Actinium Pharmaceuticals (ATNM) Life Sciences Investor Forum summary
Event summary combining transcript, slides, and related documents.
Life Sciences Investor Forum summary
15 Nov, 2025Strategic pipeline overview
Focus on targeted radiotherapy for blood cancers, solid tumors, and conditioning for cell/gene therapy, supported by over 230 patents and proprietary Actinium-225 manufacturing technology.
Lead program Actimab-A advancing to phase II-III trials for AML, with additional studies in solid tumors and combinations with PD-1 inhibitors like KEYTRUDA and OPDIVO.
Iomab-ACT program initiated in CAR-T and sickle cell disease settings, with trials at UT Southwestern and Columbia University.
New solid tumor candidate ATNM-400 targets prostate cancer, showing higher potency than PLUVICTO in preclinical models and efficacy in PLUVICTO-resistant tumors.
In-house R&D and manufacturing capabilities enable expansion into new indications and support future clinical trials.
Clinical and preclinical data highlights
Actimab-A plus CLAG-M in relapsed/refractory AML showed high response rates (>50%) and deep remissions, including MRD negativity, even in high-risk groups.
Median overall survival reached 18 months in certain subgroups, with 24 months for those proceeding to bone marrow transplant.
Actimab-A is mutation agnostic and targets CD33, expressed across AML patients, supporting its potential as a backbone therapy.
ATNM-400 demonstrated selective tumor uptake, minimal normal tissue exposure, and efficacy in PLUVICTO-resistant models.
Iomab-ACT pilot study showed low toxicity and complete responses in heavily pretreated leukemia/lymphoma patients, supporting ongoing trials.
Market opportunities and partnerships
Pipeline addresses large markets: AML, solid tumors, prostate cancer, CAR-T, and sickle cell disease, with potential patient populations exceeding several hundred thousand.
Actimab-A being studied in combination with PD-1 inhibitors for head and neck and non-small cell lung cancer, targeting resistance mechanisms via MDSC depletion.
Iomab-ACT targets the rapidly growing cell and gene therapy market, forecasted to reach 100,000 patients by 2030.
Actinium-225 manufacturing technology offers cost-effective, high-purity isotope production, with potential for external partnerships.
Actively seeking partnerships for late-stage assets, including Actimab-A and Iomab-B, to accelerate development and commercialization.
Latest events from Actinium Pharmaceuticals
- Key clinical and R&D advances position the pipeline for major milestones and data in 2025.ATNM
15th Annual LD Micro Invitational 202527 Dec 2025 - Annual Meeting to elect directors and ratify auditor, with focus on governance and risk oversight.ATNM
Proxy Filing2 Dec 2025 - Net loss narrowed on lower expenses; focus shifts to solid tumor radiotherapies amid regulatory risks.ATNM
Q3 202514 Nov 2025 - Proxy covers director elections, auditor ratification, and executive pay votes, with focus on governance.ATNM
Proxy Filing5 Nov 2025 - Q2 2025 net loss narrowed on lower expenses; focus shifts to solid tumor pipeline.ATNM
Q2 20258 Aug 2025 - Net loss narrowed, cash position strengthened, but Iomab-B faces new FDA trial requirements.ATNM
Q2 202413 Jun 2025 - Net loss narrowed as R&D spending fell, but Iomab-B faces new FDA trial requirements.ATNM
Q3 202413 Jun 2025 - Net loss narrowed to $38.2M in 2024 as Actinium advanced its radiotherapy pipeline and raised $29.3M.ATNM
Q4 20249 Jun 2025 - Q1 2025 net loss widened as Actinium advanced its pipeline and managed higher expenses.ATNM
Q1 20256 Jun 2025