KemPharm Reports First Quarter 2021 Financial Results
KemPharm reported a significant transformation in Q1 2021, highlighted by FDA approval of AZSTARYS on March 2, 2021, and successful financial restructuring resulting in $94 million in gross proceeds and a debt-free status. The company posted Q1 revenue of $12.1 million, primarily from a milestone payment, with a net loss of $10.3 million, or $0.54 per share. Cash holdings increased to $76 million. The license agreement with Gurnet Point Capital was amended to include up to $590 million in future milestone payments for AZSTARYS, enhancing shareholder value prospects.
- FDA approval of AZSTARYS marks a major milestone.
- Successful financial restructuring led to $94 million in gross proceeds.
- Net operating income improved to $7 million, a $10.7 million increase from Q1 2020.
- Cash and equivalents increased to $76 million, up from $4.3 million at end of 2020.
- Amended license agreement allows for up to $590 million in future milestone payments.
- Q1 2021 net loss of $10.3 million represents a decrease from Q1 2020's net loss.
- Non-cash loss on extinguishment of debt negatively impacted financial results.
Corporate and Regulatory Highlights
- AZSTARYSTM NDA approved by the FDA on March 2, 2021
- Announced amendment to Licensing Agreement with Gurnet Point Capital affiliate following FDA approval of AZSTARYS
- Received FDA clearance to initiate KP879 clinical program for the treatment of Stimulant Use Disorder
- Serdexmethylphenidate (SDX) classified as a Schedule IV Controlled Substance by the DEA
Financial Highlights
- Completed financial restructuring, which resulted in re-listing on The Nasdaq Capital Market, receipt of approximate gross proceeds of
$94 million and no debt - Reported Q1 2021 revenue of
$12.1 million - Q1 2021 net loss of (
$0.54) per basic share and diluted share compared to a net loss of ($1.92) per basic share and diluted share for Q1 2020 - Total cash, cash equivalents and restricted cash was
$76.0 million at March 31, 2021
CELEBRATION, Fla., May 13, 2021 (GLOBE NEWSWIRE) -- KemPharm, Inc. (NASDAQ: KMPH), a specialty pharmaceutical company focused on the discovery and development of proprietary prodrugs, today reported its financial results for the first quarter ended March 31, 2021.
“The first quarter of 2021 was nothing short of transformational for KemPharm, highlighted by the FDA approval of AZSTARYS, the completion of our financial restructuring, and the re-listing of our shares on Nasdaq,” said Travis C. Mickle, Ph.D., President and Chief Executive Officer of KemPharm. “As a result, we stand today as a company with a solid balance sheet and capital structure that is moving full force with our partners at GPC and Corium to soon launch AZSTARYS as a once-daily product for the treatment of attention deficit hyperactivity disorder (ADHD) in patients age six years and older.”
Dr. Mickle continued, “Following the close of the quarter, KemPharm further strengthened its position by agreeing to amend the License Agreement with an affiliate of GPC. We are now eligible to receive up to
Dr. Mickle continued, “As we have noted in prior communications, KemPharm believes that the product label for AZSTARYS is potentially best-in-class, with several elements in the label providing clear points of differentiation from other commercially available methylphenidate ADHD products. We were pleased with the recent determination that serdexmethylphenidate (SDX), was classified as a Schedule IV controlled substance by the Drug Enforcement Administration (DEA) following a thorough review by the U.S. Department of Health and Human Services (HHS). SDX comprises
Dr. Mickle concluded, “Further, the Schedule IV classification of SDX is a significant development for our lead clinical product candidate, KP879, an extended-duration, agonist replacement therapy for the treatment of Stimulant Use Disorder (SUD), as SDX is the only API in KP879. We now look forward to initiating the clinical program for KP879 in 2021 after receiving FDA clearance for the Investigational New Drug (IND) application. If approved, KP879 could be a Schedule IV product, and physicians who are treating patients seeking to overcome addictions to cocaine, methamphetamine or other stimulants may be able to prescribe KP879 with the knowledge that the product candidate could have a significantly lower potential for abuse.”
Q1 2021 Financial Results:
For Q1 2021, KemPharm reported revenue of
KemPharm’s net loss for Q1 2021 was
As of March 31, 2021, total cash, cash equivalents and restricted cash was
As of March 31, 2021, total shares of common stock outstanding was 28,480,156 shares, and fully diluted common shares outstanding was 38,379,718 shares, which included 9,544,693 shares issuable upon exercise of warrants. In addition, no preferred stock is outstanding as of March 31, 2021.
“KemPharm has emerged from Q1 2021 as a Nasdaq-listed company with no debt and significant cash holdings on the balance sheet,” said LaDuane Clifton, KemPharm’s Chief Financial Officer. “We have the resources needed to continue the development of KP879, and we have begun evaluating how to efficiently deploy capital to generate additional value streams for shareholders. There are many opportunities to explore, both internally and externally, and creating long-term value is top of mind.”
Conference Call Information:
Interested participants and investors may access the conference call by dialing either:
- (866) 395-2480 (U.S.)
- (678) 509-7538 (international)
- Conference ID: 4737008
An audio webcast with slide presentation will be accessible via the Investor Relations section of the Company’s website, http://investors.kempharm.com/. An archive of the webcast and presentation will be available for 90 days beginning at approximately 5:30 p.m. ET, on May 13, 2021.
About AZSTARYS™:
AZSTARYS™ is an FDA-approved, once-daily product for the treatment of attention deficit hyperactivity disorder (ADHD) in patients age six years or older. AZSTARYS consists of SDX, KemPharm’s prodrug of d-methylphenidate (d-MPH), co-formulated with immediate release d-MPH.
The complete approved prescribing information for AZSTARYS may be downloaded in PDF format here:
https://kempharm.com/wp-content/uploads/2021/03/AZSTARYS-Master-Label-Final_20210302.pdf
About KemPharm:
KemPharm is a specialty pharmaceutical company focused on the discovery and development of proprietary prodrugs to treat serious medical conditions through its proprietary LAT® (Ligand Activated Therapy) technology. KemPharm utilizes its proprietary LAT® technology to generate improved prodrug versions of FDA-approved drugs as well as to generate prodrug versions of existing compounds that may have applications for new disease indications. KemPharm’s prodrug product candidate pipeline is focused on the high need areas of attention deficit hyperactivity disorder, or ADHD, stimulant use disorder (SUD) and CNS rare diseases, including idiopathic hypersomnia (IH). KemPharm’s lead clinical development candidate for the treatment of SUD, KP879, is based on its prodrug of d-methylphenidate, known as serdexmethylphenidate (SDX). In addition, KemPharm has received FDA approval for AZSTARYSTM, a new once-daily treatment for ADHD in patents age six years and older, and for APADAZ®, an immediate-release combination product containing benzhydrocodone, a prodrug of hydrocodone, and acetaminophen. For more information on KemPharm and its pipeline of prodrug product candidates visit www.kempharm.com or connect with us on Twitter, LinkedIn, Facebook and YouTube.
Caution Concerning Forward Looking Statements:
This press release may contain forward-looking statements made in reliance upon the safe harbor provisions of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended. Forward-looking statements include all statements that do not relate solely to historical or current facts and can be identified by the use of words such as “may,” “will,” “expect,” “project,” “estimate,” “anticipate,” “plan,” “believe,” “potential,” “should,” “continue” or the negative versions of those words or other comparable words. Forward-looking statements are not guarantees of future actions or performance. These forward-looking statements, including the timing of the potential commercial launch of AZSTARYS, the market outlook for AZSTARYS, potential regulatory and sales milestone and royalty payments pursuant to the License Agreement with an affiliate of GPC, the potential benefits of AZSTARYS and the clinical development of KP879, are based on information currently available to KemPharm and its current plans or expectations and are subject to a number of uncertainties and risks that could significantly affect current plans. Risks concerning KemPharm’s business are described in detail in KemPharm’s Quarterly Report on Form 10-Q for the quarter ended March 31, 2021, and KemPharm’s other filings with the Securities and Exchange Commission. KemPharm is under no obligation to, and expressly disclaims any such obligation to, update or alter its forward-looking statements, whether as a result of new information, future events or otherwise.
KemPharm Contacts:
Jason Rando / Maureen McEnroe, CFA
Tiberend Strategic Advisors, Inc.
(212) 375-2665 / 2664
jrando@tiberend.com
mmcenroe@tiberend.com
KEMPHARM, INC.
UNAUDITED CONDENSED STATEMENTS OF OPERATIONS
(in thousands, except share and per share amounts)
| Three months ended March 31, | ||||||||
| 2021 | 2020 | |||||||
| Revenue | $ | 12,117 | $ | 2,089 | ||||
| Operating expenses: | ||||||||
| Royalty and direct contract acquisition costs | 1,000 | 663 | ||||||
| Research and development | 2,265 | 2,126 | ||||||
| General and administrative | 1,892 | 2,245 | ||||||
| Severance expense | — | 830 | ||||||
| Total operating expenses | 5,157 | 5,864 | ||||||
| Income (loss) from operations | 6,960 | (3,775 | ) | |||||
| Other (expense) income: | ||||||||
| Loss on extinguishment of debt | (16,885 | ) | — | |||||
| Interest expense related to amortization of debt issuance costs and discount | (150 | ) | (571 | ) | ||||
| Interest expense on principal | (199 | ) | (1,260 | ) | ||||
| Fair value adjustment related to derivative and warrant liability | (30 | ) | 75 | |||||
| Interest and other income (expense), net | 8 | (223 | ) | |||||
| Total other expenses | (17,256 | ) | (1,979 | ) | ||||
| Loss before income taxes | (10,296 | ) | (5,754 | ) | ||||
| Income tax benefit (expense) | — | — | ||||||
| Net loss | $ | (10,296 | ) | $ | (5,754 | ) | ||
| Deemed dividend | (37,444 | ) | — | |||||
| Net loss attributable to common stockholders | $ | (47,740 | ) | $ | (5,754 | ) | ||
| Basic and diluted net loss per share of common stock: | ||||||||
| Net loss | $ | (0.54 | ) | $ | (1.92 | ) | ||
| Net loss attributable to common stockholders | $ | (2.49 | ) | $ | (1.92 | ) | ||
| Weighted average number of shares of common stock outstanding: | ||||||||
| Basic and diluted | 19,146,270 | 3,004,559 | ||||||
KEMPHARM, INC.
CONDENSED BALANCE SHEETS
(in thousands, except share and par value amounts)
| March 31, | December 31, | |||||||
| 2021 | 2020 | |||||||
| (unaudited) | ||||||||
| Assets | ||||||||
| Current assets: | ||||||||
| Cash and cash equivalents | $ | 75,917 | $ | 4,213 | ||||
| Accounts and other receivables | 11,308 | 2,579 | ||||||
| Prepaid expenses and other current assets | 395 | 1,481 | ||||||
| Restricted cash | 109 | 109 | ||||||
| Total current assets | 87,729 | 8,382 | ||||||
| Property and equipment, net | 975 | 1,039 | ||||||
| Operating lease right-of-use assets | 1,294 | 1,350 | ||||||
| Other long-term assets | 437 | 438 | ||||||
| Total assets | $ | 90,435 | $ | 11,209 | ||||
| Liabilities and stockholders' equity (deficit) | ||||||||
| Current liabilities: | ||||||||
| Accounts payable and accrued expenses | $ | 2,855 | $ | 6,647 | ||||
| Current portion of operating lease liabilities | 336 | 327 | ||||||
| Current portion of loans payable | 683 | 390 | ||||||
| Other current liabilities | 364 | 172 | ||||||
| Total current liabilities | 4,238 | 7,536 | ||||||
| Convertible notes, less current portion, net | — | 67,658 | ||||||
| Derivative and warrant liability | 334 | 304 | ||||||
| Operating lease liabilities, less current portion | 1,500 | 1,587 | ||||||
| Loans payable | 98 | 391 | ||||||
| Other long-term liabilities | 14 | 145 | ||||||
| Total liabilities | 6,184 | 77,621 | ||||||
| Stockholders’ equity (deficit): | ||||||||
| Preferred stock, undesignated, | — | — | ||||||
| Common stock, | 3 | — | ||||||
| Additional paid-in capital | 353,018 | 192,062 | ||||||
| Accumulated deficit | (268,770 | ) | (258,474 | ) | ||||
| Total stockholders' equity (deficit) | 84,251 | (66,412 | ) | |||||
| Total liabilities and stockholders' equity (deficit) | $ | 90,435 | $ | 11,209 | ||||
FAQ
What were KemPharm's Q1 2021 revenue and net loss?
What significant FDA approvals did KemPharm achieve recently?
How did KemPharm's financial restructuring impact its stock?
What is the future outlook for KemPharm's AZSTARYS product?
What is the status of KemPharm's KP879 program?
