Full Press Release Details
VP, Investor Relations/
Corp. Communications
Minerva Neurosciences, Inc.
NEUROSCIENCES REPORTS FISCAL 2019 FOURTH QUARTER AND YEAR END
FINANCIAL RESULTS AND BUSINESS UPDATES
Company confirms timing of expected top-line results from Phase 3 roluperidone trial in Q2 2020
Management to host conference call today at 8:30 a.m. Eastern Time
Waltham, MA, March 9, 2019 Minerva Neurosciences, Inc. (NASDAQ: NERV), a clinical-stage biopharmaceutical company focused on the development of
innovative therapies to treat unmet medical needs of central nervous system (CNS) disorders, today reported key business updates and financial results for the fourth quarter and fiscal year ended December 31, 2019.
Clinical Program Updates
The Company is pleased to confirm its previous guidance that top-line results from the Phase 3 trial with roluperidone
are expected in the second quarter of 2020. As announced in February, enrollment of 515 patients has been achieved in the 12-week core phase of a pivotal trial for the treatment of negative symptoms, the
leading unmet medical need in schizophrenia.
This trial is a multicenter, randomized, double-blind, parallel-group, placebo-controlled, 12-week trial to evaluate the efficacy and safety of 32 milligram (mg) and 64 mg doses of roluperidone as measured by the Positive and Negative Syndrome Scale. The primary endpoint is the Marder negative symptoms
factor score. The core 12-week study, which the Company expects to read out in the second quarter, will be followed by an optional 40-week, open-label extension period
during which patients on the drug continue receiving their original dose and patients on placebo receive one of the two doses of roluperidone.
The Company announced positive data readouts in 3
Phase 2b studies and one Phase 1b trial with seltorexant (MIN-202) during 2019. Three of these trials were in major depressive disorder (MDD) and one was in insomnia disorder.
The Company is currently in discussions with its partner, Janssen Pharmaceutica NV, regarding the Phase 3 strategic development program for seltorexant, with
a target indication of adjunctive treatment of MDD (aMDD) in patients with insomnia symptoms. The Company and Janssen are also currently consulting with the U.S. Food and Drug Administration (FDA) and the European Medicines Agency about this target
indication and these trials, and they have recently attended the end-of-Phase 2 meeting with FDA to discuss the design of Phase 3 studies.
The Company is developing MIN-301, a pre-clinical candidate for the potential
treatment of Parkinson s disease and other neurodegenerative disorders. Building upon positive data in non-primate pre-clinical models, the Company is continuing to
conduct pre-clinical studies in preparation for regulatory filings leading toward entry into humans.
on track to read out top-line results of the roluperidone Phase 3 study in the second quarter of 2020, said Dr. Remy Luthringer, Executive Chairman and Chief Executive Officer of Minerva, and
we continue to expand our understanding of this exciting agent as a treatment for negative symptoms in schizophrenia and beyond. In parallel, we are in discussions with Janssen about moving forward into Phase 3 with seltorexant in 2020.
Fourth Quarter and Year Ended 2019 Financial Results
Minerva Neurosciences will host a conference call and live audio webcast today at 8:30 a.m. Eastern Time to discuss these results and
recent business activities. To participate, please dial (877) 312-5845 (domestic) or (765) 507-2618 (international) and refer to conference ID 7176196.
The live webcast can be accessed under Events and Presentations in the Investors and Media
section of Minerva s website at ir.minervaneurosciences.com. The archived webcast will be available on the website beginning approximately two hours after the event for 90 days.
About Minerva Neurosciences
Minerva s proprietary
compounds include: roluperidone (MIN-101), in clinical development for schizophrenia; seltorexant (MIN-202 or JNJ-42847922), in
clinical development for insomnia and MDD; and MIN-301, in pre-clinical development for Parkinson s disease. Minerva s common stock is listed on the
NASDAQ Global Market under the symbol NERV. For more information, please visit www.minervaneurosciences.com.
Forward-Looking Safe Harbor Statement
press release contains forward-looking statements which are subject to the safe harbor provisions of the Private Securities Litigation Reform Act of 1995, as amended. Forward-looking statements are statements that are not historical facts, reflect
management s expectations as of the date of this press release, and involve certain risks and uncertainties. Forward-looking statements include statements herein with respect to the timing and scope of future clinical trials and results of
clinical trials with roluperidone (MIN-101), seltorexant (MIN-202) and MIN-301; the clinical and therapeutic potential of these
compounds; the timing and outcomes of future interactions with U.S. and foreign regulatory bodies; our ability to successfully develop and commercialize our therapeutic products; the sufficiency of our current cash position to fund our operations;
and management s ability to successfully achieve its goals. These forward-looking statements are based on our current expectations and may differ materially from actual results due to a variety of factors including, without limitation, whether
roluperidone, seltorexant and MIN-301 will advance further in the clinical trials process and whether and when, if at all, they will receive final approval from the U.S. Food and Drug Administration or
equivalent foreign regulatory agencies and for which indications; whether any of our therapeutic products will be successfully marketed if approved; whether any of our therapeutic product discovery and development efforts will be successful;
management s ability to successfully achieve its goals; our ability to raise additional capital to fund our operations on terms acceptable to us; and general economic conditions. These and other potential risks and uncertainties that could
cause actual results to differ from the results predicted are more fully detailed under the caption Risk Factors in our filings with the Securities and Exchange Commission, including our Annual Report on Form 10-K for the year ended December 31, 2019, filed with the Securities and Exchange Commission on March 9, 2020. Copies of reports filed with the SEC are posted on our website at
www.minervaneurosciences.com. The forward-looking statements in this press release are based on information available to us as of the date hereof, and we disclaim any obligation to update any forward-looking statements, except as required by
CONDENSED CONSOLIDATED BALANCE SHEET DATA
| December 31, 2019 | December 31, 2018 | |||||||
| (in thousands) | ||||||||
| ASSETS | ||||||||
| Current Assets: | ||||||||
| Cash and cash equivalents | $ | 21,413 | $ | 50,235 | ||||
| Marketable securities | 24,442 | 37,763 | ||||||
| Restricted cash | 100 | 100 | ||||||
| Prepaid expenses and other current assets | 1,182 | 1,921 | ||||||
| Total current assets | 47,137 | 90,019 | ||||||
| Equipment, net | 16 | 33 | ||||||
| Other noncurrent assets | 15 | 15 | ||||||
| Operating lease right-of-use assets | 262 | |||||||
| In-process research and development | 15,200 | 34,200 | ||||||
| Goodwill | 14,869 | 14,869 | ||||||
| Total Assets | $ | 77,499 | $ | 139,136 | ||||
| LIABILITIES AND STOCKHOLDERS EQUITY | ||||||||
| Current Liabilities: | ||||||||
| Accounts payable | $ | 2,317 | $ | 1,799 | ||||
| Accrued expenses and other current liabilities | 4,139 | 1,810 | ||||||
| Operating leases | 173 | |||||||
| Total current liabilities | 6,629 | 3,609 | ||||||
| Long-Term Liabilities: | ||||||||
| Deferred taxes | 1,803 | 4,057 | ||||||
| Deferred revenue | 41,176 | 41,176 | ||||||
| Other noncurrent liabilities | 29 | |||||||
| Noncurrent operating leases | 111 | |||||||
| Total liabilities | 49,719 | 48,871 | ||||||
| Stockholders Equity: | ||||||||
| Common stock | 4 | 4 | ||||||
| Additional paid-in capital | 314,512 | 304,814 | ||||||
| Accumulated deficit | (286,736 | ) | (214,553 | ) | ||||
| Total stockholders equity | 27,780 | 90,265 | ||||||
| Total Liabilities and Stockholders Equity | $ | 77,499 | $ | 139,136 |
CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS
| Three Months Ended December 31, (in thousands, except per share amounts) | Twelve Months Ended December 31 (in thousands, except per share amounts) | |||||||||||||||
| 2019 | 2018 | 2019 | 2018 | |||||||||||||
| Revenues | $ | $ | $ | $ | ||||||||||||
| Operating expenses: | ||||||||||||||||
| Research and development | 28,524 | 9,008 | 58,123 | 34,889 | ||||||||||||
| General and administrative | 3,843 | 4,620 | 17,741 | 16,841 | ||||||||||||
| Total operating expenses | 32,367 | 13,628 | 75,864 | 51,730 | ||||||||||||
| Foreign exchange losses | (11 | ) | (5 | ) | (29 | ) | (5 | ) | ||||||||
| Investment income | 206 | 430 | 1,456 | 1,674 | ||||||||||||
| Interest expense | (110 | ) | ||||||||||||||
| Loss before income taxes | (32,172 | ) | (13,203 | ) | (74,437 | ) | (50,171 | ) | ||||||||
| Benefit for income taxes | (2,254 | ) | (2,254 | ) | ||||||||||||
| Net (loss) income | $ | (29,918 | ) | $ | (13,203 | ) | $ | (72,183 | ) | $ | (50,171 | ) | ||||
| Loss per share: | ||||||||||||||||
| Basic and diluted | $ | (0.77 | ) | $ | (0.34 | ) | $ | (1.85 | ) | $ | (1.29 | ) | ||||
| Weighted average shares: | ||||||||||||||||
| Basic and diluted | 39,037 | 38,888 | 39,014 | 38,793 |