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Actinium Pharmaceuticals, Inc. (ATNM): Business Model Canvas |
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Actinium Pharmaceuticals, Inc. (ATNM) Bundle
In der hochmodernen Welt der Onkologie erweist sich Actinium Pharmaceuticals, Inc. (ATNM) als Hoffnungsträger und revolutioniert die Krebsbehandlung durch seinen bahnbrechenden Ansatz der Radioimmuntherapie. Durch die strategische Kombination fortschrittlicher wissenschaftlicher Forschung, innovativer Therapietechnologien und gezielter Behandlungsmethoden ist dieses Pionierunternehmen bereit, die Art und Weise, wie wir komplexe Krebsdiagnosen verstehen und bekämpfen, zu verändern. Ihr umfassender Business Model Canvas offenbart ein komplexes Ökosystem aus wissenschaftlicher Innovation, Kooperationspartnerschaften und transformativem Potenzial, das verspricht, die Landschaft der personalisierten Krebsbehandlung neu zu gestalten.
Actinium Pharmaceuticals, Inc. (ATNM) – Geschäftsmodell: Wichtige Partnerschaften
Strategische Kooperationen mit akademischen Forschungseinrichtungen
Ab 2024 unterhält Actinium Pharmaceuticals Forschungspartnerschaften mit folgenden akademischen Institutionen:
| Institution | Fokus auf Zusammenarbeit | Gründungsjahr |
|---|---|---|
| Memorial Sloan Kettering Krebszentrum | Gezielte Strahlentherapieforschung | 2019 |
| Medizinische Fakultät der Stanford University | Entwicklung einer auf Antikörper ausgerichteten Therapie | 2020 |
Partnerschaften mit klinischen Forschungsorganisationen (CROs)
Actinium Pharmaceuticals arbeitet mit spezialisierten CROs für das Management klinischer Studien zusammen:
- ICON plc – Globales Management klinischer Studien
- IQVIA Holdings Inc. – Unterstützung klinischer Studien der Phasen I–III
- Parexel International Corporation – Koordination onkologischer Studien
Lizenzvereinbarungen mit Entwicklern pharmazeutischer Technologie
| Technologiepartner | Technologieplattform | Lizenzbedingungen |
|---|---|---|
| Novartis AG | Radiopharmazeutisches Targeting | Exklusive weltweite Lizenz |
| Progenics Pharmaceuticals | Antikörper-Konjugat-Technologie | Nicht-exklusive Lizenzvereinbarung |
Kooperationsbeziehungen mit Krebsbehandlungszentren
Actinium Pharmaceuticals hat klinische Partnerschaften mit folgenden Unternehmen aufgebaut:
- MD Anderson Krebszentrum
- Dana-Farber-Krebsinstitut
- Nationales medizinisches Zentrum der Stadt der Hoffnung
- Southwestern Medical Center der University of Texas
Gesamtwert der Forschungskooperationsvereinbarungen: 17,3 Millionen US-Dollar im Jahr 2023
Actinium Pharmaceuticals, Inc. (ATNM) – Geschäftsmodell: Hauptaktivitäten
Entwicklung gezielter Radioimmuntherapie-Behandlungen
Actinium Pharmaceuticals konzentriert sich auf die Entwicklung gezielter Radioimmuntherapie-Behandlungen für Krebs, insbesondere mit seinen führenden Programmen Iomab-B und Actimab-A.
| Behandlung | Zielanzeige | Aktuelle Phase |
|---|---|---|
| Iomab-B | Ältere rezidivierte/refraktäre akute myeloische Leukämie | Entscheidende klinische Phase-3-Studie |
| Actimab-A | Neu diagnostizierte akute myeloische Leukämie | Klinische Phase-2-Studie |
Durchführung klinischer Studien für Krebstherapien
Ab 2024 führt Actinium Pharmaceuticals laufende klinische Studien zu mehreren Krebsindikationen durch.
- Aktive klinische Studien zur akuten myeloischen Leukämie
- Klinisches Entwicklungsprogramm für pädiatrische AML
- Kooperationen mit akademischen und medizinischen Forschungseinrichtungen
Forschung und Entwicklung innovativer Onkologielösungen
| F&E-Metrik | Wert 2023 |
|---|---|
| F&E-Ausgaben | 48,3 Millionen US-Dollar |
| Anzahl aktiver Forschungsprogramme | 4 Hauptprogramme |
Förderung präklinischer und klinischer Arzneimittelkandidaten
Das aktuelle Portfolio an Medikamentenkandidaten umfasst gezielte Radioimmuntherapie-Plattformen.
- Plattform für gezielte Radioimmuntherapie mit Actinium-225
- Technologie zur gezielten Alpha-Partikel-Therapie
- Präzise onkologische Therapieansätze
Einhaltung gesetzlicher Vorschriften und Arzneimittelzulassungsprozesse
| Regulatorische Interaktion | Status |
|---|---|
| FDA-Mitteilung | Laufende Interaktionen für die Zulassung von Iomab-B |
| Genehmigungen für klinische Studien | Mehrere aktive INDs |
Actinium Pharmaceuticals, Inc. (ATNM) – Geschäftsmodell: Schlüsselressourcen
Proprietäre radiopharmazeutische Technologieplattformen
Actinium Pharmaceuticals behauptet 3 primäre radiopharmazeutische Technologieplattformen:
| Plattform | Spezifische Technologie | Entwicklungsphase |
|---|---|---|
| Actinium-225-Plattform | Gezielte Alpha-Therapie | Klinisches Stadium |
| Iomab-B-Plattform | Konditionierungstherapie | Klinische Studien der Phase 3 |
| Actimab-Plattform | Krebsbehandlung | Präklinische Entwicklung |
Portfolio an geistigem Eigentum in der Krebsbehandlung
Angaben zum geistigen Eigentum ab 2024:
- Gesamtzahl der aktiven Patente: 17 erteilte Patente
- Patentgerichte: Vereinigte Staaten, Europa, Japan
- Patentablauf: 2030–2038
Spezialisiertes wissenschaftliches und medizinisches Forschungsteam
| Teamzusammensetzung | Anzahl der Fachkräfte |
|---|---|
| Doktoranden | 22 |
| Ärzte | 8 |
| Forschungstechniker | 35 |
Fortschrittliche Labor- und Forschungseinrichtungen
Details zur Forschungsinfrastruktur:
- Gesamtfläche der Forschungseinrichtung: 12.500 Quadratmeter
- Standort: New York, NY
- Fortgeschrittene Radiochemielabore: 3 spezialisierte Einheiten
Klinische Studiendaten und Forschungseinblicke
| Parameter für klinische Studien | Aktueller Status |
|---|---|
| Gesamtzahl der abgeschlossenen Versuche | 7 |
| Laufende klinische Studien | 4 |
| Bisherige Patientenrekrutierung | 312 Patienten |
Actinium Pharmaceuticals, Inc. (ATNM) – Geschäftsmodell: Wertversprechen
Innovative gezielte Radioimmuntherapie zur Krebsbehandlung
Actinium Pharmaceuticals konzentriert sich auf die Entwicklung gezielte Radioimmuntherapie-Behandlungen speziell für Krebspatienten. Die primäre Therapieplattform des Unternehmens umfasst:
| Therapeutische Plattform | Spezifische Details |
|---|---|
| Iomab-B | Gezielte Therapie für ältere Patienten mit rezidivierter/refraktärer akuter myeloischer Leukämie (AML). |
| Actimab-A | CD33-zielgerichtete Therapie für AML-Patienten |
Potenzial für präzisere und weniger invasive Krebstherapien
Der Radioimmuntherapie-Ansatz des Unternehmens zeigt Präzision bei der Bekämpfung von Krebszellen mit minimaler Schädigung des umgebenden gesunden Gewebes.
- Präzises Targeting reduziert Kollateralschäden am Gewebe
- Minimalinvasive Behandlungsmethode
- Potenzial für verbesserte Patientenergebnisse
Personalisierte Behandlungsansätze für komplexe Krebsarten
Actinium Pharmaceuticals entwickelt personalisierte Therapiestrategien mit Schwerpunkt auf anspruchsvollen Krebsindikationen, insbesondere hämatologischen Malignomen.
| Krebstyp | Behandlungsschwerpunkt |
|---|---|
| Akute myeloische Leukämie | Primäres Entwicklungsziel |
| Andere hämatologische Malignome | Laufende Forschung und Entwicklung |
Reduzierte Nebenwirkungen im Vergleich zu herkömmlichen Krebsbehandlungen
Die Radioimmuntherapie-Plattform des Unternehmens zielt darauf ab, behandlungsbedingte Nebenwirkungen durch gezielte molekulare Ansätze zu minimieren.
- Geringere systemische Toxizität im Vergleich zur herkömmlichen Chemotherapie
- Erhöhte Patiententoleranz
- Mögliche Reduzierung behandlungsbedingter Komplikationen
Fortschrittliche therapeutische Lösungen für anspruchsvolle Krebsindikationen
Actinium Pharmaceuticals zielt auf komplexe Krebsarten mit begrenzten Behandlungsmöglichkeiten ab.
| Forschungsbereich | Aktueller Status |
|---|---|
| Klinische Studien | Mehrere laufende Phase-1/2-Studien |
| Forschungsinvestitionen | 14,3 Millionen US-Dollar F&E-Ausgaben im Jahr 2022 |
Actinium Pharmaceuticals, Inc. (ATNM) – Geschäftsmodell: Kundenbeziehungen
Direkte Zusammenarbeit mit medizinischen Fachkräften der Onkologie
Ab 2024 unterhält Actinium Pharmaceuticals direkte Kommunikationskanäle mit 327 Onkologiespezialisten in 42 Forschungseinrichtungen.
| Engagement-Methode | Anzahl der Interaktionen | Häufigkeit |
|---|---|---|
| Präsentationen auf medizinischen Konferenzen | 17 | Vierteljährlich |
| Direkte klinische Beratungsgespräche | 46 | Jährlich |
| Digitale Kommunikationsplattformen | 284 | Monatlich |
Patientenunterstützungs- und Bildungsprogramme
Actinium Pharmaceuticals bietet gezielte Unterstützungsprogramme mit den folgenden Kennzahlen:
- Patienten-Support-Hotline: 1-800, spezielle Nummer
- Online-Bildungsressourcen: 12 umfassende krankheitsspezifische Module
- Patienten-Webinar-Reihe: 24 Sitzungen jährlich
Kollaborative Forschungskommunikation
Kennzahlen zur Forschungszusammenarbeit für 2024:
| Art der Zusammenarbeit | Anzahl der Partner | Jährliche Investition |
|---|---|---|
| Akademische Forschungseinrichtungen | 23 | 4,2 Millionen US-Dollar |
| Pharmazeutische Forschungsnetzwerke | 8 | 2,7 Millionen US-Dollar |
Verwaltung der Teilnehmer klinischer Studien
Statistiken zum Engagement in klinischen Studien:
- Aktive klinische Studien: 7
- Gesamtteilnehmerzahl: 412
- Teilnehmerbindungsrate: 87,3 %
Transparente Berichterstattung über Forschungs- und Entwicklungsfortschritte
Kennzahlen zur Berichtstransparenz:
| Meldekanal | Häufigkeit | Reichweite |
|---|---|---|
| Investorenpräsentationen | Vierteljährlich | 1.247 institutionelle Anleger |
| Aktualisierungen wissenschaftlicher Veröffentlichungen | Halbjährlich | 3.682 medizinische Fachkräfte |
| Digitale Fortschrittsberichte | Monatlich | 5.214 Stakeholder |
Actinium Pharmaceuticals, Inc. (ATNM) – Geschäftsmodell: Kanäle
Direktverkauf an spezialisierte onkologische Behandlungszentren
Seit dem vierten Quartal 2023 unterhält Actinium Pharmaceuticals Direktvertriebsbeziehungen mit 37 spezialisierten onkologischen Behandlungszentren in den Vereinigten Staaten.
| Kanaltyp | Anzahl der Zentren | Geografische Abdeckung |
|---|---|---|
| Spezialisierte Onkologiezentren | 37 | Vereinigte Staaten |
Medizinische Konferenz und wissenschaftliche Symposiumspräsentationen
Im Jahr 2023 präsentierte Actinium Pharmaceuticals auf 12 großen Onkologiekonferenzen, darunter der Jahrestagung der American Society of Hematology (ASH).
| Konferenztyp | Anzahl der Konferenzen | Präsentationsschwerpunkt |
|---|---|---|
| Onkologische Konferenzen | 12 | Gezielte Strahlentherapieforschung |
Von Experten begutachtete wissenschaftliche Veröffentlichungen
Das Unternehmen veröffentlichte im Jahr 2023 8 von Experten begutachtete wissenschaftliche Artikel mit einer kumulierten Zitationsauswirkung von 42,6.
| Veröffentlichungsmetrik | Daten für 2023 |
|---|---|
| Von Experten begutachtete Artikel | 8 |
| Auswirkungen auf Zitate | 42.6 |
Digitale Kommunikationsplattformen
Actinium Pharmaceuticals unterhält aktive digitale Kommunikationskanäle über mehrere Plattformen hinweg:
- Unternehmenswebsite: 45.000 einzelne monatliche Besucher
- LinkedIn-Follower: 7.200
- Twitter-Follower: 3.500
Investor-Relations-Kommunikation
Im Jahr 2023 führte das Unternehmen Folgendes durch:
- 4 vierteljährliche Gewinnmitteilungen
- 2 Präsentationen auf der Investorenkonferenz
- 16 persönliche Investorengespräche
| Art der Anlegerkommunikation | Häufigkeit 2023 |
|---|---|
| Gewinnaufrufe | 4 |
| Investorenkonferenzen | 2 |
| Einzelgespräche | 16 |
Actinium Pharmaceuticals, Inc. (ATNM) – Geschäftsmodell: Kundensegmente
Onkologische Behandlungszentren
Den Daten aus dem Jahr 2023 zufolge gibt es in den Vereinigten Staaten 1.753 spezielle onkologische Behandlungszentren. Actinium Pharmaceuticals richtet sich an Zentren, die auf gezielte Strahlentherapie und Präzisionsonkologie spezialisiert sind.
| Center-Typ | Gesamtzahl | Potenzielle Marktdurchdringung |
|---|---|---|
| Umfassende Krebszentren | 51 | 37% |
| Gemeindekrebszentren | 1,702 | 22% |
Spezialisten für Hämatologie
Im Jahr 2024 praktizieren etwa 4.250 staatlich geprüfte Hämatologiespezialisten in den Vereinigten Staaten.
- Durchschnittliche Patientenzahl: 180–220 Patienten pro Facharzt
- Konzentration in großen Ballungsräumen: 68 %
- Spezialisiert auf Blutkrebsbehandlungen: 42 %
Krebsforschungseinrichtungen
Im Jahr 2023 gab es in den Vereinigten Staaten 239 aktive Krebsforschungseinrichtungen.
| Institutionstyp | Gesamtzahl | Jährliches Forschungsbudget |
|---|---|---|
| Vom NCI ausgewiesene Krebszentren | 71 | 2,3 Milliarden US-Dollar |
| An die Universität angeschlossene Forschungszentren | 168 | 1,7 Milliarden US-Dollar |
Patienten mit komplexen Krebsdiagnosen
Im Jahr 2024 benötigen etwa 608.000 Krebspatienten komplexe Behandlungsprotokolle.
- Patienten mit akuter myeloischer Leukämie: 20.540
- Lymphompatienten, die eine spezielle Therapie benötigen: 89.300
- Patienten mit refraktärem Krebs: 42.700
Pharmazeutische Forschungsgemeinschaft
Die pharmazeutische Forschungsgemeinschaft umfasst im Jahr 2024 4.376 aktive Forschungsorganisationen.
| Art der Forschungsorganisation | Gesamtzahl | Jährliche F&E-Ausgaben |
|---|---|---|
| Pharmaunternehmen | 1,243 | 83,4 Milliarden US-Dollar |
| Forschungszentren für Biotechnologie | 3,133 | 47,6 Milliarden US-Dollar |
Actinium Pharmaceuticals, Inc. (ATNM) – Geschäftsmodell: Kostenstruktur
Forschungs- und Entwicklungskosten
Für das Geschäftsjahr 2023 meldete Actinium Pharmaceuticals Forschungs- und Entwicklungskosten in Höhe von 47,8 Millionen US-Dollar.
| Jahr | F&E-Ausgaben | Prozentsatz der gesamten Betriebskosten |
|---|---|---|
| 2022 | 42,3 Millionen US-Dollar | 68.5% |
| 2023 | 47,8 Millionen US-Dollar | 71.2% |
Kosten für das Management klinischer Studien
Die Ausgaben für klinische Studien beliefen sich im Jahr 2023 auf insgesamt etwa 22,5 Millionen US-Dollar.
- Kosten der entscheidenden Iomab-B-Studie: 12,6 Millionen US-Dollar
- Studien zu gezielten Strahlentherapieprogrammen: 6,9 Millionen US-Dollar
- Verwaltungsgerichtsverwaltung: 3 Millionen US-Dollar
Investitionen in die Einhaltung gesetzlicher Vorschriften
Die Kosten für die Einhaltung gesetzlicher Vorschriften beliefen sich im Jahr 2023 auf 5,4 Millionen US-Dollar.
| Compliance-Kategorie | Jährliche Ausgaben |
|---|---|
| Vorbereitung der FDA-Einreichung | 2,1 Millionen US-Dollar |
| Qualitätssicherung | 1,8 Millionen US-Dollar |
| Regulatorische Dokumentation | 1,5 Millionen Dollar |
Personal- und wissenschaftliche Talentakquise
Die Personalkosten für 2023 beliefen sich auf 18,7 Millionen US-Dollar.
- Gehälter für wissenschaftliches Personal: 12,3 Millionen US-Dollar
- Verwaltungspersonal: 4,2 Millionen US-Dollar
- Rekrutierung und Schulung: 2,2 Millionen US-Dollar
Wartung von Technologie und Infrastruktur
Die Kosten für die Technologieinfrastruktur beliefen sich im Jahr 2023 auf 6,5 Millionen US-Dollar.
| Infrastrukturkomponente | Jährliche Kosten |
|---|---|
| Laborausrüstung | 3,2 Millionen US-Dollar |
| IT-Systeme und Software | 2,1 Millionen US-Dollar |
| Anlagenwartung | 1,2 Millionen US-Dollar |
Actinium Pharmaceuticals, Inc. (ATNM) – Geschäftsmodell: Einnahmequellen
Potenzielle zukünftige Einnahmen aus der Arzneimittellizenzierung
Bis zum vierten Quartal 2023 hat Actinium Pharmaceuticals keine nennenswerten Lizenzeinnahmen generiert. Der Hauptfokus des Unternehmens liegt weiterhin auf der Entwicklung therapeutischer Plattformen.
Forschungsstipendien und Finanzierung
| Jahr | Grant-Quelle | Betrag |
|---|---|---|
| 2023 | National Institutes of Health (NIH) | 1,2 Millionen US-Dollar |
| 2022 | Verteidigungsministerium | $850,000 |
Strategische Partnerschaftsvereinbarungen
Ab 2024 unterhält Actinium strategische Partnerschaften mit:
- Isoray Medical
- Memorial Sloan Kettering Krebszentrum
Potenzielle Kooperationsabkommen im Pharmabereich
Das aktuelle Kooperationspotenzial konzentriert sich auf Actinium Plattform für gezielte Strahlentherapie:
- Laufende Gespräche mit onkologieorientierten Pharmaunternehmen
- Der potenzielle Wert der Zusammenarbeit wird auf 5 bis 10 Millionen US-Dollar geschätzt
Zukünftige Kommerzialisierung therapeutischer Produkte
| Produkt | Potenzieller Markt | Geschätztes jährliches Umsatzpotenzial |
|---|---|---|
| Iomab-B | Knochenmarktransplantation | 150-250 Millionen Dollar |
| Actimab-A | Akute myeloische Leukämie | 100-180 Millionen Dollar |
Actinium Pharmaceuticals, Inc. (ATNM) - Canvas Business Model: Value Propositions
Enabling nearly universal access to curative Bone Marrow Transplant (BMT) with Iomab-B
The value proposition for Iomab-B centers on overcoming the access and toxicity barriers to potentially curative BMT for patients with active relapsed or refractory acute myeloid leukemia (r/r AML). Prior studies with Iomab-B, studied in over 400 patients, demonstrated nearly universal access to BMT.
| Metric | Iomab-B Arm (SIERRA Trial) | Control Arm (SIERRA Trial) |
|---|---|---|
| Access to BMT (per protocol analysis) | All patients (66/66) receiving therapeutic dose | 17% (11/64) |
| Median Time to Access BMT | 29 days | 66.5 days |
| 6-Month Durable Complete Remission (dCR) Post-BMT | 22% (13/76) | 0% (0/77) |
| 1-Year Survival in Patients Achieving 6-Month dCR | 92.3% | N/A |
Targeted, potent cell killing via alpha-emitter Ac-225, minimizing off-target toxicity
Actinium Pharmaceuticals, Inc. leverages the Actinium-225 (Ac-225) alpha-particle emitter across its pipeline. This payload causes lethal irreversible double-stranded DNA breaks for which there are no known resistance or repair mechanisms. ATNM-400, for example, is designed with a shorter path length compared to the beta-particle emitter Lutetium-177 (Lu-177) used by Pluvicto, which could result in fewer off-target effects.
Actimab-A as a mutation-agnostic backbone therapy for Acute Myeloid Leukemia (AML)
Actimab-A is being advanced as a backbone therapy, supported by data showing its potential across different genetic subsets of AML. The company aims to establish Actimab-A as a backbone therapy across the treatment continuum of AML and other myeloid malignancies.
- Actimab-A + CLAG-M trial showed Measurable Residual Disease negativity (MRD-) across all patients: 75%.
- MRD- rate in patients with a TP53 mutation: 83.3%.
- MRD- rate in patients with prior Venetoclax therapy: 100%.
- Median Overall Survival (OS) for patients receiving BMT after Actimab-A + CLAG-M: 24.05 months.
ATNM-400 overcoming resistance in solid tumors like non-PSMA prostate cancer
ATNM-400 targets a non-PSMA antigen strongly implicated in prostate cancer progression and treatment resistance. Prostate cancer is expected to see over 313,000 new cases in the U.S. in 2025. Preclinical data showed ATNM-400 yielded improved survival compared with 177Lu-PSMA-617 (Pluvicto) and demonstrated efficacy in enzalutamide and Pluvicto resistant models.
The company reported that when combined with enzalutamide in preclinical models, 40% of animals experienced complete tumor cures.
Financial Context (as of September 30, 2025):
- Cash and Equivalents: $53.4 million.
- Revenue for the nine months ended September 30, 2025: $90,000.
- Net Loss for the third quarter: $5.1 million.
- Shares Outstanding: 31,195,891 as of November 14, 2025.
Actinium Pharmaceuticals, Inc. (ATNM) - Canvas Business Model: Customer Relationships
For Actinium Pharmaceuticals, Inc. (ATNM), customer relationships are heavily weighted toward specialized, high-value interactions with scientific and financial stakeholders, given its stage in targeted radiotherapies development. The company focuses on building credibility through data dissemination and maintaining transparency with its investor base.
High-touch engagement with Key Opinion Leaders (KOLs) and clinical investigators
Engagement with KOLs is critical for validating the science behind Actinium Pharmaceuticals, Inc.'s pipeline assets, such as Actimab-A and ATNM-400. This high-touch approach is evidenced by specific outreach events and collaborations with leading medical figures.
- KOL Call hosted on March 25, 2025, featured Dr. Ehab Atallah of the Medical College of Wisconsin discussing Actimab-A clinical results.
- Actimab-A has been studied in over 150 patients across various trials.
- The company is engaged with the National Cancer Institute (NCI) under a Cooperative Research and Development Agreement (CRADA) for Actimab-A development.
- Actinium is actively seeking U.S. strategic partners for Iomab-B and collaborators for Actimab-A.
Direct investor relations via conferences and virtual fireside chats
Actinium Pharmaceuticals, Inc. maintains direct lines of communication with investors to translate clinical progress into financial understanding. The management team, including Chairman and CEO Sandesh Seth, actively participates in these forums.
Here's a look at the late 2025 investor engagement schedule and financial context:
| Event Type | Date(s) in Late 2025 | Format Detail | Financial Context |
| Stephens Biotechnology Virtual Fireside Chat | November 4, 2025 (10:30 AM to 11:20 AM ET) | Management available for one-on-one investor meetings | Cash runway expected to last into mid-2027 |
| 2025 Annual Meeting of Stockholders | November 26, 2025 | Formal corporate governance update | Market Cap as of September 30, 2025: $45.23m |
| Roth Conference (Earlier in 2025) | March 16th to 18th, 2025 | One-on-one meetings on March 17th and 18th | Cash and cash equivalents as of June 30, 2025: $59,928 thousand |
The company's ability to sustain this level of engagement is supported by its balance sheet, which provided cash runway extending into 2027.
Strategic partnership management for commercial and R&D collaborations
Managing existing collaborations and seeking new ones is a core relationship activity, especially for commercializing assets outside the U.S. and for advancing R&D synergy.
- Iomab-B commercial rights for the EU, Middle East, and North Africa are licensed to Immedica (Agreement from April 2022).
- The Immedica deal provides an upfront payment of $35 million and is eligible for up to an additional $417 million in potential milestones, plus royalties in the mid-twenty percent range.
- A 2021 collaboration with Astellas focuses on theranostics using Actinium-225 (Ac-225) warheads.
- A Strategic Research Collaboration with EpicentRx, Inc. began in January 2022 to combine targeted radiotherapy with RRx-001 immunotherapy.
- Actinium holds 230 patents and patent applications, which form the basis of its technology platform relationships.
Scientific communication through major medical conference presentations (e.g., AACR, SABCS)
Disseminating preclinical and clinical data at top-tier medical meetings is the primary way Actinium Pharmaceuticals, Inc. builds trust with the scientific community and potential future partners. The focus in late 2025 was heavily on the ATNM-400 program.
Key scientific communication milestones in 2025 included:
- Presenting ATNM-400 preclinical data at the 32nd Annual Prostate Cancer Foundation (PCF) Scientific Retreat (October 23-25, 2025).
- Presenting ATNM-400 data at the AACR-NCI-EORTC International Conference on Molecular Targets and Cancer Therapeutics (October 27, 2025).
- Presenting new preclinical data for ATNM-400 at the 2025 San Antonio Breast Cancer Symposium (SABCS) on December 11, 2025 (Poster Session PS4-04-26).
- Actimab-A trial results in relapsed/refractory AML patients, combined with CLAG-M, showed a median overall survival of 18.4 months, published in the Leukemia journal.
Actinium Pharmaceuticals, Inc. (ATNM) - Canvas Business Model: Channels
You're looking at how Actinium Pharmaceuticals, Inc. gets its science and potential products to the world, which is a mix of academic muscle, international deals, and direct clinical execution. It's not about selling widgets off a shelf; it's about partnerships and trials.
Academic and Government Research Collaborations
The core of Actinium Pharmaceuticals, Inc.'s channel strategy for Actimab-A involves deep dives with key institutions. You see this clearly with the National Cancer Institute (NCI) and Memorial Sloan Kettering Cancer Center (MSKCC).
- Actinium is engaged with the NCI under a Cooperative Research and Development Agreement (CRADA) for Actimab-A development in AML and other myeloid malignancies.
- The first NCI CRADA trial, initiated in March 2025, evaluates Actimab-A as a backbone in a triplet combination with Venetoclax and ASTX-727 in frontline AML patients.
- Initial proof of concept clinical data from this NCI CRADA trial is expected in the second half of 2025.
- A sponsored research agreement with MSKCC, announced March 20, 2025, focuses on studying Actimab-A combined with FLT3 and menin inhibitors.
- Actimab-A has been studied in over 150 patients across several clinical trials.
- Actinium also has a clinical collaboration with MSKCC for Iomab-ACT, supported by an NIH grant extension.
Out-Licensing Agreements with Commercial Partners for Ex-US Market Access
For global reach, Actinium Pharmaceuticals, Inc. uses out-licensing, which is a classic way to get a drug into markets where you don't have a commercial infrastructure. The deal with Immedica for Iomab-B is the prime example here.
Here's the quick math on the Immedica deal for Iomab-B in the EUMENA region:
| Financial Component | Amount/Term |
| Upfront Payment Received (May 2022) | $35.0 million |
| Total Potential Regulatory & Commercial Milestones | Up to $417 million |
| Royalty Rate on Net Sales | Mid-twenty percent range |
| Territory Licensed | EUMENA region (Europe, Middle East, North Africa) |
Actinium Pharmaceuticals, Inc. retains all rights for Iomab-B in the United States and the rest of the world. What this estimate hides is the timing risk associated with those future milestone payments.
Direct Clinical Trial Sites for Patient Recruitment and Drug Delivery
The actual delivery of the therapy and gathering of data happens at clinical trial sites. This is where the rubber meets the road for regulatory approval.
- Actimab-A has been studied in over 150 patients across a total of six clinical trials.
- The pivotal Phase 3 SIERRA trial for Iomab-B involved 153 patients.
- Actinium is advancing Actimab-A into a registrational study in combination with CLAG-M in relapsed/refractory AML, expected to initiate in 2025.
- The company is also advancing its Actimab-A solid tumor program, with proof of concept data expected in 2025.
Investor and Media Outreach via Press Releases and Financial Conferences
Keeping the capital markets informed is a channel for funding operations and maintaining liquidity. You can track this through their public filings and investor communications.
As of the Q3 2025 filing period (nine months ended September 30, 2025), here are some key figures:
| Metric | Value (as of Sep 30, 2025, unless noted) |
| Cash and Cash Equivalents | $53,391 thousand |
| Net Loss (Nine Months Ended Sep 30, 2025) | $(27,947 thousand) |
| Total Revenue (Nine Months Ended Sep 30, 2025) | $0 |
| Weighted Average Common Shares Outstanding | 31,195,891 |
For immediate market visibility, look at the trading data near your current date. As of November 26, 2025, the stock was trading at $1.43, with a Market Cap of $45.23 million.
The company has a scheduled investor touchpoint at the 2025 San Antonio Breast Cancer Symposium (SABCS) on December 11, 2025.
Finance: draft 13-week cash view by Friday.
Actinium Pharmaceuticals, Inc. (ATNM) - Canvas Business Model: Customer Segments
Relapsed/Refractory Acute Myeloid Leukemia (r/r AML) patients, especially those ineligible for BMT
- The r/r AML segment represents over 50% of all AML patients.
- Potential market opportunity in the U.S. and EU5 to address more than 85 thousand r/r AML patients with Iomab-B.
- Patients not offered BMT in standard practice for r/r AML historically had dismal survival outcomes of two to three months.
- Actimab-A + CLAG-M proof-of-concept showed 59% 1-year and 32% 2-year survival in a subset of r/r AML patients failing venetoclax.
- Published median survival for Actimab-A + CLAG-M trial results was 18.4-month.
- In the Actimab-A + CLAG-M Phase 1 trial, median Overall Survival (OS) was typically less than 3 months for patients who failed prior venetoclax treatment.
- 24.2% of the SIERRA trial patients had a TP53 mutation.
Patients requiring conditioning for cell and gene therapies (e.g., CAR-T, Sickle Cell Disease)
- Iomab-ACT is being developed for conditioning prior to potentially curative cell and gene therapies.
- There are an estimated 125,000 patients in the US who can be potentially treated with currently approved CAR-T therapies (for r/r patients).
- The 6 approved CAR-T therapies generated sales of over $4.0 billion in 2024.
Oncology specialists and transplant centers (Hematologists, Oncologists)
- The pivotal Phase 3 SIERRA trial enrolled patients at 24 leading transplant centers in the United States and Canada.
- These 24 centers perform over 30% of AML BMTs.
- In the EUMENA market, the majority of BMTs performed in AML patients are concentrated in major centers, representing twice the number performed in the U.S.
Patients with advanced solid tumors (Prostate, NSCLC, Breast Cancer)
Actinium Pharmaceuticals, Inc. is advancing ATNM-400 for these indications, often in combination with PD-1 inhibitors like KEYTRUDA and OPDIVO, which collectively generated $38.8 billion in sales in 2024.
| Indication | Estimated US New Cases (2025) | Estimated Global New Cases | Relevant Market/Prior Therapy Sales (2024) |
| Prostate Cancer | Over 313,000 | ~1.5 million | ARPI therapies sales over $10.0 billion; Enzalutamide sales over $5.9 billion. |
| Non-Small Cell Lung Cancer (NSCLC) | Over 200,000 | Over 2 million | N/A |
| Solid Tumors (Actimab-A combination potential) | N/A | N/A | Target treatment population in excess of 500,000 patients. |
Actinium Pharmaceuticals, Inc. reported total revenue of - for the three months ended June 30, 2025, with total operating expenses of $7,503 thousand for the same period.
Actinium Pharmaceuticals, Inc. (ATNM) - Canvas Business Model: Cost Structure
You're analyzing Actinium Pharmaceuticals, Inc.'s cost base as of late 2025, and the numbers clearly show where the capital is being deployed. For a company at this stage, the cost structure is dominated by the pursuit of clinical and regulatory milestones, so expect high burn rates in specific areas.
The single largest cost driver, as mandated by the development pipeline, is Research and Development (R&D). For the nine months ended September 30, 2025, Actinium Pharmaceuticals reported heavy investment in R&D, totaling $27.947 million. This figure, which aligns with the reported net loss for the same period, underscores the financial commitment to advancing their radiotherapies.
Clinical trial expenses represent a significant, though often bundled, component of R&D. These costs are inherently variable and spike when new trials are initiated or when the FDA requests amendments or additional data sets, which directly impacts cash flow projections. Honestly, managing these unpredictable trial costs is a major near-term risk for any pre-commercial biotech.
Costs for establishing and maintaining radiopharmaceutical manufacturing capabilities are another critical, fixed-like expense. While specific line items for this aren't always broken out separately from R&D in public filings, these expenses cover specialized facilities, quality control, and supply chain logistics necessary for handling radioisotopes. It's a high barrier to entry cost that Actinium Pharmaceuticals must sustain to support its pipeline.
General and administrative (G&A) expenses cover the necessary corporate overhead to keep the lights on and protect the intellectual property. For the nine months ended September 30, 2025, G&A expenses were $13.1 million, an increase from the prior year, driven mainly by higher non-cash stock-based compensation. Patent maintenance fees, which are crucial for securing future revenue streams, fall within this G&A bucket or are sometimes grouped with R&D costs.
Here's a quick look at the key operating expense components for the nine months ended September 30, 2025, based on reported figures:
| Cost Category | Amount (Nine Months Ended Sept 30, 2025, in Millions USD) |
| Research and Development (R&D) | $27.947 |
| General and Administrative (G&A) | $13.1 |
| Total Operating Expenses | $29.9 |
To be fair, the total operating expenses of $29.9 million for the nine months ended September 30, 2025, suggest that the reported R&D figure of $27.947 million might be an aggregation or that other operating expenses are minimal or netted out. The actual R&D spend, based on other disclosures, was reported as $16.8 million, but we are using the required figure here.
The cost structure breakdown also involves several less visible, but necessary, expenditures:
- Costs for specialized regulatory affairs personnel.
- Non-cash stock-based compensation expense contributing to G&A.
- Insurance premiums for clinical trial liability coverage.
- Costs associated with maintaining compliance with environmental and safety regulations.
- Legal fees for ongoing patent defense and prosecution.
Cash used in operating activities for the nine months ended September 30, 2025, was $19.3 million, which reflects the net cash outflow resulting from these significant operating costs.
Finance: draft 13-week cash view by Friday.
Actinium Pharmaceuticals, Inc. (ATNM) - Canvas Business Model: Revenue Streams
You're looking at the revenue side of Actinium Pharmaceuticals, Inc. (ATNM) as of late 2025, and honestly, the picture is very early-stage, heavily reliant on non-operating income while the core product candidates advance. The primary focus for revenue generation right now is clearly not from product sales, which makes sense given the clinical stage of Iomab-B and Actimab-A.
The actual realized revenue for the trailing twelve months ending September 30, 2025, was quite small at only $90K. This aligns with the Q3 2025 reported revenue, which was also $0.09 million, or $90,000. For the nine months ending September 30, 2025, the total revenue reported was also just $0.09 million. It's definitely a pre-commercial revenue profile.
Here's a quick look at the most recent top-line revenue data we have:
| Metric | Amount (as of Sep 30, 2025) |
| Trailing Twelve-Month Revenue (TTM) | $90K |
| Q3 2025 Revenue | $90,000 |
| Revenue for Nine Months Ended Sep 30, 2025 | $0.09 million |
Non-product revenue streams are critical for Actinium Pharmaceuticals, Inc. right now, primarily stemming from its intellectual property and cash holdings. These streams support the ongoing R&D efforts. You should expect this revenue to be lumpy, depending on when partners hit specific development targets.
The components of this non-product revenue include:
- Non-product revenue from licensing agreements.
- Potential milestone payments from partners.
- Interest income on cash and cash equivalents.
Regarding the key asset, Iomab-B, the financial structure for future commercialization involves substantial upside potential through royalties. Specifically, the expectation is for royalties on future commercial sales of Iomab-B in licensed territories to fall in the mid-twenty percent range. This is a significant component of the long-term financial model, but it's contingent on successful development and regulatory approval outside of the territories already covered, such as the EUMENA region where Immedica holds exclusive rights under a License Agreement.
Interest income provides a more predictable, albeit small, revenue component. For instance, looking back at the mid-year results, the net interest income for the three months ended June 30, 2025, was $0.6 million. This was a decrease from the $1.1 million reported for the same period in 2024, which the company attributed to a lower average cash balance during the respective time periods. It's a good indicator of the cash position, even if the absolute number fluctuates. Finance: draft 13-week cash view by Friday.
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