Actinium Pharmaceuticals, Inc. (ATNM) Business Model Canvas

Actinium Pharmaceuticals, Inc. (ATNM): Business Model Canvas

US | Healthcare | Biotechnology | AMEX
Actinium Pharmaceuticals, Inc. (ATNM) 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

Actinium Pharmaceuticals, Inc. (ATNM) Bundle

Get Full Bundle:
$14.99 $9.99
$14.99 $9.99
$14.99 $9.99
$14.99 $9.99
$24.99 $14.99
$14.99 $9.99
$14.99 $9.99
$14.99 $9.99
$14.99 $9.99

TOTAL:

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.


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.