ACTINIUM PHARMACEUTICALS INC

Insider Trading & Executive Data

ATNM
NYSEMKT
Healthcare
Biotechnology

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49 insider trades in the last year. Go beyond summary counts with transaction-level detail, compensation intelligence, and institutional ownership context.

Trade-level insider transactions with filing links, transaction codes, and footnotes
Executive compensation trends by role with year-over-year comparisons
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Insider Activity Summary

Insider Trades (1Y)
49
0 in last 30 days
Buy / Sell (1Y)
0/49
Acquisitions / Dispositions
Unique Insiders (1Y)
7
Active in past year
Insider Positions
5
Current holdings
Position Status
1/4
Active / Exited
Institutional Holders
60
Latest quarter
Board Members
37

Compensation & Governance

Avg Total Compensation
$1.6M
Latest year: 2024
Executives Covered
4
Comp records available
Form 8-K Events (1Y)
2
Personnel Changes (1Y)
2
Bonus Plan Events (1Y)
0
Organization Changes (1Y)
1
Board Appointments (1Y)
1
Board Departures (1Y)
0

Restricted Sales

Form 144 Filings (1Y)
0
Form 144 Insiders (1Y)
0
Planned Sale Shares (1Y)
0
Planned Sale Value (1Y)
$0.00
Price
$1.18
Market Cap
$36.8M
Volume
2,703
EPS
$-0.16
Revenue
$90000.00
Employees
31
About ACTINIUM PHARMACEUTICALS INC

Company Overview

Actinium Pharmaceuticals (ATNM) is a clinical‑stage specialty radiopharmaceutical company in the Healthcare sector, Biotechnology industry developing targeted radiotherapies that combine biologic targeting agents with radioisotope “warheads.” Its lead programs include Actimab‑A (CD33) for AML/high‑risk MDS, Iomab‑ACT (anti‑CD45) as a targeted conditioning agent for CAR‑T and gene therapies, and a preclinical Ac‑225 program (ATNM‑400) for prostate cancer. Operations are R&D and trial‑cycle driven with time‑sensitive, just‑in‑time radiochemistry logistics, a planned in‑house cyclotron build‑out (H2 2025), supply arrangements (e.g., Eckert & Ziegler), and a large patent portfolio supporting scale‑up risks and isotope supply constraints. The company currently has no commercial revenue, carries a $35.0M deferred license liability contingent on EU regulatory outcomes, and is dependent on successful clinical/regulatory milestones and additional financing.

Executive Compensation Practices

Compensation is likely heavily influenced by clinical and regulatory milestones (INDs, Phase readouts, FDA/EU approvals), partnership/licensing events (which can bring upfront and milestone payments), and execution of manufacturing scale‑up (cyclotron build‑out and CDMO performance). As a biotech in the Biotechnology industry, executives typically receive lower cash salaries with a higher proportion of stock‑based incentives and milestone‑linked bonuses to conserve cash — consistent with Actinium’s recent reliance on equity financings and the material impact from stock‑based compensation. Recent actions (March 2025 option cancellations) materially changed non‑cash compensation timing and magnitude, and the company has been cutting headcount to reduce cash burn, which suggests near‑term compensation programs may be rebalanced toward long‑dated equity or milestone awards. Management’s stated need for additional capital and the presence of contingent deferred revenue ($35M) make achievement of regulatory and partnership triggers central to any pay‑for‑performance design.

Insider Trading Considerations

Insider trading activity at Actinium will likely cluster around binary, high‑impact events: clinical readouts, FDA/EU decisions (which would also affect the $35M deferred license), IND/CRADA milestones, partner announcements, and financing rounds. Because the business is equity‑driven with no commercial revenue, insider sales may be more common for liquidity or to fund dilution‑related needs; insider purchases post‑data or post‑financing can be a stronger bullish signal. Note the March 2025 option cancellations and the pending putative securities class action — both can affect timing of disclosures and create atypical patterns in Form 4 filings (e.g., accelerated option exercises or increased non‑cash compensation). Regulatory considerations specific to the sector (FDA/BLA pathways, orphan designations, and radioisotope handling/transport rules) create predictable blackout windows around material filings and trial readouts; look for 10b5‑1 plans, Section 16 filings, and any company insider‑trading policies when interpreting transactions.

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