Thomas Thomas T. - 07 Sep 2021 Form 4 Insider Report for OPIANT PHARMACEUTICALS, INC.

Role
Director
Signature
/s/ Thomas T. Thomas
Issuer symbol
N/A
Transactions as of
07 Sep 2021
Net transactions value
-$46
Form type
4
Filing time
09 Sep 2021, 16:02:32 UTC
Previous filing
20 Aug 2021
Next filing
16 Sep 2021

Transactions Table

Type Sym Class Transaction Value $ Shares Change % * Price $ Shares After Date Ownership Footnotes
transaction OPNT Common Stock Options Exercise $14,750 +1,475 +25% $10.00 7,475 07 Sep 2021 Direct
transaction OPNT Common Stock Sale $14,796 -822 -11% $18.00 6,653 07 Sep 2021 Direct F1, F2

Derivative Securities (e.g., puts, calls, warrants, options, convertible securities)

Type Sym Class Transaction Value $ Shares Change % * Price $ Shares After Date Underlying Class Amount Exercise Price Ownership Footnotes
transaction OPNT Stock Option (right to buy) Options Exercise $0 -1,475 -18% $0.000000 6,859 07 Sep 2021 Common Stock 1,475 $10.00 Direct F3, F4
* An asterisk sign (*) next to the price indicates that the price is likely invalid.

Explanation of Responses:

Id Content
F1 The shares were sold pursuant to a Rule 10b5-1 trading plan entered into by the Reporting Person.
F2 The shares were sold to cover the $10 exercise price of the vested stock options. The net shares of 653, after selling to cover the exercise price, will be held by the Reporting Person.
F3 The option was exercised pursuant to a Rule 10b5-1 trading plan entered into by the Reporting Person.
F4 On November 4, 2016, the reporting person was granted an option to purchase 35,000 shares of Common Stock. The options vest as follows: (i) 11,667 share upon the up listing of the Issuer to The NASDAQ Stock Market (which occurred on August 29, 2017); (ii) 11,667 shares upon the cumulative funding of the Issuer in excess of $5,000,000 by institutional investors, commencing May 5, 2016 (which performance criteria was met on December 13, 2016); and (iii) 11,666 shares upon the first submission of a New Drug Application ("NDA") to the FDA for one of Issuer's products by either the Issuer or an Issuer licensee.