REVBWNasdaqPharmaceutical PreparationsUS GAAP · USD

Revelation Biosciences, Inc

Revelation Biosciences, Inc. is a U.S.-based clinical-stage life science company developing therapies built around its proprietary Gemini formulation of PHAD, an innate-immune modulator. Its pipeline includes programs for acute kidney injury, chronic kidney disease, post-surgical infection, and infection prevention in severe burn patients, with operations centered in San Diego, California.

Liikevoitto (EBIT)−9,1milj. USD
−13,7 %v/v
Nettotulos−8,9milj. USD
+40,7 %v/v
Vapaa kassavirta−8,3milj. USD
+54,8 %v/v

Tilikausi 2025 · muutos edellisvuodesta

Kehitys 2020–2025

−12,5−10,0−7,5−5,0−2,50,0milj. USD20202021: EBIT −12 milj. USD20212022: EBIT −11 milj. USD20222023: EBIT −8,7 milj. USD20232024: EBIT −8,0 milj. USD20242025: EBIT −9,1 milj. USD2025−9,1
LiikevaihtoLiikevoitto (EBIT)

Liiketoiminta

Osuus liikevaihdosta
Clinical-stage product candidates85 %

Gemini-based drug candidates being developed for kidney disease and infection-related indications.

Licensed PHAD program15 %

A worldwide licensed program using PHAD for treating or preventing infections.

Asiakkaat

Revelation does not yet sell approved products; its near-term counterparties are clinical investigators, contract research organizations, manufacturers, regulators, and licensing partners. If approved, its therapies would be used by physicians and hospitals treating acute kidney injury, chronic kidney disease, post-surgical infection, and severe burn patients.

Clinical trial ecosystem

Research sites, CROs, and vendors supporting preclinical and clinical development of Gemini programs.

Hospital and specialist physicians

Potential prescribers for AKI, CKD, post-surgical infection, and burn-related infection prevention.

Licensing and collaboration partners

Partners that could help fund, develop, or commercialize PHAD-based programs.

Regulatory and reimbursement stakeholders

FDA and future payers that determine approval timing and market access.

Strategia

Revelation’s strategy is to advance Gemini through clinical development across multiple indications while preserving optionality through licensing and partnerships. It also seeks to broaden its pipeline through internal development, acquisitions, and in-licensing, while relying on third parties for manufacturing and future commercialization.

Advance GEM-AKI and GEM-CKDLyhyt aikaväli

These are the core clinical programs and the main path to value creation.

Expand into infection-related indicationsKeskipitkä aikaväli

Broadens the platform beyond kidney disease and increases pipeline optionality.

Secure development funding and partnersLyhyt aikaväli

Clinical-stage biotech requires external capital and collaboration to progress.

Outsource manufacturing and future commercializationKeskipitkä aikaväli

Reduces capital intensity and leverages specialized third-party capabilities.

Maantiede

The company is incorporated in Delaware and based in San Diego, California, with development activities centered in the United States. Its business is currently U.S.-focused, although the Vanderbilt license is worldwide and any eventual commercialization could extend beyond the U.S.

Riskit

Revelation faces the typical risks of a clinical-stage biotech company: uncertain trial outcomes, regulatory delays, and dependence on external capital. Its business is also exposed to single-supplier and third-party manufacturing reliance, plus the possibility that licensing terms, milestone obligations, or commercialization plans do not progress as expected.

Järjestetty vakavuuden mukaan
MatalaKohtalainenKorkeaMatalaKohtalainenKorkeaVaikutus →Todennäköisyys →Clinical development failure1Regulatory delay or rejection2Capital dependence and dilution3Manufacturing and supply concentration4Commercialization and reimbursement uncertainty5
Vaikutus on riskin vakavuus ja todennäköisyys sen toteutumisen todennäköisyys lähivuosina, molemmat arvioitu yhtiön raporttien perusteella. Numerot vastaavat listaa.
  1. Clinical development failureVaikutus: KriittinenTodennäköisyys: Korkea

    Gemini programs must prove safety and efficacy in human trials before approval.

    KohdistuuGEM-AKIGEM-CKDGEM-PSIGEM-PBI
  2. Regulatory delay or rejectionVaikutus: KorkeaTodennäköisyys: Korkea

    FDA review and trial oversight determine whether programs can advance.

    Kohdistuu: All product candidates

  3. Capital dependence and dilutionVaikutus: KorkeaTodennäköisyys: Korkea

    The company funds operations through equity raises and may need more capital.

    Kohdistuu: Operating funding

  4. Manufacturing and supply concentrationVaikutus: KorkeaTodennäköisyys: Matala

    The company relies on third parties and has a single supplier for PHAD.

    Kohdistuu: PHAD and clinical supply chain

  5. Commercialization and reimbursement uncertaintyVaikutus: KeskitasoTodennäköisyys: Matala

    Even approved drugs need market access, pricing, and adoption by physicians/payers.

    Kohdistuu: Future approved products

Kirjanpito

Harkinnanvaraiset erät
Research and development expense recognition

Clinical and preclinical costs are expensed as incurred, making results highly dependent on trial activity.

Vaikutus: Drives operating loss timing and comparability across periods

Warrant liability fair value

Outstanding warrants may be marked to market, creating non-cash volatility.

Vaikutus: Can materially affect reported earnings and balance sheet values

Going concern and financing disclosures

The company depends on external funding to continue development.

Vaikutus: Important for assessing liquidity and continuity of operations

Reverse stock split accounting presentation

Multiple reverse splits affect share counts and per-share metrics.

Vaikutus: Impacts EPS, share price comparability, and market data

Julkisesti listattuja yhtiöitä, joilla on samankaltainen liiketoiminta.

Päivitetty: 24.9.2026