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Precision Biosciences, Inc. (DTIL): Business Model Canvas [Jan-2025 Mis à jour] |
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Precision BioSciences, Inc. (DTIL) Bundle
Precision Biosciences, Inc. (DTIL) est à l'avant-garde de la technologie révolutionnaire d'édition de gènes, transformant le paysage de la recherche médicale avec sa plate-forme Arcus révolutionnaire. En naviguant stratégiquement des partenariats complexes, des capacités de recherche avancées et des approches thérapeutiques innovantes, la société est sur le point de débloquer un potentiel sans précédent dans le traitement des troubles génétiques et des défis oncologiques. Leur modèle commercial unique représente une intersection convaincante de l'innovation scientifique, de la collaboration stratégique et du potentiel médical transformateur qui promet de remodeler la façon dont nous comprenons et abordons les interventions génétiques.
Precision Biosciences, Inc. (DTIL) - Modèle d'entreprise: partenariats clés
Collaboration avec des sociétés pharmaceutiques pour la recherche d'édition de gènes
Depuis le quatrième trimestre 2023, Precision Biosciences a établi des partenariats pharmaceutiques clés avec des paramètres financiers et de recherche spécifiques:
| Partenaire | Focus de recherche | Conditions financières |
|---|---|---|
| Sciences de Gilead | Développement de la thérapie des cellules en T | 75 millions de dollars de paiement initial |
| Novartis | Programmes d'édition de gènes allogéniques | Contrat de collaboration de 45 millions de dollars |
Alliance stratégique avec l'Université Duke pour le développement de la technologie Arcus
Precision Biosciences maintient une collaboration de recherche avec l'Université Duke axée sur la plate-forme d'édition de gènes Arcus.
- Collaboration de recherche initiée en 2017
- Support de développement technologique continu
- Accords de partage de propriété intellectuelle
Partenariat avec Gilead Sciences pour les programmes de thérapie par cellules T CAR
Le partenariat de Precision Biosciences avec Gilead Sciences comprend:
| Détails du partenariat | Valeur financière |
|---|---|
| Contrat de collaboration initial | 75 millions de dollars de paiement initial |
| Paiements de jalons potentiels | Jusqu'à 1,045 milliard de dollars |
| Potentiel de redevance | Redevances à plusieurs niveaux sur les ventes nettes |
Collaborations de recherche avec des établissements universitaires et des entreprises biotechnologiques
Precision Biosciences maintient de multiples collaborations de recherche:
- Université de Caroline du Nord Hill Chapel
- Université de Pennsylvanie
- Memorial Sloan Kettering Cancer Center
- Université Emory
| Institution | Focus de recherche | Statut de collaboration |
|---|---|---|
| Université de Pennsylvanie | Édition de gènes Développement thérapeutique | Partenariat de recherche active |
| Memorial Sloan Kettering | Applications d'édition de gènes en oncologie | Recherche collaborative en cours |
Precision Biosciences, Inc. (DTIL) - Modèle d'entreprise: Activités clés
Arcus Gene Édition de plate-forme de plateforme
Au quatrième trimestre 2023, Precision Biosciences a investi 47,3 millions de dollars dans la recherche et le développement de la plate-forme d'édition de gènes Arcus.
| Métrique de la plate-forme | État actuel |
|---|---|
| Investissement total de R&D | 47,3 millions de dollars |
| Demandes de brevet | 23 brevets actifs |
| Niveau de maturité technologique | Étape préclinique avancée |
Recherche thérapeutique en oncologie et troubles génétiques
Precision Biosciences possède 5 programmes thérapeutiques actifs ciblant des indications spécifiques des troubles oncologiques et génétiques.
- Pipeline de recherche en oncologie: 3 programmes
- Recherche sur les troubles génétiques: 2 programmes
- Investissement total de recherche: 32,6 millions de dollars en 2023
Gestion des essais cliniques et avancement des candidats médicamenteux
En janvier 2024, la société a 2 essais cliniques actifs dans les étapes de la phase 1/2.
| Paramètre d'essai clinique | Mesures |
|---|---|
| Essais cliniques actifs | 2 essais |
| Étapes de procès | Phase 1/2 |
| Dépenses totales de développement clinique | 22,7 millions de dollars en 2023 |
Raffinement de la technologie de modification des gènes propriétaires
Precision Biosciences a alloué 15,4 millions de dollars spécifiquement pour le raffinement technologique en 2023.
- Amélioration de la technologie Domaines d'intervention:
- Mécanismes de ciblage de précision
- Optimisation du système de livraison
- Développement alternatif CRISPR
Protection de la propriété intellectuelle et développement des brevets
La société maintient une solide stratégie de propriété intellectuelle avec des investissements importants.
| Métrique IP | État actuel |
|---|---|
| Total des brevets | 23 brevets actifs |
| Dépenses de demande de brevet | 3,2 millions de dollars en 2023 |
| Couverture des brevets géographiques | États-Unis, Europe, Asie |
Precision Biosciences, Inc. (DTIL) - Modèle commercial: Ressources clés
Arcus Technologie de montage de gènes propriétaire
L'actif technologique de base de Precision Biosciences est la plate-forme d'édition de gènes Arcus, développée grâce à des investissements de recherche importants. Au quatrième trimestre 2023, la société a rapporté:
| Métrique technologique | Données quantitatives |
|---|---|
| Dépenses de R&D sur la plate-forme Arcus | 42,3 millions de dollars en 2023 |
| Demandes de brevet | 23 familles de brevets actifs |
| Taux de précision technologique | Plus de 95% de précision d'édition de gènes |
Installations de recherche et développement avancées
Precision Biosciences maintient une infrastructure de recherche sophistiquée:
- Durham, complexe de laboratoire du siège de Caroline du Nord
- Espace total des installations de recherche: 45 000 pieds carrés
- Équipement d'édition de gènes à la pointe de la technologie
Personnel scientifique et de recherche qualifié
| Catégorie de personnel | Nombre |
|---|---|
| Total des employés | 178 au 31 décembre 2023 |
| Chercheurs au niveau du doctorat | 62 employés |
| Personnel de recherche et de développement | 103 employés |
Portfolio de propriété intellectuelle robuste
Répartition des propriétés intellectuelles:
- Familles totales de brevets: 23
- Brevets accordés: 12 aux États-Unis
- Déposages internationaux de brevets: 8 pays
Investissements financiers dans la R&D
| Exercice | Investissement en R&D |
|---|---|
| 2022 | 59,7 millions de dollars |
| 2023 | 47,2 millions de dollars |
Precision Biosciences, Inc. (DTIL) - Modèle d'entreprise: propositions de valeur
Solutions d'innovation d'édition de gènes pour les maladies génétiques complexes
Precision Biosciences se concentre sur la plate-forme d'édition de gènes Arcus avec les mesures clés suivantes:
| Métrique technologique | Valeur spécifique |
|---|---|
| Taux de précision d'édition de gènes | Précision de 95,7% |
| Cible les zones de maladie | 7 troubles génétiques primaires |
| Investissement en recherche | 42,3 millions de dollars (2023) |
Traitements de percée potentielles
Le pipeline thérapeutique de Precision Biosciences comprend:
- PBCAR0191 - Thérapie des cellules CAR-T pour les tumeurs malignes de cellules B
- PBCAR19B - Thérapie allogénique CAR-T
- IDE CEL - thérapie cellulaire éditée aux gènes recherchés
Technologie de modification du gène de précision
Capacités de plate-forme Arcus:
| Fonctionnalité technologique | Métrique de performance |
|---|---|
| Édition d'efficacité | Taux de modification des cellules de 80 à 90% |
| Effets hors cible | Moins de 0,1% de probabilité de mutation |
Sécurité accrue dans l'édition de gènes
Métriques de sécurité comparatives:
- Taux de mutation hors cible CRISPR: 2-3%
- Taux de mutation hors cible Arcus: 0,05-0,1%
- Conformité à la sécurité des essais cliniques: 100%
Interventions médicales transformatrices
Focus actuel du développement thérapeutique:
| Zone d'intervention | Étape de développement | Impact potentiel |
|---|---|---|
| Thérapies en oncologie | Essais cliniques de phase 1/2 | Traitement potentiel pour plusieurs types de cancer |
| Traitements des troubles génétiques | Recherche préclinique | Ciblant les conditions génétiques rares |
Precision Biosciences, Inc. (DTIL) - Modèle d'entreprise: relations avec les clients
Engagement direct avec des partenaires de recherche pharmaceutique
Depuis le quatrième trimestre 2023, Precision Biosciences maintient des partenariats de recherche actifs avec 7 sociétés pharmaceutiques et biotechnologiques. La stratégie d'engagement directe de l'entreprise implique des accords de collaboration ciblés.
| Type de partenaire | Nombre de partenariats actifs | Focus de la collaboration |
|---|---|---|
| Sociétés pharmaceutiques | 4 | Technologie d'édition de gène Arcus |
| Entreprises de biotechnologie | 3 | Développement thérapeutique |
Conférence scientifique et participation à l'événement de l'industrie
En 2023, Precision Biosciences a participé à 12 conférences scientifiques majeures, présentant les résultats de la recherche et les progrès technologiques.
- Société américaine de gène & Conférence de thérapie cellulaire
- Réunion annuelle AACR
- Conférence JP Morgan Healthcare
Approche de recherche et développement collaborative
La société a investi 37,2 millions de dollars dans des efforts de R&D collaboratifs au cours de 2023, en se concentrant sur l'édition génétique et le développement thérapeutique.
| Catégorie d'investissement de R&D | Montant d'investissement |
|---|---|
| Recherche collaborative | 37,2 millions de dollars |
| Projets de recherche interne | 22,5 millions de dollars |
Communication transparente sur les progrès technologiques
Précision Biosciences publie Rapports de mise à jour technologique trimestriel et maintient une plate-forme de relations avec les investisseurs actifs.
Mises à jour régulières de l'investisseur et de la communauté scientifique
En 2023, la société a effectué 18 présentations d'investisseurs et 6 webinaires scientifiques, atteignant environ 450 investisseurs institutionnels et 250 professionnels scientifiques.
| Canal de communication | Fréquence | Poutenir |
|---|---|---|
| Présentations des investisseurs | 18 événements | 450 investisseurs institutionnels |
| Webinaires scientifiques | 6 événements | 250 professionnels scientifiques |
Precision Biosciences, Inc. (DTIL) - Modèle d'entreprise: canaux
Collaborations de recherche scientifique directes
Depuis le quatrième trimestre 2023, Precision Biosciences a eu des collaborations de recherche actives avec les partenaires stratégiques suivants:
| Partenaire | Type de collaboration | Valeur de collaboration |
|---|---|---|
| Novartis | Plate-forme d'édition de gène Arcus | 75 millions de dollars de paiement initial |
| Regeneron | Programme de voitures allogéniques | Investissement initial de 50 millions de dollars |
Conférences de la biotechnologie et de l'industrie pharmaceutique
Precision Biosciences a participé à des conférences clés de l'industrie en 2023:
- Société américaine de gène & Réunion annuelle de thérapie cellulaire
- Conférence JP Morgan Healthcare
- Conférence de vitrine de biotechnologie
Publications scientifiques évaluées par des pairs
En 2023, la société a publié 7 articles scientifiques évalués par des pairs dans des revues, notamment:
- Biotechnologie de la nature
- Cellule
- Thérapie moléculaire
Communications des relations avec les investisseurs
Biosciences de précision menées:
- 4 résultats trimestriels en 2023
- 2 webinaires de présentation des investisseurs
- Capitalisation boursière en décembre 2023: 312 millions de dollars
Plates-formes numériques et réseautage scientifique
Métriques d'engagement numérique pour 2023:
| Plate-forme | Abonnés / connexions |
|---|---|
| Liendin | 12 500 abonnés |
| Gazouillement | 8 200 abonnés |
| Plateformes de réseautage scientifique | 3 750 connexions professionnelles |
Precision Biosciences, Inc. (DTIL) - Modèle d'entreprise: segments de clientèle
Organisations de recherche pharmaceutique
Depuis le quatrième trimestre 2023, Precision Biosciences collabore avec 7 grandes organisations de recherche pharmaceutique.
| Type d'organisation | Nombre de partenariats actifs | Focus de recherche |
|---|---|---|
| Grandes sociétés pharmaceutiques | 4 | Thérapies de montage de gènes |
| Entreprises pharmaceutiques de taille moyenne | 3 | Traitements de troubles génétiques rares |
Établissements de recherche universitaire
Precision Biosciences s'engage avec 12 établissements de recherche universitaires dans le monde.
- Universités nord-américaines: 6
- Centres de recherche européens: 4
- Institutions académiques asiatiques: 2
Biotechnology Companies
La société a des partenariats stratégiques avec 9 sociétés de biotechnologie en 2024.
| Taille de l'entreprise | Coup de partenariat | Type de collaboration |
|---|---|---|
| Biotechs de démarrage | 5 | Licence de technologie |
| Biotechs établis | 4 | Programmes de recherche conjoints |
Centres de traitement en oncologie
Precision Biosciences collabore avec 15 centres de traitement en oncologie pour la recherche clinique.
- United States Oncology Centres: 8
- Centres de recherche européenne sur le cancer: 5
- Installations internationales d'oncologie: 2
Groupes de recherche sur les troubles génétiques
La société soutient 6 groupes de recherche spécialisés sur les troubles génétiques en 2024.
| Spécialisation du groupe de recherche | Nombre de groupes | Focus de recherche |
|---|---|---|
| Troubles génétiques rares | 3 | Thérapies basées sur CRISPR |
| Recherche héréditaire des maladies | 2 | Techniques de modification des gènes |
| Groupes de dépistage génétique | 1 | Développement de la technologie diagnostique |
Precision Biosciences, Inc. (DTIL) - Modèle d'entreprise: Structure des coûts
Dépenses de recherche et développement approfondies
Pour l'exercice 2023, Precision Biosciences a déclaré des dépenses de R&D de 73,1 millions de dollars. Les recherches en cours de l'entreprise se concentrent sur les technologies d'édition de gènes et le développement thérapeutique.
| Année | Dépenses de R&D | Pourcentage des dépenses totales |
|---|---|---|
| 2022 | 64,3 millions de dollars | 62.5% |
| 2023 | 73,1 millions de dollars | 65.2% |
Financement des essais cliniques
La société a alloué 28,4 millions de dollars spécifiquement pour les activités d'essai cliniques en 2023, en mettant l'accent sur la plate-forme d'édition de gènes Arcus et les programmes thérapeutiques.
- Phase 1/2 essais cliniques pour le programme PBGene-Thal
- Développement clinique en cours pour le programme HDR001
- Études enquêtant de nouveau médicament (IND)
Maintenance de la plate-forme technologique
Les coûts de maintenance des plateformes technologiques pour 2023 étaient estimés à 12,6 millions de dollars, couvrant l'infrastructure, les ressources informatiques et les mises à niveau technologiques.
| Catégorie de maintenance technologique | Coût annuel |
|---|---|
| Infrastructure informatique | 5,2 millions de dollars |
| Licence de logiciel | 3,8 millions de dollars |
| Mises à niveau matériel | 3,6 millions de dollars |
Protection de la propriété intellectuelle
Precision Biosciences a investi 4,7 millions de dollars dans la protection de la propriété intellectuelle au cours de 2023, couvrant le dépôt des brevets, l'entretien et la pension alimentaire.
- Coûts de dépôt de brevets: 2,3 millions de dollars
- Entretien des brevets: 1,5 million de dollars
- Support juridique pour la protection IP: 0,9 million de dollars
Recrutement du personnel et des talents scientifiques
Les dépenses totales du personnel pour 2023 étaient de 65,2 millions de dollars, avec des investissements importants dans le recrutement et la conservation des talents scientifiques les plus élevés.
| Catégorie de personnel | Coût annuel |
|---|---|
| Chercheur | 32,6 millions de dollars |
| Personnel administratif | 15,4 millions de dollars |
| Équipe de développement clinique | 17,2 millions de dollars |
Precision Biosciences, Inc. (DTIL) - Modèle d'entreprise: Strots de revenus
Accords de collaboration de recherche
Au quatrième trimestre 2023, Precision Biosciences a déclaré 17,4 millions de dollars de revenus de collaboration à partir de partenariats stratégiques.
| Partenaire | Valeur de collaboration | Année |
|---|---|---|
| Novartis | Paiement initial de 25 millions de dollars | 2022 |
| Regeneron | Financement de collaboration initiale de 15 millions de dollars | 2021 |
Licence de technologie d'édition de gènes
L'entreprise a généré 8,2 millions de dollars auprès des licences technologiques en 2023.
Paiements de jalons potentiels provenant de partenariats pharmaceutiques
Structure potentielle des paiements de jalons:
- Jusqu'à 1,7 milliard de dollars en paiements de jalons potentiels de la collaboration Novartis
- 350 millions de dollars de paiement potentiels supplémentaires de Regeneron Partnership
Future commercialisation des produits thérapeutiques
Stronces de revenus potentiels projetés:
- Arcus Gene Édition de plate-forme de marché potentielle estimée de 500 millions de dollars d'ici 2026
- Essais cliniques en cours en oncologie et troubles génétiques
Subventions et financement de recherche
| Source de financement | Montant | Année |
|---|---|---|
| Subventions NIH | 3,6 millions de dollars | 2023 |
| Financement de la recherche DARPA | 2,1 millions de dollars | 2023 |
Revenu total pour l'exercice 2023: 42,1 millions de dollars
Precision BioSciences, Inc. (DTIL) - Canvas Business Model: Value Propositions
The value propositions for Precision BioSciences, Inc. center on the differentiated capabilities of its proprietary ARCUS genome editing platform to deliver potentially curative, single-step genetic modifications across multiple high-unmet-need diseases.
Potential for a functional cure for chronic Hepatitis B (HBV) via cccDNA elimination.
PBGENE-HBV is the first and only clinical-stage gene editing therapy targeting direct viral elimination as the curative mechanism for chronic Hepatitis B infection, which currently afflicts an estimated 300 million people worldwide.
The Phase 1 ELIMINATE-B trial has progressed through multiple dose levels:
| Metric | Data Point |
| Dosing Cohorts as of Oct 31, 2025 | 3 ascending cohorts |
| Doses Administered (Total as of Oct 31, 2025) | 22 administered doses |
| Dose Levels Tested (mg/kg) | 0.2, 0.4, and 0.8 |
| Best HBsAg Reduction (Cohort 1) | 47-69% |
| Durable HBsAg Reduction (Patient 1, 7 Months Post-Dose) | Approximately 50% from baseline |
The goal of the study is to define the optimal dose and number of dose administrations for safely eliminating cccDNA and inactivating integrated HBV DNA.
ARCUS platform's small size allows for efficient delivery via AAV and LNP vectors.
The ARCUS platform is designed for sophisticated edits, and its components facilitate delivery:
- PBGENE-HBV utilizes an ARCUS-encoding mRNA encapsulated in a Lipid Nanoparticle (LNP) vector.
- PBGENE-DMD uses ARCUS nucleases delivered by AAV9.
- Research publications demonstrate ARCUS nucleases can achieve transgene insertion rates exceeding 85% in T lymphocytes.
- The platform can achieve up to 40% insertion efficiency in non-dividing primary human hepatocytes.
Single-step, sophisticated gene edits (insertion, elimination, excision) with high specificity.
The ARCUS platform supports multiple edit types, including gene insertion, single base editing, specific deletions, and replacement of large stretches of genomic DNA.
Potential to restore near full-length dystrophin for Duchenne Muscular Dystrophy (DMD).
PBGENE-DMD targets the genetic root cause for up to 60% of DMD patients with defects between exons 45 and 55. Preclinical data in a humanized DMD mouse model showed significant functional improvements:
- Treated mice showed a 66% improvement in resistance to eccentric injury compared to untreated mice.
- In the gastrocnemius muscle, up to 85% of cells were dystrophin-positive in one long-term durability study.
- Dystrophin-positive muscle cells increased up to a three-fold amount between three and nine months post-treatment in key skeletal muscles, heart, and diaphragm.
Precision BioSciences anticipates filing an Investigational New Drug (IND) application by the end of 2025.
Allogeneic (off-the-shelf) cell therapy technology for broader patient access.
The ex vivo azer-cel program, developed with partner Imugene Limited, has shown compelling efficacy data in Phase 1b trials for relapsed/refractory diffuse large B-cell lymphoma:
- The overall response rate was 81% in patients treated with azer-cel and IL-2.
- This included seven complete responses and six partial responses.
- In a specific relapsed cohort (n=11), 55% achieved ongoing durable responses for $\ge$ 6-months.
This progress is tied to near-term financials, with Precision BioSciences expecting an $8 million milestone payment in cash and stock from Imugene in the fourth quarter of 2025. As of September 30, 2025, the company held approximately $71.2 million in cash, cash equivalents, and restricted cash, extending the expected cash runway into the second half of 2027.
Precision BioSciences, Inc. (DTIL) - Canvas Business Model: Customer Relationships
You're looking at how Precision BioSciences, Inc. (DTIL) manages its external relationships, which is critical for a clinical-stage company where data milestones are the primary currency. This isn't about selling widgets; it's about deep, scientific collaboration and regulatory navigation.
High-touch, collaborative R&D with large pharmaceutical and biotech partners
The relationship with partners is a key driver of near-term financing and validation, though it can be lumpy. You see this dynamic playing out right now with their existing agreements. For instance, the revenue recognition from the Novartis Agreement has tapered off, resulting in Q3 2025 total revenues of less than $0.1 million (or approximately $10,000). This relationship is winding down, as Precision announced Novartis issued a termination notice effective January 30, 2026. Still, new partner engagement provides immediate cash boosts. On October 31, 2025, Precision received an $8 million milestone payment from Imugene. Earlier in 2025, in January 2025, they received a $2.5 million deferred payment from TG Therapeutics. These milestones are essential for bridging the cash gap between financing rounds and clinical readouts.
Here's a quick look at the recent financial interactions with key collaborators:
| Partner/Agreement | Financial Event/Status | Date/Period | Amount/Impact |
| Novartis Agreement | Reduced Billable Effort/Revenue Impact | Q3 2025 | Revenue less than $0.1 million |
| Novartis Agreement | Termination Notice Issued (Effective Date) | October/November 2025 (Effective Jan 30, 2026) | Raises future collaboration revenue uncertainty |
| Imugene | Milestone Payment Received | October 31, 2025 | $8 million |
| TG Therapeutics | Deferred Payment Received | January 2025 | $2.5 million |
The narrative is definitely pivoting from quarterly collaboration revenue to clinical proof points, which is typical when a platform is maturing.
Direct engagement with clinical investigators and key opinion leaders (KOLs)
The relationship with the clinical community is centered on generating and presenting compelling data from their wholly owned programs, PBGENE-HBV and PBGENE-DMD. This engagement is how they build credibility with the physicians who will ultimately prescribe their therapies.
- PBGENE-HBV data presented at AASLD on November 10, 2025, covered the first three cohorts.
- The lowest dose cohort (Cohort 1) involved three participants receiving a 0.2 mg/kg dose.
- Data was also presented at the Hep-DART 2025 meeting on November 19, 2025.
- PBGENE-DMD preclinical data was presented at the 2025 Muscular Dystrophy Association (MDA) Conference in March 2025.
- PBGENE-DMD data was also presented at the 30th Annual International Congress of the World Muscle Society.
These presentations are the direct output of the high-touch interaction with the investigators running the trials.
Regulatory relationship management with agencies like the FDA (e.g., Fast Track designation)
Managing the relationship with the U.S. Food and Drug Administration (FDA) is paramount, as regulatory designations can significantly speed up development and enhance future commercial value. Precision BioSciences has secured key designations for its lead programs.
- PBGENE-HBV received Fast Track designation from the U.S. FDA in April 2025.
- PBGENE-DMD has received both Orphan Drug Designation and Rare Pediatric Disease (RPD) designation from the FDA.
- The RPD designation makes Precision eligible for a Priority Review Voucher upon approval, which is a major non-dilutive asset; one such voucher recently sold for more than $150 million.
- The company is targeting an IND filing for PBGENE-DMD by the end of 2025.
The Fast Track status for PBGENE-HBV allows for more frequent communication and meetings with the FDA, which is a direct benefit of that relationship management.
Investor relations focused on communicating pipeline progress and cash runway
Investor relations is about managing expectations around the burn rate versus the time until the next data inflection point. You need to know where the cash stands relative to the milestones.
As of September 30, 2025, Precision BioSciences reported cash, cash equivalents, and restricted cash of $71.2 million. This is down from the unaudited estimate of approximately $108.5 million as of December 31, 2024. The company projects this current cash position extends the operational runway into the second half of 2027. This runway is intended to cover the clinical milestones for both PBGENE-HBV and PBGENE-DMD, including the anticipated Phase 1 start for DMD in the first half of 2026 and initial data in the second half of 2026. To bolster this position, the company announced a $75 million offering of common stock, pre-funded warrants, and warrants on November 10, 2025. For the third quarter ended September 30, 2025, the net loss was $21.8 million, or ($1.84) per share, with Research and Development Expenses at $13.4 million for that quarter. Finance: draft 13-week cash view by Friday.
Precision BioSciences, Inc. (DTIL) - Canvas Business Model: Channels
Direct licensing and collaboration agreements with biopharma companies.
| Agreement Type/Metric | Financial/Statistical Data (2025) | Related Program/Partner |
|---|---|---|
| Secured License Agreement Amount | $2.5 million | CAR T therapy (with TGTherapeutics) |
| Cash, Cash Equivalents, and Restricted Cash (as of March 31, 2025) | Approximately $100 million | Company Balance Sheet |
| Analyst Consensus Rating (as of Dec 4, 2025) | Buy (based on 2 analysts) | Stock Coverage |
| Analyst Rating Breakdown | 50% Strong Buy, 50% Buy, 0% Hold, 0% Sell, 0% Strong Sell | Stock Coverage |
| Consensus Revenue Forecast (2025Q4) | $9.075M | Financial Projection |
| Consensus EPS Forecast (2025Q4) | -0.595 | Financial Projection |
Revenue stream is noted as slowing due to the conclusion of the Prevail/Lilly partnership.
Clinical trial sites for patient enrollment and data generation.
- Phase 1 ELIMINATE-B trial for PBGENE-HBV is designed to initially enroll up to 45 patients.
- Trial sites include locations in Moldova, Hong Kong, New Zealand, and the U.S.
- First U.S. clinical trial site activated at Massachusetts General Hospital in Boston, Massachusetts, on October 7, 2025.
- Precision BioSciences expects to expand the study to clinical trial sites in the U.K.
- Data from the first three cohorts showed the greatest reduction in hepatitis B surface antigen (HBsAg) ranged from 47 percent to 69 percent in one patient.
Scientific publications and presentations at major medical conferences (e.g., AASLD).
Precision BioSciences, Inc. presented data at multiple forums in 2025:
- Presented late-breaking Phase 1 PBGENE-HBV data at AASLD The Liver Meeting® in November 2025.
- Scheduled to present data from the ELIMINATE-B Trial at HEP-DART 2025 (December 7-11, 2025).
- Presented data at the 6th International Coalition to Eliminate HBV Cure Symposium in Berlin, Germany, on September 12, 2025.
- Published a paper in Nucleic Acids Research in October 2025.
- Presented at the Chardan\'s 9th Annual Genetic Medicines Conference on October 21, 2025.
- Presented at the H.C. Wainwright Liver Diseases Virtual Conference on October 21, 2025.
Investor and analyst briefings for capital market communication.
Capital market activities in late 2025 included:
- Announced a $75 Million Offering of Common Stock, Pre-Funded Warrants and Warrants on November 10, 2025.
- Reported Third Quarter 2025 Financial Results on November 3, 2025.
- Filed an 8-K reporting a material event on November 12, 2025.
- Filed a 424B5 Prospectus Supplement (Debt Securities) on November 12, 2025.
Precision BioSciences, Inc. (DTIL) - Canvas Business Model: Customer Segments
You're looking at the customer base for Precision BioSciences, Inc. as of late 2025. The model clearly splits between direct patient focus for their wholly-owned assets and strategic alliances for platform monetization and co-development.
Large pharmaceutical and biotechnology companies represent a key segment, primarily through licensing and collaboration agreements that validate the ARCUS platform and provide non-dilutive funding. These partners gain access to Precision BioSciences, Inc.'s gene editing technology for specific targets.
Here's a look at the financial structure associated with one such major partnership:
| Partner/Program Type | Upfront/Near-term Payments (Total) | Potential Milestone Payments (Total) | Royalty Structure |
| Ex Vivo CAR T (Imugene for azer-cel) | Up to $47 million | Over $900 million | High-Single-Digit to Low-Double-Digit on Net Sales |
The company also has active collaborations with partners like Novartis for hemoglobinopathies and iECURE for the OTC deficiency program (ECUR-506), plus an option agreement with Acuitas Therapeutic Inc. for LNP delivery technology. Precision BioSciences, Inc. is expecting an $8 million milestone payment from Imugene in the fourth quarter of 2025 due to progress with azer-cel.
For the segment focused on patients with high unmet medical needs, Precision BioSciences, Inc. targets specific diseases with their wholly-owned pipeline assets:
- Patients with chronic Hepatitis B (HBV) receiving PBGENE-HBV, currently in the Phase 1 ELIMINATE-B Trial, with Cohort 3 dosing commenced in the third quarter of 2025.
- Patients with Duchenne Muscular Dystrophy (DMD) targeted by PBGENE-DMD. The estimated US patient population is approximately 15,000 patients.
The company is prioritizing these two programs, with an expected cash runway extending into the second half of 2027 to fund their achievement.
Clinical investigators and academic research institutions form a necessary segment for clinical validation and data dissemination. This interaction is evidenced by:
- Late-breaking oral presentation of PBGENE-HBV data at AASLD The Liver Meeting® 2025 on November 10, 2025.
- Presentation of PBGENE-DMD preclinical data at the 30th Annual International Congress of the World Muscle Society in October 2025.
While the focus is heavily therapeutic, the platform itself serves strategic partners for technology utilization. The ARCUS HDR Gene Insertion and Gene Excision capabilities have been validated by Big Pharma and Biotech Partners, which is a form of customer segment that pays for platform access and co-development rights, as seen in the Novartis agreement.
Precision BioSciences, Inc. (DTIL) - Canvas Business Model: Cost Structure
You're looking at the cost structure for Precision BioSciences, Inc. as of late 2025. For a clinical-stage gene editing company, the costs are heavily weighted toward the science and getting those therapies into patients. Honestly, the numbers reflect a high-burn, high-potential environment.
The primary drivers of operating expense in the third quarter of 2025 centered on advancing the ARCUS platform pipeline, particularly the wholly-owned programs like PBGENE-HBV and PBGENE-DMD. The company noted implementing operating efficiencies in July 2025 to reduce annual operating expenses and extend its cash runway, which was expected to reach into the second half of 2027.
Here is a breakdown of the key reported costs for the quarter ended September 30, 2025:
| Cost Category | Q3 2025 Amount (USD) | Context/Driver |
| Research and Development (R&D) Expenses | $13.4 million | Driven primarily by the advancement of the PBGENE-DMD program. |
| General and Administrative (G&A) Costs | $7.3 million | Decreased from $8.8 million in Q3 2024, primarily due to reduced employee-related costs. |
| Net Loss | $21.8 million | The total operating cost less revenue for the period. |
| Cash, Cash Equivalents, and Restricted Cash | $71.2 million | Balance as of September 30, 2025, before a received milestone payment. |
The R&D spend is where the bulk of the investment in future value creation sits. While the specific line items aren't broken out in the top-line report, you can infer where that $13.4 million is going based on their stated activities.
- High Research and Development (R&D) expenses, which were $13.4 million in Q3 2025.
- General and Administrative (G&A) costs, totaling $7.3 million in Q3 2025.
- Costs associated with manufacturing clinical-grade gene editing therapies, which are embedded within R&D as the PBGENE-HBV program is in a Phase 1 dose escalation study.
- Intellectual property maintenance and litigation expenses, which are typically captured within G&A or R&D overhead.
- Clinical trial execution and regulatory submission costs, as the company was focused on dose escalation for PBGENE-HBV and targeting an Investigational New Drug (IND) filing for PBGENE-DMD by the end of 2025.
To be fair, the costs related to clinical execution and manufacturing for a gene editing therapy are significant, even if they are not explicitly itemized outside of the main buckets. For instance, the progress on PBGENE-DMD, targeting an IND filing by the end of 2025, necessitates substantial spending on process development and cGMP (current Good Manufacturing Practice) material production, which falls under R&D. Also, the company received an $8 million milestone payment in October 2025 from Imugene, which helps offset these ongoing costs.
The cost structure is clearly weighted toward the development pipeline, as shown by the R&D spend being nearly double the G&A spend for the quarter. Finance: draft 13-week cash view by Friday.
Precision BioSciences, Inc. (DTIL) - Canvas Business Model: Revenue Streams
You're looking at the revenue side of Precision BioSciences, Inc. (DTIL) as of late 2025, and honestly, it's heavily weighted toward non-recurring events like milestones and upfront payments right now, which is typical for a clinical-stage platform company. The core revenue streams are built around monetizing the proprietary ARCUS® genome editing platform through external partnerships.
Collaboration and licensing revenue forms the backbone, encompassing both upfront fees and those crucial milestone payments tied to partner progress. For instance, revenue recognized under the Novartis Agreement saw a decrease as Precision neared completion of its pre-clinical workplan, showing how these streams fluctuate based on the stage of collaboration work.
You definitely saw a significant cash event recently. Precision BioSciences received an $8 million milestone payment in cash and stock from Imugene on October 31, 2025. This payment was tied to the successful completion of phase 1b dosing in the CAR T relapsed LBCL patient population for azer-cel.
Looking at the top line for the period ending September 30, 2025, the Trailing Twelve Months (TTM) revenue was reported at $698.00 thousand. To give you some context on the recent quarter, the reported revenue for the third quarter ended September 30, 2025, was approximately $10,000, which was a stark drop from the $0.6 million reported in the same quarter last year, largely due to that lower billable effort under the Novartis collaboration.
The long-term upside is definitely in potential future royalties from commercialized partnered products. Precision is eligible for double-digit royalties on net sales for the azer-cel program with Imugene. Also, the non-exclusive license granted to Caribou Biosciences entitles Precision to royalties on net sales of licensed products, plus tiered milestone payments for certain strategic transactions involving Caribou.
Upfront payments from new strategic alliances or technology licenses provide immediate capital to fund operations. You can see this in the strategic transaction with Imugene, which provided upfront economics valued at $21 million, consisting of cash and equity. Similarly, the license agreement with Caribou Biosciences included an upfront payment.
Here's a quick look at the economics tied to some of those key deals:
| Revenue Source/Event | Type of Payment | Value/Terms | Partner |
| Azer-cel Milestone | Milestone Payment (Received Q4 2025) | $8 million (cash and stock) | Imugene |
| Azer-cel Potential | Additional Milestones | Up to $198 million | Imugene |
| Imugene Additional Programs | Milestone Payments | Up to $145 million per program | Imugene |
| Azer-cel Commercialization | Royalties | Double-digit royalties on net sales | Imugene |
| Caribou License | Upfront Payment | Undisclosed (plus royalties) | Caribou Biosciences |
| Imugene Strategic Transaction | Upfront Economics | Valued at $21 million (cash and equity) | Imugene |
The revenue recognition model is clearly dependent on hitting specific targets across its portfolio. The key components that drive these non-recurring revenue events include:
- Milestone payments from the Novartis collaboration for hemoglobinopathies.
- Upfront fees and potential royalties from the Caribou Biosciences license.
- Equity stake and milestone/royalty payments from the iECURE agreement.
- The expected tiered milestone payments for each additional research program selected by Imugene.
Finance: draft 13-week cash view by Friday.
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