ProPhase Labs Announces Financial Results for the Three Months Ended March 31, 2024, and Highlights Significant Progress in its Strategic Initiatives.
ProPhase Labs, Inc. reported financial results for Q1 2024, highlighting strategic initiatives including Project ZenQ-AI and the BE-Smart Esophageal Cancer Test. Pharmaloz Manufacturing is exploring strategic alternatives and anticipates significant revenue growth. Equivir trial results are on track for release, and Nebula Genomics is expanding its global reach.
Pharmaloz Manufacturing is engaged in negotiations for potential revenue capacity of $40-45 million once line two is operational.
Pharmaloz signed deals worth over $5 million in additional revenues, with more non-seasonal customers in the pipeline.
Nebula Genomics expanded its business development team and signed key international agreements, enhancing global growth opportunities.
BE-Smart Esophageal Cancer Test is on track for commercialization in the second half of 2024, with potential to revolutionize cancer risk assessment.
Project ZenQ-AI aims to develop new cancer therapies using the Company's genomics database and patented discoveries.
Net revenue for Q1 2024 decreased significantly compared to the same period in 2023 due to lower testing volumes.
Gross margin loss was reported for Q1 2024, attributed to decreased revenue and increased costs.
The Company reported a net loss of $6.3 million for Q1 2024, in contrast to net income of $0.6 million for Q1 2023.
Insights
The financial results for ProPhase Labs indicate a significant year-over-year decline in net revenue, from
However, it is worth highlighting the anticipated revenue capacity of Pharmaloz Manufacturing, which expects to potentially reach between
The expansion plans for Pharmaloz Manufacturing and strategic initiatives, such as the negotiations to potentially sell the plant or book future capacity, represent a strategic push to leverage existing assets for revenue generation. The claim of a
On the genomics and diagnostics front, Nebula Genomics' developments and the BE-Smart Esophageal Cancer Test's progress toward commercialization are promising, but the timeline and market acceptance remain risks to consider. The entry into liquid fill equipment manufacturing also taps into a reportedly growing market segment, diversifying ProPhase's product line which could help mitigate seasonal demand fluctuations.
From a medical innovation perspective, the BE-Smart Esophageal Cancer Test and Project ZenQ-AI represent significant advancements with potential implications for patient care and the biopharma industry. The potential commercialization of the BE-Smart test, aiming at a wide market in the range of
Pharmaloz Manufacturing explores strategic alternatives, including potential sale.
Company announces major strategic AI initiative, Project ZenQ-AI, leveraging its massive global genomics database and patented discoveries in its BE-Smart Esophageal Cancer Diagnostic Test.
BE-Smart Cancer Test continues to advance towards second half commercialization.
Company to hold a conference call Thursday, May 9, 2024, at 11:00 AM ET
Garden City, NY, May 09, 2024 (GLOBE NEWSWIRE) -- ProPhase Labs, Inc. (NASDAQ: PRPH) (“ProPhase” or the “Company”), a next-generation biotech, genomics, and diagnostics company, today reported its financial and operational results for the three months ended March 31, 2024.
The three months ended March 31, 2024, marked a continuation of the transformation of ProPhase Labs. As the expansion plans at its wholly owned subsidiary, Pharmaloz Manufacturing, gain momentum, the Company is evaluating strategic alternatives including the potential sale or securing long-term agreements to optimize the capacity of its forthcoming second production line.
The shortage of lozenge manufacturing capacity that the Company has previously highlighted shows no sign of abating. In Q1 the Company attended Expo West, the largest health and wellness expo of the year. Pharmaloz was the only attending company, to our knowledge, that was offering future lozenge manufacturing capacity. Nearly a dozen companies expressed significant interest, and we are in negotiations with several such companies. Some of the newer potential customers are seeking out functional year-round lozenges that deliver vitamins, immunity boosters or overall health and wellness. Over the next several quarters, Pharmaloz intends to enter into agreements with multiple customers that will require year-round production that should smooth out the manufacturing seasonality. The new automation equipment incorporated into line one is running smoothly and the capacity has been increased to over
Subject to market conditions, our ability to generate enhanced revenues, and other factors, the Company anticipates that there will be a significant sequential improvement in revenues and EBITDA in the second half of 2024, driven by strategic advancements across its subsidiaries.
Participants can register for the virtual conference call by navigating to:
Additional corporate highlights for the three months ended March 31, 2024, and recent positive developments, include the following:
1) Pharmaloz Manufacturing
| ● | The Company is currently engaged in late-stage negotiations to potentially either sell the plant or pre-book some or all of the future capacity of its second manufacturing line. | |
| ● | Anticipate | |
| ● | There is a significant shortage of lozenge manufacturing capacity in both the U.S. and globally. | |
| ● | The Company estimates that to build a new manufacturing facility from scratch with the capacity that Pharmaloz could have next year might cost approximately | |
| ● | Pharmaloz recently signed two significant deals representing over | |
| ● | The Company is working on several more non-seasonal customers that were sourced at the largest annual health and wellness expo. | |
| ● | Engineering completed the design of phase 1 and phase 2 plans. This could potentially take the plant from 1 lozenge line to a potential of up to 7 operational lines within the next four years and a potential of over | |
| ● | New liquid fill equipment is ahead of schedule and already enroute to the factory with manufacturing anticipated to begin by the end of May. | |
| ● | Existing customers accepted an average price increase of | |
| ● | Passed the 3-year FDA audit with no citations. | |
| ● | Recently passed the 4-Day UL Audit. |
2) Nebula Genomics
| ● | Expanded its business development team to increase global outreach and access to advanced genetic testing. | |
| ● | Automated workflows and added key technicians in the New York lab have significantly improved throughput and reduced turnaround times. | |
| ● | Nebula has built a massive database over the last six years, from whole genome sequencing tests across more than 130 countries, equivalent to roughly 150 million ancestry SNP-based tests. | |
| ● | Data is safeguarded by world-class cyber security measures to protect sensitive genetic information. | |
| ● | Nebula’s whole genome sequencing technology analyzes greater than | |
| ● | Nebula’s proprietary bioinformatics platform delivers in-depth genetic health information, identifies rare genetic mutations, and traces ancestry at highly competitive prices. | |
| ● | Signed key international business-to-business agreement with MenaDNA, Inc., a well-established global distribution company, enabling significant global growth opportunities. | |
| ● | Additional significant agreements are currently under negotiation. | |
3) BE-Smart Esophageal Cancer Test
| ● | Completed additional samples which are currently being analyzed by Stat King, a division of Genesis Drug Discovery and Development, to further validate the | |
| ● | Company on track to commercialize BE-Smart in the second half of 2024. Working with multiple consultants to secure CPT codes by the second half of 2024. | |
| ● | Discussions for commercialization continue with a potential global partner. | |
| ● | Working in conjunction with multiple groups to fully develop the ‘advanced traffic light’ approach of green, yellow, orange, and red to assess distinct levels of cancer risk, leading to optimized treatment approaches. This approach could lead to insurance companies mandating the use of the BE-Smart test for endoscopies performed on Barrett’s Esophagus patients. | |
| ● | Working with Mayo Clinic to assess additional potential areas of interest within a panel of 55 additional markers. These patterns could help in conjunction with ZenQ-AI to develop potential targeted oncology therapies. | |
4) Project ZenQ-AI
| ● | The launch of Project ZenQ-AI marks a significant leap forward in cancer treatment research, utilizing the Company’s massive global genomics database and analyzing patented discoveries from its BE-Smart Esophageal Cancer diagnostic test. | |
| ● | This initiative deploys state-of-the-art AI algorithms to discover potential new cancer therapies, specifically focusing on antibody drug conjugates. | |
5) Equivir
| ● | Anticipate that by the end of May, the 300th patient will have reached the 180-day mark thereby completing the original target of enrolling 300 or more patients and monitoring such patients over a 180-day period. | |
| ● | Currently have over 329 active patients in the study. | |
| ● | Released impressive interim preliminary results from 152 patients at the 90-day mark. | |
| ● | Remain on target for full data unlocking by the end of the second quarter. | |
| ● | The Company is planning to increase production of the Equivir capsules with a second half 2024 launch timeframe. | |
| ● | Currently working with the Company’s distribution partner to potentially leverage distribution longer term in over 40,000 food, drug and mass retail stores. | |
6) Some additional financial highlights
| ● | Ended April with over | |
| ● | Realized over | |
| ● | Raised over | |
| ● | Increased monthly accounts receivable collections with current collection partner. | |
| ● | Started to receive payment from a key insurance company representing a receivable of close to | |
Ted Karkus, ProPhase Lab’s Chief Executive Officer, commented, “Q1 continues to be transformative for ProPhase Labs. The expansion of Pharmaloz and new strategic interest, the potential commercialization of our BE-Smart Esophageal Cancer test, the continued development of Nebula Genomics and the most recent AI initiative are collectively paving the way for a very exciting future.
Pharmaloz is no longer an undiscovered gem as it was one of the stars of the expo in April. We discussed potential deals with a dozen companies that, if consummated, would fill our near term planned capacity expansion. Several key industry players have turned to Pharmaloz to help develop bench samples of products that they have not been able to develop on their own. Furthermore, the interest from a couple of the largest brands has been quite staggering as they are seeking to potentially lock up our newest line with long-term contracts. We are also excited to roll out our liquid-filled capacity, starting late in Q2, as many customers are noting growing demand in the liquid-filled segment.
ProPhase Biopharma remains a primary focus as our BE-Smart Esophageal Cancer test moves ever closer to commercialization. The Company is in discussions with multiple experts in the field to secure the CPT codes and plan for a successful commercial launch. The initial target market for BE-Smart is
We also eagerly await the results of the Equivir trial expected to be released sometime by the end of the second quarter. Once we confirm the results, the Company is poised with a commercial launch designed to coincide with the start of the upper respiratory disease season.
As we move forward, our focus remains on driving value across all subsidiaries, with a clear vision of realizing and maximizing shareholder value. As of April 30, 2024, the Company had over
Financial Results
Three Months Ended March 31, 2024 as compared to the Three Months Ended March 31, 2023
For the three months ended March 31, 2024, net revenue was
Cost of revenues for the three months ended March 31, 2024 were
We realized a gross margin loss of
Diagnostic services costs for the three months ended March 31, 2024 were zero compared to
General and administration expenses for the three months ended March 31, 2024 were
Research and development costs for the three months ended March 31, 2024 were
As a result of the effects described above, net loss for the three months ended March 31, 2024 was
Our aggregate cash and cash equivalents as of March 31, 2024 were
Webcast Details
Investors interested in participating in this live event will need to register using the link below. After the event, a replay will be available on The Company’s Investor website.
REGISTER HERE: https://www.renmarkfinancial.com/events/first-quarter-2024-results-virtual-conference-call-nasdaq-prph-2024-05-09-110000
About ProPhase Labs
ProPhase Labs Inc. (Nasdaq: PRPH) (“ProPhase”) is a next-generation biotech, genomics and diagnostics company. Our goal is to create a healthier world with bold action and the power of insight. We’re revolutionizing healthcare with industry-leading Whole Genome Sequencing solutions, while developing potential game changer diagnostics and therapeutics in the fight against cancer. This includes a potentially life-saving cancer test focused on early detection of esophageal cancer and potential breakthrough cancer therapeutics with novel mechanisms of action. Our world-class CLIA labs and cutting-edge diagnostic technology provide wellness solutions for healthcare providers and consumers. We develop, manufacture, and commercialize health and wellness solutions to enable people to live their best lives. We are committed to executional excellence, smart diversification, and a synergistic, omni-channel approach. ProPhase Labs’ valuable subsidiaries, their synergies, and significant growth underscore our multi-billion-dollar potential.
Forward Looking Statements
Except for the historical information contained herein, this document contains forward looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, including statements regarding our strategy, plans, objectives and initiatives, including our expectation to enter into new agreements for Pharmaloz, our expectations regarding the future revenue growth potential of each of our subsidiaries, our expectations regarding future liquidity events and the prospects of raising additional equity capital, the expected timeline for commercializing our BE-Smart Esophageal Cancer Test, our ability to enter into new domestic and international long-term contracts for our Nebula Genomics business and the financial impact of any such contracts, the anticipated timing for the receipt of new equipment and installation of additional lozenge lines and their ability to increase capacity and revenue, our anticipated expenses, ability to obtain funding for our operations and the sufficiency of our cash resources, and the expected timeline for the launch of Equivir capsules. Management believes that these forward-looking statements are reasonable as and when made. However, such forward-looking statements involve known and unknown risks, uncertainties, and other factors that may cause actual results to differ materially from those projected in the forward-looking statements. These risks and uncertainties include but are not limited to our ability to obtain and maintain necessary regulatory approvals, general economic conditions, consumer demand for our products and services, challenges relating to entering into and growing new business lines, the competitive environment, and the risk factors listed from time to time in our Annual Reports on Form 10-K, Quarterly Reports on Form 10-Q and any other SEC filings. The Company undertakes no obligation to update forward-looking statements except as required by applicable securities laws. Readers are cautioned that forward-looking statements are not guarantees of future performance and are cautioned not to place undue reliance on any forward-looking statements.
For more information, visit www.ProPhaseLabs.com.
ProPhase Media Relations and Institutional Investor Contact:
ProPhase Labs, Inc.
267-880-1111
investorrelations@prophaselabs.com
ProPhase Retail Investor Relations Contact:
Renmark Financial Communications
John Boidman
514-939-3989
Jboidman@renmarkfinancial.com
Source: ProPhase Labs, Inc.
ProPhase Labs, Inc. and Subsidiaries
Condensed Consolidated Balance Sheets
(in thousands, except share and per share amounts)
| March 31, 2024 | December 31, 2023 | |||||||
| (Unaudited) | ||||||||
| ASSETS | ||||||||
| Current assets | ||||||||
| Cash and cash equivalents | $ | 1,175 | $ | 1,609 | ||||
| Restricted cash | 561 | 540 | ||||||
| Marketable debt securities, available for sale | 58 | 3,127 | ||||||
| Accounts receivable, net | 35,116 | 36,313 | ||||||
| Inventory, net | 3,758 | 3,841 | ||||||
| Prepaid expenses and other current assets | 4,377 | 2,155 | ||||||
| Total current assets | 45,045 | 47,585 | ||||||
| Property, plant and equipment, net | 12,797 | 12,898 | ||||||
| Prepaid expenses, net of current portion | 732 | 832 | ||||||
| Operating lease right-of-use asset, net | 4,462 | 4,572 | ||||||
| Intangible assets, net | 11,687 | 12,333 | ||||||
| Goodwill | 5,231 | 5,231 | ||||||
| Deferred tax asset | 9,762 | 7,313 | ||||||
| Other assets | 316 | 1,163 | ||||||
| TOTAL ASSETS | $ | 90,032 | $ | 91,927 | ||||
| LIABILITIES AND STOCKHOLDERS’ EQUITY | ||||||||
| Current liabilities | ||||||||
| Accounts payable | $ | 11,759 | $ | 9,383 | ||||
| Accrued diagnostic services | 268 | 314 | ||||||
| Accrued advertising and other allowances | 8 | 24 | ||||||
| Finance lease liabilities | 1,840 | 1,840 | ||||||
| Operating lease liabilities | 959 | 953 | ||||||
| Short-term loan payable, net of discount of | 2,381 | — | ||||||
| Deferred revenue | 1,630 | 2,382 | ||||||
| Income tax payable | 3,005 | 3,278 | ||||||
| Other current liabilities | 2,057 | 2,683 | ||||||
| Total current liabilities | 23,907 | 20,857 | ||||||
| Non-current liabilities: | ||||||||
| Secured long-term debt, net of discount of | 2,926 | 2,924 | ||||||
| Unsecured promissory notes, net of discount of | 7,368 | 7,334 | ||||||
| Due to sellers (see Note 3) | 2,000 | 2,000 | ||||||
| Deferred revenue, net of current portion | 1,100 | 1,100 | ||||||
| Operating lease liabilities, net of current portion | 4,122 | 4,237 | ||||||
| Finance lease liabilities, net of current portion | 3,742 | 4,092 | ||||||
| Total non-current liabilities | 21,258 | 21,687 | ||||||
| Total liabilities | 45,165 | 42,544 | ||||||
| COMMITMENTS AND CONTINGENCIES | ||||||||
| Stockholders’ equity | ||||||||
| Preferred stock authorized 1,000,000, | — | — | ||||||
| Common stock authorized 50,000,000, | 18 | 18 | ||||||
| Additional paid-in capital | 120,283 | 118,694 | ||||||
| Accumulated deficit | (11,294 | ) | (5,029 | ) | ||||
| Treasury stock, at cost, 18,940,967 and 18,940,967 shares, respectively | (64,000 | ) | (64,000 | ) | ||||
| Accumulated other comprehensive loss | (140 | ) | (300 | ) | ||||
| Total stockholders’ equity | 44,867 | 49,383 | ||||||
| TOTAL LIABILITIES AND STOCKHOLDERS’ EQUITY | $ | 90,032 | $ | 91,927 | ||||
ProPhase Labs, Inc. and Subsidiaries
Condensed Consolidated Statements of Operations and Comprehensive Income (Loss)
(in thousands, except per share amounts)
(unaudited)
| For the three months ended | ||||||||
| March 31, 2024 | March 31, 2023 | |||||||
| Revenues, net | $ | 3,634 | $ | 19,303 | ||||
| Cost of revenues | 4,067 | 8,783 | ||||||
| Gross (loss) profit | (433 | ) | 10,520 | |||||
| Operating expenses: | ||||||||
| Diagnostic expenses | — | 1,203 | ||||||
| General and administration | 7,593 | 8,298 | ||||||
| Research and development | 272 | 144 | ||||||
| Total operating expenses | 7,865 | 9,645 | ||||||
| (Loss) Income from operations | (8,298 | ) | 875 | |||||
| Interest income, net | — | 11 | ||||||
| Interest expense | (515 | ) | (215 | ) | ||||
| Other expense | (18 | ) | (107 | ) | ||||
| (Loss) Income from operations before income taxes | (8,831 | ) | 564 | |||||
| Income tax benefit (expense) | 2,566 | (14 | ) | |||||
| (Loss) income from operations after income taxes | (6,265 | ) | 550 | |||||
| Net (loss) income | $ | (6,265 | ) | $ | 550 | |||
| Other comprehensive income (loss): | ||||||||
| Unrealized gain (loss) on marketable debt securities | 160 | (665 | ) | |||||
| Total comprehensive loss | $ | (6,105 | ) | $ | (115 | ) | ||
| Earnings (loss) per share: | ||||||||
| Basic | $ | (0.07 | ) | $ | 0.03 | |||
| Diluted | $ | (0.07 | ) | $ | 0.03 | |||
| Weighted average common shares outstanding: | ||||||||
| Basic | 90,423 | 16,748 | ||||||
| Diluted | 90,423 | 18,061 | ||||||
ProPhase Labs, Inc. and Subsidiaries
Condensed Consolidated Statements of Cash Flows
(in thousands)
(unaudited)
| For the three months ended | ||||||||
| March 31, 2024 | March 31, 2023 | |||||||
| Cash flows from operating activities | ||||||||
| Net (loss) income | $ | (6,265 | ) | $ | 550 | |||
| Adjustments to reconcile net (loss) income to net cash (used in) provided by operating activities: | ||||||||
| Realized loss on marketable debt securities | 18 | 107 | ||||||
| Depreciation and amortization | 1,686 | 1,292 | ||||||
| Amortization of debt discount | 146 | 20 | ||||||
| Amortization on operating lease right-of-use assets | 110 | 85 | ||||||
| Stock-based compensation expense | 1,589 | 947 | ||||||
| Accounts receivable allowances | — | (147 | ) | |||||
| Credit loss expense, direct write-off | — | 230 | ||||||
| Inventory reserve | (69 | ) | 1 | |||||
| Changes in operating assets and liabilities: | ||||||||
| Accounts receivable | 1,197 | (864 | ) | |||||
| Inventory | 152 | (336 | ) | |||||
| Prepaid expenses and other current assets | (2,122 | ) | (2,107 | ) | ||||
| Deferred tax asset | (2,612 | ) | (96 | ) | ||||
| Other assets | 847 | — | ||||||
| Accounts payable and accrued expenses | 2,376 | (2,661 | ) | |||||
| Accrued diagnostic services | (46 | ) | (656 | ) | ||||
| Accrued advertising and other allowances | (16 | ) | 52 | |||||
| Deferred revenue | (752 | ) | 443 | |||||
| Operating lease liabilities | (459 | ) | (80 | ) | ||||
| Income tax payable | (273 | ) | (341 | ) | ||||
| Other liabilities | (626 | ) | 4,037 | |||||
| Net cash (used in) provided by operating activities | (5,119 | ) | 476 | |||||
| Cash flows from investing activities | ||||||||
| Business acquisitions, escrow received | — | 478 | ||||||
| Asset acquisitions, net of cash acquired | — | (2,904 | ) | |||||
| Proceeds from sales of marketable securities | 3,374 | 1,291 | ||||||
| Capital expenditures | (939 | ) | (517 | ) | ||||
| Net cash provided by (used in) investing activities | 2,435 | (1,652 | ) | |||||
| Cash flows from financing activities | ||||||||
| Proceeds from issuance of note payable | 2,460 | 7,600 | ||||||
| Repurchases of common shares | — | (541 | ) | |||||
| Repurchase of common stock for payment of statutory taxes due on cashless exercise of stock option | — | (5,379 | ) | |||||
| Repayment of note payable | (189 | ) | — | |||||
| Net cash provided by financing activities | 2,271 | 1,680 | ||||||
| (Decrease) increase in cash, cash equivalents and restricted cash | (413 | ) | 504 | |||||
| Cash, cash equivalents and restricted cash at the beginning of the period | 2,149 | 9,109 | ||||||
| Cash, cash equivalents and restricted cash at the end of the period | $ | 1,736 | $ | 9,613 | ||||
| Supplemental disclosures: | ||||||||
| Cash paid for income taxes | $ | 318 | $ | 1,500 | ||||
| Interest payment on the promissory notes | $ | 642 | $ | 203 | ||||
| Supplemental disclosure of non-cash investing and financing activities: | ||||||||
| Financed capital expenditures | $ | — | $ | 1,623 | ||||
| Common stock issued in asset acquisition | $ | — | $ | 1,000 | ||||
Non-GAAP Financial Measures and Reconciliation
In an effort to provide investors with additional information regarding our results of operations as determined by accounting principles generally accepted in the United States of America (“GAAP”), we disclose certain non-GAAP financial measures. The primary non-GAAP financial measures we disclose are EBITDA and Adjusted EBITDA.
We define “EBITDA” as net income (loss) before net interest expense, income taxes, depreciation and amortization. Adjusted EBITDA further adjusts EBITDA by excluding acquisition costs, other non-cash items, and other unusual or non-recurring charges (as described in the table below).
Non-GAAP financial measures should not be considered as a substitute for, or superior to, measures of financial performance prepared in accordance with GAAP. These non-GAAP financial measures do not reflect a comprehensive system of accounting, differ from GAAP measures with the same names and may differ from non-GAAP financial measures with the same or similar names that are used by other companies. We compute non-GAAP financial measures using the same consistent method from quarter to quarter and year to year. We may consider whether other significant items that arise in the future should be excluded from the non-GAAP financial measures.
We use EBITDA and Adjusted EBITDA internally to evaluate and manage the Company’s operations because we believe they provide useful supplemental information regarding the Company’s ongoing economic performance. We believe that these non-GAAP financial measures provide meaningful supplemental information regarding our operating results primarily because they exclude amounts that are not considered part of ongoing operating results when planning and forecasting and when assessing the performance of the organization. In addition, we believe that non-GAAP financial information is used by analysts and others in the investment community to analyze our historical results and in providing estimates of future performance and that failure to report these non-GAAP measures could result in confusion among analysts and others and create a misplaced perception that our results have underperformed or exceeded expectations.
The following table sets forth the reconciliations of EBITDA and Adjusted EBITDA excluding other costs to the most comparable GAAP financial measures (in thousands):
| For the three months ended | ||||||||
| March 31, 2024 | March 31, 2023 | |||||||
| GAAP net income (1) | $ | (6,265 | ) | $ | 550 | |||
| Interest, net | 515 | 204 | ||||||
| Income tax (benefit) expense | (2,566 | ) | 14 | |||||
| Depreciation and amortization | 1,686 | 1,292 | ||||||
| EBITDA | (6,630 | ) | 2,060 | |||||
| Share-based compensation expense | 1,589 | 947 | ||||||
| Non-cash rent expense (2) | 169 | 6 | ||||||
| Bad debt expense | — | 74 | ||||||
| Adjusted EBITDA | $ | (4,872 | ) | $ | 3,087 | |||
| (1) | We believe that net income (loss) is the financial measure calculated and presented in accordance with GAAP that is most directly comparable to EBITDA and Adjusted EBITDA. EBITDA and Adjusted EBITDA measure the Company’s operating performance without regard to certain expenses. EBITDA and Adjusted EBITDA are not presentations made in accordance with GAAP and the Company’s computation of EBITDA and Adjusted EBITDA may vary from others in the industry. EBITDA and Adjusted EBITDA have important limitations as analytical tools and should not be considered in isolation or as substitutes for analysis of the Company’s results as reported under GAAP. |
| (2) | The non-cash portion of rent, which reflects the extent to which our GAAP rent expense recognized exceeds (or is less than) our cash rent payments. For newer leases, our rent expense recognized typically exceeds our cash rent payments, while for more mature leases, rent expense recognized is typically less than our cash rent payments. |
FAQ
What strategic initiatives did ProPhase Labs announce?
What is Pharmaloz Manufacturing exploring?
What is the revenue capacity anticipated for Pharmaloz Manufacturing?
