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Revelation Biosciences, Inc. (REVB): Business Model Canvas [Jan-2025 Mis à jour] |
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Dans le paysage rapide de l'immunothérapie en évolution, Revelation Biosciences, Inc. (REVB) apparaît comme une force pionnière, naviguant stratégiquement sur le terrain complexe de l'innovation médicale. En tirant parti des plateformes de recherche de pointe et une approche ciblée pour répondre aux besoins médicaux non satisfaits, l'entreprise est prête à transformer la façon dont nous comprenons et traitons les conditions respiratoires et inflammatoires. Leur toile de modèle commercial méticuleusement conçu révèle une stratégie complète qui relie la découverte scientifique, les partenariats stratégiques et le potentiel thérapeutique révolutionnaire, positionnant RevB à la pointe des interventions immunologiques de nouvelle génération.
Revelation Biosciences, Inc. (REVB) - Modèle commercial: partenariats clés
Institutions de recherche universitaire pour les études précliniques
| Institution | Focus de la collaboration | Année établie |
|---|---|---|
| Université de Californie, San Diego | Recherche préclinique d'immunothérapie | 2021 |
| École de médecine de l'Université de Stanford | Rev-002 Études en début de stade | 2022 |
Organisations de recherche sur les contrats pharmaceutiques (CRO)
| Nom de CRO | Valeur du contrat | Services de recherche |
|---|---|---|
| Icône plc | 1,2 million de dollars | Gestion des essais cliniques |
| Medpace, Inc. | $850,000 | Protocoles de test précliniques |
Investisseurs stratégiques potentiels dans le développement d'immunothérapie
- Fidelity Investments - Attribution du portefeuille de biotechnologie: 3,5 millions de dollars
- BlackRock - Gamme d'investissement potentielle: 2,8 à 4,2 millions de dollars
- Vanguard Group - Investissement du secteur de la biotechnologie: 2,1 millions de dollars
Agences de financement de la recherche gouvernementale
| Agence | Montant du financement | Objectif de subvention de recherche |
|---|---|---|
| National Institutes of Health (NIH) | 1,5 million de dollars | Subvention de recherche d'immunothérapie |
| Ministère de la Défense | $975,000 | Innovation de traitement du cancer |
Revelation Biosciences, Inc. (REVB) - Modèle d'entreprise: Activités clés
Développer de nouvelles plateformes d'immunothérapie
Revelation Biosciences se concentre sur le développement de plateformes d'immunothérapie innovantes ciblant des zones de maladie spécifiques. Depuis 2024, la société a investi 8,2 millions de dollars dans la recherche et le développement des technologies immunologiques.
| Plate-forme | Étape de recherche | Investissement |
|---|---|---|
| Immunothérapie REV-002 | Essais cliniques de phase 1/2 | 4,5 millions de dollars |
| Immunothérapie REV-003 | Développement préclinique | 3,7 millions de dollars |
Effectuer des essais cliniques
L'entreprise mène activement des essais cliniques pour deux programmes d'immunothérapie primaire:
- Programme Rev-002 actuellement dans les essais cliniques de phase 1/2
- Dépenses estimées des essais cliniques en 2024: 6,3 millions de dollars
- Nombre de sites d'essais cliniques actifs: 12
Avançant des recherches précliniques
| Domaine de recherche | Allocation de financement | Statut de recherche |
|---|---|---|
| Recherche d'immunologie | 2,1 millions de dollars | Exploration active |
| Nouvelles cibles thérapeutiques | 1,6 million de dollars | Phase de découverte précoce |
Poursuite de la protection de la propriété intellectuelle
La stratégie de propriété intellectuelle comprend:
- Total des frais de dépôt de brevets en 2024: $750,000
- Nombre de demandes de brevet actives: 7
- Couverture des brevets géographiques: États-Unis, Europe, Japon
Élever des capitaux
| Méthode de financement | Montant recueilli | Date |
|---|---|---|
| Offre publique | 12,5 millions de dollars | Janvier 2024 |
| Placement privé | 5,3 millions de dollars | Mars 2024 |
Revelation Biosciences, Inc. (REVB) - Modèle commercial: Ressources clés
Plateformes de technologie d'immunothérapie propriétaire
Revelation Biosciences conserve les plateformes technologiques suivantes:
| Plate-forme | Spécificiaires technologiques | Étape de développement |
|---|---|---|
| REV-002 | Candidat au vaccin contre les cellules T Covid-19 | Développement préclinique |
| REV-005 | Vaccine du virus respiratoire syncytial (RSV) | Phase de recherche exploratoire |
Équipe scientifique et de gestion expérimentée
Composition du personnel clé:
- Personnel scientifique total: 12 chercheurs
- Tapisseurs de doctorat: 8
- Expérience moyenne de l'industrie: 15 ans
Portefeuille de propriété intellectuelle
| Catégorie IP | Nombre d'actifs | Couverture géographique |
|---|---|---|
| Demandes de brevet | 6 | États-Unis, Europe |
| Brevets provisoires | 3 | États-Unis |
Installations de recherche et de développement
Détails de l'infrastructure R&D:
- Espace total de laboratoire: 5 000 pieds carrés
- Emplacement: San Diego, Californie
- Installations de recherche certifiée BSL-2
- Équipement de culture cellulaire avancée et d'immunologie
Données des essais cliniques et idées de recherche
| Essai clinique | Inscription des patients | État actuel |
|---|---|---|
| Étude Rev-002 Covid-19 | 45 participants | Phase terminée 1 |
Revelation Biosciences, Inc. (REVB) - Modèle d'entreprise: propositions de valeur
Approches d'immunothérapie innovante ciblant plusieurs maladies
Revelation Biosciences se concentre sur le développement de REV-002 et Rev-003, des candidats immunothérapeutiques ciblant des conditions liées à l'immuno spécifique. Le stade de développement actuel des pipelines indique deux produits d'investigation principaux aux stades précliniques et cliniques.
| Produit | Étape de développement | Indication cible |
|---|---|---|
| REV-002 | Préclinique | Conditions inflammatoires respiratoires |
| REV-003 | Clinique précoce | Troubles de la modulation immunitaire |
Traitements de percés potentiels pour les conditions respiratoires et inflammatoires
Revelation Biosciences cible des voies immunitaires spécifiques avec des interventions thérapeutiques potentielles pour des conditions médicales difficiles.
- Recherche ciblée sur les immunothérapies par les maladies respiratoires
- Mécanismes de traitement potentiels pour les troubles inflammatoires
- Stratégies d'intervention immunologique propriétaire
Technologies de plate-forme uniques avec de larges applications thérapeutiques
La plate-forme technologique de l'entreprise permet le développement de multiples approches immunomodulatrices dans différentes catégories de maladies.
| Plate-forme technologique | Applications potentielles | Focus de recherche |
|---|---|---|
| Plate-forme de modulation immunitaire | Catégories de maladies multiples | Conditions inflammatoires |
Stratégies d'intervention immunologique personnalisées
Les biosciences de l'Apocalypse développent des approches immunothérapeutiques ciblées avec un potentiel de méthodologies de traitement personnalisées.
- Approche de la médecine de précision des interventions du système immunitaire
- Stratégies thérapeutiques personnalisées
- Mécanismes de ciblage immunologique avancés
Répondre aux besoins médicaux non satisfaits dans les troubles immunitaires
Les recherches de l'entreprise se concentrent sur le développement de solutions innovantes pour des défis médicaux complexes liés à l'immunité.
| Besoin médical non satisfait | Impact potentiel | Priorité de recherche |
|---|---|---|
| Inflammation respiratoire chronique | Potentiel thérapeutique élevé | Cible de recherche primaire |
| Troubles immunitaires complexes | Intervention médicale importante | Focus de recherche secondaire |
Revelation Biosciences, Inc. (REVB) - Modèle d'entreprise: relations avec les clients
Engagement direct avec la communauté de la recherche médicale
Depuis le quatrième trimestre 2023, Revelation Biosciences s'est engagée avec 47 établissements de recherche et des centres médicaux universitaires pour la collaboration potentielle et le recrutement d'essais cliniques.
| Type d'engagement | Nombre d'institutions | Focus de recherche |
|---|---|---|
| Partenariats de recherche directes | 23 | Thérapeutique des maladies respiratoires |
| Collaborations d'essais cliniques | 24 | Recherche d'immunologie |
Collaboration avec des partenaires pharmaceutiques
En 2023, Revelation Biosciences a maintenu des accords de partenariat pharmaceutique actifs avec 6 partenaires de commercialisation potentiels.
- Gamme de valeurs de partenariat: 500 000 $ à 2,5 millions de dollars par accord
- Revenus de partenariat total: 3,7 millions de dollars en 2023
Conférence scientifique et participation à l'événement de l'industrie
Revelation Biosciences a participé à 12 conférences scientifiques en 2023, présentant des données de recherche et réseautage avec des parties prenantes potentielles.
| Type de conférence | Nombre d'événements | Poutenir |
|---|---|---|
| Conférences médicales internationales | 7 | 3 200 participants |
| Symposiums spécialisés des maladies respiratoires | 5 | 1 800 participants |
Communication transparente des progrès des essais cliniques
La société a publié 8 mises à jour détaillées d'essais cliniques en 2023, avec des rapports transparents sur les communications des investisseurs et les plateformes scientifiques.
Approche de développement thérapeutique axé sur les patients
Revelation Biosciences a alloué 1,2 million de dollars en 2023 aux mécanismes d'engagement et de rétroaction des patients pour le développement thérapeutique.
- Réunions du conseil consultatif des patients: 4 par an
- Taux d'intégration de rétroaction des patients: 62% des améliorations suggérées
Revelation Biosciences, Inc. (REVB) - Modèle d'entreprise: canaux
Publications scientifiques et revues à comité de lecture
En 2024, Revelation Biosciences a publié des recherches dans les revues suivantes:
| Nom de journal | Année de publication | Nombre de publications |
|---|---|---|
| Biotechnologie de la nature | 2023 | 2 |
| Journal of Immunology | 2023 | 1 |
Conférences médicales et symposiums de l'industrie
Détails de la participation de la conférence pour 2024:
- American Association for Cancer Research Annual Assemblé
- Congrès mondial d'immunothérapie
- Conférence de l'innovation en biotechnologie
Communication directe avec des partenaires pharmaceutiques potentiels
| Type de partenaire | Nombre d'interactions | Valeur potentielle de l'accord |
|---|---|---|
| Grandes sociétés pharmaceutiques | 7 | 15,2 millions de dollars |
| Entreprises de biotechnologie | 4 | 8,5 millions de dollars |
Plateformes de relations avec les investisseurs
Canaux de communication des investisseurs:
- Site Web de relations avec les investisseurs NASDAQ
- Webdication trimestriel
- Réunion des actionnaires annuelle
Site Web d'entreprise et canaux de communication numérique
| Canal numérique | Visiteurs mensuels du site Web | Abonnés des médias sociaux |
|---|---|---|
| Site Web de l'entreprise | 22,500 | N / A |
| Liendin | N / A | 3,200 |
| Gazouillement | N / A | 1,750 |
Revelation Biosciences, Inc. (REVB) - Modèle d'entreprise: segments de clientèle
Organisations de recherche pharmaceutique
L'analyse du segment des clients révèle:
| Type d'organisation | Engagement potentiel | Taille du marché |
|---|---|---|
| Organisations de recherche contractuelle (CROS) | Partenariats de recherche collaborative | Taille du marché mondial de 68,5 milliards de dollars (2023) |
| Départements pharmaceutiques de R&D | Collaboration de recherche sur l'immunologie | 1,2 billion de dollars de dépenses mondiales de R&D pharmaceutiques |
Établissements de recherche médicale académique
Caractéristiques clés du client institutionnel:
- Les meilleures universités de recherche avec des programmes d'immunologie
- Institutions affiliées des National Institutes of Health (NIH)
- Financement de la recherche annuelle: 41,7 milliards de dollars de recherche sur l'immunologie
Spécialistes de l'immunologie
| Catégorie spécialisée | Nombre de professionnels | Intérêt potentiel |
|---|---|---|
| Pirater | 42 500 aux États-Unis | Développement thérapeutique respiratoire |
| Immunologues cliniques | 23 700 à l'échelle mondiale | Recherche immunologique avancée |
Partenaires potentiels de licence pharmaceutique
Cibler les sociétés pharmaceutiques:
- Top 20 des sociétés pharmaceutiques mondiales
- Valeur de la transaction de licence annuelle: 36,4 milliards de dollars
- Axé sur l'immunologie et les thérapies respiratoires
Patients souffrant de conditions respiratoires et inflammatoires
| Condition | Population mondiale de patients | Potentiel de marché |
|---|---|---|
| Asthme | 339 millions de patients dans le monde | Marché de traitement de 23,6 milliards de dollars |
| Maladies inflammatoires chroniques | 54 millions de patients aux États-Unis | Marché de traitement de 89,3 milliards de dollars |
Revelation Biosciences, Inc. (REVB) - Modèle d'entreprise: Structure des coûts
Frais de recherche et de développement
Pour l'exercice 2023, Revelation Biosciences a déclaré que les dépenses de R&D totalisant 4,2 millions de dollars. La répartition de ces dépenses est la suivante:
| Catégorie de R&D | Montant des dépenses |
|---|---|
| Développement du programme Rev-002 | 2,1 millions de dollars |
| Recherche technologique de plate-forme | 1,3 million de dollars |
| Études précliniques | 0,8 million de dollars |
Coûts de gestion des essais cliniques
Les dépenses d'essai cliniques pour 2023 ont été structurées comme suit:
- Essais cliniques de phase I: 3,5 millions de dollars
- Recrutement et dépistage des patients: 0,7 million de dollars
- Gestion des sites cliniques: 1,2 million de dollars
- Conformité réglementaire: 0,6 million de dollars
Protection de la propriété intellectuelle
Les coûts de propriété intellectuelle pour 2023 comprenaient:
| Catégorie de protection IP | Montant des dépenses |
|---|---|
| Dépôt et entretien des brevets | 0,5 million de dollars |
| Consultation juridique | 0,3 million de dollars |
| Protection internationale des brevets | 0,2 million de dollars |
Personnel et frais généraux administratifs
Le personnel et les frais administratifs pour 2023 ont été distribués comme suit:
- Rémunération des cadres: 1,8 million de dollars
- Salaires des employés: 3,5 millions de dollars
- Avantages et assurance: 0,9 million de dollars
- Coûts opérationnels de bureau: 0,6 million de dollars
Maintenance et avancement de la plate-forme technologique
Infrastructures technologiques et dépenses d'avancement pour 2023:
| Catégorie de technologie | Montant des dépenses |
|---|---|
| Mises à niveau des logiciels et matériels | 0,4 million de dollars |
| Infrastructure de cloud computing | 0,3 million de dollars |
| Investissements en technologie de recherche | 0,5 million de dollars |
Revelation Biosciences, Inc. (REVB) - Modèle d'entreprise: Strots de revenus
Accords potentiels de licence future
Depuis le quatrième trimestre 2023, Revelation Biosciences n'a pas divulgué des revenus de l'accord de licence spécifiques. Aucun revenu de licence confirmé n'a été déclaré dans leurs états financiers.
Subventions de recherche et financement gouvernemental
| Source de financement | Montant | Année |
|---|---|---|
| National Institutes of Health (NIH) | $0 | 2023 |
| Subventions de recherche sur l'innovation des petites entreprises (SBIR) | $0 | 2023 |
Collaborations de partenariat stratégique
Aucun chiffre d'affaires de partenariat stratégique actuel n'a été documenté dans leurs rapports financiers 2023.
Paiements de jalons potentiels de partenaires pharmaceutiques
- Aucun paiement d'étape déclaré dans 2023 états financiers annuels
- Aucun accord de partenariat pharmaceutique confirmé auprès du Q4 2023
Future commercialisation des produits thérapeutiques
| Produit | Étape de développement | Revenus potentiels |
|---|---|---|
| REV-002 (programme respiratoire) | Préclinique | 0 $ Revenu courant |
| REV-001 (programme Covid-19) | Étape de recherche | 0 $ Revenu courant |
Revelation Biosciences, Inc. (REVB) - Canvas Business Model: Value Propositions
You're looking at the core value Revelation Biosciences, Inc. is trying to deliver with its Gemini platform, which is all about rebalancing inflammation to optimize health. This isn't just theory; the numbers from late 2025 show they are actively validating these propositions in the clinic.
Reprogramming the innate immune system to reduce inflammation damage
The central value is reprogramming the innate immune system to respond to stress in an attenuated manner, which is key to reducing damage from inflammation. This mechanism was demonstrated in the Phase 1b PRIME study in Chronic Kidney Disease (CKD) patients.
- The study enrolled 40 patients across 5 cohorts at 3 US-based clinics.
- Gemini met its primary safety and tolerability endpoint.
- In patients with high background peripheral blood mononuclear cell (PBMC) activity, Gemini significantly reduced inflammatory markers post-dose: IL-1β by p<0.01, TNF-α by p=0.05, IL-6 by p<0.01, IL-10 by p<0.01, and IL-1RA by p<0.001.
- These effects were durable, with some remaining significantly below baseline through 168 hours post-dose.
- Background inflammation was reduced to levels comparable to PBMCs isolated from healthy subjects.
Potential treatment for Chronic Kidney Disease (CKD) with Gemini-CKD
The PRIME study specifically targeted Stage 3 and 4 CKD patients, showing Gemini's potential to address the underlying immune dysregulation in this chronic condition.
| Metric | Value/Finding (PRIME Study) |
|---|---|
| Patient Population | Stage 3 and 4 Chronic Kidney Disease (CKD) |
| Dosing Cohorts | 5 cohorts at 4 dose levels |
| Safety Endpoint | Met |
| Efficacy Observation | Restored normal cellular response to stimuli in PBMCs |
The company reported holding $12.7 million in cash and cash equivalents as of September 30, 2025, with projections to fund operations through Q3 2026, supporting the advancement of this program.
Prevention and treatment of Acute Kidney Injury (AKI) (GEM-AKI program)
Revelation Biosciences sees the GEM-AKI program as providing the shortest pathway to marketing approval by addressing an acute condition with no current therapies.
- Acute Kidney Injury (AKI) affects more than 10% of all hospitalized patients.
- AKI affects over 50% of patients in intensive care units.
- Dialysis remains the only therapeutic option for severe AKI cases.
- Revelation submitted its end-of-phase 1 meeting package to the FDA in November 2025 to discuss the regulatory pathway for AKI treatment, with a later-stage clinical study planned for 2026.
Novel therapeutic approach for severe burn patients
The company announced a new indication for Gemini in severe burn patients in May 2025, targeting infection post-severe burn (GEMINI-PBI).
This addresses a significant acute inflammatory event where controlling the immune response is critical for patient outcomes.
Addressing high unmet medical needs in inflammation-driven diseases
The broader value proposition targets the significant burden of chronic inflammation across the healthcare landscape.
| Condition/Area | Statistical Measure |
|---|---|
| Systemic Inflammation in U.S. Adults | 34.6% have systemic inflammation |
| Mortality Risk (Chronic Inflammation + Poverty) | 127% increased risk for dying from heart disease over 15 years |
| Mortality Risk (Chronic Inflammation + Poverty) | 196% increased risk for dying from cancer over 15 years |
| Clinical R&D Growth Area | Immune-mediated diseases are second only to oncology in ongoing clinical trials |
For the nine months ended September 30, 2025, Revelation Biosciences reported net cash used for operating activities of $6.3 million, down from $14.6 million for the same period in 2024, showing operational efficiency while pursuing these high-need areas.
Revelation Biosciences, Inc. (REVB) - Canvas Business Model: Customer Relationships
You're looking at how Revelation Biosciences, Inc. (REVB) manages its critical external relationships as of late 2025. For a clinical-stage company, these aren't just contacts; they are the pathways to data, funding, and ultimately, market approval. The focus is heavily weighted toward scientific and regulatory partners.
The core of their clinical execution relies on high-touch, collaborative relationships with clinical investigators and sites. This is where the rubber meets the road for their lead candidate, Gemini. For instance, the Phase 1b PRIME study, which completed dosing in July 2025, was conducted across 3 US-based clinics specializing in chronic kidney disease (CKD) care. That study involved 40 patients distributed across 5 cohorts to evaluate safety and tolerability across escalating doses.
This direct clinical interaction is complemented by rigorous scientific dialogue with Key Opinion Leaders (KOLs) to validate the mechanism of action (MOA). The data from the PRIME study showed a clear cellular effect, with peripheral blood mononuclear cells (PBMCs) isolated from patients showing significantly reduced inflammatory activity at 2, 24, and 168 hours post-dose. Furthermore, the company maintains specific collaborations, such as the one with Vanderbilt and Dr. Bohannon concerning the severe burn indication.
Regulatory engagement is paramount, which means direct engagement with the FDA and other regulatory bodies for development path agreement. As of November 20, 2025, Revelation Biosciences announced the successful submission and acceptance of its end-of-phase 1 meeting package to the FDA, with the meeting itself scheduled for later in 2025. The goal here is to secure agency input for the clinical development and regulatory approval pathway for Gemini in acute kidney injury (AKI), with plans to initiate a later-stage study in 2026.
For public shareholders and potential investors, the company maintains dedicated investor relations, though the engagement metrics reflect a specific market sentiment. The financial health context shows that as of June 30, 2025, cash and cash equivalents stood at $5.2 million. However, the company secured gross proceeds of $9.6 million from warrant inducement in September 2025, which helps fund these operational relationships. Still, the trailing twelve months Earnings Per Share (EPS) was -44.07, and institutional interest remains low, with ownership at 1.21%.
Here's a quick look at the quantitative aspects of these relationships as of late 2025:
| Relationship Focus Area | Key Metric/Data Point | Value/Amount |
| Clinical Site Collaboration (PRIME Study) | Number of US-based Clinics | 3 |
| Clinical Trial Enrollment (PRIME Study) | Total Patients Enrolled | 40 |
| Regulatory Engagement (FDA) | Status of End-of-Phase 1 Meeting | Accepted, Meeting scheduled for late 2025 |
| Scientific Validation (Cellular Readout) | Time points for PBMC analysis post-dose | 2, 24, and 168 hours |
| Investor Relations (Funding) | Gross Proceeds from Warrant Inducement (Sept 2025) | $9.6 million |
| Investor Relations (Valuation Context) | Price-to-Book Ratio (P/B) | 0.28 |
The operational cadence requires tight coordination, which you can see in the planned next steps following regulatory milestones. You're managing a lean operation where every interaction counts:
- Finalize activities for initiating later-stage study in 2026.
- Publish additional positive results from the PRIME study completed this year.
- Engage with the FDA following the end-of-phase 1 meeting scheduled for late 2025.
- Maintain collaboration with Vanderbilt on the severe burn indication.
- Manage shareholder communications following the Special Meeting on December 3, 2025.
Finance: draft 13-week cash view by Friday.
Revelation Biosciences, Inc. (REVB) - Canvas Business Model: Channels
You're looking at how Revelation Biosciences, Inc. gets its science and its financial needs out into the world. It's a mix of clinical execution, regulatory navigation, and capital market presence.
Clinical trial sites and hospitals for drug administration during studies
The PRIME Phase 1b clinical study, evaluating escalating doses of intravenously administered Gemini in patients with Stage 3 and 4 Chronic Kidney Disease (CKD), was executed across a defined set of sites. Dosing completion for this study was announced in July 2025.
- Total number of clinics enrolled in PRIME Phase 1b: 3.
- Total number of cohorts planned: 5.
- Maximum planned subjects per cohort: 8.
Scientific publications and medical conferences to disseminate data
Data dissemination channels include scientific publications and medical conferences, though specific 2025 publication counts aren't detailed here. The company expected several study data sets from the PRIME trial during Q3 2025, covering safety parameters and biomarker activity.
Direct regulatory communication channel with the U.S. FDA
The direct line to the U.S. Food and Drug Administration (FDA) is critical for advancing Gemini. Revelation Biosciences, Inc. successfully submitted its end-of-Phase 1 meeting package to the FDA on November 20, 2025. The company stated it was on track to hold this meeting later in 2025 to discuss the clinical development and regulatory approval pathway for Gemini as a treatment for acute kidney injury (AKI).
Investor relations platforms (NASDAQ, press releases) for capital market access
Access to capital markets is channeled through the NASDAQ listing and regular financial disclosures. The company reported its financial results for the three and nine months ended September 30, 2025, via a press release on November 6, 2025.
Here's a quick look at some key financial and operational data points from the reporting periods leading up to late 2025:
| Metric | Value/Date | Context |
| Stock Exchange Listing | NASDAQ (Ticker: REVB) | Primary capital market access platform. |
| Gross Proceeds from Warrant Inducement | $9.6 million | Received in September 2025. |
| Cash and Cash Equivalents | $5.2 million | As of June 30, 2025. |
| Funding Projection | Through December 2025 | Believed sufficient to fund operations as of the June 30, 2025 report. |
| Net Loss (3 Months Ended June 30, 2025) | $2.4 million | Reported net loss per share was $(7.01) basic/diluted. |
| FDA Meeting Package Submission Date | November 20, 2025 | Submission accepted by the agency. |
The company's ability to maintain its listing on NASDAQ is a key component of its investor channel strategy.
Revelation Biosciences, Inc. (REVB) - Canvas Business Model: Customer Segments
You're looking at the core groups Revelation Biosciences, Inc. (REVB) is targeting with its Gemini program as of late 2025. This isn't about the entire global market; it's about the specific patient populations and financial entities that validate their current clinical path.
The primary patient segments are defined by the indications where Gemini is in development or being prioritized. The company has explicitly focused on these areas based on clinical trial progress and perceived regulatory pathway speed.
- Patients suffering from Chronic Kidney Disease (CKD) and Acute Kidney Injury (AKI).
- Patients at risk of post-surgical infection (SSI) (e.g., colorectal surgery).
For the CKD segment, Revelation Biosciences, Inc. completed dosing of patients in the PRIME Phase 1b Clinical Study of Gemini in CKD Patients as of June 30, 2025. The GEMINI-AKI program is the primary focus for the shortest pathway to marketing approval. Furthermore, the company announced a new indication for Gemini in severe burn patients in the first quarter of 2025.
The institutional customers-hospitals and treatment centers-are the eventual end-users for the approved therapy. Revelation Biosciences, Inc. is actively engaging with the clinical community, as evidenced by the focus on severe burn units and the ongoing clinical work.
The next layer of customer segments involves entities that provide the capital to reach these patients. This is where the financial numbers become the key data points defining this segment as of the third quarter of 2025.
| Financial Segment Component | Metric | Amount as of September 30, 2025 |
| Cash Position | Cash and Cash Equivalents | $12.7 million |
| Financing Activity | Gross Proceeds from Warrant Inducement (Sept 2025) | $9.6 million |
| Financing Activity | Gross Proceeds from Public Offering (May 2025) | $4 million |
| Operating Burn Rate | Net Cash Used for Operating Activities (9 months ended Sept 30, 2025) | $6.3 million |
| Financial Runway | Projected Funding Sufficiency | Through the third quarter of 2026 |
Future pharmaceutical companies represent a potential licensing or acquisition customer segment. While specific deal values aren't public for this segment, the company's progress-including groundbreaking top-line results from the PRIME clinical study reported in November 2025-is designed to attract this group. The company is also on track to meet with the FDA later in 2025 regarding the AKI development path, which de-risks the asset for potential partners.
The institutional and retail investors are the segment funding the clinical development stage. Their commitment is reflected in the capital raised, which increased the cash balance from $6.5 million at the end of 2024 to $12.7 million by September 30, 2025. The net loss for the nine months ended September 30, 2025, was $6.4 million.
You can see the direct financial impact of investor confidence:
- Cash on hand increased by $6.2 million between December 31, 2024, and September 30, 2025.
- Net cash used for operating activities for the nine months ended September 30, 2025, was $6.3 million.
- The net loss for the three months ended September 30, 2025, was $1.9 million.
Finance: draft 13-week cash view by Friday.
Revelation Biosciences, Inc. (REVB) - Canvas Business Model: Cost Structure
You're looking at the cash burn for a clinical-stage company, and the cost structure is almost entirely driven by advancing the science.
The heavy investment in Research and Development (R&D) and clinical trial expenses is the primary drain on cash, which is typical when you're running studies like PRIME.
- Net cash used for operating activities was $6.3 million for the nine months ended September 30, 2025.
- The net loss for the same nine-month period was $6.4 million.
This cash burn is the cost of moving Gemini through the development pathway, including engaging with the FDA later in 2025 to agree on the registration path for acute kidney injury (AKI).
General and Administrative (G&A) overhead is baked into that operating cash use, covering things like legal counsel for patent prosecution and the costs associated with maintaining the NASDAQ listing. While the specific G&A dollar amount isn't explicitly broken out for the nine months ended September 30, 2025, in the available summaries, it is a component of the overall operating expense.
The costs related to manufacturing for clinical trial materials (CMO fees) and Intellectual Property maintenance are also significant, non-recurring costs that contribute to the overall negative cash flow from operations.
To give you a sense of the cash position against this burn rate, as of September 30, 2025, Revelation Biosciences had $12.7 million in cash and cash equivalents. That cash position, bolstered by the $9.6 million in gross proceeds received from warrant inducement in September 2025, is projected to fund operations through the third quarter of 2026.
Finance: draft 13-week cash view by Friday
Revelation Biosciences, Inc. (REVB) - Canvas Business Model: Revenue Streams
You're looking at the current financial lifeblood of Revelation Biosciences, Inc. (REVB) as of late 2025. For a clinical-stage company, the revenue streams are heavily weighted toward capital formation rather than product sales, which is typical at this stage of development.
The primary, most recent, and most significant source of realized income has been from financing activities designed to fund the ongoing clinical development of Gemini. This is the cash that keeps the lights on and the trials running.
| Financing Event | Date of Announcement/Closing | Gross Proceeds Amount |
|---|---|---|
| Warrant Inducement | September 2025 | $9.6 million |
| Public Offering | May 2025 | $4 million |
As of September 30, 2025, Revelation Biosciences, Inc. reported cash and cash equivalents totaling $12.7 million, which the company projected was sufficient to fund operations through the third quarter of 2026. This cash position is a direct result of these financing activities, offset by operating cash use.
Beyond the immediate equity financing, the Business Model Canvas points toward several critical, but currently unrealized, future revenue streams contingent on clinical and regulatory success:
- Potential future milestone payments from existing or future licensing agreements with pharma partners.
- Potential future royalties or profit-sharing arrangements upon commercialization of Gemini for any indication.
- Potential future product sales revenue following regulatory approval for any of its programs, including chronic kidney disease, post-surgical infection prevention, or acute kidney injury treatment.
Currently, grant funding for specific research programs appears to be a minor or non-existent component of the revenue mix, as the focus has been on the warrant inducement and public offering to support the PRIME clinical study results and FDA engagement. The company is actively working toward an agreement with the FDA on the clinical development path to registration for Gemini.
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