IMMUNOME INC

Insider Trading & Executive Data

IMNM
NASDAQ
Healthcare
Biotechnology

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35 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
Institutional ownership shifts by quarter with top-holder concentration data
Form 144 and Form 8-K monitoring with AI analysis and CSV export tools

Insider Activity Summary

Insider Trades (1Y)
35
0 in last 30 days
Buy / Sell (1Y)
27/8
Acquisitions / Dispositions
Unique Insiders (1Y)
13
Active in past year
Insider Positions
16
Current holdings
Position Status
16/0
Active / Exited
Institutional Holders
153
Latest quarter
Board Members
31

Compensation & Governance

Avg Total Compensation
$3.6M
Latest year: 2024
Executives Covered
9
Comp records available
Form 8-K Events (1Y)
0
Personnel Changes (1Y)
0
Bonus Plan Events (1Y)
0
Organization Changes (1Y)
0
Board Appointments (1Y)
0
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
$21.70
Market Cap
$2.4B
Volume
23,126
EPS
$-0.65
Revenue
$0.00
Employees
168
About IMMUNOME INC

Company Overview

Immunome, Inc. (IMNM) is a clinical‑stage targeted oncology biotech focused on antibody‑drug conjugates (ADCs) and targeted radioligand therapies (RLTs) directed at underexplored cancer targets. The company advanced a diversified pipeline in 2024–2025 including a Phase 3 oral gamma‑secretase program (varegacestat, topline expected H2 2025), a ROR1‑targeted ADC (IM‑1021/IM‑11021) in Phase 1, and an IND‑stage FAP‑targeted 177Lu RLT (IM‑3050), while outsourcing all cGMP manufacturing to third‑party CMOs. Financially it shifted from discovery to heavy clinical spend—R&D and share‑based comp rose materially, net losses widened, and financings in 2024–2025 boosted cash to provide ~12 months of runway while management warns additional capital will likely be required. Key operational sensitivities include dependency on CMOs and radioisotope supply, milestone/royalty obligations to licensors, and competitive pressure from larger ADC/RLT developers.

Executive Compensation Practices

Given Immunome’s clinical‑stage profile, compensation is likely weighted toward equity‑based incentives (options/RSUs) and milestone‑linked bonuses to retain scientific and clinical leadership and to align pay with program de‑risking events (IND clears, dose escalations, Phase 3 topline, regulatory filings). The filings explicitly note higher share‑based compensation as a driver of G&A increases, and management must balance retention of Seagen‑experienced talent with investor sensitivity to dilution following multiple equity raises. Short‑term cash pay is typically modest for biotech executives; therefore program advancement, successful partnering, milestone receipts (which can fund operations) and key clinical readouts are the primary performance metrics that will drive payouts and potential extraordinary awards. Board compensation committees will also need to consider financing outcomes and contingent licensor obligations (up to ~$142M in potential BMS milestones) when setting long‑term incentive targets to avoid incentivizing excessive risk taking.

Insider Trading Considerations

Insider trading activity at Immunome should be interpreted through the lens of event‑driven biotech risk: executives and directors often trade around financings (public offerings, ATMs), major clinical milestones (INDs, dose escalation, Phase 3 topline), and disclosure of material operational constraints (manufacturing or radioisotope supply). Expect a higher frequency of option exercises and subsequent sales tied to tax/liquidity needs after financings and during periods of heavy share‑based pay; conversely, open‑market insider purchases are rare but significant when they occur and can signal management confidence. Regulatory factors—Section 16 reporting, blackout windows ahead of FDA/Phase 3 readouts, 10b5‑1 plans, and strict handling of material nonpublic clinical data—will shape timing; watch Form 4 filings clustered around financing dates, post‑earnings periods, and immediately after announced trial milestones for informative patterns.

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