PROTARA THERAPEUTICS INC

Insider Trading & Executive Data

TARA
NASDAQ
Healthcare
Biotechnology

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40 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)
40
0 in last 30 days
Buy / Sell (1Y)
26/14
Acquisitions / Dispositions
Unique Insiders (1Y)
14
Active in past year
Insider Positions
20
Current holdings
Position Status
20/0
Active / Exited
Institutional Holders
80
Latest quarter
Board Members
29

Compensation & Governance

Avg Total Compensation
$2.2M
Latest year: 2024
Executives Covered
7
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)
5
Form 144 Insiders (1Y)
3
Planned Sale Shares (1Y)
1.4M
Planned Sale Value (1Y)
$8.2M
Price
$6.40
Market Cap
$340.8M
Volume
27,626.72
EPS
$-0.31
Revenue
$0.00
Employees
33
About PROTARA THERAPEUTICS INC

Company Overview

Protara Therapeutics is a small, clinical-stage biotechnology company focused on oncology and rare diseases, with two lead programs: TARA-002 (a cell therapy based on OK-432 materials) targeting NMIBC and pediatric lymphatic malformations, and IV Choline Chloride (an intravenous therapy for parenteral support patients) with Fast Track and Orphan designations. The company outsources manufacturing to U.S. cGMP CDMOs (47 consecutive successful batches by end-2024, no recent Form 483s) and in-licenses key IP from Chugai and academic inventors. Protara has no product revenue, a history of operating losses (net loss ~$44.6M in 2024; accumulated deficit near $272M as of mid‑2025), modest headcount (~33 employees) and relies on periodic equity financings and warrant exercises to fund pivotal trials and operating needs. Near‑term value drivers are interim ADVANCED-2 and STARBORN data, the planned registrational THRIVE study for IV Choline, and enrollment/inspection milestones that will materially move the stock.

Executive Compensation Practices

As a clinical-stage biotech with no product revenue, Protara’s executive pay is likely weighted heavily toward equity-based compensation and milestone-linked incentives rather than cash salary—consistent with the company’s disclosure of $4.1M stock‑based compensation in 2024 and relatively modest personnel expense in G&A. Compensation and bonuses are expected to be tied to clinical and regulatory milestones (IND clearances, cohort enrollments, interim analyses, pivotal trial starts/completions) and to successful capital raises or partnering deals that address the company’s funding needs. Given the company’s reliance on third‑party CDMOs, licensed IP and the need to preserve runway (cash + marketable securities ~$145–170M range in 2024–mid‑2025), management incentives may also include metrics for cash stewardship, successful CDMO performance/inspections, and completion of financing tranches. Board and scientific advisors are likely compensated with options/RSUs and milestone payments to conserve cash while aligning long‑term interests with shareholders.

Insider Trading Considerations

Protara’s stock is highly event‑driven and sensitive to trial readouts, enrollment announcements, IND/registrational milestones and financing activity, so insider transactions will often cluster around these material events; watch for Form 4 filings around interim data releases (ADVANCED‑2, STARBORN, THRIVE) and after financing closings or warrant exercises. Common patterns to monitor include option exercises followed by immediate sales (liquidity/diversification), scheduled 10b5‑1 plans to manage disclosure risk around clinical data, and insider sales following public offerings (underwriter option exercises and warrant-related financing occurred in 2024). Regulatory and reputational risk is heightened in healthcare: trading on material nonpublic clinical data is strictly scrutinized by the SEC and FDA‑driven events (e.g., FDA alignment on registrational path, CDMO inspections) can be broadly material—expect blackout periods around trial data and additional restrictions tied to financing lock‑ups or collaborator agreements. Finally, because executives may hold concentrated equity positions in a no‑revenue biotech, large insider sales or consistent selling can signal liquidity needs or de‑risking and should be interpreted in the context of contemporaneous funding and clinical milestones.

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