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Minerva Neurosciences Reports First Quarter 2025 Financial Results and Business Updates

Key Takeaway: Minerva Neurosciences, Inc. has reported its financial results for the first quarter of 2025, highlighting positive developments such as regaining compliance with Nasdaq Listing Rules. The company experienced a notable reduction in net loss, reaching $3.8 million compared to $8.6 million in the same quarter last year. However, it continues to address regulatory feedback from the FDA regarding its New Drug Application for roluperidone while its cash position has slightly declined.
Price reaction · baseline $1.6311 (2025-05-12 close) · hit after-hours · clean, no other NERV news in the window
day 0 close
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Market Sentiment Analysis

POSITIVE FACTORS

  • Regained compliance with Nasdaq Listing Rule, ensuring continued listing.
  • Significant reduction in net loss compared to the previous year.
  • Lower research and development expenses, indicating cost management.

CONCERNS & RISKS

  • Continued interactions with the FDA regarding the Complete Response Letter indicate ongoing regulatory challenges.
  • Cash position decreased compared to the previous quarter, raising concerns about liquidity.

BiopharmaWatch Analysis

From our catalyst data and publicly available data · not financial advice
Best trade, last catalyst
+355%
120-day peak, hindsight
Typical move
29.3%
average across 2 past catalysts
Cash runway
~16 mo
Low dilution risk
Lead asset
MIN-117
Phase 2 · Major Depressive Disorder

Full Press Release Details

BURLINGTON, Mass., May 13, 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 first quarter of 2025 ended on March 31, 2025.
On March 17, 2025, we were formally notified by Nasdaq that we had regained compliance with Nasdaq Listing Rule 5550(b)(3), and as such, will continue to be listed on the Nasdaq Capital Market.
Interactions with the FDA continue with the goal of addressing questions raised in the Complete Response Letter (CRL) to our New Drug Application (NDA) for roluperidone for the treatment of negative symptoms in patients with schizophrenia as first disclosed in the first quarter of 2024.
First Quarter 2025 Financial Results
Research and development (R&D) expense: For the three months ended March 31, 2025 and 2024, R&D expense was $1.4 million and $4.2 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.
General and administrative (G&A) expense: For both the three months ended March 31, 2025 and 2024, G&A expense was $2.5 million.
Non-cash interest expense: For the three months ended March 31, 2025 and 2024, non-cash interest expense for the sale of future royalties was zero and $2.3 million, respectively. Non-cash interest expense was lower versus the prior year period due to revising our estimates for the timing and amount of future royalty payments to be received under the royalty arrangement. During the third quarter of 2024, we adjusted the carrying amount of our 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.
Net loss: Net loss was $3.8 million for the three months ended March 31, 2025, or a basic and diluted net loss per share of $0.50, as compared to net loss of $8.6 million for the three months ended March 31, 2024, or a basic and diluted net loss per share of $1.13.
Cash Position: Cash, cash equivalents and restricted cash at March 31, 2025 were approximately $17.4 million, as compared to $21.5 million at December 31, 2024.
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; and Minerva’s expectation that it will maintain compliance with Nasdaq’s listing standards and will be able to continue its listing on the Nasdaq Capital Market. 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, as updated by its Quarterly Report on Form 10-Q for the quarter ended March 31, 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.
Chief Financial Officer
Minerva Neurosciences, Inc.
Shik Communications LLC
CONDENSED CONSOLIDATED BALANCE SHEET DATA
(Unaudited)
March 31, 2025 December 31, 2024
(in thousands)
ASSETS
Current assets:
Cash and cash equivalents $ 17,290 $ 21,362
Restricted cash 100 100
Prepaid expenses and other current assets 535 807
Total current assets 17,925 22,269
Equipment and capitalized software, net 4 6
Goodwill 14,869 14,869
Total assets $ 32,798 $ 37,144
LIABILITIES AND STOCKHOLDERS' DEFICIT
Current liabilities:
Accounts payable $ 640 $ 1,608
Accrued expenses and other current liabilities 1,307 1,229
Total current liabilities 1,947 2,837
Long-term liabilities:
Liability related to the sale of future royalties 60,000 60,000
Total liabilities 61,947 62,837
Stockholders' deficit:
Common stock 1 1
Additional paid-in capital 369,980 369,683
Accumulated deficit (399,130 ) (395,377 )
Total stockholders' deficit (29,149 ) (25,693 )
Total liabilities and stockholders' deficit $ 32,798 $ 37,144
CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS
(Unaudited)
Three Months Ended March 31, (in thousands, except per share amounts)
2025 2024
Operating expenses:
Research and development $ 1,362 $ 4,167
General and administrative 2,541 2,515
Total operating expenses 3,903 6,682
Loss from operations (3,903 ) (6,682 )
Foreign exchange (losses) gains (8 ) 5
Investment income 158 358
Non-cash interest expense for the sale of future royalties - (2,250 )
Net loss $ (3,753 ) $ (8,569 )
Net loss per share, basic and diluted $ (0.50 ) $ (1.13 )
Weighted average shares outstanding, basic and diluted 7,569 7,569

Frequently Asked Questions

What is Minerva Neurosciences focused on?

Minerva Neurosciences develops therapies for central nervous system disorders.

How did Minerva fare with Nasdaq compliance?

Minerva regained compliance with Nasdaq Listing Rule 5550(b)(3) on March 17, 2025.

What was Minerva's net loss for Q1 2025?

The net loss for Q1 2025 was $3.8 million, or $0.50 per share.

What were Minerva's R&D expenses for Q1 2025?

R&D expenses for Q1 2025 were $1.4 million, down from $4.2 million in Q1 2024.

What future product does Minerva focus on?

Minerva is focused on roluperidone for treating negative symptoms of schizophrenia.

Last updated: May 13, 2025