Actinium Pharmaceuticals (ATNM) Investor presentation summary
Event summary combining transcript, slides, and related documents.
Investor presentation summary
16 Oct, 2026Investment thesis and financial position
Pipeline spans solid tumors, hematology and conditioning, with several 2026 readouts and cash runway into 2028.
Cash and equivalents were $36.5M at June 30, 2026; 31.4M shares outstanding, with no debt, warrants or preferred stock.
In-house R&D, manufacturing buildout planned for 2H 2026, ~250 patents and proprietary Ac-225 production technology support development and supply.
Solid tumor pipeline
ATNM-400 is a preclinical Ac-225 radiotherapy targeting an undisclosed target, with mCRPC, NSCLC and breast cancer as lead indications.
Preclinical prostate models showed 87% tumor growth inhibition for ATNM-400 versus 0% for 177Lu-PSMA-617 in a low-PSMA model; presentation cites potential to address patients with low or no PSMA expression.
In EGFR-mutant NSCLC models, ATNM-400 showed 3–5x greater tumor growth inhibition than approved therapies and 100% complete cures with osimertinib combination.
Breast cancer models showed efficacy in trastuzumab-resistant and triple-negative settings, including reported tumor growth inhibition of 97% and 100% in combination arms.
Actimab-A depletes CD33+ MDSCs; planned PD-1 combination trials target GBM and a basket of MDSC-rich tumors, with initial trial data expected in 2027.
Hematology and conditioning
Actimab-A + CLAG-M is positioned as a mutation-agnostic AML backbone; FDA alignment is reported for a Phase 2/3 trial in relapsed/refractory AML, with a collaborator sought.
In Phase 1b, Actimab-A + CLAG-M reported 80% MRD negativity and 18.4-month median OS in first/second-salvage patients; TP53-mutated patients had 83% MRD negativity and 9.6-month median OS.
lomab-B is a Phase 2/3-ready CD45-targeted BMT conditioning asset; lomab-ACT is being studied in CAR-T and sickle cell disease conditioning trials, with initial proof-of-concept data expected in 2026.
Planned 4Q 2026 milestones include initiating the Actimab-A + CLAG-M Phase 2/3 trial with a partner and a frontline AML triplet trial; CAR-T and sickle cell proof-of-concept data are targeted for 2027.
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