Lipocine Announces Financial Results for the Second Quarter Ended June 30, 2024

Rhea-AI Summary

Lipocine Inc. (NASDAQ: LPCN) reported financial results for Q2 2024 and provided a corporate update. Key highlights include:

1. Positive topline results for LPCN 1154 in postpartum depression, with NDA submission targeted for Q4 2024.

2. Encouraging Phase 2 results for LPCN 2401 in weight management, showing improved body composition.

3. Positive Phase 2 results for LPCN 1148 in cirrhosis management, presented at EASL Congress 2024.

4. Q2 2024 financial results: Net loss of $3.1 million ($0.56 per diluted share), compared to $3.6 million in Q2 2023. Revenue of $90,000 from royalties.

5. As of June 30, 2024, Lipocine had $22.5 million in cash and equivalents.

Positive

• Positive topline results for LPCN 1154 in postpartum depression, with NDA submission planned for Q4 2024
• Encouraging Phase 2 results for LPCN 2401 in weight management, showing improved body composition
• Positive Phase 2 results for LPCN 1148 in cirrhosis management, presented at EASL Congress 2024
• Increased cash position to $22.5 million as of June 30, 2024, compared to $22.0 million at December 31, 2023
• Reported net profit of $0.5 million for the six months ended June 30, 2024, compared to a net loss of $7.4 million in the same period of 2023
• Revenue increased to $7.7 million for the six months ended June 30, 2024, primarily from licensing revenue

Negative

• Reported net loss of $3.1 million for Q2 2024, although improved from $3.6 million in Q2 2023
• Research and development expenses of $1.9 million in Q2 2024, despite decrease from $2.5 million in Q2 2023
• General and administrative expenses increased to $1.5 million in Q2 2024 from $1.4 million in Q2 2023

Insights

Financial Analyst

Lipocine's Q2 2024 results show a narrowing net loss of $3.1 million compared to $3.6 million in Q2 2023. Revenue generation of $90,000 from royalties is a positive sign, albeit modest. The cash position remains stable at $22.5 million, providing a runway for ongoing operations.

The company's focus on LPCN 1154 for postpartum depression and LPCN 2401 for weight management shows promise. The planned NDA submission for LPCN 1154 by Q4 2024 could be a significant catalyst. However, investors should note that R&D expenses, while decreased, still represent a substantial $1.9 million of the quarterly spend.

The six-month profit of $0.5 million is encouraging, primarily driven by licensing revenue. This demonstrates Lipocine's ability to monetize its intellectual property, a important factor for biotech companies.

Medical Research Analyst

Lipocine's pipeline shows promising developments. LPCN 1154 for postpartum depression demonstrated positive topline results with no sedation or somnolence, potentially offering a competitive edge over existing treatments. The planned NDA submission by Q4 2024 puts it on a clear regulatory path.

LPCN 2401 for weight management showed significant improvements in body composition, including increased lean mass and decreased fat mass. Its potential for combination with GLP-1 agonists could address the unmet need of lean mass loss in current obesity treatments. This positions Lipocine in the rapidly growing obesity market.

LPCN 1148 for cirrhosis management met primary and hepatic encephalopathy endpoints, as highlighted at the EASL Congress. This recognition in a major liver disease conference underscores the potential impact of this treatment.

Overall, Lipocine's diverse pipeline targets significant unmet medical needs, potentially opening multiple revenue streams if successful in late-stage trials and regulatory approvals.

SALT LAKE CITY, Aug. 8, 2024 /PRNewswire/ -- Lipocine Inc. (NASDAQ: LPCN), a biopharmaceutical company leveraging its proprietary technology platform to augment therapeutics through effective oral delivery, today announced financial results for the second quarter ended June 30, 2024 and provided a corporate update.

LPCN 1154 for Postpartum Depression (PPD)

• In June 2024, Lipocine announced positive topline study results from the NDA enabling study of LPCN 1154. LPCN 1154 treatment was well tolerated with no sedation nor somnolence events observed
  
  
• The Company is targeting NDA submission for LPCN 1154 by the end of the fourth quarter of 2024
  
  
• LPCN 1154, oral brexanolone, is being developed as a 48-hour oral dosing duration treatment for treatment of postpartum depression. It is targeted to be a highly effective, fast-acting and outpatient treatment option

LPCN 2401 for Chronic Weight Management

• In April 2024, the Company announced positive results from the multi-center perspective, blinded Phase 2 study evaluating LPCN 2401 in participants with obesity (BMI ≥30) and participants with BMI ≥27 with at least one weight-related comorbidity
  
  
• LPCN 2401 treatment resulted in significant improvements in body composition through increased lean mass (LM) or fat free mass (FFM) and bone mineral content in addition to decreased fat mass (FM) and android fat. LPCN 2401 was well-tolerated; adverse events (AEs) including GI events were similar to placebo with no muscle spasm reported
  
  
• LPCN 2401 has potential for use in combination with incretin mimetics (GLP-1/GIP agonists) including amplification of GLP-1R insulinotropic actions supported by studies demonstrating the role of the androgen receptor agonist in regulation of GLP-1R. Target benefits of LPCN 2401 in combination with GLP-1 agonists include improved body composition with quality weight loss while attenuating lean mass loss, a serious unmet need, and quality fat loss through appreciable abdominal fat loss. LPCN 2401 could also be potentially used as monotherapy post discontinuation of GLP-1 agonist to manage weight/fat regain and durability of diabetes remission
  
  
• Lipocine plans to meet with FDA to discuss the further development of LPCN 2401 as an aid to weight management interventions

LPCN 1148 for Management of Cirrhosis

• In June, results from a Phase 2 study evaluating LPCN 1148 in cirrhosis were featured in a late breaking oral presentation at the European Association for the Study of Liver (EASL) Congress. The presentation was delivered by Arun J. Sanyal, MD, Director, Stravitz-Sanyal Institute for Liver Disease and Metabolic Health, Virginia Commonwealth University. The presentation was featured in the symposium "Revolutionary Advances in Liver Disease Research Unveiled at EASL Congress 2024" highlighting significant advances in liver disease
  • As previously announced, the study met primary and hepatic encephalopathy (HE) endpoints and LPCN 1148 was well-tolerated, with AE rates and severities similar to placebo

We continue to pursue opportunities for partnering and/or development arrangements for the continued development and/or marketing of our pipeline candidates.

Second quarter Ended June 30, 2024 Financial Results 

Lipocine reported a net loss of $3.1 million, or ($0.56) per diluted share, for the second quarter ended June 30, 2024, compared with a net loss of $3.6 million, or ($0.68) per diluted share, for the quarter ended June 30, 2023.

Revenues were approximately $90,000, ­ consisting of royalty revenue from the Verity license agreement in the second quarter of 2024.­ No revenue was recorded during the second quarter of 2023. 

Research and development expenses were $1.9 million and $2.5 million, respectively, for the quarters ended June 30, 2024 and 2023. The decrease was a result of a decrease in contract research organization expense and outside consulting costs related to the wind down of our LPCN 1148 study in 2024, a decrease in TLANDO related costs, and a decrease in personnel related costs, offset by an increase in costs related to the LPCN 1154 clinical studies, and an increase in other R&D related costs.

General and administrative expenses were $1.5 million and $1.4 million, respectively for the quarters ended June 30, 2024 and 2023.

As of June 30, 2024, Lipocine had $22.5 million of unrestricted cash, cash equivalents and marketable investment securities compared to $22.0 million at December 31, 2023. 

Six Months Ended, June 30 2024 Financial Results

Lipocine reported a net profit of $0.5 million, or $0.10 per diluted share, for the six months ended June 30, 2024, compared with a net loss of $7.4 million, or ($1.42) per diluted share, for the six months ended June 30, 2023.

Revenues for the six-month period ended June 30, 2024 were $7.7 million, primarily consisting of licensing revenue from the Verity License Agreement. This compares with licensing revenue of $55,000 during the six months ended June 30, 2023.

Research and development expenses were $4.7 million and $5.6 million, respectively, for the six months ended June 30, 2024 and 2023. The decrease was a result of a decrease in contract research organization expense and outside consulting costs related to the wind down of our LPCN 1148 study in 2024, decrease in personnel related costs, and a decrease in LPCN 1111 and LPCN 1144 clinical study costs.  These decreases were offset by an increase in costs related to our LPCN 1154 clinical studies, an increase in TLANDO related costs, and an increase in other research and development related costs.

General administrative expenses were $3.1 million and $2.7 million, respectively, for the six months ended June 30, 2024 and 2023.

For more information on Lipocine's financial results, refer to Form 10Q filed by the Company with the SEC.

About Lipocine

Lipocine is a biopharmaceutical company leveraging its proprietary technology platform to augment therapeutics through effective oral delivery to develop differentiated products.  Lipocine has drug candidates in development as well as drug candidates for which we are exploring partnerships.  Our drug candidates represent enablement of differentiated, patient friendly oral delivery options for favorable benefit to risk profile which target large addressable markets with significant unmet medical needs. 

Lipocine's clinical development candidates include: LPCN 1154, oral brexanolone, for the potential treatment of postpartum depression, LPCN 2101 for the potential treatment of epilepsy, LPCN 2203 an oral candidate targeted for the management of essential tremor, LPCN 2401 an oral proprietary combination of anabolic androgen receptor agonist and α-tocopherol, an antioxidant, as an adjunct therapy to incretin mimetics, as an aid for improved body composition in chronic weight management and LPCN 1148, a novel androgen receptor agonist prodrug for oral administration targeted for the management of symptoms associated with liver cirrhosis.  Lipocine is exploring partnering opportunities for LPCN 1107, our candidate for prevention of preterm birth, LPCN 1154, for rapid relief of postpartum depression, LPCN 2401 for chronic weight management, LPCN 1148, for the management of decompensated cirrhosis, and LPCN 1144, our candidate for treatment of non-cirrhotic NASH.  TLANDO, a novel oral prodrug of testosterone containing testosterone undecanoate developed by Lipocine, is approved by the FDA for conditions associated with a deficiency of endogenous testosterone, also known as hypogonadism, in adult males. For more information, please visit www.lipocine.com.

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 our product development efforts, our strategic plans for developing products, our ability to monetize product candidates, including through entering into partnering arrangements, our 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, and the potential uses and benefits of our product candidates.  Investors are cautioned that all such forward-looking statements involve risks and uncertainties, including, without limitation, the risks that we may not be successful in developing product candidates, we may not have sufficient capital to complete the development processes for our product candidates, we may not be able to enter into partnerships or other strategic relationships to monetize our non-core assets, 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, and our ability to utilize a streamlined approval pathway for LPCN 1154, 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 www.sec.gov. Lipocine assumes no obligation to update or revise publicly any forward-looking statements contained in this release, except as required by law.

 

 

LIPOCINE INC. AND SUBSIDIARIES
Condensed Consolidated Balance Sheets
						June 30,		December 31,
						2024		2023
Assets
Current assets:
Cash and cash equivalents						$               5,553,371		$         4,771,758
Marketable investment securities						16,995,424		17,263,788
Accrued interest income						63,636		52,254
Prepaid and other current assets						297,051		773,424
	Total current assets					22,909,482		22,861,224
Property and equipment, net of accumulated depreciation
of $1,199,215 and $1,182,191 respectively						99,071		116,095
Other assets						23,753		23,753
	Total assets					$             23,032,306		$       23,001,072
Liabilities and Stockholders' Equity
Current liabilities:
Accounts payable						$                 448,798		$         1,395,977
Accrued expenses						1,233,477		1,218,486
Warrant liability						141,668		17,166
	Total current liabilities					1,823,943		2,631,629
	Total liabilities					1,823,943		2,631,629
Stockholders' equity:
	Common stock, par value $0.0001 per share, 200,000,000
	shares authorized; 5,348,276 and 5,316,166 issued, and
	5,347,940 and 5,315,830 outstanding, respectively
	outstanding					8,863		8,860
	Additional paid-in capital					220,582,158		220,171,250
	Treasury stock at cost, 336 shares					(40,712)		(40,712)
	Accumulated other comprehensive gain (loss)					(9,719)		7,259
	Accumulated deficit					(199,332,227)		(199,777,214)
	Total stockholders' equity					21,208,363		20,369,443
	Total liabilities and stockholders' equity					$             23,032,306		$       23,001,072

 

LIPOCINE INC. AND SUBSIDIARIES
Condensed Consolidated Statements of Operations and Comprehensive Loss
						Three Months Ended June 30,				Six Months Ended June 30,
						2024		2023		2024		2023
Revenues:
	License revenue					$                        -		$                       -		$            7,500,000		$               54,990
	Royalty revenue					89,565		-		206,738		-
	Total revenues					89,565		-		7,706,738		54,990
Operating expenses:
	Research and development					1,874,721		2,515,211		4,693,646		5,621,521
	General and administrative					1,507,412		1,440,394		3,083,131		2,727,708
	Total operating expenses					3,382,133		3,955,605		7,776,777		8,349,229
	Operating loss					(3,292,568)		(3,955,605)		(70,039)		(8,294,239)
Other income (expense):
	Interest and investment income					308,845		379,521		640,209		749,991
	Unrealized gain (loss) on warrant liability					(84,430)		27,455		(124,502)		125,589
	Total other income, net					224,415		406,976		515,707		875,580
	Income (loss) before income tax expense					(3,068,153)		(3,548,629)		445,668		(7,418,659)
Income tax expense						(481)		-		(681)		(200)
	Net income (loss)					(3,068,634)		(3,548,629)		444,987		(7,418,859)
	Issuance of Series B preferred stock dividend					-		-		-		(89)
	Net income (loss) attributable to common shareholders					$          (3,068,634)		$         (3,548,629)		$              444,987		$         (7,418,948)
Basic earnings (loss) per share attributable to common stock						$                  (0.57)		$                 (0.68)		$                   0.08		$                 (1.42)
Weighted average common shares outstanding, basic						5,343,922		5,234,830		5,329,876		5,234,830
Diluted earnings (loss) per share attributable to common stock						$                  (0.56)		$                 (0.68)		$                   0.10		$                 (1.44)
Weighted average common shares outstanding, diluted						5,343,922		5,234,830		5,459,204		5,234,830
Comprehensive income (loss):
	Net income (loss)					$          (3,068,634)		$         (3,548,629)		$              444,987		$         (7,418,859)
	Net unrealized gain (loss) on marketable investment securities					885		(19,053)		(16,978)		4,509
	Comprehensive income  (loss)					$          (3,067,749)		$         (3,567,682)		$              428,009		$         (7,414,350)

 

 

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SOURCE Lipocine Inc.

FAQ

What were Lipocine's (LPCN) financial results for Q2 2024?

Lipocine reported a net loss of $3.1 million, or $0.56 per diluted share, for Q2 2024. Revenue was approximately $90,000 from royalties. The company had $22.5 million in cash and equivalents as of June 30, 2024.

What progress has Lipocine (LPCN) made with LPCN 1154 for postpartum depression?

Lipocine announced positive topline results from the NDA enabling study of LPCN 1154 for postpartum depression in June 2024. The company is targeting NDA submission by the end of Q4 2024.

What were the results of Lipocine's (LPCN) Phase 2 study for LPCN 2401 in weight management?

The Phase 2 study showed that LPCN 2401 treatment resulted in significant improvements in body composition, including increased lean mass and decreased fat mass. The treatment was well-tolerated with adverse events similar to placebo.

How did Lipocine's (LPCN) financial performance in the first half of 2024 compare to 2023?

Lipocine reported a net profit of $0.5 million for the six months ended June 30, 2024, compared to a net loss of $7.4 million in the same period of 2023. Revenue increased to $7.7 million, primarily from licensing revenue.