Alimera Sciences Reports First Quarter 2024 Results
Alimera Sciences reported a 70% increase in net revenue, reaching $23 million in Q1 2024, compared to $13.5 million in Q1 2023. U.S. net revenue surged 92% to $14.6 million, while international revenue grew 42% to $8.5 million. Despite a net loss of $6.3 million, Alimera achieved a positive adjusted EBITDA of $1.8 million. Key milestones include the completion of enrollment in the Synchronicity Study and NICE’s recommendation for ILUVIEN access in the UK. However, total operating expenses rose to $22 million, driven by sales, marketing, and amortization costs.
- Net revenue increased by 70% to $23 million in Q1 2024.
- U.S. net revenue surged 92% to $14.6 million.
- International net revenue grew 42% to $8.5 million.
- Positive adjusted EBITDA of $1.8 million compared to a loss of $2.4 million in Q1 2023.
- Global end user demand increased by 23% to 4,028 units.
- Completed enrollment in the Synchronicity Study.
- NICE recommendation for ILUVIEN in the UK for chronic DME patients.
- Increased term loan agreement by $5 million.
- Net loss increased to $6.3 million from $5 million in Q1 2023.
- Total operating expenses rose to $22 million from $14.8 million.
- Increased sales and marketing expenses by $3.3 million.
- Additional amortization expense of $2.4 million due to YUTIQ acquisition.
- General administrative expenses increased by $1.3 million.
Insights
Alimera Sciences has reported significant growth in its Q1 2024 financial results, with net revenue jumping by
Remarkably, U.S. net revenue grew by
Despite the impressive revenue growth, Alimera still reported a net loss of
Additionally, the company's cash position improved slightly to
The completion of enrollment in the Synchronicity Study and the randomization of the first patient in the DRCR Retina Network study are key clinical milestones for Alimera. These studies are important for expanding the indications of ILUVIEN and YUTIQ, potentially opening new markets and increasing the products' value propositions.
ILUVIEN is being studied as a treatment for radiation retinopathy, a condition for which there are currently no FDA-approved pharmacotherapies. Successful results could not only address an unmet medical need but also establish ILUVIEN as a unique therapeutic option, potentially driving future revenue growth.
Furthermore, the NICE recommendation allowing chronic DME patients with a natural lens to access ILUVIEN in the UK is a noteworthy development. Since phakic patients represent a significant portion of the DME population, this could lead to increased adoption and sales in the UK market, enhancing Alimera’s international revenue stream.
- Net Revenue up
70% to$23 Million vs. Q1 2023 - Global End User Demand Up
23% vs. Q1 2023 - Reiterates Improved 2024 Net Revenue and Adjusted EBITDA Guidance
ATLANTA, May 14, 2024 (GLOBE NEWSWIRE) -- Alimera Sciences, Inc. (Nasdaq: ALIM) (“Alimera”), a global pharmaceutical company whose mission is to be invaluable to patients, physicians and partners concerned with retinal health and maintaining better vision longer, today announced financial results for the first quarter of 2024. Alimera will host a conference call today at 9:00 a.m. EDT to discuss these results.
“Our results in this quarter were consistent with our expectations as we continue to integrate YUTIQ into our U.S. business and support the acceleration of growth in international markets, providing further confidence in our ability to achieve
Key First Quarter Financial Highlights:
- Net revenue of
$23.0 million up70% vs Q1 2023 - Net loss of
$6.3 million compared to a net loss of$5.0 million in Q1 2023 - Positive adjusted EBITDA of
$1.8 million vs. adjusted EBITDA loss of$(2.4) million in Q1 2023 - U.S. net revenue of
$14.6 million up92% vs. Q1 2023 - International net revenue of
$8.5 million up42% vs. Q1 2023 - Global end user demand up
23% over Q1 2023 at 4,028 units for the quarter - Increased term loan agreement with its current lenders, investment affiliates managed by SLR Capital Partners, LLC, by
$5.0 million
First Quarter Corporate Highlights:
- First patient randomized in Protocol AL, a DRCR Retina Network study with ILUVIEN or faricimab injections versus observation in patients at risk of radiation retinopathy. Over
40% of radiation retinopathy patients have been shown to experience the devastating vision loss associated with radiotherapy within three years of treatment, and currently there are no FDA approved pharmacotherapies for radiation retinopathy. - Received positive final draft guidance from the National Institute for Health and Care Excellence (NICE) recommending that chronic diabetic macular edema patients with a natural lens (phakic patients) be given access to ILUVIEN. Phakic patients represent up to
75% of the broader DME population in the United Kingdom. - Completed enrollment of 110 patient eyes across 25 sites in the Synchronicity Study, a prospective, open-label clinical study evaluating the safety and efficacy of YUTIQ (fluocinolone acetonide intravitreal implant 0.18mg) in the treatment of chronic non-infectious uveitis and related intraocular inflammation. The study included a broader retinal physician base to better understand the way they treat chronic non-infectious uveitis affecting the posterior segment.
First Quarter 2024 Financial Results
Net Revenue
Consolidated global net revenue was up
U.S. net revenue increased
International net revenue increased
Operating Expenses
Total operating expenses were approximately
Cash and Cash Equivalents
As of March 31, 2024, Alimera had cash and cash equivalents of approximately
About Alimera Sciences, Inc.
Alimera Sciences is a global pharmaceutical company whose mission is to be invaluable to patients, physicians and partners concerned with retinal health and maintaining better vision longer. For more information, please visit www.alimerasciences.com
Non-GAAP Financial Measures
This press release presents Adjusted EBITDA, as defined below, which is a non-GAAP financial measure. Alimera uses this measure to supplement the financial information presented on a GAAP basis. Alimera believes that excluding certain items from its GAAP financial results allows management to better understand its ongoing operations and analyze its financial performance from period to period and provides meaningful supplemental information to its investors.
Alimera defines “Adjusted EBITDA” as earnings before interest, taxes, depreciation, amortization, stock-based compensation expenses, net unrealized gains and losses from foreign currency exchange transactions, gains on extinguishment of debt, preferred stock dividends, severance expenses and change in fair value of warrant asset.
Alimera believes that Adjusted EBITDA, when taken together with its corresponding GAAP financial measure, provides meaningful supplemental information to its investors regarding its performance by excluding certain items that may not be indicative of its business, results of operations, or outlook. Accordingly, Adjusted EBITDA for the three months ended March 31, 2024, and 2023, together with a reconciliation to GAAP net income or loss, its most directly comparable GAAP financial measure, has been presented in the table entitled “Reconciliation of GAAP Loss to Non-GAAP Adjusted EBITDA.”
This non-GAAP financial measure may not be comparable to similarly titled measures reported by other companies, including companies in Alimera’s industry, because not all companies calculate Adjusted EBITDA in an identical manner or may use other financial measures to evaluate their performance. Therefore, this non-GAAP financial measure may be limited in usefulness for comparison between companies.
The presentation of this non-GAAP financial measure is not intended to be considered in isolation from or as a substitute for other financial performance measures prepared in accordance with GAAP and should be read only in conjunction with financial information presented on a GAAP basis. The principal limitation of this non-GAAP financial measure is that it excludes significant elements required by GAAP to be recorded in Alimera’s financial statements. In addition, this non-GAAP financial measure is subject to inherent limitations because it reflects the exercise of judgments by management. Investors are encouraged not to rely on any single financial measure to evaluate Alimera’s business.
Forward Looking Statements
This press release, includes “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995 regarding, among other things, Alimera’s expectations with respect to growth opportunities, the commencement, enrollment, timing and outcome of its and others' clinical studies, the effect of an expanded label, demand for its product, its business strategy, future operations, future financial position including the timeline for achieving positive Adjusted EBITDA, future revenues, projected costs, prospects, plans and objectives. Words such as “anticipate,” “believe,” “estimate,” “expect,” “intend,” “may,” “plan,” “contemplates,” “predict,” “project,” “target,” “likely,” “potential,” “continue,” “ongoing,” “will,” “would,” “should,” “could,” or the negative of these terms and similar expressions or words, identify forward-looking statements. Forward-looking statements are based on current expectations and involve inherent risks and uncertainties (some of which are beyond Alimera’s control), including factors that could delay, divert or change any of them, and could cause actual results to differ materially from those projected in these forward-looking statements. These risks and uncertainties include, but are not limited to, those factors discussed in the “Risk Factors” and “Management’s Discussion and Analysis of Financial Condition and Results of Operations” sections of Alimera’s most recently filed Annual Report on Form 10-K, most recently filed Quarterly Report on Form 10-Q, and any of Alimera’s subsequent filings with the Securities and Exchange Commission (SEC) and available on the SEC’s website at www.sec.gov.
All forward-looking statements contained in this press release are expressly qualified by the cautionary statements contained or referred to herein. Alimera cautions investors not to rely on the forward-looking statements Alimera makes or that are made on its behalf as predictions of future events. These forward-looking statements speak only as of the date of this press release. Alimera undertakes no obligation to publicly update or revise any of the forward-looking statements made in this press release, whether as a result of new information, future events or otherwise, except as may be required under applicable securities laws.
| For investor inquiries: | For media inquiries: |
| Scott Gordon | Jules Abraham |
| for Alimera Sciences | for Alimera Sciences |
| scottg@coreir.com | julesa@coreir.com |
| ALIMERA SCIENCES, INC. | |||||||
| CONSOLIDATED BALANCE SHEETS | |||||||
| (UNAUDITED) | |||||||
| March 31, | December 31, | ||||||
| 2024 | 2023 | ||||||
| (In thousands, except share and per share data) | |||||||
| Assets | |||||||
| Current assets: | |||||||
| Cash and cash equivalents | $ | 14,314 | $ | 12,058 | |||
| Restricted cash | 32 | 32 | |||||
| Accounts receivable, net | 34,224 | 34,545 | |||||
| Prepaid expenses and other current assets | 3,693 | 3,909 | |||||
| Inventory | 2,206 | 1,879 | |||||
| Total current assets | 54,469 | 52,423 | |||||
| Property and equipment, net | 2,377 | 2,466 | |||||
| Right-of-use assets, net | 1,060 | 1,124 | |||||
| Intangible assets, net | 94,471 | 97,355 | |||||
| Deferred tax asset | 102 | 104 | |||||
| Warrant asset | 6 | 52 | |||||
| Total assets | $ | 152,485 | $ | 153,524 | |||
| Liabilities and Stockholders’ Equity | |||||||
| Current liabilities: | |||||||
| Accounts payable | $ | 10,307 | $ | 8,252 | |||
| Accrued expenses | 4,780 | 6,192 | |||||
| Accrued licensor payment | 5,482 | 7,275 | |||||
| Finance lease obligations | 220 | 194 | |||||
| Total current liabilities | 20,789 | 21,913 | |||||
| Long-term liabilities: | |||||||
| Notes payable, net of discount | 69,436 | 64,489 | |||||
| Accrued licensor payments | 15,616 | 15,136 | |||||
| Other non-current liabilities | 5,991 | 5,816 | |||||
| Total liabilities | 111,832 | 107,354 | |||||
| Commitments and contingencies | |||||||
| Stockholders’ equity: | |||||||
| Preferred stock, $.01 par value — 10,000,000 shares authorized at March 31, 2024 and December 31, 2023, none issued | — | — | |||||
| Common stock, $.01 par value — 150,000,000 shares authorized, 52,374,687 shares issued and outstanding at March 31, 2024 and 52,354,450 shares issued and outstanding at December 31, 2023 | 524 | 524 | |||||
| Common stock warrants | 4,396 | 4,396 | |||||
| Additional paid-in capital | 463,328 | 462,446 | |||||
| Accumulated deficit | (424,741 | ) | (418,490 | ) | |||
| Accumulated other comprehensive loss | (2,854 | ) | (2,706 | ) | |||
| Total stockholders’ equity | 40,653 | 46,170 | |||||
| Total liabilities and stockholders’ equity | $ | 152,485 | $ | 153,524 | |||
| ALIMERA SCIENCES, INC. | |||||||
| CONSOLIDATED STATEMENTS OF OPERATIONS | |||||||
| (UNAUDITED) | |||||||
| Three Months Ended | |||||||
| March 31, | |||||||
| 2024 | 2023 | ||||||
| (In thousands, except share and per share data) | |||||||
| Net revenue | $ | 23,011 | $ | 13,546 | |||
| Cost of goods sold, excluding depreciation and amortization | (3,353 | ) | (2,028 | ) | |||
| Gross profit | 19,658 | 11,518 | |||||
| Operating expenses: | |||||||
| Research, development and medical affairs expenses | 4,361 | 4,164 | |||||
| General and administrative expenses | 5,432 | 4,171 | |||||
| Sales and marketing expenses | 9,082 | 5,804 | |||||
| Depreciation and amortization | 3,085 | 681 | |||||
| Total operating expenses | 21,960 | 14,820 | |||||
| Loss from operations | (2,302 | ) | (3,302 | ) | |||
| Interest expense and other, net | (3,739 | ) | (1,667 | ) | |||
| Unrealized foreign currency loss, net | (196 | ) | (13 | ) | |||
| Change in fair value of warrant asset | (46 | ) | 14 | ||||
| Net loss before income taxes | (6,283 | ) | (4,968 | ) | |||
| Income tax benefit | 32 | — | |||||
| Net loss | (6,251 | ) | (4,968 | ) | |||
| Preferred stock dividends | — | (14 | ) | ||||
| Net loss applicable to common stockholders | $ | (6,251 | ) | $ | (4,982 | ) | |
| Net loss per share — basic and diluted | $ | (0.12 | ) | $ | (0.71 | ) | |
| Weighted average shares outstanding — basic and diluted | 54,356,828 | 7,032,231 | |||||
| RECONCILIATION OF GAAP NET LOSS TO NON-GAAP ADJUSTED EBITDA | |||||||
| (UNAUDITED) | |||||||
| Three Months Ended | |||||||
| March 31, | |||||||
| 2024 | 2023 | ||||||
| (In thousands) | |||||||
| U.S. GAAP net loss | $ | (6,251 | ) | $ | (4,968 | ) | |
| Adjustments to U.S. GAAP net loss: | |||||||
| Interest expense and other, net | 3,739 | 1,667 | |||||
| Income tax benefit | (32 | ) | — | ||||
| Depreciation and amortization | 3,085 | 681 | |||||
| Stock-based compensation | 845 | 226 | |||||
| Foreign currency exchange losses | 196 | 13 | |||||
| Change in fair value of warrant asset | 46 | (14 | ) | ||||
| Severance expenses | 176 | — | |||||
| Non-GAAP adjusted EBITDA | $ | 1,804 | $ | (2,395 | ) | ||
FAQ
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