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Public company intelligence preview

THERIVA BIOLOGICS INC

4 insider trades surfaced from the last year. This page shows only aggregate signals, not the underlying transactions, people, filings, filters, or AI workspace.

Snapshot

A narrow read on a much deeper workspace.

The preview gives search visitors enough signal to understand coverage. It does not expose transaction records, person-level profiles, filters, comparisons, or analyst workflows.

Insider trades, last 12 months
4
0 filed in the last 30 days
Acquisition / disposition count
4/0
Buy / Sell
Unique insiders active in the last year
4
Current insider positions tracked
4
4 active, 0 exited

Insider compensation

Public aggregate: $1.1M average total compensation across covered insiders.

Governance movement

Public aggregate: 1 governance events in the last year.

Institutional ownership

Public aggregate: 21 holders from the latest quarter.

Restricted sales and governance

Public counts, not the investigation layer.

The full product opens the underlying filings, insider context, historical holdings, comparison tools, and AI analysis.

Restricted-sale filings, 1Y
0
Restricted-sale insiders, 1Y
0
Planned sale shares, 1Y
0
Planned sale value, 1Y
$0.00
Insiders covered
4
Latest year: 2024
Personnel changes, 1Y
0
Board appointments, 1Y
0
Board departures, 1Y
0

Market context

Basic quote context for the preview.

Price
$0.28
Market cap
$13.0M
Volume
1,697,989
EPS
$-0.05
Revenue
$300000.00
Employees
16

Company note

Context before the data.

Company Overview

Theriva Biologics Inc. is a clinical-stage biotechnology company in the Healthcare sector and Biotechnology industry, now focused primarily on oncology. Its lead asset, VCN-01, is an oncolytic adenovirus designed to selectively replicate in tumor cells and enhance penetration of chemo- and immunotherapies, with development centered on metastatic pancreatic ductal adenocarcinoma and retinoblastoma. The company has also been advancing next-generation oncolytic virus programs and a manufacturing platform, while divesting or partnering non-core gastrointestinal and microbiome assets to conserve capital. Recent disclosures show the company remains highly dependent on regulatory progress, third-party manufacturing, and external funding, but it has received encouraging development milestones including positive Phase 2b data and FDA alignment on a proposed Phase 3 design.

Executive Compensation Practices

Executive compensation at Theriva is likely influenced heavily by clinical, regulatory, and financing milestones rather than traditional revenue growth, since the company is still pre-commercial and posting operating losses. In a biotech company like this, pay packages often emphasize base salary, annual bonuses, equity awards, and milestone-based incentives tied to trial execution, FDA feedback, financing success, and strategic transactions such as licensing deals. The filings suggest compensation and expense trends may also be affected by headcount reductions, lower clinical trial spend, and restructuring actions, while indirect compensation costs declined alongside reduced R&D activity. Because management has highlighted contingent consideration adjustments and the need to preserve cash, compensation decisions are likely shaped by runway extension, successful partnering, and progress toward advancing VCN-01 into later-stage development.

Insider Trading Considerations

Insider trading activity in Theriva should be viewed through the lens of a small, cash-constrained biotechnology company where news flow is highly binary and stock performance can react sharply to clinical or financing events. Insider purchases may signal confidence in VCN-01’s Phase 3 path, the company’s ability to secure funding, or the value of licensing arrangements like SYN-020, while sales may more often reflect liquidity needs, tax planning, or diversification rather than a negative outlook. Because the company regularly raises capital through ATM sales, equity offerings, and warrant exercises, insider trading patterns may also be influenced by dilution risk and ongoing financing overhang. Regulatory and blackout considerations are especially important here given the sensitivity of FDA interactions, trial data releases, and partnership announcements that can materially move the stock.

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