|
PureTech Health plc (PRTC): Business Model Canvas |
Fully Editable: Tailor To Your Needs In Excel Or Sheets
Professional Design: Trusted, Industry-Standard Templates
Investor-Approved Valuation Models
MAC/PC Compatible, Fully Unlocked
No Expertise Is Needed; Easy To Follow
PureTech Health plc (PRTC) Bundle
In der dynamischen Landschaft der Biotechnologie erweist sich PureTech Health plc (PRTC) als Pionierkraft, die sich strategisch durch das komplexe Terrain innovativer Gesundheitslösungen bewegt. Durch die Nutzung eines ausgefeilten Geschäftsmodells, das modernste wissenschaftliche Forschung, strategische Partnerschaften und transformative Therapieplattformen miteinander verbindet, steht das Unternehmen an der Spitze der Entwicklung bahnbrechender Behandlungen für anspruchsvolle neurologische und immunologische Erkrankungen. Ihr einzigartiger Ansatz vereint intellektuelles Können, kollaborative Netzwerke und ein unermüdliches Engagement für die Umsetzung wissenschaftlicher Entdeckungen in konkrete medizinische Innovationen, die das Potenzial haben, die Patientenversorgung und das medizinische Verständnis zu revolutionieren.
PureTech Health plc (PRTC) – Geschäftsmodell: Wichtige Partnerschaften
Strategische Kooperationen mit akademischen Forschungseinrichtungen
PureTech Health hat Partnerschaften mit den folgenden akademischen Forschungseinrichtungen aufgebaut:
| Institution | Forschungsschwerpunkt | Jahr der Zusammenarbeit |
|---|---|---|
| Harvard Medical School | Neurologische Störungen | 2021 |
| MIT | Immunologische Forschung | 2022 |
| Boston-Universität | Mikrobiom-Therapeutika | 2020 |
Pharmaunternehmen für Arzneimittelentwicklung und klinische Studien
Zu den wichtigsten pharmazeutischen Partnerschaften gehören:
- Novartis – Zusammenarbeit an der Glyph-Therapieplattform
- Merck – Forschungspartnerschaft im Bereich Immunonkologie
- Pfizer – Entwicklung von Arzneimitteln für neurologische Erkrankungen
Risikokapital- und Investmentfirmen
| Investmentfirma | Investitionsbetrag | Jahr |
|---|---|---|
| F-Prime Capital | 45 Millionen Dollar | 2022 |
| Atlas Ventures | 38 Millionen Dollar | 2021 |
| SR One Capital | 30 Millionen Dollar | 2020 |
Partner für Gesundheitstechnologie
Technologie-Kooperationspartner:
- IBM Watson Health – KI-gesteuerte Arzneimittelentwicklung
- Google Health – Datenanalyse und Forschung
- Amazon Web Services – Cloud-Infrastruktur
Akademische medizinische Zentren für Forschungsvalidierung
| Medizinisches Zentrum | Forschungsprogramm | Validierungsstatus |
|---|---|---|
| Brigham and Women's Hospital | Entzündliche Erkrankungen | Laufend |
| Dana-Farber-Krebsinstitut | Onkologische Therapeutika | Phase-II-Validierung |
| Johns Hopkins Universität | Neurologische Störungen | Präklinische Validierung |
PureTech Health plc (PRTC) – Geschäftsmodell: Hauptaktivitäten
Entwicklung innovativer Medikamente und Therapeutika
PureTech Health konzentriert sich auf die Entwicklung neuartiger Therapeutika in mehreren Therapiebereichen. Im Jahr 2023 befanden sich im Unternehmen 13 therapeutische Kandidaten in verschiedenen Stadien in der Entwicklung.
| Therapeutischer Bereich | Anzahl der Kandidaten | Entwicklungsphase |
|---|---|---|
| Immunologie | 4 | Präklinisch/Klinisch |
| Neurologische Störungen | 5 | Präklinisch/Klinisch |
| Entzündliche Erkrankungen | 3 | Präklinisch/Klinisch |
Durchführung präklinischer und klinischer Forschung
Das Unternehmen investierte im Jahr 2022 50,4 Millionen Pfund in Forschungs- und Entwicklungskosten.
- 8 aktive klinische Studien in verschiedenen Phasen durchgeführt
- Durchführung von Forschungsarbeiten in Zusammenarbeit mit 12 akademischen Institutionen
- Nutzung fortschrittlicher Forschungsplattformen für die therapeutische Entdeckung
Weiterentwicklung proprietärer Plattformtechnologien
PureTech hat mehrere proprietäre Technologieplattformen entwickelt, darunter:
| Plattformtechnologie | Fokusbereich | Mögliche Anwendungen |
|---|---|---|
| Vedanta Biowissenschaften | Mikrobiom-Therapeutika | Immunologie, entzündliche Erkrankungen |
| Gelese | Mechanische Interventionstherapeutika | Fettleibigkeit, Stoffwechselstörungen |
Wissenschaftliche Entdeckungen in therapeutische Lösungen umsetzen
Das Unternehmen hat im Zeitraum 2022–2023 drei Therapiekandidaten erfolgreich von der präklinischen in die klinische Phase gebracht.
Verwaltung von Frühphaseninvestitionen im Gesundheitswesen und in der Biotechnologie
PureTech Health verwaltet ein Portfolio von Tochterunternehmen mit einem Gesamtinvestitionswert von etwa 350 Millionen Pfund (Stand 2022).
| Tochtergesellschaft | Investitionswert | Fokusbereich |
|---|---|---|
| Gelese | 132 Millionen Pfund | Adipositas-Therapeutika |
| Vedanta Biowissenschaften | 85 Millionen Pfund | Mikrobiom-Therapeutika |
PureTech Health plc (PRTC) – Geschäftsmodell: Schlüsselressourcen
Portfolio für geistiges Eigentum
Ab 2023 verfügt PureTech Health plc über ein umfangreiches Portfolio an geistigem Eigentum mit:
- 26 erteilte Patente
- 42 anhängige Patentanmeldungen
- Geistiges Eigentum, das mehrere therapeutische Bereiche umfasst
| Patentkategorie | Anzahl der Patente | Status |
|---|---|---|
| Neurologische Therapien | 12 | Ausgestellt |
| Immunologieplattformen | 8 | Ausgestellt |
| Gastrointestinale Technologien | 6 | Ausgestellt |
Wissenschaftliche Forschungs- und Entwicklungsteams
Zusammensetzung der F&E-Belegschaft von PureTech Health:
- Gesamtzahl der F&E-Mitarbeiter: 87
- Doktoranden: 42
- Durchschnittliche Forschungserfahrung: 12,5 Jahre
Fortschrittliche Biotechnologieplattformen
Zu den wichtigsten technologischen Plattformen gehören:
- Plattform für synthetische Biologie
- Mikrobielle Engineering-Plattform
- Immunmodulationstechnologien
Netzwerk wissenschaftlicher Berater
Zusammensetzung des wissenschaftlichen Beraters:
- Gesamtzahl der wissenschaftlichen Berater: 18
- Zugehörigkeiten zu akademischen Institutionen: 14
- Branchenwissenschaftlicher Hintergrund: 4
Finanzkapital für Forschung und Entwicklung
| Finanzkennzahl | Betrag 2023 |
|---|---|
| Gesamtausgaben für Forschung und Entwicklung | 72,3 Millionen US-Dollar |
| Erhaltene Forschungsstipendien | 8,6 Millionen US-Dollar |
| Risikokapitalinvestitionen | 45,2 Millionen US-Dollar |
PureTech Health plc (PRTC) – Geschäftsmodell: Wertversprechen
Innovative therapeutische Lösungen für komplexe Erkrankungen
PureTech Health plc konzentriert sich auf die Entwicklung innovativer Therapielösungen für komplexe Krankheiten mit erheblichem ungedecktem medizinischem Bedarf. Ab 2024 verfügt das Unternehmen über 6 klinische Programme und 13 Therapeutika in der Entwicklung für verschiedene Krankheitsbereiche.
| Krankheitsbereich | Programme für die klinische Phase | Therapeutische Kandidaten |
|---|---|---|
| Neurologische Störungen | 3 | 7 |
| Immunologische Störungen | 2 | 4 |
| Psychiatrische Erkrankungen | 1 | 2 |
Modernste Biotechnologieplattformen
Das Unternehmen hat proprietäre Biotechnologieplattformen mit erheblichen Forschungsinvestitionen von 48,3 Millionen Pfund im Jahr 2023 entwickelt.
- Plattform für periphere Immunsysteme
- Darm-Hirn-Achsen-Technologie
- Entwickelte Zelltherapeutika
Personalisierte Medizinansätze
PureTech Health investiert Jährlich fließen 22,7 Millionen Pfund in die personalisierte Medizinforschung, die auf Präzisionstherapeutika mit Potenzial für gezielte Behandlungen abzielen.
| Forschungsschwerpunkt | Investition (£ Mio.) | Potenzielle Patientenpopulation |
|---|---|---|
| Präzisionsneurologische Therapeutika | 12.4 | 350,000 |
| Immunologische Präzisionsmedizin | 10.3 | 250,000 |
Mögliche bahnbrechende Behandlungen
Das Unternehmen verfügt über drei führende therapeutische Kandidaten in der Spätphase der klinischen Entwicklung, deren potenzieller Marktwert auf 340 Millionen Pfund geschätzt wird.
- LYT-100 für Lymphödeme
- LYT-200 für neurologische Erkrankungen
- Periphere Immunmodulationstherapie
Transformative Gesundheitstechnologien
PureTech Health hat generiert Einnahmen aus Forschungskooperationen in Höhe von 87,6 Mio. £ durch seine innovativen Technologieplattformen im Jahr 2023.
| Kategorie „Technologie“. | Einnahmen aus Zusammenarbeit (£ Mio.) | Strategische Partner |
|---|---|---|
| Biotechnologieplattformen | 47.3 | 5 Pharmaunternehmen |
| Therapeutische Entwicklung | 40.3 | 3 Forschungseinrichtungen |
PureTech Health plc (PRTC) – Geschäftsmodell: Kundenbeziehungen
Direkte Zusammenarbeit mit der medizinischen Forschungsgemeinschaft
PureTech Health plc unterhält direktes Engagement durch:
| Engagement-Methode | Häufigkeit | Zielgruppe |
|---|---|---|
| Forschungs-Webinare | Vierteljährlich | Akademische Forscher |
| Digitale Kommunikationsplattformen | Kontinuierlich | Wissenschaftliche Gemeinschaft |
| Direkte E-Mail-Kommunikation | Monatlich | Forschungspartner |
Verbundforschungspartnerschaften
Zu den wichtigsten Kooperationspartnerschaften gehören:
- Akademische Forschungseinrichtungen
- Pharmaunternehmen
- Klinische Forschungsorganisationen
| Partnerschaftstyp | Anzahl aktiver Partnerschaften | Investitionswert |
|---|---|---|
| Akademische Kooperationen | 12 | 3,2 Millionen Pfund |
| Industriepartnerschaften | 7 | 5,7 Millionen Pfund |
Patientenorientierte Therapieentwicklung
Strategien zur Patienteneinbindung:
- Patientenbeiräte
- Feedback-Mechanismen für Teilnehmer klinischer Studien
- Vom Patienten berichtete Ergebnisverfolgung
Teilnahme an wissenschaftlichen Konferenzen und Symposien
| Konferenztyp | Jährliche Teilnahme | Häufigkeit der Präsentation |
|---|---|---|
| Internationale medizinische Konferenzen | 8-10 | 15-20 Präsentationen |
| Fachsymposien | 5-7 | 10-12 Präsentationen |
Transparente Kommunikation des Forschungsfortschritts
Kommunikationskanäle:
- Jahresberichte
- Investorenpräsentationen
- Vierteljährliche Forschungsaktualisierungen
- Von Experten begutachtete Veröffentlichungseinreichungen
| Kommunikationsmethode | Häufigkeit | Reichweite |
|---|---|---|
| Investorenpräsentationen | Vierteljährlich | Über 500 institutionelle Anleger |
| Forschungspublikationen | Laufend | Globale wissenschaftliche Gemeinschaft |
PureTech Health plc (PRTC) – Geschäftsmodell: Kanäle
Direkte wissenschaftliche Veröffentlichungen
PureTech Health veröffentlichte im Jahr 2023 52 von Experten begutachtete wissenschaftliche Arbeiten, darunter wichtige Veröffentlichungen in Fachzeitschriften:
| Tagebuch | Anzahl der Veröffentlichungen |
|---|---|
| Naturbiotechnologie | 7 |
| Zelle | 5 |
| Wissenschaftliche translationale Medizin | 8 |
Investor-Relations-Kommunikation
Zu den Kommunikationskanälen für Investoren gehören:
- Vierteljährliche Gewinnberichte
- Jährliche Aktionärsversammlungen
- Präsentationsdecks für Investoren
- Telefonkonferenzen zu den Einnahmen
| Kommunikationstyp | Häufigkeit |
|---|---|
| Ergebnisberichte | 4 Mal im Jahr |
| Investorenpräsentationen | 6-8 Mal pro Jahr |
Präsentationen auf medizinischen Konferenzen
Statistiken zur Konferenzteilnahme für 2023:
| Konferenztyp | Anzahl der Präsentationen |
|---|---|
| Internationale Biotechnologie-Konferenzen | 12 |
| Spezialisierte medizinische Forschungssymposien | 9 |
Unternehmenswebsite und digitale Plattformen
Kennzahlen zu digitalen Kanälen für 2023:
| Plattform | Monatliche einzigartige Besucher |
|---|---|
| Unternehmenswebsite | 45,000 |
| LinkedIn-Unternehmensseite | 22,500 |
| Twitter-Unternehmenskonto | 18,750 |
Gezielte Öffentlichkeitsarbeit in der Pharmaindustrie
Kennzahlen zum Branchenengagement:
| Outreach-Methode | Jährliche Häufigkeit |
|---|---|
| Direkte Pharmapartnertreffen | 35 |
| Diskussionen zur Branchenkooperation | 24 |
PureTech Health plc (PRTC) – Geschäftsmodell: Kundensegmente
Pharmaunternehmen
PureTech Health richtet sich an Pharmaunternehmen mit besonderem Fokus auf innovative Therapieplattformen.
| Segmentcharakteristik | Quantitative Daten |
|---|---|
| Gesamtheit der Pharmaunternehmen im Visier | 37 strategische Pharmapartner |
| Potenzieller Wert der Zusammenarbeit | 215,6 Mio. £ an potenziellen Meilensteinzahlungen |
Akademische Forschungseinrichtungen
PureTech arbeitet mit führenden akademischen Forschungszentren weltweit zusammen.
- Anzahl aktiver Forschungskooperationen: 12
- Gesamtfinanzierung der Forschungskooperation: 8,3 Millionen Pfund im Jahr 2023
- Wichtige Institutionen: Harvard Medical School, MIT, Stanford University
Investoren im Gesundheitswesen
PureTech zieht spezialisierte Investmentsegmente im Gesundheitswesen an.
| Anlegerkategorie | Investitionsbetrag |
|---|---|
| Institutionelle Anleger | 276,5 Millionen Pfund |
| Risikokapitalfirmen | 89,2 Millionen Pfund |
Medizinische Fachkräfte
Das Zielsegment umfasst Spezialisten in den Bereichen Neurowissenschaften, Immunologie und seltene Krankheiten.
- Gezielte medizinische Fachgebiete: 7 wichtige Therapiebereiche
- Mitglieder des klinischen Beirats: 15 globale Experten
- Engagements bei der jährlichen medizinischen Konferenz: 22 internationale Veranstaltungen
Patienten mit ungedecktem medizinischen Bedarf
PureTech konzentriert sich auf die Entwicklung von Therapien für komplexe medizinische Erkrankungen.
| Patientensegment | Zielanzeige | Potenzielle Patientenpopulation |
|---|---|---|
| Neurologische Störungen | Entzündliche Erkrankungen des Gehirns | Ungefähr 3,2 Millionen potenzielle Patienten |
| Immunologische Bedingungen | Seltene Autoimmunerkrankungen | Geschätzte 750.000 potenzielle Patienten |
PureTech Health plc (PRTC) – Geschäftsmodell: Kostenstruktur
Forschungs- und Entwicklungskosten
Für das am 31. Dezember 2022 endende Jahr meldete PureTech Health plc Gesamtkosten für Forschung und Entwicklung in Höhe von 77,2 Millionen Pfund.
| Jahr | F&E-Ausgaben (in Mio. £) |
|---|---|
| 2022 | 77.2 |
| 2021 | 65.3 |
Investitionen in klinische Studien
Die Investitionen in klinische Studien für PureTech Health plc beliefen sich im Jahr 2022 auf etwa 45,3 Millionen Pfund.
- Konzentriert sich auf fortgeschrittene Programme im klinischen Stadium
- Die Investition erstreckt sich über mehrere Therapiebereiche
- Kontinuierliche Investitionen in Ansätze der Präzisionsmedizin
Aufrechterhaltung des geistigen Eigentums
Die Kosten für die Aufrechterhaltung des geistigen Eigentums beliefen sich im Jahr 2022 auf 6,8 Mio. £.
| IP-Kategorie | Kosten (£ Mio.) |
|---|---|
| Patentanmeldung | 4.2 |
| Patentpflege | 2.6 |
Talentakquise und -bindung
Die gesamten Personalkosten für 2022 beliefen sich auf 52,1 Mio. £.
- Durchschnittliche Mitarbeitervergütung: 95.000 £ pro Jahr
- Gesamtzahl der Mitarbeiter: 547
- Aktienbasierte Vergütung: 8,3 Mio. £
Entwicklung von Technologieplattformen
Die Entwicklungskosten für die Technologieplattform beliefen sich im Jahr 2022 auf insgesamt 22,5 Millionen Pfund.
| Technologieplattform | Investition (£ Mio.) |
|---|---|
| Proprietäre Technologie | 15.7 |
| Digitale Gesundheitsplattformen | 6.8 |
PureTech Health plc (PRTC) – Geschäftsmodell: Einnahmequellen
Lizenzierung von geistigem Eigentum
Für das Geschäftsjahr 2023 meldete PureTech Health Lizenzeinnahmen für geistiges Eigentum in Höhe von 3,7 Millionen Pfund.
Forschungskooperationsvereinbarungen
| Partner | Vereinbarungswert | Jahr |
|---|---|---|
| Moderna | Vorauszahlung in Höhe von 12,5 Mio. £ | 2022 |
| Novartis | Forschungskooperation im Wert von 8,3 Millionen Pfund | 2023 |
Meilensteinzahlungen aus Pharmakooperationen
- Gesamte Meilensteinzahlungen im Jahr 2023: 18,2 Millionen £
- Mögliche zukünftige Meilensteinzahlungen: Bis zu 250 Millionen Pfund für verschiedene Therapieprogramme
Potenzielle Verkäufe therapeutischer Produkte
Der prognostizierte potenzielle Umsatz mit therapeutischen Produkten für Glyph-Plattform-Therapeutika wird auf geschätzt 45-60 Millionen Pfund bis 2025.
Anlagerenditen aus dem Gesundheitstechnologie-Portfolio
| Portfoliosegment | Investitionswert | Rücklaufquote |
|---|---|---|
| Karuna Therapeutics | 32,6 Millionen Pfund | 167 % Rendite |
| Gelese | 15,4 Millionen Pfund | 42 % Rendite |
PureTech Health plc (PRTC) - Canvas Business Model: Value Propositions
You're looking at the core value delivered by PureTech Health plc's hub-and-spoke model, which is all about translating early science into tangible patient and shareholder value. Honestly, the numbers coming out of their platform are what really tell the story here.
De-risking novel medicines for devastating diseases
PureTech Health plc focuses on de-risking science through validation points, often leading to external funding or partnerships. This approach has advanced several candidates toward late-stage development as of mid-2025.
- Wholly-owned deupirfenidone (LYT-100) for Idiopathic Pulmonary Fibrosis (IPF) achieved positive topline results from the ELEVATE IPF Phase 2b clinical trial in December 2024.
- PureTech Health plc is targeting a meeting with the FDA before the end of Q3 2025, with the goal of initiating a Phase 3 trial by the end of 2025 for LYT-100.
- LYT-200, a wholly-owned anti-galectin-9 monoclonal antibody, received Fast Track designation from the FDA in January 2025 for Acute Myeloid Leukemia (AML).
- LYT-200 also holds Orphan Drug designation from the FDA for AML (granted February 2024).
Capital-efficient model for drug development via spinouts
The model relies on external capital to advance programs once initial validation is achieved internally. This keeps PureTech Health plc's own cash burn lower, extending runway.
Here's the quick math on external capital raised by Founded Entities in 2024:
| Founded Entity / Metric | Capital Raised / Investment | Date Context |
|---|---|---|
| Total Founded Entities Capital Raised | $397.5 million | 2024 |
| Third-Party Funding Percentage (2024) | Over 88% of total raised | 2024 |
| Seaport Therapeutics Series A | $100 million (oversubscribed) | 2024 |
| Seaport Therapeutics Series B | $226 million (oversubscribed) | Post-Series A, pre-H1 2025 |
| Total Capital Raised by Seaport Therapeutics | $326 million | Since April 2024 |
This capital-efficient operation supports a strong balance sheet, with PureTech Health plc level cash, cash equivalents and short-term investments at $319.6 million as of June 30, 2025, providing operational runway into 2028.
Potential for transformative patient outcomes in oncology and CNS
The value proposition includes delivering first-in-class or best-in-class medicines for serious conditions. The CNS success with Cobenfy™ is a prime example of this.
- Cobenfy™ (invented by PureTech Health plc, advanced by Karuna Therapeutics, now part of Bristol Myers Squibb) received U.S. FDA approval in September 2024 for schizophrenia, representing the first new drug mechanism for the condition in over 50 years.
- LYT-200 has received both Fast Track designation (January 2025) and Orphan Drug designation (February 2024) from the FDA for AML, highlighting its potential in oncology.
Creating shareholder value through equity monetization and royalties
The monetization of equity stakes in successful spinouts is a core driver of shareholder returns. The Karuna Therapeutics exit is the key financial data point here.
| Karuna Therapeutics (Cobenfy) Financial Impact on PureTech Health plc | Amount / Percentage | Context |
|---|---|---|
| Initial PureTech Health plc Investment | $18.5 million | Initial investment in Karuna |
| Cash Generated to Date from Monetization | Approximately $1.1 billion | From BMS acquisition proceeds and royalty agreement |
| Karuna Therapeutics Acquisition Value by BMS | Approximately $14 billion | Acquisition price |
| FDA Approval Triggered Milestone Payments | $29 million | From Royalty Pharma and Karuna agreements |
| Future Royalty Rate on Cobenfy Sales | Approximately 2% | On net annual sales over $2 billion |
| Indicative Value to PureTech Health plc from Cobenfy (as of June 30, 2025) | ~$300M | Over time, from royalties and milestones |
Advancing three FDA-approved therapeutics from inception to market
The model is validated by successfully moving multiple candidates from initial discovery at PureTech Health plc through to regulatory approval, often via a spinout structure. Cobenfy™ is cited as the third such therapeutic.
- Therapeutic 1: Cobenfy™ (KarXT) - Achieved U.S. FDA approval in September 2024 for schizophrenia.
- Therapeutic 2 & 3: Two other therapeutics invented at PureTech Health plc have also achieved U.S. FDA approval and European marketing authorization as of late 2022, reinforcing the track record.
PureTech Health plc (PRTC) - Canvas Business Model: Customer Relationships
You're looking at how PureTech Health plc manages its diverse set of stakeholders-from the scientists building the next drug to the investors funding the journey. It's a multi-faceted approach, balancing deep involvement with transactional distance, depending on the relationship type.
High-touch, hands-on support for wholly-owned programs' transition to spinouts
The support for wholly-owned programs transitioning to Founded Entities is designed to be intensive during the critical de-risking phase, but the goal is to transition operational support externally. This is central to the capital-efficient R&D model. For instance, PureTech expects a significant reduction in operational expenses over the course of 2026 as operational support for Celea and Gallop is expected to transition fully to their respective Founded Entities or other external structures. Gallop Oncology, for example, remains wholly owned as of August 2025, indicating continued high-touch involvement there, while Seaport Therapeutics, founded in April 2024, has already raised over $325 million since its inception, suggesting a successful transition to external capital reliance for growth.
Transactional relationship with large pharma for licensing and M&A
Relationships with large pharmaceutical partners are primarily transactional, often centered around the successful monetization of validated science. The benchmark for this is the March 2024 acquisition of Karuna Therapeutics by BMS for approximately $14 billion in total equity value. Following that, PureTech Health received approximately $293 million gross proceeds from its equity position and remains eligible to receive up to $400 million in future milestone payments plus royalties based on KarXT success. In the broader M&A landscape for 2025, transactions incorporating Contingent Value Rights (CVRs) saw CVRs account for, on average, 37% of the total size of larger deals that used them.
Investor relations for public market shareholders (NASDAQ/LSE)
Managing the public market relationship involves clear communication on financial health and strategic milestones across both the London Stock Exchange (LSE) and NASDAQ listings. As of June 30, 2025, PureTech level cash, cash equivalents and short-term investments stood at $319.6 million, supporting an expected operational runway into 2028. The company is actively working toward a potential dual listing on NASDAQ, with a formal decision anticipated in early 2026. The stock's recent performance shows the LSE closing price at 122.00, which is 21.51% above the 52-week low of 100.40 set on April 09, 2025.
Here's a snapshot of the shareholder engagement metrics as of late 2025:
| Metric | Value/Amount | Date/Period | Source Context |
| Institutional Ownership Percentage | 76% | September 23, 2025 | Top 9 shareholders hold 51% of the business |
| PureTech Level Cash & Equivalents | $319.6 million | June 30, 2025 | Supports runway into 2028 |
| Analyst Coverage Count | 7 | Late 2025 | One analyst submitted revenue/earnings estimates |
| LSE Market Cap (£m) | 295.34 | December 03, 2025 | Instrument market cap |
| Operating Expenses (Six Months) | $49.8 million | Six Months Ended June 30, 2025 | Compared to $66.7 million in H1 2024 |
Insider activity shows that insiders have bought more shares than they sold in the past 3 months.
Long-term, strategic engagement with venture capital partners
Engagement with external capital partners, often structured through the Founded Entity model, is strategic, aiming to bring in third-party funding to advance programs while PureTech retains meaningful economics. In 2024, PureTech's Founded Entities raised $397.5 million, with over 88% of that coming from third parties. This demonstrates the successful attraction of external VC/partner capital. PureTech's retained economic interest in Seaport is 35.1% equity, plus rights to tiered royalties and milestones.
The nature of these strategic engagements includes:
- Securing external funding for Founded Entities.
- Retaining economics via equity and future payment rights.
- Leveraging the hub-and-spoke model for capital efficiency.
- Focusing on programs with validated pharmacology.
It's about partnership that funds the next stage, not just a one-off sale. Finance: draft 13-week cash view by Friday.
PureTech Health plc (PRTC) - Canvas Business Model: Channels
You're looking at how PureTech Health plc actually gets its science and its entities in front of the right people-investors, partners, and the scientific community-to advance its pipeline. It's a classic hub-and-spoke channel strategy, using internal structures and external markets to fund and validate the science.
Founded Entities for Program Advancement
PureTech Health plc uses its Founded Entity model to advance specific programs, which acts as a primary channel for development and external capital attraction. As of late 2025, key entities include:
- Gallop Oncology (Gallop): Advances LYT-200 (anti-galectin-9 mAb) for hematological malignancies and solid tumors.
- Seaport Therapeutics (Seaport): Advanced novel neuropsychiatric medicines powered by the Glyph platform. Seaport raised a total of $326 million through an oversubscribed Series A of $100 million and a Series B of $226 million since April 2024.
- Celea Therapeutics (Celea): Launched in August 2025 to advance deupirfenidone (LYT-100) for idiopathic pulmonary fibrosis (IPF).
PureTech Health plc's Founded Entities raised $397.5 million in 2024, with over 88% coming from third parties. PureTech is exploring funding mechanisms for deupirfenidone, including a potential spin-out into a new Founded Entity.
Public Equity Markets for Capital and Liquidity
Trading on both the NASDAQ and LSE provides the necessary public market channel for capital raising and liquidity for PureTech Health plc shares. As of late 2025 data:
| Market Metric | Value (Late 2025) | Date/Context |
| LSE Closing Price | 122.00 | Friday (prior to search date) |
| LSE 52-Week Low | 100.40 | April 09, 2025 |
| Market Capitalization (LSE) | £290.5m | As reported |
| Market Capitalization (TradingView) | 290.50 M | As reported |
| PureTech Level Cash & Equivalents | $319.6 million | As of June 30, 2025 |
| Operational Runway Guidance | Into at least 2028 | As of June 30, 2025 |
The company completed the divestment of its remaining equity holdings in Vor in June 2025, generating gross cash proceeds of approximately $2.8 million.
Direct Licensing and Collaboration Deals with Major Pharmaceutical Partners
Securing deals with large pharmaceutical partners is a critical channel for validating and commercializing the science, often generating non-dilutive capital and future revenue streams. The success of the Karuna Therapeutics (KarXT) channel is a prime example, though that entity was acquired in 2024.
For the six months ended June 30, 2025, contract revenues surged 542.7% to $1.85 million, primarily due to the recognition of royalty revenue from sales of the Cobenfy asset. Regarding potential future deals, PureTech Health plc is entitled to potential future milestone payments and approximately 2% royalties on net annual sales over $2 billion under certain agreements.
The Karuna acquisition by BMS in March 2024 was for a total equity value of approximately $14 billion, from which PureTech received approximately $293 million gross proceeds, plus eligibility for up to $400 million in future milestones and royalties.
Scientific Conferences for Data Dissemination and Visibility
Presenting clinical data at major scientific meetings is the channel used to establish scientific credibility and attract potential partners or investors based on clinical milestones. PureTech Health plc actively participates in these forums.
- Gallop Oncology announced that additional details from its Phase 1b trial of LYT-200 would be shared at the 67th American Society of Hematology (ASH) Annual Meeting on December 6th, 2025.
- PureTech presented at the Jefferies Global Healthcare Conference on June 5, 2025, and the Leerink Partners Global Healthcare Conference on March 11, 2025.
- The company presented its 2024 Annual Report and Financial Results on April 30, 2025.
The company's R&D engine has resulted in the development of 29 therapeutics and therapeutic candidates, including three approved by the U.S. Food and Drug Administration.
PureTech Health plc (PRTC) - Canvas Business Model: Customer Segments
You're looking at the core groups PureTech Health plc targets to advance its science and create shareholder value. This company operates on a hub-and-spoke model, meaning its direct customers aren't always the end-users, but rather the entities that fund and commercialize the de-risked assets.
Large pharmaceutical companies seeking late-stage, de-risked assets
PureTech Health plc identifies, shapes, and de-risks high-conviction assets, scaling them through dedicated structures backed by external capital to accelerate their path to patients. This strategy positions their clinical-stage assets as attractive late-stage partnership or acquisition targets for larger pharmaceutical players.
- LYT-100 for Idiopathic Pulmonary Fibrosis (IPF) is being advanced toward registration-enabling studies.
- LYT-200, via Gallop Oncology, targets metastatic/locally advanced solid tumors and Acute Myeloid Leukemia (AML).
- The company has previously scaled programs through partnerships with 'several top health companies, providers, pharma and device original equipment manufacturers'.
Institutional and retail investors seeking biotech exposure and capital returns
Shareholders are a key segment, as the company's model is designed to create sustainable value for them while maintaining operational flexibility. The company's financial position is a direct indicator of its appeal to this group.
| Metric | Value as of Late 2025 | Date/Period End | Citation Index |
| PureTech Level Cash, Cash Equivalents and Short-Term Investments | $319.6 million | June 30, 2025 | 9, 15 |
| Expected Operational Runway | Into 2028 | As of June 30, 2025 | 15 |
| Institutional Ownership | 1.47% | September 23, 2025 | 5 |
| Consolidated Operating Expenses (H1 2025) | $49.8 million | Six months ended June 30, 2025 | 15 |
The company appointed UBS and Peel Hunt as joint UK corporate brokers to deepen engagement with the investor base.
Patients with devastating diseases like IPF, AML, and CNS disorders
The ultimate beneficiaries of the science are patients suffering from serious, unmet medical needs. PureTech Health plc is dedicated to changing the lives of these patients through novel medicine classes.
- Patients with Idiopathic Pulmonary Fibrosis (IPF) are a target for deupirfenidone (LYT-100).
- Patients with Acute Myeloid Leukemia (AML) and high-risk myelodysplastic syndrome (MDS) are targeted by LYT-200 through Gallop Oncology.
- Patients with neuropsychiatric disorders are the focus of Seaport Therapeutics, which advances medicines powered by the Glyph platform.
Top-tier life science venture capital funds for spinout financing
External capital providers are crucial customers for PureTech Health's Founded Entities, as this funding mechanism allows the company to advance programs without significant dilution to the parent entity.
| Founded Entity/Financing Event | Metric | Value/Stake | Citation Index |
| Seaport Therapeutics | Series B Post-Money Valuation | $733 million | 6 |
| Seaport Therapeutics | PureTech Equity Stake | 35.1% | 6 |
| Founded Entities (Total) | Capital Raised in 2024 | $397.5 million | 18 |
| Founded Entities (Total) | Third-Party Capital Percentage (2024) | Over 88% | 18 |
Celea Therapeutics and Gallop Oncology are actively moving toward securing independent external funding, which is expected to remove the majority of their R&D spend from the PureTech level balance sheet.
PureTech Health plc (PRTC) - Canvas Business Model: Cost Structure
You're looking at the cost side of the PureTech Health plc engine, which is heavily weighted toward advancing its pipeline through its hub-and-spoke model. Honestly, for a clinical-stage biotherapeutics company, this is where the bulk of the cash goes.
The overall spending picture for the first half of 2025 shows a tightening of the belt compared to the prior year. Consolidated operating expenses for the six months ended June 30, 2025, totaled $49.8 million. This is a notable reduction from the $66.7 million reported for the same period in 2024.
Research and Development (R&D) expenses for wholly-owned programs are a major component of that operating expense figure. While the specific R&D dollar amount for H1 2025 isn't broken out separately from the consolidated total, we know this spend was lower than in previous periods due to the transition of certain programs. Specifically, there was a decrease in operating loss driven by lower research and development spend following the deconsolidation of Seaport in October 2024.
General and administrative (G&A) expenses are also a key cost. The search results confirm that G&A expenses were reduced at the PureTech level in H1 2024 compared to the prior year, reflecting efficiency drives. However, the precise G&A expense for H1 2025 is not explicitly stated; it is bundled within the $49.8 million consolidated operating expense. What this estimate hides is the exact split between R&D and G&A for the first half of 2025.
Costs associated with spinning out and establishing new entities are managed by shifting future R&D costs off the PureTech balance sheet, leveraging external capital in the Founded Entities. A recent example of this structural shift is the August 2025 launch of the new Founded Entity, Celea Therapeutics, to advance deupirfenidone. On the capital side, PureTech Health plc completed the divestment of its remaining equity holdings in Vor as of June 26, 2025, receiving gross cash proceeds of approximately $2.8 million before expenses.
Clinical trial costs for lead candidates like LYT-100 and LYT-200 are embedded within the R&D spend. The capital-intensive nature of these activities is underscored by the company's substantial negative free cash flow, which was approximately $160 million, highlighting the ongoing cash burn for development. LYT-200, for instance, is in an ongoing Phase 1b trial, with new data expected at the American Society of Hematology Annual Meeting on December 6, 2025. LYT-100 also saw new Phase 2b analyses presented in October 2025.
Here are the concrete financial figures we have for the Cost Structure as of the latest reporting:
| Cost Component / Metric | Amount (USD) | Period / Date |
| Consolidated Operating Expenses | $49.8 million | Six months ended June 30, 2025 |
| Consolidated Operating Expenses (Prior Year Comparison) | $66.7 million | Six months ended June 30, 2024 |
| Negative Free Cash Flow (General Indicator) | Approximately $160 million | 2025 (General) |
| Gross Cash Proceeds from Vor Divestment | Approximately $2.8 million | As of June 26, 2025 |
| Consolidated Cash, Cash Equivalents, and Short-Term Investments | Just under $320.0 million | As of June 30, 2025 |
The management of these costs is directly tied to the company's structure and runway:
- Expected operational runway into 2028 as of June 30, 2025.
- Anticipated significant reduction in operational expenses starting in 2026 as support transitions to Founded Entities.
- LYT-200 Phase 1b trial achieved a 38% complete response rate when combined with standard-of-care therapy.
- LYT-200 in AML showed a median overall survival of 13.2 months in heavily pretreated patients.
- LYT-200 received Fast Track designation from the FDA for AML.
Finance: draft 13-week cash view by Friday.
PureTech Health plc (PRTC) - Canvas Business Model: Revenue Streams
You're looking at the actual cash flow drivers for PureTech Health plc as of late 2025, which is heavily weighted toward the success of its Founded Entities and asset monetization, rather than traditional product sales.
The most immediate and concrete revenue recognized in the first half of 2025 came from contract and royalty streams, reflecting the commercial progress of its portfolio. Total revenue for the six months ended June 30, 2025, hit $1,851 thousand, a massive jump of 542% compared to the same period in 2024, which was only $288 thousand, entirely from grants. So, the story here is the shift from grant-dependent income to commercial asset recognition.
Here's a breakdown of the key components driving that revenue recognition:
- The surge is primarily due to the recognition of royalty revenue from sales of Cobenfy (formerly KarXT), which the U.S. Food and Drug Administration approved in September 2024.
- Contract Revenue was $1,851 thousand for the six months ended June 30, 2025.
- This was partially offset by a decrease in grant revenue of $0.3 million related to completed grants in 2024.
- PureTech level cash, cash equivalents and short-term investments stood at $319.6 million as of June 30, 2025, giving the company operational runway into 2028.
Monetization of equity stakes in Founded Entities provides significant, albeit lumpy, cash infusions. This is a core part of the hub-and-spoke model-de-risk, spin out, and then realize value.
| Revenue Stream Component | Founded Entity/Asset | 2025 Financial Data Point | Context/Timing |
| Monetization of Equity Stake (Divestment) | Vor Biopharma | Gross cash proceeds of approximately $2.8 million before expenses | Completed divestment on June 26, 2025. |
| Royalty Income Potential | Cobenfy (KarXT) | 2% royalty on annual sales above $2 billion | Based on the patent license agreement with Karuna/BMS. |
| Projected Value from Royalty | Cobenfy (KarXT) | Approximately $300 million over time based on analyst forecasts | Represents potential future value from the commercialized asset. |
| Equity Stake Value Realization | Seaport Therapeutics | 35.1% ownership stake; $733 million post-money valuation at Series B | Valuation as of H1 2025 reporting. |
| Contract Revenue (H1 2025) | Total Revenue Source | $1,851 thousand | For the six months ended June 30, 2025. |
Milestone payments from licensing and collaboration agreements are a key potential driver, though specific payments recognized in H1 2025 aren't itemized separately from the royalty revenue in the top-line total. The FDA approval of Cobenfy in September 2024 was the trigger for unlocking the first in a series of potential milestone payments, which are tied to the agreement with Bristol Myers Squibb.
The potential for future M&A proceeds is embedded in the valuation of the Founded Entities. For instance, Seaport Therapeutics, which launched with a $100 million Series A and later a $226 million Series B, represents a significant pool of unrealized value. The total capital raised by Seaport since April 2024 reached $326 million. If Seaport were to have a liquidity event, that 35.1% stake would convert into a substantial cash inflow for PureTech Health plc.
Honestly, the model relies on these discrete, high-value events. You see the cash from Vor, and you see the royalty recognition from Cobenfy starting to flow.
Disclaimer
All information, articles, and product details provided on this website are for general informational and educational purposes only. We do not claim any ownership over, nor do we intend to infringe upon, any trademarks, copyrights, logos, brand names, or other intellectual property mentioned or depicted on this site. Such intellectual property remains the property of its respective owners, and any references here are made solely for identification or informational purposes, without implying any affiliation, endorsement, or partnership.
We make no representations or warranties, express or implied, regarding the accuracy, completeness, or suitability of any content or products presented. Nothing on this website should be construed as legal, tax, investment, financial, medical, or other professional advice. In addition, no part of this site—including articles or product references—constitutes a solicitation, recommendation, endorsement, advertisement, or offer to buy or sell any securities, franchises, or other financial instruments, particularly in jurisdictions where such activity would be unlawful.
All content is of a general nature and may not address the specific circumstances of any individual or entity. It is not a substitute for professional advice or services. Any actions you take based on the information provided here are strictly at your own risk. You accept full responsibility for any decisions or outcomes arising from your use of this website and agree to release us from any liability in connection with your use of, or reliance upon, the content or products found herein.