Recent Updates
Recently added Catalysts
SPRB Positive Sentiment Score: 83/100

Spruce Biosciences Reports Third Quarter 2025 Financial Results and Provides Corporate Updates Granted Breakthrough Therapy Designation for Tralesinidase Alfa Enzyme Replacement Therapy (TA-ERT) for the Treatment of Sanf

Key Takeaway: Spruce Biosciences reported its financial results for Q3 2025 and provided updates on its development efforts. The company received FDA Breakthrough Therapy Designation for its enzyme replacement therapy, TA-ERT, aimed at treating MPS IIIB. Furthermore, Spruce completed a $50 million private equity financing, which is expected to support the development and regulatory submission of TA-ERT, planned for early 2026. Overall, the company is positioning itself for significant advancements in the treatment of children impacted by this condition.

Market Sentiment Analysis

POSITIVE FACTORS

  • Received Breakthrough Therapy Designation from the FDA for TA-ERT.
  • Successfully raised $50 million in private placement financing.
  • Plans for a biologics license application submission in early 2026.
  • Anticipation of TA-ERT as a potential life-changing treatment for MPS IIIB.

Full Press Release Details

Spruce Biosciences Reports Third Quarter 2025 Financial Results and Provides Corporate Updates
Granted Breakthrough Therapy Designation for Tralesinidase Alfa Enzyme Replacement Therapy (TA-ERT) for the Treatment of Sanfillipo Syndrome Type B (MPS IIIB)
Biologics License Application Submission of TA-ERT for the Treatment of MPS IIIB on Track for the First Quarter of 2026
Completed $50.0 Million Private Placement Financing Backed by Dedicated Healthcare Investors
South San Francisco, Calif. November 10, 2025 Spruce Biosciences, Inc. (Nasdaq: SPRB), a late-stage biopharmaceutical company focused on developing and commercializing novel therapies for neurological disorders with significant unmet medical need, today reported financial results for the third quarter ended September 30, 2025 and provided corporate updates.
We have made significant progress this year with the receipt of Breakthrough Therapy Designation from the U.S. Food and Drug Administration (FDA) for our tralesinidase alfa enzyme replacement therapy (TA-ERT), followed by the syndication of a $50 million private placement financing backed by an impressive group of healthcare investors. These important corporate milestones underscore the transformative moments in our collective efforts to advance TA-ERT as potentially the first disease-modifying therapy to treat children with MPS IIIB, said Javier Szwarcberg, M.D., M.P.H., Chief Executive Officer of Spruce Biosciences. The recent financing provides the capital resources to advance TA-ERT well beyond a biologics license application (BLA) submission expected in the first quarter of 2026.
Dr. Szwarcberg continued, I am very proud of our team for the advancements we have made this year, appreciative of the unwavering support from our Board and investors, and grateful to the patients and families who took part in the TA-ERT clinical trials. We look forward to an impactful 2026 as we move towards bringing to market a new, life-changing treatment option for children affected by MPS IIIB.
-$50.0 Million Private Placement Financing Backed by Dedicated Healthcare Investors. In October 2025, the company entered into a definitive securities purchase agreement for a private placement that resulted in gross proceeds of approximately $50.0 million, before deducting offering expenses. Under the securities purchase agreement, the investors purchased 502,181 shares of the company's common stock. In lieu of shares of common stock, as a portion of their investment, certain investors purchased prefunded warrants to purchase up to 233,144 shares of common stock. The prefunded warrants are exercisable for a period of five years following the date of issuance.
-U.S. FDA Breakthrough Therapy Designation Granted to TA-ERT for the Treatment of MPS IIIB. Granted to Spruce in October 2025, the FDA Breakthrough Therapy Designation is designed to expedite the development and regulatory review of promising therapies for serious or life-threatening conditions where preliminary clinical evidence suggests the potential for substantial improvement over existing treatments. The designation facilitates more intensive FDA guidance, cross-disciplinary collaboration, and eligibility for rolling submission and priority review.
-Relisted SPRB on the Nasdaq Capital Market. In September 2025, the company resumed trading on the Nasdaq Capital Market under the ticker symbol SPRB and CUSIP 85209E 208, following a one-for-75 reverse stock split.
Third Quarter 2025 Financial Results
-Cash and Cash Equivalents: Cash and cash equivalents as of September 30, 2025, were $10.7 million, which does not include approximately $50.0 million in gross proceeds from the October 2025 private placement financing. Cash and cash equivalents as of September 30, 2025, plus proceeds from the October 2025 private placement financing are expected to fund the company's current operating plan into the fourth quarter of 2026.
-Research and Development (R&D) Expenses: R&D expenses for the three and nine months ended September 30, 2025, were $5.0 million and $15.4 million, respectively, compared to $6.6 million and $25.0 million for the same periods in 2024. The decrease in R&D expenses was primarily related to the cessation of development activities of tildacerfont for the treatment of congenital adrenal hyperplasia (CAH), offset by development activities related to TA-ERT for the treatment of MPS IIIB.
-General and Administrative (G&A) Expenses: G&A expenses for the three and nine months ended September 30, 2025, were $3.2 million and $10.0 million, respectively, compared to $3.5 million and $11.3 million for the same periods in 2024, primarily driven by a decrease in stock-based compensation expense.
-Total Operating Expenses: Total operating expenses for the three and nine months ended September 30, 2025, were $8.2 million and $25.4 million, respectively, compared to $10.0 million and $36.3 million for the same periods in 2024. Operating expenses include non-cash stock-based compensation expenses of $0.4 million and $0.9 million for the three and nine months ended September 30, 2025, respectively, compared to $1.1 million and $4.4 million for the same periods in 2024.
-Net Loss: Net loss for the three and nine months ended September 30, 2025, was $8.2 million and $24.3 million, respectively, compared to $8.7 million and $29.5 million for the same periods in 2024.
-Capital Structure: Common shares outstanding as of September 30, 2025, were 563,491, which excludes 25,512 outstanding restricted stock units and 28,118 outstanding prefunded warrants to purchase common stock. In connection with the October 2025 private placement financing, 502,181 shares of common stock and 233,144 prefunded warrants to purchase common stock were issued to certain investors.
About Spruce Biosciences
Forward-Looking Statements
Statements contained in this press release regarding matters that are not historical facts are forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Such forward-looking statements include statements regarding, among other things, the timing and likelihood of regulatory filings and approvals for TA-ERT, including the anticipated biologics license application submission of TA-ERT for MPS IIIB in the first quarter of 2026; TA-ERT's potential to be the first disease-modifying therapy to treat MPS IIIB; TA-ERT's potential to be a new, life-changing treatment option for children affected by MPS IIIB; and the Company's ability to fund its operating plan into the fourth quarter of 2026. Because such statements are subject to risks and uncertainties, actual results may differ materially from those expressed or implied by such forward-looking statements. Words such as anticipate , will , potential , intend , expect and similar expressions are intended to identify forward-looking statements. These forward-looking statements are based upon Spruce's current expectations and involve assumptions that may never materialize or may prove to be incorrect. Actual results could differ materially from those anticipated in such forward-looking statements as a result of various risks and uncertainties, which include, without limitation, risks and uncertainties associated with Spruce's business in general, the impact of geopolitical and macroeconomic events, and the other risks described in Spruce's filings with the U.S. Securities and Exchange Commission. All forward-looking statements contained in this press release speak only as of the date on which they were made and are based on management's assumptions and estimates as of such date. Spruce undertakes no obligation to update such statements to reflect events that occur or circumstances that exist after the date on which they were made, except as required by law.
Spruce Biosciences, Inc.
+++ tables to follow +++
SPRUCE BIOSCIENCES, INC.
CONDENSED BALANCE SHEETS
(in thousands, except share and per share amounts)
September 30, December 31,
2025 2024
ASSETS
Current assets:
Cash and cash equivalents $ 10,669 $ 38,753
Prepaid expenses 932 3,177
Other current assets 2,915 2,276
Total current assets 14,516 44,206
Right-of-use assets 735 934
Other assets 62 69
Total assets $ 15,313 $ 45,209
LIABILITIES AND STOCKHOLDERS' EQUITY
Current liabilities:
Accounts payable $ 1,386 $ 1,295
Accrued expenses and other current liabilities 7,502 12,329
Term loan, current portion 539 1,622
Total current liabilities 9,427 15,246
Lease liabilities, net of current portion 500 736
Term loan, net of current portion 124
Other liabilities 282
Total liabilities 9,927 16,388
Commitments and contingencies
Stockholders' equity:
Preferred stock, $0.0001 par value; 10,000,000 shares authorized and no shares issued or outstanding as of September 30, 2025 and December 31, 2024
Common stock, $0.0001 par value; 200,000,000 shares authorized as of September 30, 2025 and December 31, 2024; 563,491 and 563,042 shares issued and outstanding as of September 30, 2025 and December 31, 2024, respectively
Additional paid-in capital 279,974 279,089
Accumulated deficit (274,588 ) (250,268 )
Total stockholders' equity 5,386 28,821
Total liabilities and stockholders' equity $ 15,313 $ 45,209
SPRUCE BIOSCIENCES, INC.
CONDENSED STATEMENTS OF OPERATIONS AND COMPREHENSIVE LOSS
(in thousands, except share and per share amounts)
Three Months Ended September 30, Nine Months Ended September 30,
2025 2024 2025 2024
Collaboration revenue $ $ 602 $ $ 4,214
Operating expenses:
Research and development 5,011 6,554 15,418 24,961
General and administrative 3,218 3,456 9,995 11,330
Total operating expenses 8,229 10,010 25,413 36,291
Loss from operations (8,229 ) (9,408 ) (25,413 ) (32,077 )
Interest expense (19 ) (71 ) (84 ) (251 )
Interest and other income, net 36 808 1,177 2,851
Net loss and comprehensive loss (8,212 ) (8,671 ) (24,320 ) (29,477 )
Net loss per share, basic and diluted $ (14.58 ) $ (15.75 ) $ (41.25 ) $ (53.68 )
Weighted-average shares of common stock outstanding, basic and diluted 563,066 550,645 589,520 549,116

Frequently Asked Questions

What therapy received Breakthrough Therapy Designation from the FDA?

Tralesinidase alfa enzyme replacement therapy (TA-ERT) for MPS IIIB.

When is the BLA submission for TA-ERT expected?

The submission is on track for the first quarter of 2026.

How much did Spruce raise in private placement financing?

Spruce Biosciences completed a $50 million private placement financing.

What is the net loss for Q3 2025?

The net loss was $8.2 million for the third quarter of 2025.

When did Spruce relist its stock on Nasdaq?

Spruce resumed trading on Nasdaq in September 2025 under the ticker SPRB.

Last updated: Nov 10, 2025