John A. Roberts - 15 Mar 2022 Form 4 Insider Report for Vyant Bio, Inc.

Source evidence Original filing metadata and source links for verification. 5 source fields
SEC form
4
Accepted by SEC
17 Mar 2022, 16:15:44 UTC
Prior SEC filing
24 Nov 2021
Next SEC filing
14 Feb 2024
Source filing
View source filing
Reporting owner 1 detail
Reporting owner signature
/s/ Andrew LaFrence, attorney-in-fact

Key filing fact

John A. Roberts filed Form 4 for Vyant Bio, Inc. on 17 Mar 2022.

Key facts

  • This page summarizes John A. Roberts's Form 4 filing for Vyant Bio, Inc..
  • 1 reported transaction and 1 derivative row are listed below.
  • Accepted by SEC: 17 Mar 2022, 16:15.

Change

  • Previous filing in this sequence was filed on 24 Nov 2021.
  • Current net transaction value: $0.

Research use

  • This tells you what this filing adds before you inspect full transaction and derivative tables.
  • You can trace every row back to the original SEC filing document.

Evidence

Filed on Form 4

Ownership activity is grounded in SEC Form 4 disclosures.

View source filing

Reported derivative securities

Options, warrants, convertible securities, or similar derivative positions disclosed in the filing.

VYNT transaction Derivative

Stock option (right to buy)

Award

Transaction value
$0
Shares
+150,000
Change %
Price
$0.000000
Shares after
150,000
Date
15 Mar 2022
Ownership
Direct
Underlying class
Common Stock
Underlying amount
150,000
Exercise price
$1.00
Footnotes
F1
* marks a reported price that did not pass the local price check.

Additional SEC filing notes

Filing notes and footnotes

Explanation of responses 1 footnote

Footnote F1

The option shall become exercisable with respect to twenty five percent (25%) of the shares underlying the option upon the date of grant, with respect to thirty seven and a half percent (37.5)% upon the filing by the Company of an Investigational New Drug Application ("IND") with the U.S. Food and Drug Administration ("FDA") for a New Chemical Entity ("NCE") candidate to treat Rett Syndrome and with respect to the remaining thirty seven and a half percent (37.5)% upon the filing by the Company of an IND with the FDA for an NCE candidate to treat CDKL5 Deficiency Disorders; provided that the participant remains a service provider to the Company through each applicable vesting date.

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