StockNews.AI
NERV
StockNews.AI
175 days

Minerva Neurosciences Reports Fourth Quarter and Fiscal Year 2024 Financial Results and Business Updates

1. FDA issued CRL for roluperidone NDA; company addressing feedback. 2. R&D and G&A expenses decreased due to lower compensation and study costs. 3. Third quarter adjustments yielded non-cash income, converting net loss to net income. 4. Cash reserves declined significantly, indicating capital pressure.

Earnings
-1.12%Current Return
VS
-0.82%S&P 500
$1.7902/25 07:11 AM EDTEvent Start
$1.7702/26 02:06 PM EDTLatest Updated
10m saved
Insight
Article

FAQ

Why Neutral?

The FDA CRL introduces regulatory uncertainty that may pressure the stock, but improved expense management and non-cash adjustments partially offset concerns. Similar biotech cases have shown mixed investor reactions when non-recurring items drive net income improvements.

How important is it?

The update is significant due to the ongoing FDA issues and financial adjustments, which are pivotal for future clinical progress and capital management. Investors will closely monitor regulatory responses and funding needs, making this update materially important for NERV.

Why Long Term?

The resolution of regulatory issues and long-term clinical milestones will likely determine future performance. Historical biotech trajectories illustrate that FDA setbacks often have prolonged impact on valuation.

Related Companies

BIIBALKS
BURLINGTON, Mass., Feb. 25, 2025 (GLOBE NEWSWIRE) -- Minerva Neurosciences, Inc. (Nasdaq: NERV), a clinical-stage biopharmaceutical company focused on the development of therapies to treat central nervous system disorders, today reported business updates and financial results for the fourth quarter and year ended December 31, 2024.    Corporate Update As previously disclosed in the first quarter of 2024, the U.S. Food and Drug Administration (FDA) issued a Complete Response Letter (CRL) to our New Drug Application (NDA) for roluperidone for the treatment of negative symptoms in patients with schizophrenia. The company continues to have interactions with the FDA with the goal of addressing questions raised in the CRL.  Fourth Quarter and Year End Financial Results Research and development (R&D) expense: For the three months ended December 31, 2024 and 2023, R&D expense was $2.0 million and $ 4.7 million, respectively. R&D expense was lower versus the prior year period primarily due to costs associated with the FDA’s review of our NDA for roluperidone, costs for the C18 study, and lower compensation expenses. For the years ended December 31, 2024 and 2023, R&D expense was $ 11.9 million and $12.7 million, respectively. R&D expense was lower versus the prior year period primarily due to costs associated with the C18 study and lower compensation expenses, partially offset by higher costs associated with our drug substance validation campaign. General and administrative (G&A) expense: For both of the three months ended December 31, 2024 and 2023, G&A expense was $2.5 million. For the years ended December 31, 2024 and 2023, G&A expense was $9.9 million and $10.4 million, respectively. G&A expense was lower versus the prior year period primarily due to lower compensation expenses, partially offset by higher professional service fees. Non-cash interest expense: For the three months and year ended December 31, 2024, non-cash interest expense for the sale of future royalties was $0 and $4.6 million, respectively, as compared to $2.2 million and $8.3 million for the three months and year ended December 31, 2024, respectively. Non-cash interest expense was lower versus the prior year periods as a result of the Company revising its estimates for the timing and amount of future royalty payments to be received under the royalty arrangement. During the third quarter of 2024, the Company adjusted the carrying amount of its Liability related to the sale of future royalties to the initial payment of $60 million. This adjustment resulted in the recognition of $26.6 million in Other Income during the third quarter of 2024, representing the amount of non-cash interest expense amortized through June 30, 2024. Other income: For both the three months ended December 31, 2024 and 2023, other income was $0. For the years ended December 31, 2024 and 2023, other income was $26.6 million and $0, respectively. The Company recognized Other Income in the third quarter of 2024 as a result of the adjustment to the carrying amount of the Liability related to the sale of future royalties. Net income (loss): Net loss was $4.3 million for the three months ended December 31, 2024, or net loss per share of $0.56 basic and diluted, as compared to net loss of $9.0 million, or net loss per share of $1.19 basic and diluted, for the three months ended December 31, 2023. Net income was $1.4 million for the year ended December 31, 2024, or net income per share of $0.19 basic and diluted, as compared to net loss of $30.0 million, or net loss per share of $4.61 basic and diluted for the year ended December 31, 2023. As noted above, the adjustment to the carrying amount of the Liability related to the sale of future royalties during the third quarter of 2024 resulted in net income for the year ended December 31, 2024. Cash Position: Cash, cash equivalents and restricted cash at December 31, 2024, were approximately $21.5 million, as compared to $41.0 million at December 31, 2023. About Minerva Neurosciences Minerva Neurosciences, Inc. is a clinical-stage biopharmaceutical company focused on developing product candidates to treat CNS diseases. Minerva’s goal is to transform the lives of patients with improved therapeutic options, including roluperidone for negative symptoms of schizophrenia and MIN-301 for Parkinson’s disease. For more information, please visit the Company’s website. Forward-Looking Safe Harbor Statement This 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, but are not limited to, statements herein with respect to Minerva’s ability to remediate or otherwise resolve issues and deficiencies identified in the CRL and the outcome of its interactions with the FDA. 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, Minerva’s ability to address FDA’s feedback and timing thereof; uncertainties associated with regulatory processes, including the content and timing of decisions by the FDA; general risks associated with developing biopharmaceutical product candidates; management’s ability to successfully achieve its goals; our ability to raise additional capital to fund its clinical development plans, operations and corporate objectives on terms acceptable to Minerva; general economic conditions; and other factors that are described under the caption “Risk Factors” in Minerva’s filings with the Securities and Exchange Commission, including its Annual Report on Form 10-K for the year ended December 31, 2024, filed with the Securities and Exchange Commission on February 25, 2025. Copies of reports filed with the SEC are posted on Minerva’s website at http://ir.minervaneurosciences.com/. The forward-looking statements in this press release are based on information available to the Company as of the date hereof, and the Company disclaims any obligation to update any forward-looking statements, except as required by law. Contact: Investor inquiries:Frederick AhlholmChief Financial OfficerMinerva Neurosciences, Inc.info@minervaneurosciences.com Media inquiries: Helen ShikPrincipalShik Communications LLChelen@shikcommunications.com  CONDENSED CONSOLIDATED BALANCE SHEET DATA(Unaudited) December 31, 2024December 31, 2023 (in thousands)ASSETSCurrent assets:  Cash and cash equivalents$21,362 $40,913 Restricted cash 100  100 Prepaid expenses and other current assets 807  989 Total current assets 22,269  42,002 Equipment and capitalized software, net 6  29 Goodwill 14,869  14,869 Total assets$37,144 $56,900    LIABILITIES AND STOCKHOLDERS' DEFICITCurrent liabilities:  Accounts payable$1,608 $1,805 Accrued expenses and other current liabilities 1,229  1,535 Total current liabilities 2,837  3,340 Long-term liabilities:  Liability related to the sale of future royalties 60,000  82,017 Total liabilities 62,837  85,357 Stockholders' deficit:  Common stock 1  1 Additional paid-in capital 369,683  368,357 Accumulated deficit (395,377) (396,815)Total stockholders' deficit (25,693) (28,457)Total liabilities and stockholders' deficit$37,144 $56,900     CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS(Unaudited)        Three Months Ended December 31,(in thousands, except per share amounts) Twelve Months Ended December 31,(in thousands, except per share amounts)   2024  2023   2024  2023 Operating expenses:      Research and development $1,983 $4,721  $11,899 $12,705 General and administrative  2,539  2,451   9,949  10,414 Total operating expenses  4,522  7,172   21,848  23,119 Loss from operations  (4,522) (7,172)  (21,848) (23,119)       Foreign exchange gains (losses)  10  (19)  (2) (40)Investment income  240  359   1,272  1,437 Non-cash interest expense for the sale of future royalties  -  (2,190)  (4,562) (8,283)Other income  -  -   26,579  - Net income (loss) $(4,272)$(9,022) $1,439 $(30,005)       Net income (loss) per share, basic $(0.56)$(1.19) $0.19 $(4.61)Weighted average shares outstanding, basic  7,569  7,569   7,569  6,506 Net income (loss) per share, diluted $(0.56)$(1.19) $0.19 $(4.61)Weighted average shares outstanding, diluted  7,569  7,569   7,574  6,506        

Related News