Recent Updates
Recently added Catalysts
REVB Positive Sentiment Score: 68/100

Revelation Biosciences, Inc. Announces Financial Results for the Three Months Ended

Key Takeaway: Revelation Biosciences, Inc. reported its financial results for the quarter ending March 31, 2025, highlighting a focus on a new indication for Gemini and the completion of the first patient dosing in the PRIME Phase 1b study. The company has acknowledged a decrease in cash reserves to $3.7 million, with a net loss of $2.1 million for the quarter. Despite these challenges, Revelation is optimistic about the therapeutic potential of Gemini and anticipates topline data for its studies this summer.

Market Sentiment Analysis

POSITIVE FACTORS

  • Announced a new indication for Gemini in severe burn patients
  • Completed dosing of the first patient in Phase 1b Clinical Study
  • Expecting topline data from the Phase 1b study this summer
  • Positive Phase 1 clinical data for intravenous treatment with Gemini

CONCERNS & RISKS

  • Decrease in cash and cash equivalents from $6.5 million to $3.7 million
  • Net loss of $2.1 million for the quarter, though improved from last year
  • Operating activities continue to use cash at a high rate

Full Press Release Details

Revelation Biosciences, Inc. Announces Financial Results for the Three Months Ended March 31, 2025
San Diego, CA May 8, 2025 Revelation Biosciences, Inc. (NASDAQ: REVB) (the Company or Revelation ), a clinical-stage life sciences company that is focused on rebalancing inflammation to optimize health, today reported its three months ended March 31, 2025 financial results.
Corporate Highlights
-Announced a new indication for Gemini in severe burn patients
-Released data showing Gemini priming attenuated inflammation in peripheral blood mononuclear cells
-Completed dosing of first patient in PRIME Phase 1b Clinical Study of Gemini in CKD Patients
While we continue to expand the pipeline here at Revelation, we are excited to continue our collaboration with Vanderbilt and Dr. Bohannon in the area of severe burns. said James Rolke, Chief Executive Officer of Revelation. We are also looking forward to the Phase 1b PRIME clinical study topline data this summer.
Results of Operations
As of March 31, 2025, Revelation had $3.7 million in cash and cash equivalents, compared to $6.5 million as of December 31, 2024. The decrease in cash and cash equivalents was primarily due to cash used for operating activities. Based on current operating plans and projections, Revelation believes that its current cash and cash equivalents are sufficient to fund operations through June 2025.
Revelation's net cash used for operating activities for the three months ended March 31, 2025 was $2.8 million compared to net cash used for operating activities of $2.8 million for the same period in 2024. Revelation's net loss for the three months ended March 31, 2025 was $2.1 million, or $(2.11) basic and diluted net loss per share compared to a net loss of $2.7 million, or $(39.37) basic and diluted net loss per share for the same period in 2024.
Gemini is an intravenously administrated, proprietary formulation of phosphorylated hexaacyl disaccharide (PHAD ) that reduces the damage associated with inflammation by reprograming the innate immune system to respond to stress (trauma, infection, etc.) in an attenuated manner. Revelation has conducted multiple preclinical studies demonstrating the therapeutic potential of Gemini in the target indications. Revelation previously announced positive Phase 1 clinical data for intravenous treatment with Gemini. The primary safety endpoint was met in the Phase 1 study, and results demonstrated statistically significant pharmacodynamic activity as observed through expected changes in multiple biomarkers including upregulation of IL-10.
Gemini is being developed for multiple indications including as a pretreatment to prevent or reduce the severity and duration of acute kidney injury (GEMINI-AKI program), and as pretreatment to prevent or reduce the severity and duration of post-surgical infection (GEMINI-PSI program). In addition, Gemini may be a treatment to stop or slow the progression of chronic kidney disease (GEMINI-CKD program).
About Revelation Biosciences, Inc.
Revelation Biosciences, Inc. is a clinical stage life sciences company focused on harnessing the power of trained immunity for the prevention and treatment of disease using its proprietary formulation Gemini. Revelation has multiple ongoing programs to evaluate Gemini, including as a prevention for post-surgical infection, as a prevention for acute kidney injury, and for the treatment of chronic kidney disease.
For more information on Revelation, 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 March 31,
2025 2024
Operating expenses:
Research and development $ 858,830 $ 717,582
General and administrative 1,236,157 1,184,556
Total operating expenses 2,094,987 1,902,138
Loss from operations (2,094,987 ) (1,902,138 )
Other income (expense):
Change in fair value of warrant liability 1,417 68,427
Other income (expense), net 42,485 (847,722 )
Total other income (expense), net 43,902 (779,295 )
Net loss $ (2,051,085 ) $ (2,681,433 )
Net loss per share, basic and diluted $ (2.11 ) $ (39.37 )
Weighted-average shares used to compute net loss per share, basic and diluted 971,313 68,115
REVELATION BIOSCIENCES, INC.
Consolidated Balance Sheets
March 31, 2025 December 31, 2024
ASSETS
Current assets:
Cash and cash equivalents $ 3,704,611 $ 6,499,018
Prepaid expenses and other current assets 223,270 66,699
Total current assets 3,927,881 6,565,717
Property and equipment, net 42,390 56,332
Total assets $ 3,970,271 $ 6,622,049
LIABILITIES AND STOCKHOLDERS' EQUITY
Current liabilities:
Accounts payable $ 625,058 $ 783,621
Accrued expenses 463,632 1,127,800
Warrant liability 829 2,246
Total current liabilities 1,089,519 1,913,667
Total liabilities 1,089,519 1,913,667
Commitments and Contingencies (Note 4)
Stockholders' equity:
Common Stock, $0.001 par value; 500,000,000 shares authorized; 963,796 and 522,223 issued and outstanding at March 31, 2025 and December 31, 2024, respectively 964 522
Additional paid-in-capital 45,436,511 45,213,498
Accumulated deficit (42,556,723 ) (40,505,638 )
Total stockholders' equity 2,880,752 4,708,382
Total liabilities and stockholders' equity $ 3,970,271 $ 6,622,049
Porter LeVay & Rose Inc.
Chester S. Zygmont, III
Chief Financial Officer
Revelation Biosciences Inc.

Frequently Asked Questions

What are the latest financial results from Revelation Biosciences?

For Q1 2025, Revelation reported a net loss of $2.1 million and $3.7 million in cash.

What is the purpose of the Gemini formulation?

Gemini is designed to reduce inflammation by reprogramming the innate immune system.

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

Revelation had $3.7 million in cash and cash equivalents as of March 31, 2025.

What is the Phase 1b PRIME study focused on?

The PRIME Phase 1b study is evaluating Gemini in chronic kidney disease patients.

Which programs is Gemini being developed for?

Gemini is being developed for post-surgical infections, acute kidney injury, and CKD.

Last updated: May 8, 2025