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Item 1.01
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Entry Into a Material Definitive Agreement.
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Paycheck Protection Program Loan
On April 27, 2020,
TherapeuticsMD, Inc., a Nevada corporation (the “Company”), received a loan pursuant to the Paycheck Protection
Program under the Coronavirus Aid, Relief, and Economic Security Act (the “CARES Act”), as administered by the
U.S. Small Business Administration (the “SBA”). The loan in the principal amount of $6,477,094 (the “PPP
Loan”) was disbursed by Bank of America, NA, a national banking association (“Lender”), pursuant to a
promissory note issued by the Company (the “Promissory Note”).
The PPP Loan matures
on the two-year anniversary of the funding date and bears interest at a fixed rate of 1.00% per annum. Monthly principal and
interest payments, less the amount of any potential forgiveness (discussed below), will commence after the six-month
anniversary of the funding date. The Company did not provide any collateral or guarantees for the PPP Loan, nor did the Company
pay any facility charge to obtain the PPP Loan. The Promissory Note provides for customary events of default, including,
among others, those relating to failure to make payment, bankruptcy, breaches of representations and material adverse
effects. The Company may prepay the principal of the PPP Loan at any time without incurring any prepayment charges.
All or a portion of the
PPP Loan may be forgiven by the SBA and the Lender upon application by the Company beginning 60 days but not later than 90 days
after the funding date of the PPP Loan. Under the CARES Act, loan forgiveness is available for the sum of documented payroll costs,
covered rent payments, and covered utilities during the eight-week period beginning on the approval date of the PPP Loan. For purposes
of the CARES Act, payroll costs exclude compensation of an individual employee in excess of $100,000, prorated annually. Not more
than 25% of the forgiven amount may be for non-payroll costs. Forgiveness is reduced if full-time headcount declines, or if salaries
and wages for employees with salaries of $100,000 or less annually are reduced by more than 25%. Although the Company currently
believes that its use of the PPP Loan will meet the conditions for forgiveness of the loan, the Company cannot assure that the
PPP Loan will be forgiven, in whole or in part.
The
foregoing summary of the terms of the Promissory Note does not purport
to be complete and is subject to, and qualified in its entirety by, the full text of the Promissory Note,
a copy of which will be filed as an exhibit to the Company’s Quarterly Report on Form 10-Q for the quarter ending June 30,
2020.
Amendment
to Financing Agreement
In
connection with incurring the PPP Loan, the Company, together with its subsidiaries, amended that certain Financing
Agreement, dated as of April 24, 2019, by and among the Company, certain of the Company’s subsidiaries party thereto
from time to time as guarantors, the administrative agent and the various lenders from time to time party thereto, to, among
other things, permit the Company to incur the PPP Loan and add certain affirmative covenants relating thereto. The
foregoing summary of the terms of the amendment does not purport to be complete and is subject to, and qualified in its
entirety by, the full text of the amendment, a copy of which will be filed as an exhibit to the Company’s Quarterly
Report on Form 10-Q for the quarter ending June 30, 2020.
Item 2.03
Creation of a Direct Financial Obligation or an
Obligation under an Off-Balance Sheet Arrangement of a Registrant.
The disclosure in Item
1.01 of this Current Report on Form 8-K is incorporated into this Item 2.03 by reference.
Forward-Looking
Statements
This
Current Report on Form 8-K may contain forward-looking statements. Forward-looking statements may include, but are not limited
to, statements relating to the Company’s objectives, plans and strategies as well as statements, other than historical facts,
that address activities, events or developments that the Company intends, expects, projects, believes or anticipates will or may
occur in the future. These statements are often characterized by terminology such as “believes,” “hopes,”
“may,” “anticipates,” “should,” “intends,” “plans,” “will,”
“expects,” “estimates,”
“projects,” “positioned,” “strategy” and similar expressions and are based on assumptions and
assessments made in light of the Company’s management’s experience and perception of historical trends, current conditions,
expected future developments and other factors believed to be appropriate. Forward-looking statements in this Form 8-K are made
as of the date of this Form 8-K, and the Company undertakes no duty to update or revise any such statements, whether as a result
of new information, future events or otherwise, except as required by law or by the rules and regulations of the U.S. Securities
and Exchange Commission (the “SEC”). Forward-looking statements are not guarantees of future performance and are subject
to risks and uncertainties, many of which are outside of the Company’s control. Important factors that could cause actual
results, developments and business decisions to differ materially from forward-looking statements are described in the sections
titled “Risk Factors” in the Company’s Annual Report on Form 10-K for the year ended December 31, 2019, filed
with the SEC on February 24, 2020, as well as this Form 8-K, and include the following: the effects of the COVID-19 pandemic; whether
the Company will be able to comply with the covenants and conditions under PPP Loan, including the conditions for forgiveness of
the loan; the Company’s ability to maintain or increase sales of its products; the Company’s ability to successfully
commercialize IMVEXXY®, ANNOVERA®, and BIJUVA® and develop and commercialize its hormone therapy drug candidates and
obtain additional financing necessary therefor; the Company’s commercialization, marketing and manufacturing capabilities
and strategy for its approved products; the size of markets and the potential market opportunity for which the Company’s
products are approved and its ability to penetrate such markets; the rate and degree of market acceptance of the Company’s
products; the willingness of healthcare providers to prescribe and patients to use the Company’s products; the Company’s
ability to obtain additional financing when needed; the Company’s competitive position and the success of competing products
that are or become available for the indications that it is pursuing; the Company’s intellectual property position; whether
the Company will be able to comply with the covenants and conditions under its term loan facility, including the conditions to
draw an additional tranche thereunder and whether the lender will make such tranche available; the potential of adverse side effects
or other safety risks that could adversely affect the commercialization of the Company’s current or future approved products
or preclude the approval of the Company’s future drug candidates; whether the U.S. Food and Drug Administration (FDA) will
approve the efficacy supplement for the lower dose of BIJUVA; the Company’s ability to protect its intellectual property,
including with respect to the Paragraph IV notice letters the Company received regarding IMVEXXY and BIJUVA; the length, cost and
uncertain results of future clinical trials; the Company’s reliance on third parties to conduct its manufacturing, research
and development and clinical trials; the ability of the Company’s licensees to commercialize and distribute the Company’s
products; the ability of the Company’s marketing contractors to market ANNOVERA; the availability of reimbursement from government
authorities and health insurance companies for the Company’s products; the impact of product liability lawsuits; the influence
of extensive and costly government regulation; the volatility of the trading price of the Company’s common stock and the
concentration of power in its stock ownership.