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UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
FORM 8-K
CURRENT REPORT
Pursuant to Section 13 OR 15(d) of the Securities
Exchange Act of 1934
Date of Report (Date of earliest event reported):
August 14, 2023
Emmaus Life Sciences,
Inc.
(Exact name of registrant as specified in its charter)
Delaware |
|
001-35527 |
|
87-0419387 |
(State or other jurisdiction
of incorporation) |
|
(Commission File Number) |
|
(I.R.S. Employer
Identification No.) |
21250 Hawthorne Boulevard, Suite 800, Torrance, CA |
|
90503 |
(Address of principal executive offices) |
|
(Zip Code) |
Registrant’s telephone number, including area
code (310) 214-0065
(Former name or former address, if changed, since last
report.)
Check the appropriate box below if the Form 8-K filing
is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions:
| ☐ | Written
communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425) |
| ☐ | Soliciting
material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12) |
| ☐ | Pre-commencement
communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b)) |
| ☐ | Pre-commencement
communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13a-4(c)) |
Securities registered pursuant to Section 12(b) of the Act:
Title of each class |
|
Trading Symbol |
|
Name of each exchange on which registered |
None |
|
|
|
|
Indicate by check mark whether the registrant is an
emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§230.405 of this chapter) or Rule 12b-2 of the Securities
Exchange Act of 1934 (§240.12b-2 of this chapter).
Emerging growth company ☐
If an emerging growth company, indicate by check mark
if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards
provided pursuant to Section 13(a) of the Exchange Act. ☐
Item 2.02 Results of Operation and Financial Condition.
On August 14, 2023, Emmaus
Life Sciences, Inc. issued a press release announcing the results of operations and financial condition as of and for the six months
ended June 30, 2023. A copy of the press release is included as Exhibit 99.1 to this Current Report and incorporated herein by reference.
The
information included in this Item 2.02 and in Exhibit 99.1 shall not be deemed “filed” for purposes of Section 18 of the Securities
Exchange Act of 1934 (“Exchange Act”) or otherwise subject to the liabilities of that section, nor shall it be deemed incorporated
by reference in any filing under the Securities Act of 1933 or the Exchange Act, except as expressly set forth by specific reference in
such a filing.
Item 9.01 Financial Statements and Exhibits
(d) Exhibits
See the accompanying Index to Exhibits, which information
is incorporated herein by reference.
SIGNATURES
Pursuant to the requirements of
the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto
duly authorized.
Date: August 14, 2023 |
Emmaus Life Sciences, Inc. |
|
|
|
|
By: |
/s/ YASUSHI NAGASAKI |
|
|
Name: |
Yasushi Nagasaki |
|
|
Title: |
Chief Financial Officer |
INDEX
TO EXHIBITS
Exhibit 99.1
Emmaus Life Sciences Reports Q2 2023 Financial Results
Record Net Revenues Contributed to Income
from Operations
Sixth Straight Quarterly Increase in Net Revenues
Torrance CA, August 14, 2023 - Emmaus Life
Sciences, Inc. (OTCQX: EMMA), a commercial-stage biopharmaceutical company and leader in the treatment of sickle cell disease, today
reported on its financial condition and results of operations as of and for the three and six months ended June 30, 2023.
Recent Highlights
“We are pleased to report record net revenues
for the quarter and six months ended June 30 owing to a jump in sales in the Middle East North Africa region and continuing recovery in
U.S. sales compared to 2022. As a result, we were able to generate over $3.3 million in quarterly income from operations. Net revenue
growth accelerated in the quarter, and we hope to continue this trend through the end of the year even without regard to the prospects
for potential marketing approval of Endari in the Kingdom of Saudi Arabia,” remarked Yutaka Niihara, M.D., M.P.H., Chairman and
Chief Executive Officer of Emmaus.
Financial and Operating Results
Net Revenues. Net revenues for the three months
and six months ended June 30, 2023 were $10.8 million and $17.5 million, respectively, compared to $4.3 million and $7.5 million, respectively,
for same periods in 2022. The increased net revenues were primarily attributable to a $4.1 million increase in net revenues from sales
in the Middle East North Africa (MENA) region in Q2 2023. Net revenues in Q2 and the three months and six months ended June 30, 2023 also
were positively affected by increased U.S. sales compared to the same periods in 2022.
Operating Expenses. Total operating expenses
for the three months ended June 30, 2023 were $6.9 million, compared with $5.3 million for the same periods in 2022. Of the increased
operating expenses in Q2 2023, $0.6 million was attributable to an increase in payroll expenses related to sales personnel and $1.0 million
increase in general and administrative expenses. Total operating expenses for the six months ended June 30, 2023 were $14.4 million, compared
with $10.6 million for the same period in 2022. The increase was due to a $1.2 million increase in share-based compensation, a $0.8 million
increase in payroll expenses and a $0.6 million increase in consulting fees.
Income From Operations. Income from operations
for the three months ended June 30, 2023 was $3.3 million, compared to a loss from operations of $1.4 million in the same periods in 2022.
Income from operations for the six months ended June 30, 2023 increased to $2.2 million, compared to a loss from operations of $4.5 million
for the same period last year. The increase income from operation resulted from higher new revenues in 2023 compared to 2022. Income from
operations in Q2 2023 also increased by $4.5 million, or 385%, from $1.2 million loss from operations in Q1 2023 as a result of the increase
in net revenues in Q2 2023.
Other Expense. Other expenses decreased to
$4.8 million for the three months ended June 30, 2023, compared to $7.3 million in the same period in 2022. Other expenses for the six
months ended June 30, 2023 increase to $7.2 million from $5.8 million in the same period in 2022. Other expenses in Q2 2023 included a
decrease of $2.6 million in change in fair value of embedded conversion option of convertible promissory notes, partially offset by a
$0.5 million increase in interest expense compared to Q2 2022.
Net Loss. For the quarter, the company
realized a net loss of $1.5 million, or $0.03 per share based on approximately 52.9 million weighted average basic and diluted common
shares. This compares to a net loss of $8.9 million, or $0.18 per share based on approximately 49.3 million weighted average basic and
diluted common shares for the second quarter of 2022. The decrease in net loss was primarily attributable to the increase in income from
operations and decrease in other expenses discussed above.
For the six months ended June 30, 2023, the company
reported a net loss of $5.0 million, or $0.10 per share, based on approximately 51.8 million weighted average basic and
diluted common shares. This compares to a net loss of $10.4 million, or $0.21 per share, based on approximately 49.3 million
weighted average basic and diluted common shares for the six months ended June 30, 2022. The decrease was due to the increase in
net revenues, partially offset by the increase in operating expenses.
Liquidity and Capital Resources. On June 30,
2023, the company had cash and cash equivalents of $1.4 million, compared with $2.0 million on December 31, 2022.
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 the United States, Israel, Kuwait, Qatar,
the United Arab Emirates, Bahrain and Oman and is available on a named patient or early access basis in France, the Netherlands, and the
Kingdom of Saudi Arabia, where Emmaus’ application for marketing authorization is awaiting final action by the Saudi Food &
Drug Authority. For more information, please visit www.emmausmedical.com.
About Endari® (prescription grade
L-glutamine oral powder) Endari®, Emmaus’ prescription grade L-glutamine oral powder, was approved by the U.S. Food and
Drug Administration (FDA) in July 2017 for treating sickle cell disease in adult and pediatric patients five years of age and
older.
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 U.S. and need for related-party loans or other financing needed to meet our
current liabilities and fund our business and operations. These forward-looking statements are subject to numerous assumptions, risks
and uncertainties which change over time, including factors disclosed in the company’s Annual Report on Form 10-K for the year ended
December 31, 2022 and Quarterly Reports on Form 10-Q for the quarters ended March 31, 2023 and June 30, 2023 filed with the Securities
and Exchange Commission on March 31, 2023, May 15, 2023 and August 14, 2023, respectively, and actual results may differ materially. Such
forward-looking statements speak only as of the date they are made, and Emmaus assumes no duty to update them, except as may be required
by law.
Company Contact:
Emmaus Life Sciences, Inc.
Willis Lee
Chief Operating Officer
(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
June 30 | | |
Six Months Ended
June 30 | |
| |
2023 | | |
2022 | | |
2023 | | |
2022 | |
Revenues, Net | |
$ | 10,759 | | |
$ | 4,287 | | |
$ | 17,512 | | |
$ | 7,521 | |
Cost of Goods Sold | |
| 508 | | |
| 396 | | |
| 937 | | |
| 1,403 | |
Gross Profit | |
| 10,251 | | |
| 3,891 | | |
| 16,575 | | |
| 6,118 | |
Operating Expenses | |
| 6,925 | | |
| 5,331 | | |
| 14,414 | | |
| 10,626 | |
Income (Loss) from Operations | |
| 3,326 | | |
| (1,440 | ) | |
| 2,161 | | |
| (4,508 | ) |
Total Other Expenses | |
| (4,842 | ) | |
| (7,270 | ) | |
| (7,155 | ) | |
| (5,847 | ) |
Net Loss | |
| (1,482 | ) | |
| (8,892 | ) | |
| (5,009 | ) | |
| (10,434 | ) |
Comprehensive Income (Loss) | |
| 1,381 | | |
| (12,664 | ) | |
| (2,504 | ) | |
| (13,518 | ) |
Net Loss Per Share | |
($ | 0.03 | ) | |
($ | 0.18 | ) | |
($ | 0.10 | ) | |
($ | 0.21 | ) |
Weighted Average Common Shares Outstanding | |
| 52,865,353 | | |
| 49,319,995 | | |
| 51,793,445 | | |
| 49,315,952 | |
Emmaus Life Sciences, Inc.
Condensed Consolidated Balance Sheets
(In thousands)
| |
As of | |
| |
June 30,
2023 | | |
December 31,
2022 | |
| |
(Unaudited) | | |
| |
Assets | |
| | |
| |
Current Assets: | |
| | |
| |
Cash and cash equivalents | |
$ | 1,361 | | |
$ | 2,021 | |
Accounts receivable, net | |
| 5,573 | | |
| 375 | |
Inventories, net | |
| 1,814 | | |
| 2,379 | |
Prepaid expenses and other current assets | |
| 1,099 | | |
| 1,514 | |
Total Current Assets | |
| 9,847 | | |
| 6,289 | |
Property and equipment, net | |
| 68 | | |
| 75 | |
Equity method investment | |
| 18,302 | | |
| 18,828 | |
Right of use assets | |
| 2,585 | | |
| 2,799 | |
Investment in convertible bond | |
| 19,210 | | |
| 19,971 | |
Other Assets | |
| 276 | | |
| 263 | |
Total Assets | |
$ | 50,288 | | |
$ | 48,225 | |
| |
| | | |
| | |
Liabilities and Stockholders’ Deficit | |
| | | |
| | |
Current Liabilities: | |
| | | |
| | |
Accounts payable and accrued expenses | |
$ | 15,200 | | |
$ | 13,549 | |
Conversion feature derivative, notes payable | |
| 4,217 | | |
| 3,248 | |
Notes payable, current portion | |
| 8,462 | | |
| 6,814 | |
Convertible notes payable, net of discount | |
| 14,306 | | |
| 14,655 | |
Other current liabilities | |
| 19,362 | | |
| 16,057 | |
Total Current Liabilities | |
| 61,547 | | |
| 54,323 | |
Notes payable, less current portion | |
| 0 | | |
| 380 | |
Other long-term liabilities | |
| 23,773 | | |
| 27,613 | |
Total Liabilities | |
| 85,320 | | |
| 82,316 | |
Stockholders’ Deficit | |
| (35,032 | ) | |
| (34,091 | ) |
Total Liabilities & Stockholders’ Deficit | |
$ | 50,288 | | |
$ | 48,225 | |
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