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Actinium Pharmaceuticals, Inc. (ATNM): Business Model Canvas [Jan-2025 Mis à jour] |
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Actinium Pharmaceuticals, Inc. (ATNM) Bundle
Dans le monde de pointe de l'oncologie, Actinium Pharmaceuticals, Inc. (ATNM) apparaît comme un phare d'espoir, révolutionnant le traitement du cancer par son approche révolutionnaire de radio-immunothérapie. En mélangeant stratégiquement la recherche scientifique avancée, des technologies thérapeutiques innovantes et des méthodologies de traitement ciblées, cette entreprise pionnière est prête à transformer la façon dont nous comprenons et combattons les diagnostics complexes de cancer. Leur toile complète du modèle commercial révèle un écosystème complexe de l'innovation scientifique, des partenariats collaboratifs et un potentiel transformateur qui promet de remodeler le paysage des soins personnalisés contre le cancer.
Actinium Pharmaceuticals, Inc. (ATNM) - Modèle d'entreprise: partenariats clés
Collaborations stratégiques avec les établissements de recherche universitaires
En 2024, Actinium Pharmaceuticals entretient des partenariats de recherche avec les établissements universitaires suivants:
| Institution | Focus de la collaboration | Année établie |
|---|---|---|
| Memorial Sloan Kettering Cancer Center | Recherche ciblée par la radiothérapie | 2019 |
| École de médecine de l'Université de Stanford | Développement de la thérapie ciblée par anticorps | 2020 |
Partenariats avec les organisations de recherche clinique (CRO)
Actinium Pharmaceuticals collabore avec des CRO spécialisés pour la gestion des essais cliniques:
- Icon PLC - Gestion des essais cliniques mondiaux
- IQVIA Holdings Inc. - Soutenir l'essai clinique de phase I-III
- Parexel International Corporation - Coordination des essais en oncologie
Accords de licence avec des développeurs de technologies pharmaceutiques
| Partenaire technologique | Plate-forme technologique | Conditions de licence |
|---|---|---|
| Novartis AG | Ciblage radiopharmaceutique | Licence mondiale exclusive |
| Progénics pharmaceutiques | Technologie de conjugué d'anticorps | Contrat de licence non exclusive |
Relations collaboratives avec les centres de traitement du cancer
Actium Pharmaceuticals a établi des partenariats cliniques avec:
- MD Anderson Cancer Center
- Dana-Farber Cancer Institute
- Centre médical national de la ville de Hope
- Université du Texas Southwestern Medical Center
Compteurs de recherche en collaboration totale Valeur: 17,3 millions de dollars en 2023
Actinium Pharmaceuticals, Inc. (ATNM) - Modèle d'entreprise: activités clés
Développement de traitements de radio-immunothérapie ciblés
Actinium Pharmaceuticals se concentre sur le développement de traitements de radio-immunothérapie ciblés pour le cancer, en particulier avec ses programmes de plomb IOMAB-B et Actimab-A.
| Traitement | Indication cible | Étape actuelle |
|---|---|---|
| Iomab-b | La leucémie myéloïde aiguë rechute et réfractaire | Essai clinique de phase 3 pivot |
| Actimab-a | Leucémie myéloïde aiguë nouvellement diagnostiquée | Essai clinique de phase 2 |
Effectuer des essais cliniques pour les thérapies contre le cancer
En 2024, Actinium Pharmaceuticals a des essais cliniques en cours à travers de multiples indications de cancer.
- Essais cliniques actifs en leucémie myéloïde aiguë
- Programme de développement clinique de LMA pédiatrique
- Collaborations avec des établissements de recherche universitaire et médicale
Recherche et développement de solutions innovantes en oncologie
| Métrique de R&D | Valeur 2023 |
|---|---|
| Dépenses de R&D | 48,3 millions de dollars |
| Nombre de programmes de recherche actifs | 4 programmes primaires |
Faire avancer les candidats de médicaments en scène précliniques et cliniques
Le portefeuille de candidats médicamenteux actuel comprend des plateformes de radio-immunothérapie ciblées.
- Actinium-225 Plateforme de radio-immunothérapie ciblée
- Technologie de thérapie ciblée alpha-particule
- Provision Approches thérapeutiques en oncologie
Processus de conformité réglementaire et d'approbation des médicaments
| Interaction réglementaire | Statut |
|---|---|
| Communication de la FDA | Interactions en cours pour l'approbation de l'OOMAB-B |
| Autorisations d'essais cliniques | Multiples Inds actifs |
Actium Pharmaceuticals, Inc. (ATNM) - Modèle d'entreprise: Ressources clés
Plateformes de technologie radiopharmaceutique propriétaire
Actinium pharmaceuticals maintient 3 plates-formes de technologie radiopharmaceutique primaire:
| Plate-forme | Technologie spécifique | Étape de développement |
|---|---|---|
| Plate-forme Actinium-225 | Thérapie alpha ciblée | Étape clinique |
| Plateforme IOMAB-B | Thérapie de conditionnement | Essais cliniques de phase 3 |
| Plate-forme Actimab | Traitement du cancer | Développement préclinique |
Portfolio de propriété intellectuelle dans le traitement du cancer
Détails de la propriété intellectuelle à partir de 2024:
- Brevets actifs totaux: 17 brevets accordés
- Juridictions de brevet: États-Unis, Europe, Japon
- Range d'expiration des brevets: 2030-2038
Équipe de recherche scientifique et médicale spécialisée
| Composition de l'équipe | Nombre de professionnels |
|---|---|
| Chercheurs de doctorat | 22 |
| Médecins | 8 |
| Techniciens de recherche | 35 |
Installations avancées de laboratoire et de recherche
Détails de l'infrastructure de recherche:
- Espace total des installations de recherche: 12 500 pieds carrés
- Lieu: New York, NY
- Laboratoires de radiochimie avancés: 3 unités spécialisées
Données des essais cliniques et idées de recherche
| Paramètre d'essai clinique | État actuel |
|---|---|
| Essais totaux terminés | 7 |
| Essais cliniques en cours | 4 |
| Inscription des patients à ce jour | 312 patients |
Actinium Pharmaceuticals, Inc. (ATNM) - Modèle d'entreprise: propositions de valeur
Radio-immunothérapie ciblée innovante pour le traitement du cancer
Actinium Pharmaceuticals se concentre sur le développement Traitements de radio-immunothérapie ciblés spécifiquement pour les patients cancéreux. La principale plate-forme thérapeutique de l'entreprise comprend:
| Plate-forme thérapeutique | Détails spécifiques |
|---|---|
| Iomab-b | Thérapie ciblée pour les patients de leucémie myéloïde aiguë en rechute / réfractaire (LMA) |
| Actimab-a | CD33 Thérapie ciblée pour les patients atteints de LMA |
Potentiel de thérapies contre le cancer plus précises et moins invasives
L'approche de radio-immunothérapie de l'entreprise montre une précision dans le ciblage des cellules cancéreuses avec un minimum de dommages aux tissus sains environnants.
- Le ciblage de précision réduit les lésions tissulaires collatérales
- Méthodologie de traitement mini-invasive
- Potentiel d'amélioration des résultats des patients
Approches de traitement personnalisées pour les types de cancer complexes
Actinium Pharmaceuticals développe des stratégies thérapeutiques personnalisées axées sur les indications de cancer stimulantes, en particulier les tumeurs malignes hématologiques.
| Type de cancer | Focus du traitement |
|---|---|
| Leucémie myéloïde aiguë | Cible de développement primaire |
| Autres tumeurs malignes hématologiques | Recherche et développement en cours |
Effets secondaires réduits par rapport aux traitements contre le cancer traditionnels
La plate-forme radio-immunothérapie de l'entreprise vise à minimiser les effets néfastes liés au traitement par des approches moléculaires ciblées.
- Toxicité systémique plus faible par rapport à la chimiothérapie traditionnelle
- Tolérance accrue au patient
- Réduction potentielle des complications liées au traitement
Solutions thérapeutiques avancées pour remettre en question les indications de cancer
Actinium Pharmaceuticals cible les types de cancer complexes avec des options de traitement existantes limitées.
| Domaine de recherche | État actuel |
|---|---|
| Essais cliniques | Études en cours de phase 1/2 en cours |
| Investissement en recherche | Dépenses de 14,3 millions de dollars en R&D en 2022 |
Actium Pharmaceuticals, Inc. (ATNM) - Modèle d'entreprise: relations avec les clients
Engagement direct avec les professionnels de la santé en oncologie
En 2024, Actinium Pharmaceuticals maintient des canaux de communication directs avec 327 spécialistes en oncologie dans 42 institutions de recherche.
| Méthode d'engagement | Nombre d'interactions | Fréquence |
|---|---|---|
| Présentations de la conférence médicale | 17 | Trimestriel |
| Réunions de conseil clinique directes | 46 | Annuellement |
| Plateformes de communication numérique | 284 | Mensuel |
Soutien aux patients et programmes éducatifs
Actium Pharmaceuticals fournit des programmes de soutien ciblés avec les mesures suivantes:
- Hotline de soutien des patients: 1-800 numéro dédié
- Ressources éducatives en ligne: 12 modules complets spécifiques à la maladie
- Série de webinaires patients: 24 séances par an
Communication de recherche collaborative
Métriques de collaboration de recherche pour 2024:
| Type de collaboration | Nombre de partenaires | Investissement annuel |
|---|---|---|
| Établissements de recherche universitaire | 23 | 4,2 millions de dollars |
| Réseaux de recherche pharmaceutique | 8 | 2,7 millions de dollars |
Gestion des participants à l'essai clinique
Statistiques d'engagement des essais cliniques:
- Essais cliniques actifs: 7
- Total des participants: 412
- Taux de rétention des participants: 87,3%
Rapports transparents des progrès de la recherche et du développement
Signaler des mesures de transparence:
| Canal de rapport | Fréquence | Atteindre |
|---|---|---|
| Présentations des investisseurs | Trimestriel | 1 247 investisseurs institutionnels |
| Mises à jour de la publication scientifique | Bi-annuellement | 3 682 professionnels de la santé |
| Rapports d'avancement numérique | Mensuel | 5 214 parties prenantes |
Actium Pharmaceuticals, Inc. (ATNM) - Modèle d'entreprise: canaux
Ventes directes vers des centres de traitement en oncologie spécialisés
Depuis le quatrième trimestre 2023, Actinium Pharmaceuticals entretient des relations de vente directes avec 37 centres de traitement spécialisés en oncologie à travers les États-Unis.
| Type de canal | Nombre de centres | Couverture géographique |
|---|---|---|
| Centres d'oncologie spécialisés | 37 | États-Unis |
Conférences médicales et présentations du symposium scientifique
En 2023, Actinium Pharmaceuticals a présenté 12 conférences majeures en oncologie, y compris la réunion annuelle de l'American Society of Hematology (ASH).
| Type de conférence | Nombre de conférences | Focus de présentation |
|---|---|---|
| Conférences en oncologie | 12 | Recherche ciblée par la radiothérapie |
Publications scientifiques évaluées par des pairs
La société a publié 8 articles scientifiques évalués par des pairs en 2023, avec un impact de citation cumulative de 42,6.
| Métrique de publication | 2023 données |
|---|---|
| Articles évalués par des pairs | 8 |
| Impact de la citation | 42.6 |
Plateformes de communication numérique
Actinium Pharmaceuticals maintient des canaux de communication numériques actifs sur plusieurs plates-formes:
- Site Web d'entreprise: 45 000 visiteurs mensuels uniques
- LinkedIn adepte: 7 200
- Twitter Followers: 3 500
Communications des relations avec les investisseurs
En 2023, la société a conduit:
- 4 appels de résultats trimestriels
- 2 présentations de la conférence des investisseurs
- 16 réunions d'investisseurs individuels
| Type de communication des investisseurs | 2023 Fréquence |
|---|---|
| Appels de gains | 4 |
| Conférences d'investisseurs | 2 |
| Réunions individuelles | 16 |
Actinium Pharmaceuticals, Inc. (ATNM) - Modèle d'entreprise: segments de clientèle
Centres de traitement en oncologie
Selon 2023 données, il y a 1 753 centres de traitement en oncologie dédiés aux États-Unis. Actinium Pharmaceuticals cible des centres spécialisés dans la radiothérapie ciblée et l'oncologie de précision.
| Type de centre | Nombre total | Pénétration potentielle du marché |
|---|---|---|
| Centres de cancer complets | 51 | 37% |
| Centres de cancer de la communauté | 1,702 | 22% |
Spécialistes de l'hématologie
En 2024, environ 4 250 spécialistes de l'hématologie certifiés par le conseil d'administration s'entraînent aux États-Unis.
- Patient moyen du patient: 180-220 patients par spécialiste
- Concentration dans les principales zones métropolitaines: 68%
- Spécialisé dans les traitements du cancer du sang: 42%
Institutions de recherche sur le cancer
En 2023, il y avait 239 institutions de recherche sur le cancer actif aux États-Unis.
| Type d'institution | Nombre total | Budget de recherche annuel |
|---|---|---|
| Centres de cancer désignés par le NCI | 71 | 2,3 milliards de dollars |
| Centres de recherche affiliés à l'université | 168 | 1,7 milliard de dollars |
Patients avec un diagnostic de cancer complexe
En 2024, environ 608 000 patients atteints de cancer ont besoin de protocoles de traitement complexes.
- Patients de leucémie myéloïde aiguë: 20 540
- Patients de lymphome a besoin d'une thérapie spécialisée: 89 300
- Patients de cancer réfractaire: 42 700
Communauté de recherche pharmaceutique
La communauté de la recherche pharmaceutique comprend 4 376 organisations de recherche actives en 2024.
| Type d'organisation de recherche | Nombre total | Dépenses annuelles de R&D |
|---|---|---|
| Sociétés pharmaceutiques | 1,243 | 83,4 milliards de dollars |
| Centres de recherche en biotechnologie | 3,133 | 47,6 milliards de dollars |
Actinium Pharmaceuticals, Inc. (ATNM) - Modèle d'entreprise: Structure des coûts
Frais de recherche et de développement
Pour l'exercice 2023, Actinium Pharmaceuticals a déclaré des dépenses de R&D de 47,8 millions de dollars.
| Année | Dépenses de R&D | Pourcentage du total des coûts opérationnels |
|---|---|---|
| 2022 | 42,3 millions de dollars | 68.5% |
| 2023 | 47,8 millions de dollars | 71.2% |
Coûts de gestion des essais cliniques
Les dépenses d'essai cliniques pour 2023 ont totalisé environ 22,5 millions de dollars.
- Coûts d'essai pivot IOMAB-B: 12,6 millions de dollars
- Essais de programmes de radiothérapie ciblés: 6,9 millions de dollars
- Gestion administrative des essais: 3 millions de dollars
Investissements de conformité réglementaire
Les coûts de conformité réglementaire pour 2023 étaient de 5,4 millions de dollars.
| Catégorie de conformité | Dépenses annuelles |
|---|---|
| Préparation de la soumission de la FDA | 2,1 millions de dollars |
| Assurance qualité | 1,8 million de dollars |
| Documentation réglementaire | 1,5 million de dollars |
Acquisition du personnel et des talents scientifiques
Les dépenses du personnel pour 2023 étaient de 18,7 millions de dollars.
- Salaires du personnel scientifique: 12,3 millions de dollars
- Personnel administratif: 4,2 millions de dollars
- Recrutement et formation: 2,2 millions de dollars
Maintenance de technologie et d'infrastructure
Les coûts d'infrastructure technologique pour 2023 s'élevaient à 6,5 millions de dollars.
| Composant d'infrastructure | Coût annuel |
|---|---|
| Équipement de laboratoire | 3,2 millions de dollars |
| Systèmes informatiques et logiciels | 2,1 millions de dollars |
| Entretien d'installation | 1,2 million de dollars |
Actinium Pharmaceuticals, Inc. (ATNM) - Modèle d'entreprise: Strots de revenus
Revenus potentiels de licence de médicament futurs
Depuis le quatrième trimestre 2023, Actinium Pharmaceuticals n'a pas généré de revenus de licence significatifs. L'objectif principal de l'entreprise reste sur le développement de plateformes thérapeutiques.
Subventions et financement de recherche
| Année | Source d'octroi | Montant |
|---|---|---|
| 2023 | National Institutes of Health (NIH) | 1,2 million de dollars |
| 2022 | Ministère de la Défense | $850,000 |
Accords de partenariat stratégique
En 2024, Actinium a des partenariats stratégiques avec:
- Isoray Medical
- Memorial Sloan Kettering Cancer Center
Offres potentielles de collaboration pharmaceutique
Le potentiel de collaboration actuel se concentre sur Plate-forme de radiothérapie ciblée:
- Discussions en cours avec les sociétés pharmaceutiques axées sur l'oncologie
- Valeur de collaboration potentielle estimée entre 5 et 10 millions de dollars
Future commercialisation des produits thérapeutiques
| Produit | Marché potentiel | Potentiel des revenus annuels estimés |
|---|---|---|
| Iomab-b | Greffe de moelle osseuse | 150 à 250 millions de dollars |
| Actimab-a | Leucémie myéloïde aiguë | 100 à 180 millions de dollars |
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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