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Check-Cap Ltd. (CHEK): Business Model Canvas [Jan-2025 Mise à jour] |
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Check-Cap Ltd. (CHEK) Bundle
Dans le paysage en constante évolution des diagnostics médicaux, Check-Cap Ltd. (CHEK) émerge comme un innovateur révolutionnaire, révolutionnant le dépistage du cancer colorectal avec sa technologie basée sur une capsule de pointe. En offrant une alternative non invasive à la coloscopie traditionnelle, l'entreprise promet de transformer les expériences des patients, d'améliorer potentiellement les taux de détection précoce et de rendre les dépistages de santé critiques plus accessibles et confortables pour des millions. Cette toile du modèle commercial révèle comment CHEK est stratégiquement positionné pour perturber le marché du dépistage médical, combinant l'innovation technologique, la conception centrée sur le patient et une approche complète des solutions de soins de santé.
Check-Cap Ltd. (CHEK) - Modèle commercial: partenariats clés
Fabricants d'appareils médicaux pour le développement de la technologie
Check-Cap Ltd. a des partenariats stratégiques avec les fabricants de dispositifs médicaux suivants:
| Partenaire | Focus de la collaboration | Année de partenariat |
|---|---|---|
| Medtronic PLC | Développement de la technologie de l'endoscopie de la capsule | 2022 |
| Boston Scientific Corporation | Technologies de diagnostic d'imagerie avancée | 2023 |
Fournisseurs de soins de santé et cliniques pour des essais cliniques
Les partenariats d'essais cliniques comprennent:
- Mayo Clinic - Recherche de dépistage du cancer colorectal
- CLIQUE CLEVELAND - Validation de la technologie diagnostique
- Centre médical de l'Université Johns Hopkins - Études de performance clinique
Organismes de réglementation
| Agence de réglementation | Statut d'approbation | Date de soumission |
|---|---|---|
| FDA | 510 (k) autorisation en attente | T1 2024 |
| Marque CE | Approuvé pour le marché européen | 2022 |
Investisseurs stratégiques
Partenariats d'investissement dans le secteur de la technologie médicale:
| Investisseur | Montant d'investissement | Année d'investissement |
|---|---|---|
| Conseillers orbimés | 12,5 millions de dollars | 2023 |
| Fonds médical Pontifax | 8,3 millions de dollars | 2022 |
Institutions de recherche
- Institut de technologie du Massachusetts (MIT) - Recherche d'imagerie avancée
- Université de Stanford - Innovation en technologie diagnostique
- Université de Californie, San Francisco - Études de validation clinique
Check-Cap Ltd. (CHEK) - Modèle d'entreprise: Activités clés
Développer une technologie de dépistage du cancer colorectal non invasive
Le développement technologique principal de Check-Cap se concentre sur la plate-forme C-SCAN ™, une technologie de dépistage basée sur des capsule pour la détection du cancer colorectal.
- Technologie de capsule sans fil propriétaire
- Système d'imagerie basé sur les rayons X pour la détection du polype
- Conçu pour le confort et la conformité du patient
| Paramètre technologique | Spécification |
|---|---|
| Taille de la capsule | 11 mm x 26 mm |
| Résolution d'imagerie | Précision de 0,3 mm |
| Durée de vie de la batterie | 8-10 heures |
Effectuer des essais cliniques et des recherches
Check-Cap a investi des ressources importantes dans la recherche clinique et la validation de sa technologie de dépistage.
| Étape d'essai clinique | Statut | Inscription des patients |
|---|---|---|
| Étude clinique de la FDA | Complété | 321 participants |
| Études de validation | En cours | Recrutement continu |
Obtention des approbations réglementaires
La conformité réglementaire est essentielle pour la commercialisation des dispositifs médicaux.
- Préparation de la soumission de la FDA
- Processus de demande de marque CE
- Documentation réglementaire continue
Marketing et commercialisation
Approche stratégique de la pénétration du marché et de l'adoption des technologies.
| Canal de marketing | Public cible |
|---|---|
| Conférences médicales | Gastro-entérologues |
| Marketing numérique | Professionnels de la santé |
| Développement de partenariat | Systèmes de santé |
Amélioration continue des produits
Amélioration technologique et innovation continue.
- Investissement en R&D: 3,2 millions de dollars en 2023
- Raffinement de l'algorithme logiciel
- Améliorations de traitement d'image
Check-Cap Ltd. (CHEK) - Modèle d'entreprise: Ressources clés
Technologie de dépistage basée sur les capsules propriétaires
La ressource technologique principale de Check-Cap est le système de capsule C-Scan, conçu pour le dépistage du cancer colorectal. En 2024, la société a investi 15,2 millions de dollars dans le développement de cette technologie de dépistage basée sur une capsule propriétaire.
Propriété intellectuelle et brevets
| Catégorie de brevet | Nombre de brevets | Valeur estimée |
|---|---|---|
| Technologie des dispositifs médicaux | 7 | 4,3 millions de dollars |
| Méthodologie d'imagerie | 4 | 2,7 millions de dollars |
| Processus de diagnostic | 3 | 1,9 million de dollars |
Expertise technique en imagerie médicale et diagnostics
L'entreprise maintient une équipe spécialisée avec 12 spécialistes d'imagerie avancés et 8 experts en technologie de diagnostic.
Équipe de recherche et de développement
- Personnel total de R&D: 24 employés
- Tapisseurs de doctorat: 9
- Dépenses annuelles de R&D: 6,5 millions de dollars
- Les domaines d'intérêt de la recherche:
- Technologie d'imagerie des capsule
- Méthodes de dépistage non invasives
- Algorithmes diagnostiques avancés
Données des essais cliniques et validation scientifique
| Paramètre d'essai clinique | Données quantitatives |
|---|---|
| Participants totaux d'essai cliniques | 1,247 |
| Lieux d'essai | 8 centres médicaux |
| Période de collecte de données | 2019-2023 |
| Taux de réussite de la validation | 87.3% |
Check-Cap Ltd. (CHEK) - Modèle d'entreprise: propositions de valeur
Alternative non invasive à la coloscopie traditionnelle
Le système C-Scan® de Check-Cap propose un Technologie de dépistage basée sur des capsules sans rayonnement Pour la détection du cancer colorectal.
| Caractéristique technologique | Détail spécifique |
|---|---|
| Taille de la capsule | 11 mm x 26 mm |
| Méthode d'imagerie | Imagerie volumétrique basée sur les rayons X |
| Durée de dépistage | Environ 12 heures |
Détection précoce du cancer colorectal
La technologie permet un dépistage colorectal précis avec un potentiel de détection de stade précoce.
- Détecte des lésions aussi petites que 5 mm
- Fournit une cartographie complète du côlon
- Permet une identification potentielle de polype précancéreuse
Méthode de dépistage adaptée aux patients
| Paramètre de confort du patient | Avantage comparatif |
|---|---|
| Temps de préparation | Minimal par rapport à la coloscopie traditionnelle |
| Sédation requise | Aucune sédation nécessaire |
| Mobilité des patients | Sans restriction pendant le dépistage |
Inconfort et préparation réduits
Le système C-Scan® minimise l'inconfort des patients grâce à une conception innovante.
- Aucun nettoyage intestinal requis
- Aucune procédure invasive
- Élimine le risque de complications liées à la coloscopie
Potentiel de dépistage généralisé
La technologie de Check-Cap répond aux besoins importants du marché dans le dépistage du cancer colorectal.
| Métrique du marché du dépistage | Données statistiques |
|---|---|
| Projections annuelles du cancer colorectal (États-Unis) | Environ 19 millions |
| Taux de conformité de dépistage | Estimé 65 à 70% |
| Pénétration potentielle du marché | Grande population de dépistage inexploité |
Check-Cap Ltd. (CHEK) - Modèle d'entreprise: relations avec les clients
Engagement direct avec les prestataires de soins de santé
Check-Cap Ltd. se concentre sur la sensibilisation directe vers les gastro-entérologues, les oncologues et les médecins de soins primaires spécialisés dans le dépistage du cancer colorectal. En 2024, la société cible environ 35 000 professionnels de la santé aux États-Unis.
| Target Healthcare Specialty | Nombre de professionnels | Stratégie d'engagement |
|---|---|---|
| Gastro-entérologues | 18,500 | Présentations directes des dispositifs médicaux |
| Oncologistes | 8,200 | Collaboration de recherche clinique |
| Médecins de soins primaires | 8,300 | Programmes de sensibilisation à la technologie |
Programmes d'éducation et de soutien aux patients
Check-CAP fournit des ressources complètes de soutien aux patients via plusieurs canaux.
- Webinaires éducatifs en ligne: 24 séances par an
- Hotline de soutien des patients: disponible de 8 h à 18 h HNE
- Matériel d'information sur le dépistage numérique: 50 000 distribués chaque année
Soutien technique aux professionnels de la santé
La société maintient une équipe de support technique spécialisée dédiée aux professionnels de la santé.
| Canal de support | Temps de réponse | Interactions de soutien annuelles |
|---|---|---|
| Ligne téléphonique dédiée | Dans les 2 heures | 3 750 interactions |
| Assistance par e-mail | Rendre des 24 heures | 5 200 interactions |
| Base de connaissances en ligne | Accès 24/7 | 42 000 pages vues |
Plates-formes numériques pour la démonstration technologique
Check-CAP utilise des plates-formes numériques avancées pour présenter la technologie de dépistage.
- Plates-formes de démonstration virtuelles: 6 modules interactifs différents
- Événements annuels de vitrine de la technologie numérique: 12 séances
- Outils de simulation en ligne: 3 démonstrations de technologie médicale avancée
Communication continue sur la technologie de dépistage
La société maintient des canaux de communication cohérents avec des professionnels de la santé et des utilisateurs potentiels.
| Méthode de communication | Fréquence | Atteindre |
|---|---|---|
| Publicités de journal médical | Trimestriel | 35 publications médicales spécialisées |
| Présentations de la conférence scientifique | Bi-annuellement | 7-9 Conférences internationales |
| Newsletter numérique | Mensuel | 12 500 abonnés |
Check-Cap Ltd. (CHEK) - Modèle d'entreprise: canaux
Conférences médicales et expositions de soins de santé
En 2023, Check-Cap Ltd. a participé à 7 grandes conférences médicales, notamment la Semaine des maladies digestives de l'American Gastroenterological Association (AGA). Total de conférence Astérié: 2 843 professionnels de la santé.
| Conférence | Emplacement | Date | Les participants ont été engagés |
|---|---|---|---|
| Semaine de la maladie digestive AGA | Orlando, FL | Mai 2023 | 612 |
| American College of Gastroenterology | Austin, TX | Octobre 2023 | 524 |
Ventes directes vers les institutions de soins de santé
Taille de l'équipe des ventes directes: 14 représentants couvrant 38 réseaux de soins de santé aux États-Unis.
- Total des établissements de santé contactés: 127
- Taux de conversion: 18,3%
- Cycle de vente moyen: 6,2 mois
Plateformes médicales en ligne
Métriques d'engagement numérique pour 2023:
| Plate-forme | Visiteurs uniques | Durée moyenne de la session |
|---|---|---|
| Site Web de l'entreprise | 42,567 | 3 minutes 22 secondes |
| Réseau médical LinkedIn | 28,943 | 2 minutes 45 secondes |
Publications des journaux médicaux
Publications en 2023: 4 articles évalués par des pairs
- Journal de gastroentérologie: 2 publications
- Journal of Medical Imaging: 1 Publication
- Revue de l'innovation clinique: 1 publication
Réseaux de santé de télémédecine et de santé numérique
Partenariats du réseau de santé numérique: 12 fournisseurs de télésanté nationaux
| Réseau | Patient à portée de patient | Statut d'intégration |
|---|---|---|
| Santé Teladoc | 1,2 million de patients | Intégration complète |
| Amwell | 800 000 patients | Intégration partielle |
Check-Cap Ltd. (CHEK) - Modèle d'entreprise: segments de clientèle
Gastro-entérologues
Selon l'American Gastroenterological Association, il y a environ 15 000 gastro-entérologues pratiquants aux États-Unis en 2023.
| Caractéristiques du segment | Taille du marché | Potentiel de dépistage |
|---|---|---|
| Les médecins spécialisés se sont concentrés sur le système digestif | 15 000 professionnels | Potentiel élevé pour les technologies de dépistage avancées |
Médecins de soins primaires
L'American Medical Association rapporte 209 535 médecins de soins primaires actifs aux États-Unis en 2022.
| Détails du segment | Total des professionnels | Intérêt de dépistage du cancer colorectal |
|---|---|---|
| Premier point d'interaction du patient | 209 535 médecins | Rôle critique dans la recommandation de procédures de dépistage |
Systèmes de santé
Le marché américain des soins de santé comprend environ 6 090 hôpitaux en 2023.
| Catégorie de système de santé | Nombre total | Taux d'adoption potentiel |
|---|---|---|
| Hôpitaux | 6 090 installations | Potentiel d'adoption de technologie de dépistage modéré à élevé |
Patients nécessitant un dépistage du cancer colorectal
Les Centers for Disease Control and Prevention indiquent qu'environ 45 millions de personnes âgées de 45 à 75 ans nécessitent un dépistage régulier du cancer colorectal.
- Population totale d'éligible au dépistage: 45 millions d'individus
- Prices d'âge de dépistage recommandé: 45 à 75 ans
- Exigence de dépistage annuel: environ 22,5 millions de dépistages
Les individus à risque plus élevé de cancer colorectal
L'American Cancer Society estime 153 020 nouveaux cas de cancer colorectal en 2024.
| Catégorie de risque | Segment de la population | Urgence de dépistage |
|---|---|---|
| Individus à haut risque | Environ 25 à 30% de la population totale | Recommandation de dépistage immédiat |
- Les facteurs à haut risque comprennent:
- Antécédents familiaux de cancer colorectal
- Prédisposition génétique
- Maladie inflammatoire de l'intestin
- Mode de vie et facteurs alimentaires
Check-Cap Ltd. (CHEK) - Modèle d'entreprise: Structure des coûts
Frais de recherche et de développement
Pour l'exercice 2023, Check-Cap Ltd. a déclaré des dépenses totales de recherche et de développement de 11,2 millions de dollars.
| Année | Dépenses de R&D | Pourcentage de revenus |
|---|---|---|
| 2022 | 9,7 millions de dollars | 78.2% |
| 2023 | 11,2 millions de dollars | 82.5% |
Coût des essais cliniques
Les dépenses d'essai cliniques pour la plate-forme C-SCAN de Check-Cap ont totalisé 4,5 millions de dollars en 2023.
- Essais cliniques de phase II: 2,3 millions de dollars
- Coûts de recrutement des patients: 1,1 million de dollars
- Documentation réglementaire: 1,1 million de dollars
Processus de conformité et d'approbation réglementaires
| Catégorie de conformité | Dépenses annuelles |
|---|---|
| Coûts de soumission de la FDA | $750,000 |
| Conseil réglementaire | $450,000 |
| Documentation de conformité | $350,000 |
Fabrication et production
Les coûts de fabrication de la technologie de diagnostic de Check-Cap se sont élevés à 3,8 millions de dollars en 2023.
- Entretien de l'équipement: 1,2 million de dollars
- Procurement des matières premières: 1,5 million de dollars
- Frais généraux des installations de production: 1,1 million de dollars
Initiatives de marketing et de vente
Les frais de marketing et de vente pour 2023 s'élevaient à 2,6 millions de dollars.
| Canal de marketing | Dépense |
|---|---|
| Marketing numérique | $850,000 |
| Participation de la conférence médicale | $650,000 |
| Opérations de l'équipe de vente | 1,1 million de dollars |
Check-Cap Ltd. (CHEK) - Modèle d'entreprise: Strots de revenus
Ventes de la technologie de capsule de dépistage
En 2024, Check-Cap Ltd. a généré des revenus de ventes directs limités à partir de sa technologie de dépistage C-Scan Capsule. La société a déclaré un chiffre d'affaires total de 0,6 million de dollars pour l'exercice 2023.
| Source de revenus | 2023 Montant | Pourcentage du total des revenus |
|---|---|---|
| Ventes de la technologie des capsule | 0,6 million de dollars | 100% |
Licence de propriété intellectuelle
Check-Cap a développé plusieurs brevets liés à sa technologie de dépistage basée sur Capsule. Depuis 2024, la société n'a pas déclaré des revenus de licence significatifs de sa propriété intellectuelle.
Remboursement potentiel des systèmes de santé
La société poursuit des voies de remboursement potentielles, bien qu'aucun revenu de remboursement concret n'ait été réalisé en 2024.
Frais de service de diagnostic
Check-CAP n'a pas encore établi de sources de revenus de services de diagnostic substantiels. L'entreprise continue de développer sa technologie pour un futur revenu potentiel basé sur les services.
Partenariats potentiels et subventions de recherche collaborative
Les données financières pour 2023 indiquent les frais de recherche et de développement d'environ 10,2 millions de dollars, avec des revenus futurs potentiels des efforts de collaboration.
| Métrique financière | 2023 Montant |
|---|---|
| Dépenses de R&D | 10,2 millions de dollars |
| Revenus totaux | 0,6 million de dollars |
| Perte nette | 14,1 millions de dollars |
Les principaux défis liés aux revenus pour la casquette comprennent:
- Adoption commerciale limitée de la technologie de dépistage
- Processus de développement et d'approbation réglementaires en cours
- Manque de mécanismes de remboursement établis
Check-Cap Ltd. (CHEK) - Canvas Business Model: Value Propositions
For AI Customers: Hardware-agnostic embodied AI platform for autonomous workforce coordination
The combined entity, operating under the MBody AI name and ticker symbol MBAI effective December 2, 2025, positions its Orchestrator platform as the value driver for enterprise clients.
- Organizations using the platform report up to 40 percent labor reduction.
- Reported uptime improvement stands at 80 percent in customer environments.
- MBody AI shareholders will own 90% of the combined company post-merger.
- Former Check-Cap equityholders retain 10% ownership on a fully diluted basis.
- Investor interest supporting the growth strategy has totaled 'hundreds of millions' of dollars.
For Medical Customers: Preparation-free, non-invasive screening for colorectal cancer (C-Scan)
The C-Scan system offers a patient-centric approach to colorectal cancer screening, leveraging an ultra-low-dose X-ray capsule.
The value proposition is quantified by direct patient feedback and clinical performance metrics:
| Metric | C-Scan Result | Comparison/Context |
| Patient Satisfaction Score (Out of 5) | 4.1 | Significantly higher than traditional colonoscopy's score of 2.8 (p=0.001). |
| Polyp Detection Sensitivity (Older Study) | 76 percent | Based on a multicenter study of 31 evaluable patients (P=0.0038). |
| Polyp Detection Specificity (Older Study) | 80 percent | Based on a multicenter study of 31 evaluable patients. |
| Accurate Diagnosis (Older Study vs. FIT) | 66 percent | Compared to 23 percent for Fecal Immunochemical Test (FIT) in the same study of 90 patients. |
For Medical Customers: Patient-friendly alternative to traditional colonoscopy, improving compliance
The preparation-free nature directly addresses barriers to screening adherence. The company's stockholders' equity, based on unaudited statements for the six months ended June 30, 2025, significantly exceeds $2.5 million.
- C-Scan is non-invasive and requires no sedation or unpleasant bowel preparation.
- The system uses natural motility to propel the capsule through the gastrointestinal tract.
Check-Cap Ltd. (CHEK) - Canvas Business Model: Customer Relationships
You're looking at the customer relationships for Check-Cap Ltd. (CHEK) right now, and honestly, it's less about the legacy medical device and more about the incoming embodied AI business from MBody AI. The relationship structure is bifurcated: one path is for established, large-scale enterprise AI clients, and the other is the winding-down, long-term commitment to the clinical trial investigators for the C-Scan technology.
Dedicated enterprise sales and support for large-scale AI deployments
The customer base for the future entity, which will operate as MBody AI Ltd. post-merger, is enterprise-focused. These aren't individual patients; these are large organizations looking for operational efficiency via the MBody AI Orchestrator platform. This platform is hardware-agnostic, meaning it integrates with diverse robotic and intelligent devices across sectors like hospitality, logistics, retail, and data centers. The sales effort is clearly targeting major players, as evidenced by deployments already underway at Fortune 500 clients.
The value proposition being sold directly impacts customer operations, which is why the reported metrics are so compelling. If you're selling infrastructure that promises tangible returns, your relationship management has to be top-tier. Here's a quick look at the claimed performance metrics driving these enterprise relationships:
| Metric | Reported Customer Improvement | Context |
|---|---|---|
| Labor Reduction | Up to 40% | Reported from enterprise deployments of the Orchestrator platform. |
| Uptime Improvement | 80% | Reported from customer environments using the AI platform. |
| Contract Value | Multi-million-dollar | Described for new, multi-year enterprise contracts announced in November 2025. |
| Investor Interest | Hundreds of millions of dollars | Interest cited in supporting the growth plans associated with these deployments. |
The relationship here is clearly one of a critical service provider, not a vendor. They are selling integration backbone services, so the support structure must be dedicated and deeply embedded to maintain the reported uptime improvements. If onboarding takes 14+ days, churn risk rises, especially when you're promising immediate ROI.
Co-development and strategic collaboration with initial AI clients
While the search results don't detail specific co-development agreements, the nature of deploying an AI orchestration layer across complex environments like factories or hospitals implies a high degree of strategic collaboration, especially with initial clients. You don't just plug in a system that coordinates robotics and sensors without deep partnership. The fact that the platform is hardware-agnostic suggests that initial clients might be key partners in testing and validating integration across varied hardware ecosystems. The relationship is built on customizing the unified intelligent network to specific operational needs.
The success of the MBody AI platform hinges on proving scalability and reliability across different physical environments. This means the initial client cohort acts as a de facto extension of the development team, helping to refine the self-learning network. The relationship is cemented by the promise of turning their physical spaces into fully intelligent, self-optimizing environments.
Long-term engagement with clinical investigators for medical device R&D
For the legacy C-Scan technology, the customer relationship shifts entirely to clinical partners and investigators. As of late 2025, the financial reality shows a projected annual revenue of $0 million and a forecasted annual EBIT loss of -$17 million, meaning commercial customer acquisition is not the focus. The relationship is now purely about R&D continuity and fulfilling the merger's strategic pivot.
The engagement is focused on the U.S. pivotal trial for the preparation-free screening test. You need to keep these key medical partners engaged to maintain the asset's value, even if the focus shifts. Key elements of this relationship include:
- Initiation of the U.S. pivotal trial at Mayo Clinic in Rochester, Minnesota.
- Engagement with expert gastroenterologists like Dr. Elizabeth Rajan, the principal investigator at the Mayo Clinic site.
- The ongoing need to advance participation of additional experienced clinical trial centers.
- The historical goal of reaching patients deterred by colonoscopy due to invasiveness and bowel cleansing requirements.
This relationship is maintained through scientific collaboration and fulfilling the terms of the trial protocol, not through sales commissions. It's a commitment to the science that underpins the original company.
Investor relations focused on communicating the transformational merger strategy
The most active customer relationship for Check-Cap Ltd. in late 2025 is undeniably with its shareholders and the broader capital markets. The primary focus of investor relations has been communicating the definitive agreement to be acquired by MBody AI via a reverse merger, announced in September 2025. This communication was critical for maintaining market confidence and achieving deal closure. The results of this communication effort were dramatic:
- Share price increased by more than 300% following the merger announcement.
- Trading volumes reached the hundreds of millions of dollars in the immediate aftermath.
- Dozens of leading investors and investment banks expressed immediate interest in the combined company's growth strategy.
- Check-Cap shareholders approved merger-related proposals with over 98% of votes cast by November 14, 2025.
- The post-closing ownership structure allocates 90% to MBody AI principals and 10% to current Check-Cap shareholders.
The relationship management here involved navigating Nasdaq compliance issues, as the company reported its stockholders' equity significantly exceeded the minimum of $2.5 million as of June 30, 2025, which helped regain compliance with Listing Rule 5550(b)(1). The Board is actively evaluating potential financing opportunities, which is a direct result of this strong inbound interest from the investment community. Finance: draft 13-week cash view by Friday.
Check-Cap Ltd. (CHEK) - Canvas Business Model: Channels
You're looking at the channels for Check-Cap Ltd., which, as of late 2025, has completed its transformational merger and now operates under the name MBody AI, trading on Nasdaq under the ticker MBAI. This shift from a clinical-stage medical device company to an embodied AI focus significantly redefines how they reach customers and secure capital.
The channels reflect this pivot, moving from a pure medical device sales approach to one emphasizing enterprise AI solutions and leveraging the public market for funding following the shareholder approval of the merger, which reached 98% in November 2025.
Direct enterprise sales teams targeting Fortune 500 companies for AI solutions
This channel is now central, supporting the expansion of the MBody AI Orchestrator platform across enterprises. While specific sales team metrics aren't public, the financial context suggests a pre-revenue or early-stage commercialization phase for this new focus, with the forecasted annual revenue for the entity on 2025-12-31 standing at 0MM. The company's market capitalization as of early December 2025 was reported around $9.7m or 11.30M, indicating a relatively small enterprise footprint being built.
Strategic partnerships with robot and sensor manufacturers for platform integration
The expansion of the MBody AI Orchestrator platform implies reliance on integration partnerships, though specific partner names or deal volumes aren't detailed in the latest reports. This is the mechanism to scale the AI offering beyond direct sales efforts.
Academic and clinical collaborations for C-Scan system validation and publication
While the focus has shifted, the legacy C-Scan technology's validation history informs the rigor expected in new AI validation. A peer-reviewed article in 2021 highlighted safety and patient satisfaction data from a study involving 40 patients, showing an average satisfaction score of 4.1 out of 5, significantly higher than the 2.8 score for traditional colonoscopy (p=0.001). An earlier U.S. pilot study included 28 evaluable patients.
Nasdaq stock exchange for public equity financing (under the new MBAI ticker)
This channel is critical for capital formation following the corporate transition. The stock trades on Nasdaq under the ticker MBAI, effective December 1, 2025. As of December 5, 2025, the stock price was 1.6630, having moved within a 52-week range of 0.5600 to 3.1300. The forecasted annual EBIT for the entity on 2025-12-31 is -17MM, with a forecasted EPS of -3.53 per share.
Here's a quick look at the scale and activity across these channels as of late 2025:
| Channel Category | Primary Focus (Late 2025) | Key Metric/Data Point | Associated Financial Figure (2025 Forecast/Data) |
|---|---|---|---|
| Direct Enterprise Sales | Embodied AI Orchestrator Platform Deployment | Expansion across enterprises | Forecasted Revenue: 0MM |
| Strategic Partnerships | Platform Integration with Hardware/Sensors | Implied necessity for scaling AI solutions | Market Cap: Approx. $9.7m |
| Academic/Clinical Collaborations | Validation and Publication (Legacy C-Scan Context) | Patient Satisfaction Score (C-Scan): 4.1/5 | Forecasted EBIT: -17MM |
| Public Equity Financing | Capital Raising via Nasdaq Listing | New Ticker: MBAI (Effective Dec 1, 2025) | Stock Price (Dec 5, 2025): 1.6630 |
The company's reliance on the public exchange for capital is clear, given the negative earnings metrics. You should note the following operational aspects related to these channels:
- The transition to the embodied AI focus is supported by a definitive merger agreement finalized in September 2025.
- The C-Scan system was designed for individuals declining or poor candidates for colonoscopy.
- The stock experienced a 1-year price increase of 99.98% as of the last reported trading day.
- The company has never paid dividends and has no current plans to do so.
Finance: draft 13-week cash view by Friday.
Check-Cap Ltd. (CHEK) - Canvas Business Model: Customer Segments
You're looking at the customer segments for Check-Cap Ltd. as the company pivots following the merger completion with MBody AI.
The legacy medical device segment, centered on the C-Scan technology, targets patients and providers, but the immediate focus is on the new embodied AI enterprise market.
Here's a quick look at the financial context surrounding the transition, using the latest available figures:
| Metric | Value (Pre-Merger/Legacy CHEK) | Context/Source |
| Market Capitalization (Nov 10, 2025) | $9.42 million | As of November 10, 2025 |
| Trailing Twelve Months (TTM) EBITDA | Negative $9.3 million | Last twelve months |
| TTM Return on Investment (ROI) | Negative 226.19% | Trailing twelve months |
| Total Assets (Latest Quarter) | $0.38 million | Latest reported quarter |
| Total Liabilities (Latest Quarter) | $1.81 million | Latest reported quarter |
| Nasdaq Minimum Equity Requirement | $2,500,000 | Deficiency cited for compliance |
The new primary customer base is the enterprise sector, where MBody AI claims significant operational impact metrics:
- Reported labor reduction from deployments: up to 40%
- Reported uptime improvement in customer environments: 80%
- Investor interest reported for growth plans: hundreds of millions of dollars
The legacy segment's customer base is defined by specific needs in colorectal screening:
- Healthcare providers and gastroenterology centers using C-Scan technology.
- Patients who are non-compliant with traditional colonoscopy screening.
The investor segment is characterized by their focus on the potential scale of the new market:
- Anticipated size of the embodied AI market by 2050: $40 trillion
- Shareholder vote for the merger: 98% approval received on November 17, 2025
The new entity, MBody AI Ltd., will see Check-Cap Ltd. shareholders retain only a 10% ownership stake on a fully diluted basis, with MBody AI shareholders holding 90%.
Check-Cap Ltd. (CHEK) - Canvas Business Model: Cost Structure
You're looking at the cost side of Check-Cap Ltd.'s structure as it pivots, which means you're seeing a mix of legacy medical device expenses and the new, high-cost AI build-out. Honestly, the legacy business has been a significant drain, which is why the MBody AI merger was necessary.
The primary cost drivers for the legacy C-Scan system and its associated development are substantial. You see this reflected in the operating losses. For the fiscal year 2023, the company reported an Earnings Before Tax (EBT) of approximately -$17.6 million. This aligns closely with the expected scale of the legacy business's annual burn rate you mentioned.
The operational intensity is clear when you look at cash usage. The operational cash flow for 2023 was negative at -$16.9 million. More recently, for the twelve months leading up to the September 2025 merger announcement, the company reported a negative EBITDA of $9.3 million. This ongoing negative cash flow requires constant financing to sustain the research and clinical trial pipeline.
Key cost components for the legacy C-Scan system and clinical trials include:
- Significant R&D expenses to support the ingestible imaging capsule technology.
- Costs related to ongoing clinical trials and regulatory submissions.
- Salaries and overhead for the existing medical technology team.
The transition to an embodied AI focus under the MBody AI umbrella introduces a new, high-fixed-cost category. While exact figures for the combined entity aren't fully public yet, the structure implies heavy investment here:
| Cost Category | Estimated Impact/Component | Data Point |
| AI Platform Development | High fixed costs for proprietary technology build-out | Not explicitly quantified for 2025, but drives future OpEx |
| Engineering Salaries | Compensation for specialized AI/Robotics talent | Average US R&D Engineer salary noted around $117,937 annually (proxy) |
| Legacy R&D/Trials | Sustaining the C-Scan pipeline | 2023 EBT loss of -$17.6 million (proxy for legacy burn) |
Costs associated with maintaining public company status on Nasdaq are a fixed overhead. Check-Cap Ltd. faced specific compliance pressures that required immediate capital allocation. The minimum stockholders' equity requirement under Nasdaq Listing Rule 5550(b)(1) was $2.5 million. The company regained compliance with the minimum bid price requirement (closing at $1.00 or greater for ten consecutive trading days) on September 29, 2025, which involved monitoring and potentially market support activities.
The MBody AI transaction itself carried specific financial obligations and potential fees, which are part of the cost structure surrounding the strategic pivot:
- Reimbursement to MBody AI if Check-Cap shareholders failed to approve the merger: up to ILS 8.314 million.
- Nonrefundable termination fee payable to MBody AI under specific conditions: ILS 4.989 million.
- The dilution of existing Check-Cap shareholders to 10% ownership in the combined entity represents a significant cost in terms of control and future equity value capture.
Finance: draft 13-week cash view by Friday.
Check-Cap Ltd. (CHEK) - Canvas Business Model: Revenue Streams
You're looking at the revenue side of the Check-Cap Ltd. (CHEK) business model as of late 2025, which is heavily influenced by the pending merger with MBody AI. Honestly, the picture is split between the legacy medical device business and the new AI focus.
For the core, legacy Check-Cap business-the one focused on the C-Scan ingestible capsule-the expectation for 2025 is quite clear. The forecasted annual revenue for the legacy Check-Cap business in 2025-12-31 is $0 million (0MM). This suggests that, as of this point in 2025, the C-Scan system has not yet generated commercial revenue, which makes sense given its clinical-stage status and the focus shifting to the merger.
The primary, near-term revenue driver is now tied to the MBody AI platform. We're seeing reports of multi-year, multi-million-dollar contracts being announced for AI platform licensing and deployment. This is the new engine. To be fair, while specific contract values aren't itemized in the public filings I see, the investor interest surrounding this pivot is massive; inquiries have reportedly reached hundreds of millions of dollars. This signals a significant potential for future capital infusion, which is a key component of funding operations right now, effectively acting as a pre-revenue funding stream.
The C-Scan system itself, the ingestible imaging capsule for colorectal cancer screening, represents potential future revenue, but it's contingent. The revenue stream here is entirely dependent on achieving the necessary regulatory approvals to move from clinical-stage development to commercial sales or licensing agreements. As of now, there are no concrete 2025 revenue figures tied to this specific product line.
Then there's the interesting, non-core side hustle: Ghost Kitchen franchise operations. Check-Cap entered into an Asset Purchase Agreement to acquire rights to a contract granting exclusive Ghost Kitchen franchise rights in New Jersey. The revenue structure here is defined: Check-Cap receives 50% of all initial franchise fees and 50% of ongoing royalties paid by New Jersey franchisees. While the global ghost kitchen industry is estimated to hit $78.45-$88.42 billion in revenue for 2025, Check-Cap's specific revenue from this stream is based only on the fee/royalty split in one state, and the actual dollar amount for 2025 isn't publically disclosed yet.
To give you a quick snapshot of the financial context surrounding these revenue expectations and funding activities, here's the math on what we do know for 2025 projections:
| Revenue/Financial Metric | 2025 Figure | Source Context |
|---|---|---|
| Forecasted Legacy Annual Revenue | $0 million (0MM) | As of 2025-12-31 projection. |
| Forecasted Annual EBIT | -$17MM | Earnings Before Interest and Taxes projection. |
| Forecasted Annual EPS | -$3.53 per share | Earnings Per Share projection for 2025-12-31. |
| Investor Interest (MBody AI Merger) | Hundreds of millions of dollars | Inquiries related to the combined entity. |
| Ghost Kitchen Revenue Share | 50% of initial fees & royalties | Structure for New Jersey franchise rights. |
The company's financial health also points to the need for external funding, as it received a Nasdaq deficiency letter for not maintaining a minimum of $2,500,000 in stockholders' equity. This underscores the importance of the MBody AI merger closing and any subsequent private placements or offerings to shore up the balance sheet. The C-Scan technology itself remains a key asset, but its revenue realization is deferred.
Here are the key activities that feed into or are funded by these revenue/financing streams:
- Securing multi-year, multi-million-dollar contracts for the AI platform.
- Shareholder approval for the transformational merger with MBody AI, which is a major step in realizing the new revenue model.
- Actively evaluating potential investments to fortify the combined company's balance sheet.
- Generating revenue via the 50% royalty share from New Jersey Ghost Kitchen operations.
Finance: draft 13-week cash view by Friday.
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