[144] Guardant Health, Inc. SEC Filing
Rhea-AI Filing Summary
Form 144 notice for Guardant Health, Inc. (GH) shows an intended sale of 116 common shares via Charles Schwab on 09/17/2025 with an aggregate market value of $6,453. The shares were acquired on 09/15/2025 through a restricted stock lapse under equity compensation. The filing lists prior open-market sales by the same account in the past three months: 3,213 shares for $158,947 on 06/18/2025, and two smaller sales of 116 shares$5,591 and $6,846 on 07/17/2025 and 08/19/2025, respectively. The signer affirms no undisclosed material adverse information.
Positive
- Discloses acquisition source (restricted stock lapse), improving transparency
- Includes recent sales history for the same account, aiding compliance and investor visibility
- Identifies broker and planned sale date, giving execution clarity
Negative
- Insider liquidity activity — multiple recent sales including a 3,213-share sale, which may concern some investors
Insights
TL;DR: Insider selling activity includes a new small sale tied to restricted stock lapse and multiple recent open-market dispositions.
The filing documents a proposed sale of 116 shares following a restricted stock lapse, with execution through a retail brokerage. Recent transactions show substantial prior selling (3,213 shares for $158,947) plus two 116-share sales, indicating ongoing monetization of holdings rather than a single disposition. For investors, this is a disclosure of insider liquidity rather than a corporate operational signal; the amounts disclosed here are small relative to large-cap volumes but are material for transparency and compliance monitoring.
TL;DR: The Form 144 appears procedurally complete and cites equity compensation as the acquisition source.
The notice properly identifies the nature of acquisition as a restricted stock lapse and names the broker and planned sale date. It also summarizes prior sales by the same person in the last three months, fulfilling Rule 144 disclosure expectations. The signer’s representation about lack of undisclosed material adverse information is included, aligning with regulatory attestation norms.