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REVB Positive Sentiment Score: 75/100

Revelation Biosciences, Inc. Announces Financial Results For the Three and Twelve Months Ended

Key Takeaway: Revelation Biosciences, Inc. announced its financial results for the year ending December 31, 2025, reporting a net loss of $8.9 million. The company highlighted a positive outcome from its PRIME clinical study focused on chronic kidney disease and secured FDA agreement for an adaptive Phase 2/3 study for its product Gemini, aimed at treating acute kidney injury. Additionally, the company received $6.7 million through a warrant inducement, increasing its cash reserves to $10.7 million, projected to support operations into early 2027. Despite showing progress in clinical trials, the company continues to face significant financial losses.

Market Sentiment Analysis

POSITIVE FACTORS

  • Positive results from PRIME clinical study in chronic kidney disease patients.
  • Agreement with FDA on single adaptive Phase 2/3 study for Gemini.
  • Received $6.7 million from warrant inducement, improving financial position.
  • Gemini shows potential therapeutic benefits for acute and chronic kidney conditions.

CONCERNS & RISKS

  • A net loss of $8.9 million for the year shows ongoing financial challenges.
  • Loss per share increased significantly compared to the previous year.
  • Future clinical study outcomes are uncertain and may vary.
  • Operational burn rate remains a concern given the losses reported.

Full Press Release Details

Revelation Biosciences, Inc. Announces Financial Results
For the Three and Twelve Months Ended December 31, 2025
SAN DIEGO February 26, 2026 Revelation Biosciences, Inc. (NASDAQ: REVB) (the Company or Revelation ), a clinical-stage life sciences company focused on rebalancing inflammation to optimize health, today reported its financial results for the three and twelve months ended December 31, 2025.
Corporate Highlights
-Announced Positive Results from PRIME Clinical Study in late-stage chronic kidney disease patients
-Announced agreement with FDA on a single adaptive Phase 2/3 study for approval of Gemini for treatment of acute kidney injury
-Received net proceeds of $6.7 million from warrant inducement in January 2026
-Clinical data on the potential therapeutic benefit of Gemini for the treatment of acute kidney injury (AKI) and chronic kidney disease (CKD) will be presented at the International Conference on Advances in Critical Care Nephrology in San Diego (March 29 - April 1, 2026)
2025 was a positive year for Revelation with significant advancement of the Gemini program, said James Rolke, Chief Executive Officer of Revelation. We look forward to building on this momentum in 2026 to expeditiously bring Gemini to patients in need and adding to shareholder value.
Results of Operations
As of December 31, 2025, Revelation had $10.7 million in cash and cash equivalents, compared to $6.5 million as of December 31, 2024. The increase in cash and cash equivalents was primarily due to net cash proceeds from the May 2025 public offering and the September 2025 warrant inducement, offset by cash used for operating activities. Based on current operating plans and projections, Revelation believes its current cash and cash equivalents are sufficient to fund operations into the first quarter of 2027.
Net cash used for operating activities for the twelve months ended December 31, 2025 was $8.3 million compared to net cash used for operating activities of $18.3 million for the same period in 2024. Net loss for the three months ended December 31, 2025 was $2.5 million, or $(1.65) basic and diluted net loss per share, compared to a net loss of $1.7 million, or $(59.76) basic and diluted net loss per share for the same period in 2024. Net loss for the year ended December 31, 2025 was $8.9 million, or $(23.95) basic and diluted net loss per share compared to net loss of $15.0 million, or $(1,052.16) basic and diluted net loss per share for the year ended December 31, 2024.
Gemini is the Company's proprietary formulation of phosphorylated hexaacyl disaccharide (PHAD ), a toll-like receptor 4 (TLR4) agonist. TLR4 stimulation with Gemini rebalances the innate immune response and has been demonstrated to have the potential to treat acute and chronic diseases associated with dysregulated inflammation. Gemini is currently being evaluated as a potential treatment for acute kidney injury (GEM-AKI); Gemini is also being developed as a treatment for chronic kidney disease (GEM-CKD), as a treatment to reduce hyperinflammation and
infection associated with severe burn (GEM-PBI), and as a treatment to prevent post-surgical infection (GEM-PSI). The potential of Gemini to correct dysregulated inflammation has been demonstrated in multiple preclinical models of AKI, CKD, and infection, as well as in two phase 1 clinical studies. See additional detail here.
About Revelation Biosciences, Inc.
Revelation Biosciences, Inc. is a clinical stage life sciences company focused on rebalancing inflammation using its proprietary formulation, Gemini. Revelation has multiple ongoing programs to evaluate Gemini as a treatment for acute kidney injury, a treatment of chronic kidney disease, prevention of post-surgical infection, and a treatment to reduce hyperinflammation and infection associated with severe burn.
For more information, please visit www.RevBiosciences.com.
Forward-Looking Statements
This press release contains forward-looking statements as defined in the Private Securities Litigation Reform Act of 1995, as amended. Forward-looking statements are statements that are not historical facts. These forward-looking statements are generally identified by the words anticipate , believe , expect , estimate , plan , outlook , and project and other similar expressions. We caution investors that forward-looking statements are based on management's expectations and are only predictions or statements of current expectations and involve known and unknown risks, uncertainties and other factors that may cause actual results to be materially different from those anticipated by the forward-looking statements. Revelation cautions readers not to place undue reliance on any such forward looking statements, which speak only as of the date they were made. The following factors, among others, could cause actual results to differ materially from those described in these forward-looking statements: the ability of Revelation to meet its financial and strategic goals, due to, among other things, competition; the ability of Revelation to grow and manage growth profitability and retain its key employees; the possibility that the Revelation may be adversely affected by other economic, business, and/or competitive factors; risks relating to the successful development of Revelation's product candidates; the ability to successfully complete planned clinical studies of its product candidates; the risk that we may not fully enroll our clinical studies or enrollment will take longer than expected; risks relating to the occurrence of adverse safety events and/or unexpected concerns that may arise from data or analysis from our clinical studies; changes in applicable laws or regulations; expected initiation of the clinical studies, the timing of clinical data; the outcome of the clinical data, including whether the results of such study is positive or whether it can be replicated; the outcome of data collected, including whether the results of such data and/or correlation can be replicated; the timing, costs, conduct and outcome of our other clinical studies; the anticipated treatment of future clinical data by the FDA, the EMA or other regulatory authorities, including whether such data will be sufficient for approval; the success of future development activities for its product candidates; potential indications for which product candidates may be developed; the ability of Revelation to maintain the listing of its securities on NASDAQ; the expected duration over which Revelation's balances will fund its operations; and other risks and uncertainties described herein, as well as those risks and uncertainties discussed from time to time in other reports and other public filings with the SEC by Revelation.
REVELATION BIOSCIENCES, INC.
Consolidated Statements of Operations
Three Months Ended December 31, Year Ended December 31,
2025 2024 2025 2024
Operating expenses:
Research and development $ 964,189 $ 605,504 $ 4,063,857 $ 3,548,996
General and administrative 1,607,398 1,148,384 5,006,957 4,426,113
Total operating expenses 2,571,587 1,753,888 9,070,814 7,975,109
Loss from operations (2,571,587 ) (1,753,888 ) (9,070,814 ) (7,975,109 )
Other income (expense):
Change in fair value of warrant liability 87 2,557 2,158 81,441
Other income (expense), net 60,493 25,612 155,007 (7,144,868 )
Total other income (expense), net 60,580 28,169 157,165 (7,063,427 )
Net loss $ (2,511,007 ) $ (1,725,719 ) $ (8,913,649 ) $ (15,038,536 )
Deemed dividends (5,951,528 )
Net loss attributable to common stockholders (2,511,007 ) (1,725,719 ) (14,865,177 ) (15,038,536 )
Net loss per share, basic and diluted $ (1.65 ) $ (59.76 ) $ (23.95 ) $ (1,052.16 )
Weighted-average shares used to compute net loss per share, basic and diluted 1,524,011 28,876 620,785 14,293
REVELATION BIOSCIENCES, INC.
Consolidated Balance Sheets
December 31, 2025 December 31, 2024
ASSETS
Current assets:
Cash and cash equivalents $ 10,700,331 $ 6,499,018
Prepaid expenses and other current assets 111,297 66,699
Total current assets 10,811,628 6,565,717
Property and equipment, net 18,067 56,332
Operating lease right-of-use asset 722,288
Other assets 30,941
Total assets $ 11,582,924 $ 6,622,049
LIABILITIES AND STOCKHOLDERS' EQUITY
Current liabilities:
Accounts payable $ 577,501 $ 783,621
Accrued expenses 1,397,644 1,130,046
Operating lease liability 23,013
Total current liabilities 1,998,158 1,913,667
Operating lease liability, net of current portion 723,771
Total liabilities 2,721,929 1,913,667
Commitments and Contingencies (Note 4)
Stockholders' equity:
Common Stock, $0.001 par value; 500,000,000 shares authorized at December 31, 2025 and December 31, 2024 and 1,583,969 and 43,526 issued and outstanding at December 31, 2025 and December 31, 2024, respectively 1,584 44
Additional paid-in-capital 58,278,698 45,213,976
Accumulated deficit (49,419,287 ) (40,505,638 )
Total stockholders' equity 8,860,995 4,708,382
Total liabilities and stockholders' equity $ 11,582,924 $ 6,622,049
Porter LeVay & Rose Inc.
Chester Zygmont, III
Chief Financial Officer
Revelation Biosciences Inc.

Frequently Asked Questions

What are Revelation Biosciences' positive results?

Revelation announced positive results from the PRIME Clinical Study for late-stage chronic kidney disease.

What is Gemini in Revelation's pipeline?

Gemini is a proprietary formulation aimed at treating acute kidney injury and chronic kidney disease.

How much cash did Revelation have at the end of 2025?

As of December 31, 2025, Revelation had $10.7 million in cash and cash equivalents.

What was the net loss for Revelation in 2025?

The net loss for the year ended December 31, 2025, was $8.9 million.

When will data on Gemini be presented?

Clinical data on Gemini will be presented at a conference from March 29 to April 1, 2026.

Last updated: Feb 26, 2026