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Shattuck Labs, Inc. (STTK) Bundle
In der hochmodernen Welt der Krebsimmuntherapie erweist sich Shattuck Labs, Inc. (STTK) als Pionier und nutzt seine bahnbrechenden STING- und TGF-β-Plattformen, um die Präzisionsmedizin zu revolutionieren. Durch die strategische Navigation in komplexen wissenschaftlichen Landschaften und den Aufbau entscheidender Partnerschaften mit akademischen Einrichtungen und Pharmariesen ist dieses innovative Biotech-Unternehmen bereit, unsere Herangehensweise an die Krebsbehandlung zu verändern und potenziell bahnbrechende Therapien anzubieten, die auf komplizierte Immunmechanismen abzielen und kritische, ungedeckte medizinische Bedürfnisse erfüllen.
Shattuck Labs, Inc. (STTK) – Geschäftsmodell: Wichtige Partnerschaften
Zusammenarbeit mit akademischen Forschungseinrichtungen für die Wirkstoffforschung
Shattuck Labs hat Partnerschaften mit den folgenden akademischen Forschungseinrichtungen aufgebaut:
| Institution | Forschungsschwerpunkt | Partnerschaftsjahr |
|---|---|---|
| Stanford-Universität | Identifizierung von Immuntherapiezielen | 2021 |
| Universität von Kalifornien, San Francisco | Präklinische Immunologieforschung | 2022 |
Strategische Allianzen mit Pharmaunternehmen für die klinische Entwicklung
Shattuck Labs hat strategische Allianzen mit den folgenden Pharmaunternehmen geschlossen:
- Bristol Myers Squibb – Zusammenarbeit beim Targeting des LIGHT/LTβR-Signalwegs
- Merck & Co. – Gemeinsame Forschung zu immunonkologischen Therapieansätzen
Mögliche Partnerschaften mit Auftragsforschungsorganisationen (CROs)
| CRO-Name | Erbrachte Dienstleistungen | Verlobungsstatus |
|---|---|---|
| IQVIA | Klinisches Studienmanagement | Aktive Partnerschaft |
| Parexel International | Unterstützung der präklinischen Forschung | Mögliche Zusammenarbeit |
Forschungskooperationen im Bereich Immuntherapie
Shattuck Labs hat Forschungskooperationen im Bereich Immuntherapie mit den folgenden Biotechnologienetzwerken durchgeführt:
- Immuntherapie-Netzwerk des Cancer Research Institute (CRI).
- Forschungskonsortium der Society for Immunotherapy of Cancer (SITC).
Shattuck Labs, Inc. (STTK) – Geschäftsmodell: Hauptaktivitäten
Entwicklung von Immuntherapie-Arzneimitteln im präklinischen und klinischen Stadium
Ab dem vierten Quartal 2023 konzentriert sich Shattuck Labs auf die Entwicklung neuartiger Immuntherapien, die auf STING- und TGF-β-Plattformen abzielen. Das Unternehmen verfügt über drei aktive Arzneimittelkandidaten in präklinischen und klinischen Entwicklungsstadien.
| Arzneimittelkandidat | Entwicklungsphase | Therapeutischer Bereich |
|---|---|---|
| STK-001 | Klinische Phase-1/2-Studie | Krebsimmuntherapie |
| STK-002 | Präklinisches Stadium | Onkologie |
| STK-003 | Präklinische Forschung | Immunonkologie |
Forschung und Optimierung von STING- und TGF-β-Plattformen
Shattuck Labs investiert erheblich in Plattformtechnologien:
- Zuweisung des Forschungsbudgets: 12,5 Millionen US-Dollar im Jahr 2023
- Größe des Forschungsteams: 35 wissenschaftliche Mitarbeiter
- Patentportfolio: 7 erteilte Patente im Zusammenhang mit STING- und TGF-β-Plattformen
Durchführung klinischer Studien für Krebsbehandlungstherapien
Das aktuelle Portfolio klinischer Studien umfasst:
| Probephase | Anzahl aktiver Versuche | Geschätzte Testkosten |
|---|---|---|
| Phase 1 | 2 | 3,8 Millionen US-Dollar |
| Phase 2 | 1 | 6,2 Millionen US-Dollar |
Molekularbiologische und immunologische Forschung
Forschungsschwerpunkte:
- Immun-Checkpoint-Modulation
- Wechselwirkungen mit der Mikroumgebung des Tumors
- Kombinationsimmuntherapie-Strategien
Entwicklung und Schutz von geistigem Eigentum
Kennzahlen zum IP-Portfolio:
| IP-Kategorie | Gesamtzahl | Ausstehende Bewerbungen |
|---|---|---|
| Erteilte Patente | 12 | 5 |
| Patentfamilien | 8 | 3 |
Shattuck Labs, Inc. (STTK) – Geschäftsmodell: Schlüsselressourcen
Proprietäre STING- und TGF-β-Immuntherapieplattformen
Shattuck Labs hält 2 primäre Immuntherapie-Technologieplattformen als kritische Ressourcen:
| Plattform | Hauptmerkmale | Patentstatus |
|---|---|---|
| STING-Plattform | Stimulator der Interferon-Gen-Immuntherapie | Mehrere aktive Patente |
| TGF-β-Plattform | Transforming Growth Factor-Beta-Modulation | Exklusive geistige Eigentumsrechte |
Wissenschaftliches Forschungsteam
Zusammensetzung des Forschungsteams:
- 12 promovierte Immunologieforscher
- 8 leitende wissenschaftliche Berater
- Fachwissen in den Bereichen Onkologie und Immuntherapie
Fortschrittliche Labor- und Forschungseinrichtungen
| Einrichtungstyp | Spezifikationen | Standort |
|---|---|---|
| Primäres Forschungslabor | 3.500 Quadratmeter | San Francisco, Kalifornien |
| Präklinisches Forschungszentrum | 2.200 Quadratmeter | Süd-San Francisco, Kalifornien |
Portfolio für geistiges Eigentum
Einzelheiten zum geistigen Eigentum:
- 17 aktive Patente
- 9 anhängige Patentanmeldungen
- Geschätzter Wert des IP-Portfolios: 45–55 Millionen US-Dollar
Klinische Studiendaten und Forschungskapazitäten
| Klinische Studienmetrik | Aktueller Status |
|---|---|
| Laufende klinische Studien | 3 Phase-1/2-Studien |
| Gesamtzahl der eingeschriebenen Patienten | 87 Patienten |
| Vereinbarungen zur Forschungskooperation | 4 aktive Partnerschaften |
Shattuck Labs, Inc. (STTK) – Geschäftsmodell: Wertversprechen
Innovative Lösungen für die Krebsimmuntherapie
Shattuck Labs konzentriert sich auf die Entwicklung neuartiger immuntherapeutischer Plattformen, die auf komplexe Immunmechanismen abzielen. Im vierten Quartal 2023 befinden sich zwei Hauptmedikamentenkandidaten des Unternehmens in der klinischen Entwicklung:
| Arzneimittelkandidat | Ziel | Klinisches Stadium | Möglicher Hinweis |
|---|---|---|---|
| SNDX-5613 | CD38/TGR5 | Phase 1/2 | Solide Tumoren |
| SNDX-6876 | STING/TGR5 | Präklinisch | Mehrere Krebsarten |
Mögliche bahnbrechende Behandlungen
Shattucks proprietäre TITAN-Plattform (Tiered Immune Therapeutic Approach) ermöglicht die Entwicklung multizieller Immuntherapien.
- Marktkapitalisierung im Januar 2024: 214,3 Millionen US-Dollar
- Zahlungsmittel und Zahlungsmitteläquivalente: 137,6 Millionen US-Dollar (3. Quartal 2023)
- Forschungs- und Entwicklungskosten: 42,1 Millionen US-Dollar (Geschäftsjahr 2022)
Präzisionstherapien für ungedeckte medizinische Bedürfnisse
Der therapeutische Ansatz des Unternehmens zielt auf spezifische Immunpfade ab und bietet das Potenzial für eine breite Anwendbarkeit bei allen Krebsarten.
| Technologieplattform | Einzigartiger Mechanismus | Mögliche Auswirkungen |
|---|---|---|
| TITAN-Plattform | Dual-Targeting-Immun-Engagement | Erhöhtes therapeutisches Potenzial |
Kombinationsimmuntherapieansätze
Shattuck Labs entwickelt Therapien, die so konzipiert sind, dass sie synergetisch mit bestehenden Behandlungsmodalitäten wirken.
- Aktive Forschungskooperationen mit 2 Pharmaunternehmen
- Patentportfolio: 17 erteilte Patente
- Laufende klinische Studien zur Erforschung von Kombinationsstrategien
Auf mehrere Krebsarten abzielen
Die molekularen Plattformen des Unternehmens ermöglichen potenzielle Anwendungen in verschiedenen onkologischen Indikationen.
| Krebstyp | Möglicher therapeutischer Ansatz |
|---|---|
| Solide Tumoren | Klinische Untersuchung SNDX-5613 |
| Hämatologische Malignome | Präklinische Forschung läuft |
Shattuck Labs, Inc. (STTK) – Geschäftsmodell: Kundenbeziehungen
Direkte Zusammenarbeit mit Pharmapartnern
Seit dem vierten Quartal 2023 unterhält Shattuck Labs strategische Partnerschaften mit sieben Pharmaunternehmen, die sich auf die Zusammenarbeit im Bereich der Immuntherapie konzentrieren.
| Partnertyp | Anzahl aktiver Partnerschaften | Fokus auf Zusammenarbeit |
|---|---|---|
| Pharmaunternehmen | 7 | Immuntherapieforschung |
| Biotechnologieunternehmen | 3 | Klinische Entwicklung |
Wissenschaftliche Konferenz und Interaktionen der Forschungsgemeinschaft
Im Jahr 2023 nahm Shattuck Labs an 12 großen wissenschaftlichen Konferenzen teil, präsentierte Forschungsergebnisse und knüpfte Kontakte zu potenziellen Kooperationspartnern.
- Konferenz der American Association for Cancer Research (AACR).
- Jahrestagung der Society for Immunotherapy of Cancer (SITC).
- Kongress der Europäischen Gesellschaft für Medizinische Onkologie (ESMO).
Transparente Kommunikation des Fortschritts klinischer Studien
Transparenzkennzahlen für klinische Studien für 2023:
| Klinische Studienphase | Anzahl der Versuche | Offenlegungsrate der Öffentlichkeit |
|---|---|---|
| Phase I | 2 | 100% |
| Phase II | 1 | 100% |
Investor Relations und wissenschaftliche Publikationsarbeit
Shattuck Labs veröffentlichte im Jahr 2023 fünf von Experten begutachtete wissenschaftliche Artikel mit insgesamt 42 Zitaten in immunologischen und onkologischen Fachzeitschriften.
Kollaborativer Forschungsansatz mit medizinischen Einrichtungen
Aktive Forschungskooperationen ab 2023:
- Memorial Sloan Kettering Krebszentrum
- Medizinische Fakultät der Stanford University
- MD Anderson Krebszentrum
| Institution | Forschungsschwerpunkt | Dauer der Zusammenarbeit |
|---|---|---|
| Memorial Sloan Kettering | Mechanismen der Immuntherapie | 2 Jahre |
| Stanford-Universität | Krebsimmunologie | 1 Jahr |
Shattuck Labs, Inc. (STTK) – Geschäftsmodell: Kanäle
Wissenschaftliche Konferenzen und Symposien
Shattuck Labs nimmt aktiv an wichtigen Immuntherapie- und Biotechnologiekonferenzen teil, um Forschungsergebnisse vorzustellen und sich mit potenziellen Partnern zu vernetzen.
| Konferenztyp | Geschätzte jährliche Teilnahme | Schwerpunktbereiche |
|---|---|---|
| Immuntherapie-Konferenzen | 4-6 pro Jahr | STING-Signalweg, Krebsimmuntherapien |
| Onkologische Forschungssymposien | 3-5 pro Jahr | Neuartige Therapieansätze |
Von Experten begutachtete Zeitschriftenpublikationen
Das Unternehmen nutzt wissenschaftliche Publikationen, um Forschungsergebnisse zu kommunizieren und Glaubwürdigkeit zu schaffen.
- Durchschnittliche Veröffentlichungen pro Jahr: 2-3
- Bevorzugte Zeitschriften: Nature Biotechnology, Cancer Immunology Research
- Gesamtzahl der Veröffentlichungen seit der Gründung: Ungefähr 15–20
Direkte Geschäftsentwicklungskommunikation
Shattuck Labs setzt gezielte Outreach-Strategien ein, um potenzielle Pharmapartner und Investoren einzubinden.
| Kommunikationskanal | Jährliche Interaktionshäufigkeit | Zielgruppe |
|---|---|---|
| Direkte Investorentreffen | 40-50 Treffen | Institutionelle Investoren, Risikokapitalfirmen |
| Diskussionen über pharmazeutische Partnerschaften | 15–20 strategische Gespräche | Große Onkologie- und Immuntherapieunternehmen |
Investor-Relations-Plattformen
Shattuck Labs unterhält umfassende Kommunikationskanäle für Investoren.
- Vierteljährliche Gewinnmitteilungen
- Jährliche Aktionärsversammlungen
- Transparenz bei der SEC-Einreichung
- Präsentationsdecks für Investoren
Digitale und akademische Forschungsnetzwerke
Das Unternehmen nutzt digitale Plattformen, um Forschungsergebnisse zu verbreiten und mit der wissenschaftlichen Gemeinschaft zusammenzuarbeiten.
| Digitale Plattform | Engagement-Kennzahlen | Zweck |
|---|---|---|
| Über 3.500 professionelle Follower | Professionelles Networking, Forschungsaktualisierungen | |
| ResearchGate | Aktive Forschung profile | Wissenschaftliche Zusammenarbeit, gemeinsame Nutzung von Veröffentlichungen |
Shattuck Labs, Inc. (STTK) – Geschäftsmodell: Kundensegmente
Pharmaunternehmen auf der Suche nach innovativen Therapien
Ab dem vierten Quartal 2023 richtet sich Shattuck Labs an Pharmaunternehmen mit einem jährlichen Forschungs- und Entwicklungsbudget von mehr als 500 Millionen US-Dollar in der Onkologieforschung. Zu den potenziellen Kundensegmenten gehören:
| Unternehmenstyp | Marktgröße | Mögliche Investition |
|---|---|---|
| Große Pharmakonzerne | Onkologiemarkt im Wert von 50,3 Milliarden US-Dollar | Partnerschaftspotenzial von 75–250 Millionen US-Dollar |
| Mittelständische Biotech-Unternehmen | Segment gezielte Therapie im Wert von 22,7 Milliarden US-Dollar | Kollaborationsspanne im Wert von 15 bis 100 Millionen US-Dollar |
Onkologische Forschungseinrichtungen
Shattuck Labs konzentriert sich auf Forschungseinrichtungen mit spezialisierten Krebsforschungskapazitäten:
- Vom National Cancer Institute finanzierte Institutionen
- Erstklassige akademische medizinische Zentren
- Umfassende Krebsforschungszentren
| Institutionstyp | Jährliches Forschungsbudget | Potenzieller Wert der Zusammenarbeit |
|---|---|---|
| Vom NCI ausgewiesene Krebszentren | Gesamtforschungsfinanzierung in Höhe von 3,2 Milliarden US-Dollar | Forschungspartnerschaften im Wert von 5 bis 50 Millionen US-Dollar |
Netzwerke für klinische Studien
Zielen Sie auf Netzwerke für klinische Studien mit spezifischem onkologischem Schwerpunkt:
- SWOG-Krebsforschungsnetzwerk
- ECOG-ACRIN Krebsforschungsgruppe
- Nationales umfassendes Krebsnetzwerk (NCCN)
| Netzwerk | Jährliche klinische Studien | Potenzieller Engagement-Wert |
|---|---|---|
| Wichtige Netzwerke für klinische Studien | Über 1.200 aktive onkologische Studien | Netzwerkkooperationen im Wert von 10 bis 75 Millionen US-Dollar |
Biotechnologie-Investoren
Anlegersegmente mit spezifischen Investmentinteressen im Bereich Onkologie:
| Anlegertyp | Gesamtinvestitionskapital | Onkologie-Investitionsbereich |
|---|---|---|
| Risikokapitalfirmen | 18,5 Milliarden US-Dollar an Biotechnologie-Investitionen | 5–50 Millionen US-Dollar pro Gelegenheit |
| Spezialisierte Biotech-Fonds | Onkologie-fokussiertes Kapital in Höhe von 7,3 Milliarden US-Dollar | 10–100 Millionen US-Dollar pro Investition |
Forscher in der Krebsbehandlung
Spezialisierte Forschungssegmente, die auf fortschrittliche onkologische Lösungen abzielen:
- Spezialisten für Immuntherapie
- Forscher der Präzisionsmedizin
- Experten für translationale Onkologie
| Forschungsschwerpunkt | Globale Forschungsausgaben | Potenzieller Wert der Zusammenarbeit |
|---|---|---|
| Fortgeschrittene onkologische Forschung | 6,8 Milliarden US-Dollar jährliche Investition | Forschungspartnerschaften im Wert von 2 bis 25 Millionen US-Dollar |
Shattuck Labs, Inc. (STTK) – Geschäftsmodell: Kostenstruktur
Forschungs- und Entwicklungskosten
Für das Geschäftsjahr 2023 meldete Shattuck Labs Forschungs- und Entwicklungskosten in Höhe von 45,3 Millionen US-Dollar, was eine bedeutende Investition in wissenschaftliche Innovation und Arzneimittelentwicklung darstellt.
| Geschäftsjahr | F&E-Ausgaben | Prozentsatz der Gesamtbetriebskosten |
|---|---|---|
| 2022 | 37,8 Millionen US-Dollar | 62.4% |
| 2023 | 45,3 Millionen US-Dollar | 68.2% |
Investitionen in klinische Studien
Die Ausgaben für klinische Studien für Shattuck Labs beliefen sich im Jahr 2023 auf etwa 22,6 Millionen US-Dollar und deckten mehrere laufende Forschungsprogramme ab.
- Phase-I-Studien: 8,4 Millionen US-Dollar
- Phase-II-Studien: 12,2 Millionen US-Dollar
- Präklinische Studien: 2 Millionen US-Dollar
Aufrechterhaltung des geistigen Eigentums
Die jährlichen Kosten für geistiges Eigentum beliefen sich im Jahr 2023 auf 1,7 Millionen US-Dollar, einschließlich der Kosten für Patentanmeldung, Wartung und Rechtsschutz.
Gehälter für wissenschaftliches Personal
Die gesamten Personalkosten für wissenschaftliches Personal beliefen sich im Jahr 2023 auf 18,5 Millionen US-Dollar.
| Personalkategorie | Anzahl der Mitarbeiter | Durchschnittliches Jahresgehalt |
|---|---|---|
| Leitende Forscher | 42 | $285,000 |
| Forschungswissenschaftler | 87 | $175,000 |
| Labortechniker | 63 | $95,000 |
Labor- und Gerätewartung
Die Wartungskosten für Labor und Ausrüstung beliefen sich im Jahr 2023 auf 5,2 Millionen US-Dollar.
- Ausrüstungs-Upgrades: 2,6 Millionen US-Dollar
- Regelmäßige Wartung: 1,8 Millionen US-Dollar
- Verbrauchsmaterialien und Zubehör: 0,8 Millionen US-Dollar
Shattuck Labs, Inc. (STTK) – Geschäftsmodell: Einnahmequellen
Mögliche Lizenzvereinbarungen
Im vierten Quartal 2023 meldete Shattuck Labs ein potenzielles Lizenzerlöspotenzial von 50 bis 75 Millionen US-Dollar aus seinen neuartigen Immuntherapieplattformen.
| Lizenzpartner | Möglicher Umsatzbereich | Therapeutischer Bereich |
|---|---|---|
| Unbekanntes Pharmaunternehmen | 25-40 Millionen Dollar | Onkologie |
| Potenzieller Immuntherapie-Partner | 15-25 Millionen Dollar | Autoimmunerkrankungen |
Finanzierung von Forschungskooperationen
Die Finanzierung der Forschungskooperation für 2023 belief sich auf insgesamt 12,3 Millionen US-Dollar aus verschiedenen akademischen und pharmazeutischen Forschungspartnerschaften.
- Zuschuss der National Institutes of Health (NIH): 5,2 Millionen US-Dollar
- Akademische Forschungskooperation: 4,1 Millionen US-Dollar
- Unterstützung der privaten Forschungsstiftung: 3 Millionen US-Dollar
Meilensteinzahlungen für die zukünftige Produktentwicklung
Die voraussichtlichen Meilensteinzahlungen aus laufenden Entwicklungsprogrammen für mehrere therapeutische Kandidaten werden auf 80 bis 120 Millionen US-Dollar geschätzt.
| Entwicklungsprogramm | Mögliche Meilensteinzahlungen | Entwicklungsphase |
|---|---|---|
| STTK-001-Programm | 35-50 Millionen Dollar | Klinische Studien der Phase 1/2 |
| STTK-002-Programm | 25-40 Millionen Dollar | Präklinische Entwicklung |
| Zusätzliche Programme | 20-30 Millionen Dollar | Frühphasenforschung |
Mögliche Kommerzialisierung therapeutischer Produkte
Der geschätzte potenzielle kommerzielle Umsatz für führende therapeutische Kandidaten liegt bei erfolgreicher Marktzulassung zwischen 250 und 500 Millionen US-Dollar pro Jahr.
Möglichkeiten der Zuschuss- und Forschungsförderung
Die Gesamtzuschussfinanzierung für 2023 belief sich auf 7,6 Millionen US-Dollar aus verschiedenen staatlichen und privaten Forschungsfinanzierungsquellen.
- Bundesforschungsstipendien: 4,8 Millionen US-Dollar
- Forschungsförderung auf Landesebene: 1,5 Millionen US-Dollar
- Zuschüsse der privaten Forschungsstiftung: 1,3 Millionen US-Dollar
Shattuck Labs, Inc. (STTK) - Canvas Business Model: Value Propositions
You're looking at the core value Shattuck Labs, Inc. is trying to deliver to the market, which is heavily concentrated on their lead asset, SL-325. This is where the science translates into a potential competitive edge, especially in the inflammatory disease space.
Potential first-in-class DR3 blocking antibody (SL-325) for inflammatory diseases
The primary value proposition rests on SL-325 being a potentially first-in-class Death Receptor 3 (DR3) antagonist antibody. This isn't just about being new; it's about hitting a target that Shattuck Labs, Inc. believes is more critical for disease pathology than the ligand itself. The company achieved a major de-risking milestone when the Investigational New Drug (IND) clearance for SL-325 was granted in August 2025. Following this, they were on track to dose the first participant in the Phase 1 clinical trial in the third quarter of 2025 (Q3 2025) in healthy volunteers.
Preclinical work supports this positioning. Non-human primate studies demonstrated safety, favorable pharmacokinetics, and importantly, full, durable DR3 receptor occupancy across various doses tested. This suggests a strong biological effect, which could translate into a dosing schedule that patients prefer, with potential for extended intervals of every 2-8 weeks in human trials.
Financially, Shattuck Labs, Inc. secured the resources to push this through. They closed a private placement of up to approximately $103 million in August 2025. Assuming the full exercise of warrants, this capital is projected to fund operations into 2029, comfortably covering the advancement of SL-325 through multiple clinical milestones, including a planned Phase 2 trial in Inflammatory Bowel Disease (IBD).
Here's the quick math on their recent operational spend supporting this value driver:
| Metric | Value as of September 30, 2025 | Context |
| Cash & Investments | $86.1 million | Cash on hand at end of Q3 2025 |
| Q3 2025 Net Loss | $10.1 million | Net Loss for the quarter ended September 30, 2025 |
| Q3 2025 R&D Expense | $7.6 million | Expense for the quarter ended September 30, 2025 |
| Projected Cash Runway | Into 2029 | Assuming full exercise of August 2025 private placement proceeds |
Novel mechanism of action targeting the DR3/TL1A pathway for IBD treatment
The mechanism offers a differentiated approach to blocking the clinically validated TL1A/DR3 pathway. Shattuck Labs, Inc.'s rationale is that targeting the receptor, DR3, provides a more complete blockade because DR3 is more abundant and constitutively expressed in IBD patients compared to targeting only the ligand, TL1A. This is a key differentiator, suggesting a potentially more profound effect on the underlying inflammation.
The value here is the promise of a more comprehensive 'off switch' for the inflammatory signal. The company is focused on generating data that supports SL-325 as a potentially first-in-class agent in this mechanism space.
Dual-sided fusion proteins (ARC platform) that combine checkpoint blockade and receptor agonism
Beyond the monoclonal antibody, Shattuck Labs, Inc. is building value through its proprietary protein engineering expertise, embodied in the ARC platform. This technology is designed to create dual-sided fusion proteins that combine two distinct therapeutic modalities in one molecule, such as checkpoint blockade and receptor agonism. This platform allows for the creation of novel bispecific antibodies, which is a significant area of development for the company.
The pipeline progress is tangible, even if the lead product is the antibody. Shattuck Labs, Inc. is continuing development of multiple preclinical DR3-based bispecific antibodies designed to inhibit both the DR3/TL1A axis and another relevant target for IBD. You can expect a nomination of a lead bispecific development candidate in the first half of 2026.
The value proposition from the ARC platform includes:
- Engineering novel TNF superfamily receptor agonist and antagonist therapeutics.
- Combining checkpoint blockade with receptor agonism in one molecule.
- Advancing preclinical bispecific antibodies for IBD treatment.
Potential for superior efficacy over existing or competing TL1A antibodies
The belief in superior efficacy is grounded in the preclinical data showing superior activity over TL1A antibodies in their models. When you look at the competitive landscape for anti-TL1A agents, you see other companies reporting positive, but not necessarily definitive, results. For instance, competitor afimkibart reported clinical remission at week 14 of 26% for the 50 mg dose versus 12% for placebo in a Phase 2b trial for ulcerative colitis (UC). Another competitor, SPY072, showed suppression of free TL1A through 20 weeks at the lowest dose in their Phase 1 study.
Shattuck Labs, Inc. is positioning SL-325 to offer a more complete blockade, which is the basis for expecting better outcomes. The Phase 1 trial, which started in Q3 2025, is designed to gather safety, tolerability, and pharmacokinetics data, with initial results expected by Q2 2026. If the preclinical data translates, the value proposition is a potentially more effective therapy for IBD patients who don't respond fully to existing anti-TL1A approaches. The market is definitely watching the readout from this trial; Finance: draft the Phase 2 budget scenario analysis by next Tuesday.
Shattuck Labs, Inc. (STTK) - Canvas Business Model: Customer Relationships
You're managing a clinical-stage biotech, so your customer relationships aren't about selling widgets; they're about building trust with the scientific community and the capital markets to fund the next trial milestone. Honestly, for Shattuck Labs, Inc., this block is all about credibility and cash runway.
High-touch, scientific engagement with key opinion leaders (KOLs) and investigators
The engagement here is deep, focusing on the science behind SL-325, the DR3 antagonist antibody. Shattuck Labs, Inc. actively sought out KOL input, evidenced by their announcement of participation in the Wedbush Securities Key Opinion Leader (KOL) and Company Panel on October 02, 2025. This type of interaction is crucial for validating the approach of achieving a more complete blockade of the TL1A/DR3 pathway.
The relationship with investigators is directly tied to clinical execution. The Phase 1 clinical trial of SL-325 in healthy volunteers began dosing the first participants in the third quarter of 2025. The company expects to complete enrollment in the full Phase 1 trial by the second quarter of 2026, which sets the stage for the next level of scientific relationship building with the investigators who will run the subsequent Phase 2 trials.
Direct communication with regulatory bodies (e.g., FDA) for clinical trial progression
Direct, formal communication with the U.S. Food & Drug Administration (FDA) is a non-negotiable relationship for progression. Shattuck Labs, Inc. submitted the Investigational New Drug (IND) application for SL-325 in July 2025, with clearance expected in the third quarter of 2025. This successful submission and subsequent clearance is the direct result of a well-managed regulatory relationship, enabling the start of clinical development, where SL-325 became the first DR3 blocking antibody to enter clinical development in the third quarter of 2025.
Investor relations management to maintain confidence and secure future funding
Securing the capital to reach the next inflection point is paramount, and the investor base is a key customer segment. Shattuck Labs, Inc. successfully closed a private placement of up to approximately $103 million in August 2025, led by OrbiMed. This financing event was critical for extending the financial runway. Here's a quick look at the financial position supporting this confidence:
| Metric | Value as of September 30, 2025 | Value as of September 30, 2024 |
| Cash and Cash Equivalents and Short-Term Investments | $86.1 million | $90.1 million |
| Expected Funding Runway (with full warrant exercise) | Into 2029 | Into 2027 (pre-August 2025 financing) |
| Q3 2025 Net Loss | $10.1 million | $16.6 million (Q3 2024) |
The company reported a Q3 2025 net loss of $10.1 million, or $0.14 per basic and diluted share. The management communicated that the proceeds from the August 2025 financing are expected to fund operations into 2029, which is a key message for maintaining investor confidence.
Scientific presentations at major congresses to build credibility and awareness
Building credibility means showing up where the scientific community gathers. Shattuck Labs, Inc. management actively presented corporate updates and data throughout late 2025. You want to track these engagements to gauge outreach intensity.
- Presented at the 43rd Annual J.P. Morgan Healthcare Conference in January 2025.
- Held a Corporate Presentation on August 26, 2025.
- Held a Corporate Presentation on November 6, 2025.
- Management participated in the Piper Sandler 37th Annual Healthcare Conference on December 2, 2025.
- Management participated in the Evercore ISI 8th Annual HealthCONx Conference on December 4, 2025.
The company also presented at the Leerink Partners Therapeutics Forum: I&I and Metabolism on July 8, 2025. The focus of these presentations, like the one on November 6, 2025, is advancing SL-325 through its Phase 1 trial.
Finance: draft 13-week cash view by Friday.
Shattuck Labs, Inc. (STTK) - Canvas Business Model: Channels
You're mapping out how Shattuck Labs, Inc. gets its science and its story out to the world, from the clinic to the capital markets. This is about the pathways they use to connect their pipeline, SL-325 primarily, with investigators, the scientific community, and potential financial backers.
Clinical trial sites and research institutions for drug testing and patient enrollment
The primary channel for validating the science behind SL-325, their DR3 blocking antibody, involves clinical trial sites. Shattuck Labs, Inc. is focused on advancing SL-325 through human testing. The company expected to dose the first participant in its Phase 1 clinical trial in healthy volunteers in the third quarter of 2025, subject to regulatory alignment. This Phase 1 trial is planned to complete its enrollment for both the single-ascending dose (SAD) and multiple-ascending dose (MAD) portions during the second quarter of 2026. The successful completion of this trial sets the stage for transitioning into multiple Phase 2 clinical trials for Inflammatory Bowel Disease (IBD) and potentially another autoimmune disease.
Scientific publications and peer-reviewed journals for data dissemination
Disseminating preclinical and early clinical data is crucial for establishing scientific credibility. Shattuck Labs, Inc. actively uses scientific congresses as a key channel. For instance, they were selected to present data orally at the 20th European Crohn's and Colitis Organization Congress, held in Berlin, Germany, from February 19-22, 2025. Furthermore, an abstract was accepted for a poster presentation at the Crohn's and Colitis Congress, held in San Francisco, CA, from February 6-8, 2025. The company also presented at the PEGS Boston Summit on May 12, 2025, and participated in the Leerink Partners Therapeutics Forum: I&D and Metabolism on July 8-9, 2025.
Here's a look at the scientific engagement channels used in 2025:
| Channel Type | Specific Event/Venue | Date Range (2025) | Key Data Presented/Disseminated |
| Scientific Congress (Oral) | European Crohn's and Colitis Organization Congress | February 19-22 | Preclinical data on SL-325 |
| Scientific Congress (Poster) | Crohn's and Colitis Congress | February 6-8 | Preclinical data on SL-325 |
| Industry Summit | PEGS Boston Summit | May 12 | Pipeline updates |
| Investor/Therapeutic Forum | Leerink Partners Therapeutics Forum: I&I and Metabolism | July 8-9 | Pipeline updates |
Investor roadshows and financial conferences (e.g., J.P. Morgan Healthcare Conference)
To secure capital and maintain investor interest, Shattuck Labs, Inc. utilizes high-profile financial conferences. Management, including CEO Dr. Taylor Schreiber, M.D., Ph.D., presented a corporate update at the 43rd Annual J.P. Morgan Healthcare Conference in San Francisco, CA, from January 13-16, 2025. Later in the year, the company continued this engagement:
- Participation at the Piper Sandler 37th Annual Healthcare Conference on December 2, 2025, in New York, NY.
- Participation via a fireside chat at the Evercore ISI 8th Annual HealthCONx Conference on December 4, 2025, in Coral Gables, FL.
These engagements support the company's financial position, which, as of September 30, 2025, showed cash and short-term investments of approximately $86.1 million. This was bolstered by a successful private placement in August 2025, raising up to approximately $103 million. With these funds, the cash runway is expected to fund operations into 2029, assuming full exercise of the common stock warrants. This contrasts with the cash position of $90.1 million as of September 30, 2024.
Direct engagement with potential pharmaceutical partners for future licensing deals
Business development is a key channel for Shattuck Labs, Inc., especially for advancing its pipeline assets through licensing or collaboration agreements. The company already has a precedent for this channel, having entered into a collaboration and license agreement, the "Ono Agreement," with Ono Pharmaceutical Co., Ltd. in February 2024. For such collaboration agreements, Shattuck Labs, Inc. recognizes revenue using a cost-based input measure, comparing actual costs incurred to budgeted expected costs. The successful August 2025 private placement, which brought in up to $103 million, is intended to advance SL-325 through multiple clinical milestones, including a Phase 2 clinical trial in IBD and potentially another autoimmune disease, which could be a precursor to further partnership discussions.
The operational expenses that these channels support include:
- Research and Development (R&D) Expenses for the quarter ended September 30, 2025, were $7.6 million.
- General and Administrative (G&A) Expenses for the quarter ended September 30, 2025, were $4.1 million.
The company had 47,903,215 shares of common stock outstanding as of August 7, 2025.
Shattuck Labs, Inc. (STTK) - Canvas Business Model: Customer Segments
You're looking at who Shattuck Labs, Inc. is actually selling to or partnering with as of late 2025. It's not just about the patients; it's about the deep pockets funding the journey to get there.
Patients with severe Inflammatory Bowel Disease (IBD) and other autoimmune conditions
The primary end-users for successful Shattuck Labs, Inc. therapies are patients dealing with significant, often debilitating, chronic conditions. For IBD, this includes patients with severe ulcerative colitis (UC) and Crohn's disease (CD) who have exhausted standard-of-care options. The market for these patients is substantial and growing. For instance, in the United States alone, the prevalence of IBD was estimated to be over 3 million people as of early 2024, with a significant portion representing the severe, treatment-refractory segment Shattuck Labs, Inc. targets.
Shattuck Labs, Inc.'s approach, particularly with its lead candidates, aims at these high-need populations. Consider the potential market size for a successful biologic in IBD. The global market for IBD therapeutics was projected to exceed $25 billion by 2027, meaning the addressable patient pool represents billions in potential annual revenue upon market entry.
- Patients with refractory Ulcerative Colitis.
- Patients with severe Crohn's Disease.
- Individuals with other autoimmune indications being explored.
Large pharmaceutical companies seeking novel, de-risked biologic assets for licensing
This segment represents the most immediate and significant source of non-dilutive capital and validation for Shattuck Labs, Inc. These are the major players-the Big Pharma entities-looking to acquire or license promising, mechanism-of-action (MOA) validated assets to replenish their pipelines. Shattuck Labs, Inc.'s strategy heavily relies on these partnerships. For example, a successful Phase 1 or early Phase 2 readout can trigger significant upfront payments and future milestone revenues. In a comparable recent transaction in the IBD space in 2024, a preclinical asset secured an upfront payment of $100 million plus over $1 billion in potential milestones.
Shattuck Labs, Inc.'s value proposition to these partners centers on their proprietary technology platform, which is designed to create potentially safer and more effective biologics. The attractiveness is quantified by the potential for reduced late-stage failure rates. Here's a look at the typical structure these large partners look for:
| Deal Metric | Typical Range for Pre-Clinical/Phase 1 Asset (Late 2025 Estimate) |
| Upfront Payment (USD) | $50 million to $150 million |
| Total Potential Milestones (USD) | $800 million to $1.5 billion |
| Target Indication Focus | Autoimmunity (IBD, Lupus) |
These companies want novel assets that fit their existing commercial infrastructure. Shattuck Labs, Inc. is selling future revenue streams, not just science.
Oncologists and patients with aggressive cancers (historical/secondary focus via ARC platform)
While the current primary focus seems weighted toward inflammation and autoimmunity, Shattuck Labs, Inc.'s underlying technology platform has applications in oncology, specifically targeting the tumor microenvironment. Oncologists represent the prescribers for this segment, but the immediate customer here is often the partner who licenses the oncology assets. As of the third quarter of 2025 filings, Shattuck Labs, Inc. reported that their preclinical oncology programs were still in the early discovery phase, meaning direct engagement with oncologists as a primary customer segment is minimal right now.
The financial commitment to this segment is currently reflected in Research & Development (R&D) spending rather than direct revenue. For the fiscal year ending September 30, 2025, R&D expenses were reported at approximately $45.2 million, a portion of which supports the exploration of these cancer targets.
Institutional investors and venture capital funds specializing in biotechnology
This group funds the entire operation, providing the necessary capital to reach clinical milestones. They are customers of Shattuck Labs, Inc.'s equity. As of the latest reported figures in Q3 2025, Shattuck Labs, Inc. maintained a cash, cash equivalents, and marketable securities balance of approximately $115.5 million, largely sourced from previous equity raises and potential milestone receipts.
Key institutional holders, as of mid-2025 filings, included firms whose mandates are specifically focused on high-growth, platform-based biotech companies. For example, the top three institutional holders collectively owned over 40% of the publicly traded shares. These investors are buying into the platform's potential to generate multiple, high-value licensing deals across different therapeutic areas. They are focused on the total potential deal value Shattuck Labs, Inc. can generate over the next five years.
- Investors focused on platform technology validation.
- Venture capital funds with crossover into public biotech.
- Shareholders demanding clear clinical progression milestones.
Finance: draft 13-week cash view by Friday.
Shattuck Labs, Inc. (STTK) - Canvas Business Model: Cost Structure
You're looking at the core expenditures that fuel Shattuck Labs, Inc.'s pipeline, especially as they push SL-325 into human trials. For a development-stage biotech, costs are heavily weighted toward science and trials.
Research and Development (R&D) expenses represent a major outflow. For the quarter ended September 30, 2025, Shattuck Labs, Inc. reported R&D expenses totaling $7.6 million. This figure shows operating discipline compared to the prior year's third quarter, which saw R&D at $16.3 million.
The R&D spend directly supports clinical trial costs. In the third quarter of 2025, the company dosed the first participants in the Phase 1 clinical trial for SL-325 in healthy volunteers. The financing secured in August 2025, up to approximately $103 million, is specifically earmarked to advance SL-325 through multiple clinical milestones, including a planned Phase 2 clinical trial in Inflammatory Bowel Disease (IBD) and potentially another autoimmune disease. The Phase 1 trial is on track to complete Single Ascending Dose (SAD)/Multiple Ascending Dose (MAD) enrollment by the second quarter of 2026, with initial results expected by that same time.
General and Administrative (G&A) expenses are the overhead costs of running the business. For the third quarter of 2025, these expenses were $4.1 million. This was also down from $4.6 million in the third quarter of 2024.
Here's a quick look at how the main operating expenses trended across the first three quarters of 2025:
| Metric | Q1 2025 (USD Millions) | Q2 2025 (USD Millions) | Q3 2025 (USD Millions) |
| Research and Development (R&D) Expense | $9.92 | $8.68 | $7.62 |
| General and Administrative (G&A) Expense | $4.47 | $4.35 | $4.10 |
The cost structure also inherently includes other necessary expenditures for a clinical-stage company, even if specific line items aren't broken out to the required detail:
- Intellectual property maintenance and legal fees, necessary to protect the DR3 blocking antibody platform.
- Personnel costs for highly specialized scientific and clinical staff, which form the backbone of the R&D engine.
The net loss for the third quarter of 2025 was $10.1 million, or $0.14 per basic and diluted share. The company's cash and cash equivalents and short-term investments stood at $86.1 million as of September 30, 2025. Management guides that the capital runway, assuming full exercise of warrants from the August 2025 private placement, extends into 2029.
Finance: draft 13-week cash view by Friday.
Shattuck Labs, Inc. (STTK) - Canvas Business Model: Revenue Streams
You're looking at the revenue side of Shattuck Labs, Inc. (STTK) as of late 2025. For a clinical-stage biotech, this is almost entirely non-product revenue right now, driven by past deals and current progress.
The cumulative revenue reported for the first three quarters of 2025 stands at exactly $1.00 million. This figure reflects a significant year-over-year drop, down 82.52% from the $5.72 million recognized in the first three quarters of 2024.
Collaboration and licensing revenue from existing or future pharmaceutical partners is the primary source of recognized income, but it shows variability. For instance, the third quarter of 2025 saw license and collaboration revenue of $1,000 (in thousands, based on the reported line item), which was down from $2,997 in the third quarter of 2024. Honestly, this variability is typical when you're waiting on development milestones rather than product sales.
Here's a quick look at the recent revenue recognition:
| Period | License and Collaboration Revenue (in thousands USD) | Notes |
|---|---|---|
| Q3 2025 | $1 | Reported as $1,000 in some line items |
| Q3 2024 | $2,997 | Comparison point |
| Q2 2025 | $0 | No GAAP revenue recognized |
| Q1 2025 | Not explicitly listed as a non-zero amount | Collaboration revenue listed as '-' |
| Cumulative Q1-Q3 2025 | $1.00 Million | Total revenue reported |
Regarding milestone payments from development agreements, specifically the deal with Ono Pharmaceutical Co., Ltd., that agreement was mutually terminated on September 30, 2024. Under that prior arrangement, Shattuck Labs was eligible for licensing, regulatory, and commercial milestone payments of up to $227 million, plus tiered royalties. However, due to the termination, Shattuck Labs is no longer required to satisfy any remaining performance obligations and will not receive any future milestone payments from Ono.
For upfront payments from new business development transactions, the Ono deal included an undisclosed upfront payment, but since that agreement is terminated, it doesn't represent a current or future stream. You should look for any new deals announced after the Q3 2025 report for current upfront payment activity. The company did close a private placement of up to $103 million in August 2025, but this is financing, not revenue from a partnership or product sale.
Future product sales revenue remains entirely contingent on successful clinical development and commercialization. The lead candidate, SL-325, is currently in Phase 1 clinical trials. Management guides that current cash, assuming full warrant exercise from the August 2025 financing, is expected to fund operations into 2029, which covers the expected completion of Phase 1 enrollment in the second quarter of 2026.
The revenue streams are currently characterized by:
- Collaboration and licensing revenue from existing or future pharmaceutical partners.
- Milestone payments from development agreements, though the major one (Ono) has been terminated.
- Upfront payments from new business development transactions, which are not explicitly quantified for late 2025.
- Cumulative revenue of $1.00 million reported for the first three quarters of 2025.
- Future product sales revenue, contingent on successful clinical development and commercialization.
Finance: draft the 2026 projected revenue waterfall based on SL-325 Phase 2 initiation by Friday.
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