Emmaus Life Sciences Reports Q3 2023 Financial Results
- Increased net revenues from sales in the MENA region and increased U.S. sales compared to the same periods in 2022.
- Income from operations for the three months ended September 30, 2023 was $0.02 million, compared to a loss from operations of $0.7 million in the same period in 2022.
- The company reported a net loss of $4.9 million for the nine months ended September 30, 2023, compared to a net loss of $10.8 million for the nine months ended September 30, 2022.
- None.
Recent Highlights
"We experienced lower net revenues in the third quarter compared to the second quarter due to a shortage of finished inventory of Endari, which has been remedied, and we expect our sales to recover in this quarter. Even so, we were able to generate modest net income as we curtailed spending on activities unrelated to Endari sales," remarked Willis Lee, Chairman of the Board and Co-president of Emmaus.
Financial and Operating Results
Net Revenues. Net revenues for the three months and nine months ended September 30, 2023 were
Operating Expenses. Total operating expenses for the three months ended September 30, 2023 were
Income From Operations. Income from operations for the three months ended September 30, 2023 was
Other Income (Expense). The company realized other income of
Net Income (Loss). For the quarter, the company realized net income of
For the nine months ended September 30, 2023, the company reported a net loss of
Liquidity and Capital Resources. At September 30, 2023, the company had cash and cash equivalents of
About Emmaus Life Sciences
Emmaus Life Sciences, Inc. is a commercial-stage biopharmaceutical company and leader in the treatment of sickle cell disease. Endari® (L-glutamine oral powder), indicated to reduce the acute complications of sickle cell disease in adults and children 5 years and older, is approved for marketing in
About Endari® (prescription grade L-glutamine oral powder)
Endari®, Emmaus' prescription grade L-glutamine oral powder, was approved by the
Indication
Endari® is indicated to reduce the acute complications of sickle cell disease in adult and pediatric patients five years of age and older.
Important Safety Information
The most common adverse reactions (incidence >10 percent) in clinical studies were constipation, nausea, headache, abdominal pain, cough, pain in extremities, back pain, and chest pain.
Adverse reactions leading to treatment discontinuation included one case each of hypersplenism, abdominal pain, dyspepsia, burning sensation, and hot flash.
The safety and efficacy of Endari® in pediatric patients with sickle cell disease younger than five years of age has not been established.
For more information, please see full Prescribing Information of Endari® at: www.ENDARIrx.com/PI.
About Sickle Cell Disease
There are approximately 100,000 people living with sickle cell disease (SCD) in the United States and millions more globally. The sickle gene is found in every ethnic group, not just among those of African descent; and in the United States an estimated 1-in-365 African Americans and 1-in-16,300 Hispanic Americans are born with SCD.1 The genetic mutation responsible for SCD causes an individual's red blood cells to distort into a "C" or a sickle shape, reducing their ability to transport oxygen throughout the body. These sickled red blood cells break down rapidly, become very sticky, and develop a propensity to clump together, which causes them to become stuck and cause damage within blood vessels. The result is reduced blood flow to distal organs, which leads to physical symptoms of incapacitating pain, tissue and organ damage, and early death.2
1Source: Data & Statistics on Sickle Cell Disease – National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, December 2020.
2Source: Committee on Addressing Sickle Cell Disease – A Strategic Plan and Blueprint for Action -- National Academy of Sciences Press, 2020.
Forward-looking Statements
This press release contains forward-looking statements made pursuant to the safe harbor provisions of the Private Securities Litigation Reform Act of 1995, as amended, including statements regarding the trend in sales in the MENA region and in the
Company Contact:
Emmaus Life Sciences, Inc.
Willis Lee
Chairman and Co-president
(310) 214-0065, Ext. 1130
wlee@emmauslifesciences.com
(Financial Tables Follow)
Emmaus Life Sciences, Inc. | |||||||
Condensed Consolidated Statement of Operations and Comprehensive Income Loss | |||||||
(In thousands, except share and per share amounts) (Unaudited) | |||||||
Three Months Ended | Nine Months Ended | ||||||
2023 | 2022 | 2023 | 2022 | ||||
Revenues, Net | |||||||
Cost of Goods Sold | 214 | 540 | 1,151 | 1,943 | |||
Gross Profit | 4,804 | 4,399 | 21,379 | 10,517 | |||
Operating Expenses | 4,780 | 5,059 | 19,194 | 15,685 | |||
Income (Loss) from Operations | 24 | (660) | 2,185 | (5,168) | |||
Total Other Income (Expenses) | 81 | 234 | (7,074) | (5,613) | |||
Net Income (Loss) | 67 | (391) | (4,942) | (10,825) | |||
Comprehensive Loss | (1,322) | (2,957) | (3,826) | (16,475) | |||
Net Income (Loss) Per Share - Basic | ( | ( | ( | ||||
Net Loss Per Share - Diluted | ( | ( | ( | ( | |||
Weighted Average Common Shares Outstanding - Basic | 53,637,554 | 49,558,501 | 52,414,903 | 49,397,690 | |||
Weighted Average Common Shares Outstanding - Diluted | 138,375,065 | 49,558,501 | 52,414,903 | 49,397,690 |
Emmaus Life Sciences, Inc. | ||||||
Condensed Consolidated Balance Sheets | ||||||
(In thousands) | ||||||
As of | ||||||
September 30, | December 31, | |||||
Assets | ||||||
Current Assets: | ||||||
Cash and cash equivalents | ||||||
Accounts receivable, net | 4,587 | 375 | ||||
Inventories, net | 1,650 | 2,379 | ||||
Prepaid expenses and other current assets | 1,515 | 1,514 | ||||
Total Current Assets | 9,257 | 6,289 | ||||
Property and equipment, net | 60 | 75 | ||||
Equity method investment | 17,737 | 18,828 | ||||
Right of use assets | 2,510 | 2,799 | ||||
Investment in convertible bond | 17,596 | 19,971 | ||||
Other Assets | 293 | 263 | ||||
Total Assets | ||||||
Liabilities and Stockholders' Deficit | ||||||
Current Liabilities: | ||||||
Accounts payable and accrued expenses | ||||||
Conversion feature derivative, notes payable | 1,251 | 3,248 | ||||
Notes payable, current portion | 8,488 | 6,814 | ||||
Convertible notes payable, net of discount | 15,819 | 14,655 | ||||
Other current liabilities | 19,074 | 16,057 | ||||
Total Current Liabilities | 60,917 | 54,323 | ||||
Notes payable, less current portion | 156 | 380 | ||||
Other long-term liabilities | 22,710 | 27,613 | ||||
Total Liabilities | 83,783 | 82,316 | ||||
Stockholders' Deficit | (36,330) | (34,091) | ||||
Total Liabilities & Stockholders' Deficit |
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SOURCE Emmaus Life Sciences, Inc.
FAQ
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