Item 1.01 Entry into a Material Definitive Agreement
Note Purchase Agreement and Note
On January 19, 2021, Jaguar Health, Inc. (Jaguar or the Company) and Napo Pharmaceuticals, Inc., a wholly-owned subsidiary of Jaguar (Napo and, together with Jaguar, the Borrower), entered into a note purchase agreement (the Purchase Agreement) with Streeterville Capital, LLC (Investor), an affiliate of Chicago Venture Partners, L.P. (CVP), pursuant to which the Borrower issued to Investor a secured promissory note (the Note) in the aggregate principal amount of $6,220,812.50 (the Note Offering). The initial principal balance of the Note includes $195,812.50 representing prepaid interest for the first twelve months and $25,000 to cover Investors transaction expenses. The Company will use the proceeds to fund development of the Companys NP-300 (lechlemer) drug product candidate for the indication of the symptomatic relief of diarrhea from cholera (the Cholera Indication) and general corporate purposes, including the Companys product pipeline activities. The Note bears interest at 3.25% per annum and matures on January 20, 2025. Interest will be prepaid each 12 months at the beginning of the period.
Under the Purchase Agreement, if a tropical disease priority review voucher (TDPRV) is granted to the Company by the U.S. Food & Drug Administration in connection with the Companys development of lechlemer for the Cholera Indication and the Company sells the TDPRV, then Investor will be entitled to a specified percentage of the gross proceeds from such sale, ranging from 18% to 1%, depending on the percentage of the original balance of the Note that remains outstanding as of the date of the sale of the TDPRV, which percentage will decrease to 1% once the Note is paid in full.
In addition, beginning on the earlier of (i) six months following the closing of the Note Offering and (ii) the initiation of human clinical trials with lechlemer, (the Optional Prepayment Period), the Company will have the right, from time to time at in its sole discretion, to prepay all or any portion of the Note (such amount, the Principal Prepayment Amount) at a price equal to 112.5% multiplied by the Principal Prepayment Amount (the Optional Prepayment Amount). Beginning on the date that the last patient is enrolled in a pivotal trial with lechlemer for the Cholera Indication, the Company must receive Investor approval before prepaying the Note.
In the event that, prior to redeeming the Note, (i) the Company abandons the clinical trial with lechlemer for the Cholera Indication, (ii) the Company fails to start the Phase 1 clinical trial of lechlemer for the Cholera Indication by July 1, 2022 or (iii) the Company fails to meet all primary endpoints in the pivotal trial for lechlemer for the Cholera Indication with statistical significant (such event, a Trial Failure), then Investor has the right to multiply the outstanding balance of the Note as of the date of the Trial Failure by 125% and accelerate the Note. The Purchase Agreement and the Note also contain representations, warranties, covenants, events of default (in the case of the Note) and other provisions customary for transactions of this nature.
Security Agreement
Napo also entered into a security agreement (the Security Agreement) with Investor, pursuant to which Investor will receive a first priority security interest in all existing and future lechlemer technology, and Napo will agree, with certain exceptions, not to grant any lien on any of the collateral securing the Note and not to grant any license under any of the intellectual property relating to such collateral. Notwithstanding the foregoing, the grant of security interest under the Security Agreement will not be effective until such time as the Company receives required consent from a third party.
The foregoing summaries of the Note, the Purchase Agreement and the Security Agreement do not purport to be complete and are subject to, and qualified in their entirety by, the Note, the Purchase Agreement and the Security Agreement attached as Exhibits 1.1 and 10.1, and 10.2 respectively, to this Current Report on Form 8-K, which exhibits are incorporated herein by reference.