ImmuCell Announces Unaudited Financial Results for the Third Quarter Ended September 30, 2021
ImmuCell Corporation (Nasdaq: ICCC) reported a net income of $148,000 for Q3 2021, a significant turnaround from the net loss of ($323,000) in Q3 2020. Total product sales rose 38% to $5.2 million, while nine-month sales increased 19% to $13.8 million. The company achieved a gross margin of 47% in Q3 2021 and improved EBITDA to approximately $852,000. Cash reserves grew to $10.5 million as of September 30, 2021, up from $7.9 million at year-end 2020. ImmuCell plans to submit another Technical Section to the FDA for its product Re-Tain® by year-end 2021.
- Net income of $148,000 versus a net loss of ($323,000) in Q3 2020.
- Product sales increased by 38% to $5.2 million in Q3 2021.
- Gross margin improved to 47% in Q3 2021.
- EBITDA rose to approximately $852,000 for Q3 2021.
- Net loss of ($152,000) for the nine-month period ended September 30, 2021.
- Product development expenses decreased only slightly from $1.1 million to $1.0 million.
Q3 2021 Net Income of
PORTLAND, Maine, Nov. 15, 2021 (GLOBE NEWSWIRE) -- ImmuCell Corporation (Nasdaq: ICCC) (“ImmuCell” or the “Company”), a growing animal health company that develops, manufactures and markets scientifically-proven and practical products that improve the health and productivity of dairy and beef cattle, today announced its unaudited financial results for the third quarter and the nine-month period ended September 30, 2021.
Product Sales Results:
- During the three-month period ended September 30, 2021, total product sales increased by
38% , or$1.4 million , to$5.2 million versus the three-month period ended September 30, 2020. - During the nine-month period ended September 30, 2021, total product sales increased by
19% , or$2.2 million , to$13.8 million versus the nine-month period ended September 30, 2020.
Management’s Discussion:
“A
“We are delivering both increased product sales and increased production output,” added Mr. Brigham. “We were able to increase production output of the First Defense® product line to the annualized rate of approximately
“We are on plan to make a second submission of the last of five significant Technical Section submissions pertaining to Re-Tain® to the FDA before year end,” concluded Mr. Brigham. “The response from the FDA after their six-month review will determine whether we will be able to commence an initial, limited market launch of Re-Tain® at the end of the third quarter of 2022.”
Other Financial Results:
- Gross margin earned was
47% and46% of product sales during the quarters ended September 30, 2021 and 2020, respectively, and44% and45% of product sales during the nine-month periods ended September 30, 2021 and 2020, respectively. - Product development expenses were
$1 million and$1.1 million during the quarters ended September 30, 2021 and 2020, respectively, and$3.1 million and$3.2 million during the nine-month periods ended September 30, 2021 and 2020, respectively. - Net income was
$148,000 , or$0.02 per share, during the quarter ended September 30, 2021 in contrast to a net loss of ($323,000) , or ($0.04) per share, during the quarter ended September 30, 2020. Net loss was ($152,000) , or ($0.02) per share, during the nine-month period ended September 30, 2021 in comparison to a net loss of ($1,211,000) , or ($0.17) per share, during the nine-month period ended September 30, 2020. - EBITDA (a non-GAAP financial measure, see page 4 of this press release) was approximately
$852,000 and$354,000 during the quarters ended September 30, 2021 and 2020, respectively, and approximately$1,953,000 and$1,008,000 during the nine-month periods ended September 30, 2021 and 2020, respectively.
Balance Sheet Data as of September 30, 2021:
- Cash, cash equivalents and short-term investments increased to
$10.5 million as of September 30, 2021 from$7.9 million as of December 31, 2020. - Net working capital increased to
$13.9 million as of September 30, 2021 from$9.9 million as of December 31, 2020. - Stockholders’ equity increased to
$32.5 million as of September 30, 2021 from$28.3 million as of December 31, 2020.
Conference Call:
The Company will host a conference call on Tuesday, November 16, 2021 to discuss these financial results for the quarter ended September 30, 2021. Interested parties can access the conference call by dialing (844) 855-9502 (toll free) or (412) 317-5499 (international) at 9:00 AM ET. A teleconference replay of the call will be available for seven days at (877) 344-7529 (toll free) or (412) 317-0088 (international), utilizing confirmation #10160879. Investors are encouraged to review the Company’s updated Corporate Presentation slide deck that provides an overview of the Company’s business and is available under the “Investors” tab of the Company’s website at www.immucell.com, or by request to the Company.
About ImmuCell:
ImmuCell Corporation's (Nasdaq: ICCC) purpose is to create scientifically-proven and practical products that improve the health and productivity of dairy and beef cattle. ImmuCell manufactures and markets First Defense®, providing Immediate Immunity™ to newborn dairy and beef calves, and is in the late stages of developing Re-Tain®, a novel treatment for subclinical mastitis in dairy cows without a milk discard requirement that provides an alternative to traditional antibiotics. Press releases and other information about the Company are available at: http://www.immucell.com.
Condensed Statements of Operations (Unaudited)
| During the Three-Month | During the Nine-Month | ||||||||||||||
| Periods Ended September 30, | Periods Ended September 30, | ||||||||||||||
| (In thousands, except per share amounts) | 2021 | 2020 | 2021 | 2020 | |||||||||||
| Product sales | |||||||||||||||
| Costs of goods sold | 2,731 | 2,001 | 7,704 | 6,357 | |||||||||||
| Gross margin | 2,419 | 1,722 | 6,095 | 5,242 | |||||||||||
| Product development expenses | 1,048 | 1,123 | 3,078 | 3,184 | |||||||||||
| Sales, marketing and administrative expenses | 1,100 | 851 | 2,905 | 2,804 | |||||||||||
| Operating expenses | 2,148 | 1,974 | 5,983 | 5,988 | |||||||||||
| NET OPERATING INCOME (LOSS) | 271 | (252 | ) | 112 | (746 | ) | |||||||||
| Other expenses, net | 115 | 71 | 256 | 480 | |||||||||||
| INCOME (LOSS) BEFORE INCOME TAXES | 156 | (323 | ) | (144 | ) | (1,226 | ) | ||||||||
| Income tax expense (benefit) | 8 | - | 8 | (15 | ) | ||||||||||
| NET INCOME (LOSS) | ( | ) | ( | ) | ( | ) | |||||||||
| Basic weighted average common shares outstanding | 7,742 | 7,213 | 7,542 | 7,213 | |||||||||||
| Basic net income (loss) per share | ( | ) | ( | ) | ( | ) | |||||||||
| Diluted weighted average common shares outstanding | 7,820 | 7,213 | 7,542 | 7,213 | |||||||||||
| Diluted net income (loss) per share | ( | ) | ( | ) | ( | ) | |||||||||
Selected Balance Sheet Data (In thousands) (Unaudited)
| As of | As of | |||
| September 30, 2021 | December 31, 2020 | |||
| Cash, cash equivalents and short-term investments | ||||
| Net working capital | 13,910 | 9,946 | ||
| Total assets | 44,231 | 40,350 | ||
| Stockholders’ equity |
Non-GAAP Financial Measures:
Generally, a non-GAAP financial measure is a numerical measure of a company’s performance, financial position or cash flow that either excludes or includes amounts that are not normally excluded or included in the most directly comparable measure calculated and presented in accordance with GAAP. The non-GAAP measures included in this press release should be considered in addition to, and not as a substitute for or superior to, the comparable measure prepared in accordance with GAAP. We believe that considering the non-GAAP income before income taxes and certain non-cash expenses assists management and investors by looking at our performance across reporting periods on a consistent basis excluding these certain charges that are not uses of cash from our reported income (loss) before income taxes. We start with our reported income (loss) before income taxes because presently we are not paying cash for income taxes and do not anticipate paying significant cash for income taxes in the near-term future. We calculate non-GAAP income before income taxes and certain non-cash expenses as indicated in the table below:
| During the Three-Month | During the Nine-Month | ||||||||||||||
| Periods Ended September 30, | Periods Ended September 30, | ||||||||||||||
| (In thousands) | 2021 | 2020 | 2021 | 2020 | |||||||||||
| Income (loss) before income taxes | ( | ) | ( | ) | ( | ) | |||||||||
| Depreciation | 613 | 597 | 1,846 | 1,721 | |||||||||||
| Amortization and write-off of debt issuance costs | 7 | 6 | 20 | 115 | |||||||||||
| Stock-based compensation | 45 | 62 | 103 | 196 | |||||||||||
| Income before income taxes and certain non-cash expenses | |||||||||||||||
Earnings (Loss) Before Interest, Taxes, Depreciation and Amortization (EBITDA) increased to
1) We have not added back interest expense or interest rate swap termination fees because we do pay cash for these expenses; and
2) We have added back stock-based compensation expense because this is a non-cash expense that is not added back to the calculation of EBITDA.
Cautionary Note Regarding Forward-Looking Statements (Safe Harbor Statement):
This Press Release contains “forward-looking statements” within the meaning of Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934. Such statements include, but are not limited to, any statements relating to: our plans and strategies for our business; projections of future financial or operational performance; the timing and outcome of pending or anticipated applications for regulatory approvals; factors that may affect the dairy and beef industries and future demand for our products; the extent, nature and duration of the COVID-19 pandemic and its consequences, and their direct and indirect impacts on our production activities, operating results and financial condition and on the customers and markets that we serve; the impact of the global supply-chain disruptions on our ability to obtain, in a timely and cost-effective fashion, all the supplies and components we need to produce our products; the scope and timing of ongoing and future product development work and commercialization of our products; future costs of product development efforts; the estimated prevalence rate of subclinical mastitis and producers’ level of interest in treating subclinical mastitis given the current economic and market conditions; the expected efficacy of new products; estimates about the market size for our products; future market share of and revenue generated by current products and products still in development; our ability to increase production output and reduce costs of goods sold per unit; the future adequacy of our own manufacturing facilities or those of third parties with which we have contractual relationships to meet demand for our products on a timely basis; the impacts of backlogs on customer relationships; the anticipated costs of (or time to complete) planned expansions of our manufacturing facilities and the adequacy of our funds available for these projects; the continuing availability to us on reasonable terms of third-party providers of critical products or services; the robustness of our manufacturing processes and related technical issues; estimates about our production capacity, efficiency and yield, which are highly subject to biological variability and the product format mix of our sales; the future adequacy of our working capital and the availability and cost of third-party financing; future regulatory requirements relating to our products; future expense ratios and margins; future compliance with bank debt covenants; costs associated with sustaining compliance with current Good Manufacturing Practice (cGMP) regulations in our current operations and attaining such compliance for our facilities to produce the Nisin Drug Substance and Drug Product; our effectiveness in competing against competitors within both our existing and our anticipated product markets; the cost-effectiveness of additional sales and marketing expenditures and resources; anticipated changes in our manufacturing capabilities and efficiencies; the value of our net deferred tax assets; projections about depreciation expense and its impact on income for book and tax return purposes; and any other statements that are not historical facts. Forward-looking statements can be identified by the use of words such as “expects”, “may”, “anticipates”, “aims”, “intends”, “would”, “could”, “should”, “will”, “plans”, “believes”, “estimates”, “targets”, “projects”, “forecasts”, “seeks” and similar words and expressions. In addition, there can be no assurance that future developments affecting us will be those that we anticipate. Such statements involve risks and uncertainties, including, but not limited to, those risks and uncertainties relating to: difficulties or delays in development, testing, regulatory approval, production and marketing of our products (including the First Defense® product line and Re-Tain®), competition within our anticipated product markets, customer acceptance of our new and existing products, product performance, alignment between our manufacturing resources and product demand (including the consequences of backlogs or excess inventory buildup), uncertainty associated with the timing and volume of customer orders as we come out of a prolonged backlog, adverse impacts of supply chain disruptions on our operations and customer relationships, our reliance upon third parties for financial support, products and services, our small size and dependence on key personnel, changes in laws and regulations, decision making and delays by regulatory authorities, a recurrence of inflation and its impact on our customers’ order patterns, currency values and fluctuations and other risks detailed from time to time in filings we make with the Securities and Exchange Commission (SEC), including our Quarterly Reports on Form 10-Q, our Annual Reports on Form 10-K and our Current Reports on Form 8-K. Such statements involve risks and uncertainties and are based on our current expectations, but actual results may differ materially due to various factors, including the risk factors summarized above.
| Contacts: | Michael F. Brigham, President and CEO |
| ImmuCell Corporation | |
| (207) 878-2770 | |
| Joe Diaz, Robert Blum and Joe Dorame | |
| Lytham Partners, LLC | |
| (602) 889-9700 | |
| iccc@lythampartners.com | |
FAQ
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