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We are a clinical-stage biopharmaceutical company focused on metabolic and endocrine disorders. We improve compliance, absorption, and more with our proprietary drug delivery technology.

Lipocine Announces Financial Results for the First Quarter Ended March 31, 2022

SALT LAKE CITY, May 9, 2022 /PRNewswire/ -- Lipocine Inc. (NASDAQ: LPCN), a biopharmaceutical company focused on developing innovative products for neuroendocrine and metabolic disorders, today announced financial results for the quarter ended March 31, 2022 and provided a corporate update.

Program Highlights

  • TLANDO™ was approved and granted Market Exclusivity by the U.S. Food and Drug Administration ("FDA") for hypogonadism and our licensee expects commercial launch in second quarter of 2022
  • Lipocine is currently enrolling subjects in a Phase 2 proof-of-concept study to evaluate the therapeutic potential of LPCN 1148 for the management of cirrhosis, with enrollment in the study expected to be complete by the end of the third quarter of 2022
  • Lipocine has requested an End of Phase 2 meeting to discuss the Phase 3 study and confirmatory trial design for LPCN 1144 in non-cirrhotic non-alcoholic steatohepatitis ("NASH")
  • An open label extension ("OLE") study in non-cirrhotic NASH has been completed and topline results are expected in May 2022

Board Appointments

The company appointed Jill M. Jene, Ph.D. and Spyros Papapetropoulos, M.D., Ph.D. to its board of directors in April 2022

First Quarter Ended March 31, 2022 Financial Results

Lipocine reported a net loss of $3.5 million or ($0.04 per diluted share), for the quarter ended March 31, 2022, compared with a net loss of $3.4 million, or ($0.04) per diluted share, in the quarter ended March 31, 2021.

Research and development expenses were $1.9 million for the quarter ended March 31, 2022, compared with $1.6 million for the quarter ended March 31, 2021. The increase in research and development expenses for the quarter ended March 31, 2022, was a result of increases in contract research organization expenses related to the ongoing Phase 2 clinical study for LPCN 1148, PK and food effect studies for LPCN 1107 and LPCN 1154, manufacturing scale up expenses for LPCN 1111, and an increase in personnel and other R&D expenses.  These increases were offset by a decrease in contract research organization expense and outside consulting costs related to the LPCN 1144 LiFT Phase 2 clinical study and a decrease in costs related to TLANDO.

General and administrative expenses were $1.2 million for the quarter ended March 31, 2022, compared with $1.5 million for the quarter ended March 31, 2021. The decrease in general and administrative expenses for the quarter ended March 31, 2022, was primarily due to decreases in legal costs, personnel costs and other general and administrative costs. These decreases were offset by increases in professional fees related to various consulting and proxy solicitation services as well as an increase in corporate insurance expenses.

As of March 31, 2022, the company had $42.0 million of unrestricted cash, cash equivalents and marketable investment securities compared to $46.6 million as of December 31, 2021. 

About Lipocine

Lipocine Inc. is a biopharmaceutical company focused on neuroendocrine and metabolic disorders using its proprietary drug delivery technologies. Lipocine's clinical development pipeline includes: LPCN 1148, LPCN 1144, LPCN 1111, LPCN 1107 and oral neuroactive steroids including LPCN 1154 and LPCN 2101. TLANDO, a novel oral prodrug of testosterone containing testosterone undecanoate, is approved by the FDA for conditions associated with a deficiency of endogenous testosterone, also known as hypogonadism, in adult males. LPCN 1148 is an oral prodrug of bioidentical testosterone targeted for the management of symptoms associated with liver cirrhosis.  LPCN 1144, an oral prodrug of bioidentical testosterone, recently completed a Phase 2 clinical study demonstrating potential utility in the treatment of non-cirrhotic NASH.  LPCN 1111, a novel oral prodrug of testosterone, originated and is being developed by Lipocine as a next-generation oral testosterone product with potential for once-daily dosing. In a phase 2 clinical evaluation when administered as once or twice daily, LPCN 1111 met primary and secondary endpoints.  LPCN 1107 is potentially the first oral hydroxyprogesterone caproate product candidate indicated for the prevention of recurrent preterm birth and has been granted orphan drug designation by the FDA.  Neuroactive steroids are currently being evaluated including LPCN 1154 for the potential treatment of postpartum depression and LPCN 2101 for the potential treatment of epilepsy. For more information, please visit

Forward-Looking Statements

This release contains "forward-looking statements" that are made pursuant to the safe harbor provisions of the Private Securities Litigation Reform Act of 1995 and include statements that are not historical facts regarding Lipocine's product candidates and related clinical trials, the achievement of milestones within and completion of clinical trials, the timing and completion of regulatory reviews, outcomes of clinical trials of our product candidates, the potential uses and benefits of our product candidates, and our product development efforts. Investors are cautioned that all such forward-looking statements involve risks and uncertainties, including, without limitation, the risks that the FDA will not approve any of our products, risks related to our products, expected product benefits not being realized, clinical and regulatory expectations and plans not being realized, new regulatory developments and requirements, risks related to the FDA approval process including the receipt of regulatory approvals, the results and timing of clinical trials, patient acceptance of Lipocine's products, the manufacturing and commercialization of Lipocine's products, and other risks detailed in Lipocine's filings with the SEC, including, without limitation, its Form 10-K and other reports on Forms 8-K and 10-Q, all of which can be obtained on the SEC website at Lipocine assumes no obligation to update or revise publicly any forward-looking statements contained in this release, except as required by law.

*TLANDO® is a registered trademark assigned to Antares Pharma.



Condensed Consolidated Balance Sheets


March 31,

December 31,




Current assets:

Cash and cash equivalents

$              5,733,231

$     2,950,552

Marketable investment securities



Accrued interest income



Prepaid and other current assets



Total current assets



Marketable investment securities



Contract asset



Property and equipment, net of accumulated depreciation 

of $1,145,796 and $1,144,077, respectively



Other assets



Total assets

$            47,603,591

$   52,482,439

Liabilities and Stockholders' Equity

Current liabilities:

Accounts payable

$                469,887

$     1,289,342

Accrued expenses



Debt - current portion



Litigation settlement liability - current portion



Total current liabilities



Warrant liability



Litigation settlement liability - non-current portion



Total liabilities



Commitments and contingencies

Stockholders' equity:

Preferred stock, par value $0.0001 per share, 10,000,000 

shares authorized; zero issued and outstanding



Common stock, par value $0.0001 per share, 100,000,000 

shares authorized; 88,504,634 and 88,296,360 issued

and 88,498,924 and 88,290,650 outstanding



Additional paid-in capital



Treasury stock at cost, 5,710 shares



Accumulated other comprehensive loss



Accumulated deficit



Total stockholders' equity



Total liabilities and stockholders' equity

$            47,603,591

$   52,482,439




Condensed Consolidated Statements of Operations and Comprehensive Loss


Three Months Ended March 31,




$                        -

$                       -

Operating expenses:

Research and development



General and administrative



Total operating expenses



Operating loss



Other income (expense):

Interest and investment income



Interest expense



Unrealized loss on warrant liability



Total other expense, net



Loss before income tax expense



Income tax expense



Net loss

$          (3,487,781)

$         (3,368,082)

Basic loss per share attributable to common stock

$                  (0.04)

$                 (0.04)

Weighted average common shares outstanding, basic



Diluted loss per share attributable to common stock 

$                  (0.04)

$                 (0.04)

Weighted average common shares outstanding, diluted



Comprehensive loss:

Net loss

$          (3,487,781)

$         (3,368,082)

Net unrealized loss on available-for-sale securities



Comprehensive loss

$          (3,537,181)

$         (3,390,541)



SOURCE Lipocine Inc.

For further information: Krista Fogarty, Phone: (801) 994-7383, or Investors: Hans Vitzthum, Phone: (617) 430-7875,