REVIVA PHARMACEUTICALS HOLDINGS INC

Insider Trading & Executive Data

RVPH
NASDAQ
Healthcare
Biotechnology

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4 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)
4
0 in last 30 days
Buy / Sell (1Y)
4/0
Acquisitions / Dispositions
Unique Insiders (1Y)
4
Active in past year
Insider Positions
5
Current holdings
Position Status
5/0
Active / Exited
Institutional Holders
41
Latest quarter
Board Members
11

Compensation & Governance

Avg Total Compensation
$632733.00
Latest year: 2024
Executives Covered
3
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
$0.22
Market Cap
$25.1M
Volume
24,329
EPS
N/A
Revenue
$0.00
Employees
14
About REVIVA PHARMACEUTICALS HOLDINGS INC

Company Overview

Reviva Pharmaceuticals Holdings, Inc. is a late‑stage biotechnology company developing next‑generation small‑molecule therapies for central nervous system, inflammatory and cardiometabolic diseases, with two proprietary NCEs: brilaroxazine (RP5063) for schizophrenia and other neuropsychiatric/ pulmonary indications and RP1208 for depression and obesity. The company is asset‑light (14 full‑time employees) and relies on CROs, contract manufacturers and consultants to run global clinical programs; key recent milestones include a positive Phase 3 RECOVER‑1 topline and encouraging 1‑year OLE data. Reviva has substantial patent coverage (63 granted, 10 pending) and orphan designations for certain indications, but lacks commercialization infrastructure and is milestone‑and financing‑driven, targeting further registrational activity and a potential NDA in 2026 conditional on additional funding. Financially, cash has declined ( ~$10–13M range in 2024–H1 2025), management disclosed going‑concern risk, and management estimates roughly $67M of clinical spend may be required over the next ~3 years.

Executive Compensation Practices

Given Reviva’s late‑stage, milestone‑driven profile and constrained liquidity, executive pay is likely skewed toward equity‑based incentives (stock options/warrants and restricted stock) tied to clinical and regulatory milestones (RECOVER‑series outcomes and NDA milestones), with lower base salaries relative to larger biopharma peers. The filings show material use of stock‑based compensation and warrant instruments (including non‑cash warrant remeasurement gains/losses), and management has explicitly used equity financings in 2024–2025, which creates strong alignment between executives and shareholders but also increases dilution risk. Compensation metrics for management will be centered on trial enrollment/completion rates, pivotal efficacy/safety endpoints, FDA interactions and financing execution rather than near‑term revenue or sales targets. Material weaknesses in internal controls and tight cash runway can compress cash pay and increase reliance on long‑dated equity or milestone‑contingent pay structures.

Insider Trading Considerations

Insider trading in Reviva should be monitored for financings, warrant exercises and equity grants since recent years featured registered offerings, ATM sales and warrant activity — insiders may exercise warrants or sell shares contemporaneous with capital raises, producing observable Form 4/144 activity. Because the stock is milestone‑sensitive and float is small, even modest insider buys/sells can move the price materially; traders should watch Form 4 filings closely around clinical readouts (RECOVER OLE and RECOVER‑2), FDA meetings/submissions, and announced financing windows. Expect formal blackout periods surrounding material nonpublic information (trial data and regulatory submissions) and a higher likelihood of 10b5‑1 plans or scheduled sales tied to financing needs; also note Section 16 short‑swing rules and that internal control weaknesses could delay timely filings or create additional regulatory scrutiny.

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