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Revelation Biosciences, Inc. Announces Financial Results for the Three and Six Months Ended June 30, 2026

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Revelation Biosciences (NASDAQ:REVB) reported financial results for the three and six months ended June 30, 2026, and highlighted progress with its Gemini program. The company formed and expanded an Acute Kidney Injury (AKI) Advisory Board for its planned Phase 2/3 Gemini AKI trial and continued study start-up activities. An independent market assessment indicated a potential $94 billion total addressable market for Gemini across target indications.

As of June 30, 2026, Revelation held $11.5 million in cash and cash equivalents, up from $10.7 million at December 31, 2025, primarily from January 2026 warrant inducement proceeds. According to Revelation, existing cash is expected to fund operations through the first quarter of 2027. For Q2 2026, net cash used in operating activities was $2.6 million versus $1.9 million a year earlier. Net loss for Q2 2026 was $3.3 million (basic and diluted loss per share of $0.87) compared with $2.4 million ($28.04 per share) in Q2 2025. For the six-month period, net loss was $6.3 million, or $3.41 per share, versus $4.5 million, or $54.39 per share, in the prior-year period.

Total operating expenses for Q2 2026 were $3.7 million, driven by research and development expense of $1.9 million and general and administrative expense of $1.7 million. At June 30, 2026, total assets were $12.5 million and stockholders' equity was $10.1 million, with 3,908,420 common shares outstanding, up from 1,583,969 at year-end 2025.

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Positive

  • Cash and cash equivalents of $11.5 million at June 30, 2026, up from $10.7 million at December 31, 2025
  • Runway guidance: company expects existing cash to fund operations through the first quarter of 2027
  • Phase 2/3 Gemini AKI program advancing, with advisory board formed and study start-up activities ongoing
  • Stockholders' equity increased to $10.1 million at June 30, 2026 from $8.9 million at December 31, 2025

Negative

  • Net loss of $3.3 million in Q2 2026 vs. $2.4 million in Q2 2025
  • Six-month net loss widened to $6.3 million from $4.5 million year over year
  • Operating cash use rose to $2.6 million in Q2 2026 from $1.9 million in Q2 2025
  • Total operating expenses increased to $3.7 million in Q2 2026 from $2.5 million in Q2 2025
  • Common shares outstanding grew to 3.9 million at June 30, 2026 from 1.6 million at December 31, 2025, indicating dilution
  • Accumulated deficit reached $55.8 million as of June 30, 2026

Market Context

Across five tag-specific earnings events, the average 24-hour reaction was -2.71%; that record adds ...
Analysis

Across five tag-specific earnings events, the average 24-hour reaction was -2.71%; that record adds a historical divergence lens to this report, while cash runway and quarterly losses remain the key risk-monitoring anchors.

Key Figures

Cash and equivalents: $11.5 million Cash runway: Through the first quarter of 2027 Operating cash use: $2.6 million +5 more
8 metrics
Cash and equivalents $11.5 million June 30, 2026, versus $10.7 million at December 31, 2025
Cash runway Through the first quarter of 2027 Based on current operating plans and projections
Operating cash use $2.6 million Three months ended June 30, 2026, versus $1.9 million in 2025
Quarterly net loss $3.3 million Three months ended June 30, 2026
Quarterly loss per share $0.87 basic and diluted net loss per share Three months ended June 30, 2026
Six-month net loss $6.3 million Six months ended June 30, 2026
Six-month loss per share $3.41 basic and diluted net loss per share Six months ended June 30, 2026
Total addressable market $94 billion Independent market assessment for Gemini

Previous Earnings Reports

5 past events · Latest: May 07 (Positive)
Same Type Pattern 5 events
Date Event Sentiment 24h Move Catalyst
May 07 First-quarter earnings Positive -5.9% FDA agreement and clinical progress accompanied cash and quarterly financial results
Feb 26 Full-year earnings Positive -0.8% Year-end cash, warrant proceeds, clinical progress, and FDA pathway were reported
Nov 06 Third-quarter earnings Positive -2.9% Top-line PRIME results and financing proceeds accompanied cash and loss disclosures
Aug 08 Second-quarter earnings Positive -6.7% PRIME dosing completion and public offering accompanied reduced cash runway
May 08 First-quarter earnings Positive +2.7% Gemini program progress and first patient dosing accompanied quarterly financial results

24h Move is the share-price change in the day after each event; other market factors may also have contributed.

Pattern Detected

Tag-specific earnings announcements were followed by negative 24-hour reactions in four of five events, including releases describing clinical or financial progress.

Key Terms

phosphorylated hexaacyl disaccharide, tlr4, agonist, phase 2/3 clinical trial, +1 more
5 terms
phosphorylated hexaacyl disaccharide technical
"Gemini is the Company's proprietary formulation of phosphorylated hexaacyl disaccharide"
A phosphorylated hexaacyl disaccharide is a synthetic fat-like molecule made of two sugar units, six fatty chains, and a phosphate group that mimics part of a bacterial surface molecule to stimulate the immune system. It is used as a vaccine adjuvant or immune-stimulating ingredient to help vaccines produce a stronger, more consistent response—think of it as a booster that helps the body notice and react to a vaccine. Its use matters to investors because it affects a vaccine candidate’s effectiveness, manufacturing complexity, regulatory review, and potential market value.
tlr4 medical
"a toll-like receptor 4 (TLR4) agonist"
TLR4 (Toll‑like receptor 4) is a protein on the surface of immune cells that senses certain bacterial molecules and sets off an inflammatory response, acting like a smoke detector that raises the alarm when it detects danger. Investors watch TLR4 because medicines that block or stimulate this sensor can change disease outcomes, safety profiles, or vaccine effectiveness, so clinical results or regulatory news about TLR4‑targeted therapies can affect biotech valuations.
agonist medical
"a toll-like receptor 4 (TLR4) agonist"
An agonist is a drug or molecule that binds to a specific cell receptor and activates it, producing a biological effect—like a key that not only fits a lock but also turns it to open a door. For investors, knowing whether a therapy is an agonist helps predict how it might work in the body, its potential benefits and side effects, and how it could affect a company’s clinical success, regulatory outlook, and market value.
phase 2/3 clinical trial medical
"for the upcoming Phase 2/3 AKI clinical trial"
A phase 2/3 clinical trial is a single, combined study that first tests whether a treatment works and is safe in a modest number of patients, then expands seamlessly into a larger, confirmatory stage if early results are promising. Think of it like a prototype test that can quickly move into full production without starting over; for investors, it concentrates risk and time, because positive results can speed regulatory approval while negative results can be a major setback.
total addressable market financial
"a potential $94 billion total addressable market for Gemini"
Total addressable market is the total potential sales opportunity for a product or service if it were to reach every possible customer. It helps investors understand the maximum size of the market and the growth potential for a business. Think of it as the entire pie available to be shared, indicating how big the opportunity could be.

AI-generated analysis. How Rhea-AI works. Not financial advice.

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SAN DIEGO, CA / ACCESS Newswire / August 6, 2026 / Revelation Biosciences, Inc. (NASDAQ:REVB) (the "Company" or "Revelation"), a clinical-stage life sciences company developing innovative solutions to treat acute and chronic disease, today reported its financial results for the three and six months ended June 30, 2026.

Corporate Highlights

"Start-up activities for our pivotal clinical study of Gemini in acute kidney injury patients continue to progress," said James Rolke, Chief Executive Officer of Revelation. "Our focus remains on starting enrollment by year-end, for the benefit of those patients and, ultimately, to deliver value for our shareholders."

Results of Operations

As of June 30, 2026, Revelation had $11.5 million in cash and cash equivalents, compared to $10.7 million as of December 31, 2025. The increase in cash and cash equivalents was primarily due to net cash proceeds from the January 2026 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 through the first quarter of 2027.

Net cash used for operating activities for the three months ended June 30, 2026 was $2.6 million compared to net cash used for operating activities of $1.9 million for the same period in 2025. Net loss for the three months ended June 30, 2026 was $3.3 million, or $0.87 basic and diluted net loss per share compared to net loss of $2.4 million, or $28.04 basic and diluted net loss per share for the three months ended June 30, 2025. Net loss for the six months ended June 30, 2026 was $6.3 million, or $3.41 basic and diluted net loss per share compared to net loss of $4.5 million, or $54.39 basic and diluted net loss per share for the six months ended June 30, 2025.

About Gemini

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 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 studies are positive or whether they 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
June 30,

Six Months Ended
June 30,

2026

2025

2026

2025

Operating expenses:





Research and development

$

1,918,424

$

1,317,980

$

3,295,285

$

2,176,810

General and administrative

1,743,817

1,143,249

3,459,456

2,379,406

Total operating expenses

3,662,241

2,461,229

6,754,741

4,556,216

Loss from operations

(3,662,241

)

(2,461,229

)

(6,754,741

)

(4,556,216

)

Other income (expense), net:
Other income (expense), net

338,857

16,803

422,306

59,289

Change in fair value of warrant liability

-

44

-

1,460

Total other income (expense), net

338,857

16,847

422,306

60,749

Net loss

$

(3,323,384

)

$

(2,444,382

)

$

(6,332,435

)

$

(4,495,467

)

Deemed dividends

-

(3,181,786

)

(5,681,616

)

(3,181,786

)

Net loss attributable to common stockholders

(3,323,384

)

(5,626,168

)

(12,014,051

)

(7,677,253

)

Net loss per share, basic and diluted

$

(0.87

)

$

(28.04

)

$

(3.41

)

$

(54.39

)

Weighted-average shares used to compute net loss per share, basic and diluted

3,829,363

200,668

3,520,259

141,140

REVELATION BIOSCIENCES, INC.
Consolidated Balance Sheets

June 30,
2026

December 31,
2025

ASSETS



Current assets:



Cash and cash equivalents

$

11,482,792

$

10,700,331

Prepaid expenses and other current assets

201,724

111,297

Total current assets

11,684,516

10,811,628

Property and equipment, net

172,032

18,067

Operating lease right-of-use asset

610,443

722,288

Other assets

30,941

30,941

Total assets

$

12,497,932

$

11,582,924

LIABILITIES AND STOCKHOLDERS' EQUITY
Current liabilities:
Accounts payable

$

931,093

$

577,501

Accrued expenses

759,937

1,397,644

Operating lease liability

189,370

23,013

Total current liabilities

1,880,400

1,998,158

Operating lease liability, net of current portion

550,546

723,771

Total liabilities

2,430,946

2,721,929

Commitments and Contingencies (Note 4)
Stockholders' equity:
Common Stock, $0.001 par value; 500,000,000 shares authorized; 3,908,420 and 1,583,969 issued and outstanding at June 30, 2026 and December 31, 2025, respectively

3,908

1,584

Additional paid-in-capital

65,814,800

58,278,698

Accumulated deficit

(55,751,722

)

(49,419,287

)

Total stockholders' equity

10,066,986

8,860,995

Total liabilities and stockholders' equity

$

12,497,932

$

11,582,924

Company Contacts

Mike Porter
Investor Relations
Porter LeVay & Rose, Inc.
Email: mike@plrinvest.com

Chester Zygmont, III
Chief Financial Officer
Revelation Biosciences, Inc.
Email: czygmont@revbiosciences.com

SOURCE: Revelation Biosciences, Inc.



View the original press release on ACCESS Newswire

FAQ

How did Revelation Biosciences (NASDAQ:REVB) perform financially in Q2 2026?

Revelation Biosciences reported a Q2 2026 net loss of $3.3 million, or $0.87 per share. According to Revelation, total operating expenses were $3.7 million, and net cash used in operating activities was $2.6 million, higher than the prior-year quarter.

What is Revelation Biosciences' cash runway as of June 30, 2026 (REVB)?

As of June 30, 2026, Revelation Biosciences held $11.5 million in cash and cash equivalents. According to Revelation, based on current operating plans and projections, this cash is expected to fund operations through the first quarter of 2027, assuming current assumptions hold.

How much did Revelation Biosciences spend on operating activities in Q2 2026?

Net cash used for operating activities in Q2 2026 was $2.6 million for Revelation Biosciences. According to the company, this compares with $1.9 million of net cash used for operating activities in the same quarter of 2025, reflecting increased spending.

What progress has Revelation Biosciences made on the Gemini acute kidney injury trial?

Revelation Biosciences has formed and expanded an Acute Kidney Injury Advisory Board for its planned Phase 2/3 Gemini trial. According to Revelation, start-up activities for this pivotal Gemini study in acute kidney injury patients are ongoing, with a focus on beginning enrollment by year-end.

How many shares of Revelation Biosciences common stock were outstanding in mid-2026?

At June 30, 2026, Revelation Biosciences had 3,908,420 common shares issued and outstanding. According to the company, this compares with 1,583,969 shares outstanding at December 31, 2025, indicating a significant increase in the share count over the period.

What is the potential market size for Revelation Biosciences' Gemini program?

An independent market assessment indicated a potential $94 billion total addressable market for the Gemini program. According to Revelation, Gemini is being developed for acute kidney injury, chronic kidney disease, severe burn-related hyperinflammation and infection, and prevention of post-surgical infection.

What are Revelation Biosciences' total assets and equity as of June 30, 2026?

As of June 30, 2026, Revelation Biosciences reported $12.5 million in total assets and $10.1 million in stockholders' equity. According to the company, cash and cash equivalents were the largest component of current assets, at $11.5 million.