the possible side effects that you may experience with KEVEYIS. Talk to your doctor if you have any symptoms that bother you or do not go away. You are encouraged to report side effects to Strongbridge Biopharma at 1-855-324-8912, or to the FDA at 1-800-FDA-1088 or visit www.fda.gov/medwatch. For additional KEVEYIS important safety information and the full prescribing information visit www.keveyis.com. 

 

About RECORLEV

RECORLEV® (levoketoconazole) is an investigational cortisol synthesis inhibitor in development for the treatment of patients with endogenous Cushing’s syndrome, a rare but serious and potentially lethal endocrine disease caused by chronic elevated cortisol exposure. RECORLEV is the pure 2S,4R enantiomer of ketoconazole, a steroidogenesis inhibitor. RECORLEV is believed to significantly suppress serum cortisol in healthy subjects and has the potential to be a next-generation cortisol inhibitor.

The Phase 3 program for RECORLEV consists of SONICS and LOGICS: two multinational studies designed to evaluate the safety and efficacy of RECORLEV when used to treat endogenous Cushing’s syndrome. The SONICS study met its primary and secondary endpoints, demonstrating a statistically significant normalization rate of urinary free cortisol at six months. The ongoing LOGICS study is a double-blind, placebo-controlled randomized-withdrawal study of RECORLEV that is designed to

supplement the long-term efficacy and safety information supplied by SONICS.

RECORLEV has received orphan drug designation from the FDA and the European Medicines Agency for the treatment of endogenous Cushing's syndrome.

 

Forward-Looking Statements

This press release contains forward-looking statements within the meaning of the federal securities laws. The words “anticipate,” “estimate,” “expect,” “intend,” “may,” “plan,” “potential,” “project,” “target,” “will,” “would,” or the negative of these terms or other similar expressions are intended to identify forward-looking statements, although not all forward-looking statements contain these identifying words. All statements, other than statements of historical facts, contained in this press release, are forward-looking statements, including statements related to the Company’s 2020 revenue guidance, expected cash runway, future cash balances, the potential advantages of RECORLEV, status of clinical trials, the anticipated timing for completion of enrollment and the release of top-line data from the LOGICS study and the submission of an NDA for RECORLEV to the FDA, the anticipated effects of the coronavirus (COVID-19) pandemic on our business, operating results and financial condition, Strongbridge’s strategy, plans, status and results of clinical trials, outcomes of product development efforts and objectives of management for future operations. Forward-looking statements involve risks and uncertainties that could cause actual results to differ materially from those expressed in such statement, including risks and uncertainties associated with clinical development and the regulatory approval process, the reproducibility of any reported results showing the benefits of RECORLEV, the adoption of RECORLEV by physicians, if approved, as treatment for any disease and the emergence of unexpected adverse events following regulatory approval and use of the product by patients.  Additional risks and uncertainties relating to Strongbridge and its business can be found under the heading “Risk Factors” in Strongbridge’s Annual Report on Form 10-K for the year ended December 31, 2019 and subsequent filings with the SEC. These forward-looking statements are based on current expectations, estimates, forecasts and projections and are not guarantees of future performance or development and involve known and unknown risks, uncertainties and other factors. The forward-looking statements contained in this press release are made as of the date of this press release, and Strongbridge Biopharma does not assume any obligation to update any forward-looking statements except as required by applicable law.

 

Contacts:

 

Corporate and Media Relations
Elixir Health Public Relations
Lindsay Rocco
+1 862-596-1304
lrocco@elixirhealthpr.com

 

Investor Relations
Solebury Trout
Mike Biega

+1 617-221-9660
mbiega@soleburytrout.com