Revelation Biosciences (REVB) Q3 2025 earnings summary
Event summary combining transcript, slides, and related documents.
Q3 2025 earnings summary
12 Jun, 2026Executive summary
Clinical-stage life science company focused on inflammation modulation with proprietary Gemini formulation; pipeline includes GEM-AKI, GEM-CKD, GEM-PSI, and GEM-PBI product candidates.
Reported positive top-line results from the PRIME clinical study, supporting the potential of the Gemini program.
No revenue generated to date; operations funded by $69.2 million in equity and warrant financings since inception.
Net loss of $6.4 million for the nine months ended September 30, 2025, compared to $13.3 million for the same period in 2024.
Cash and cash equivalents increased to $12.7 million as of September 30, 2025, from $6.5 million at December 31, 2024.
Financial highlights
Net loss for Q3 2025 was $1.9 million, or $(1.77) per share, compared to $2.2 million, or $(40.15) per share, in Q3 2024.
Net cash used in operating activities was $6.3 million for the nine months ended September 30, 2025, down from $14.6 million in the prior year period.
Total operating expenses for the nine months ended September 30, 2025 were $6.5 million, up from $6.2 million year-over-year.
Net cash provided by financing activities was $12.5 million for the nine months ended September 30, 2025.
Total assets: $12.9 million; total liabilities: $1.85 million; stockholders' equity: $11.0 million as of September 30, 2025.
Outlook and guidance
Expects continued significant operating and net losses, and negative cash flows from operations for the foreseeable future.
Current cash position expected to fund operations through Q3 2026.
Plans to seek further funding through public or private equity or debt financings.
Plans to meet with the FDA later in 2025 to discuss the clinical development path for Gemini.
Focus remains on advancing Gemini for acute kidney injury, with additional programs in chronic kidney disease and infection prevention.
Latest events from Revelation Biosciences
- Pivotal adaptive phase II/III trial for Gemini in AKI set for late 2026, with FDA backing.REVB
38th Annual Roth Conference16 Jun 2026 - Net loss of $11.1M, positive Gemini phase 1 data, and cash covers operations through 2024.REVB
Q2 202412 Jun 2026 - Net loss of $13.3 million and new financing highlight urgent funding needs and ongoing risks.REVB
Q3 202412 Jun 2026 - Cash fell, losses widened, and Gemini clinical milestones advanced with key data expected mid-2025.REVB
Q4 202412 Jun 2026 - Q1 2025 net loss of $2.1M, $3.7M cash, and cash runway projected through June 2025.REVB
Q1 202512 Jun 2026 - Net loss narrowed, cash runway extends to year-end, but funding and regulatory risks persist.REVB
Q2 202512 Jun 2026 - Biotech seeks $8.96M for clinical pipeline, but faces dilution and ongoing financial risk.REVB
Registration filing12 Jun 2026 - Improved financials and clinical progress position Gemini for further development into 2027.REVB
Q4 202512 Jun 2026 - Biotech seeks $4.3M via share/warrant offering to fund early-stage immune-modulating therapies.REVB
Registration filing12 Jun 2026