Citius Pharmaceuticals, Inc. Reports Fiscal First Quarter 2024 Financial Results and Provides Business Update
- Resubmission of LYMPHIR™ BLA to the FDA for potential approval in 2024.
- Completion of Mino-Lok® Phase 3 trial enrollment with topline results expected in Q2 2024.
- Execution of a merger agreement with TenX Keane Acquisition to form Citius Oncology, Inc.
- Nomination of Robert Smith to Citius Board of Directors.
- Cash and cash equivalents of $20.3 million as of December 31, 2023, providing runway through August 2024.
- R&D expenses decreased to $2.6 million in Q1 2024 compared to $3.4 million in Q1 2023.
- G&A expenses increased to $3.7 million in Q1 2024 compared to $2.6 million in Q1 2023.
- Stock-based compensation expense increased to $3.1 million in Q1 2024 from $1.2 million in Q1 2023.
- Net loss was $9.2 million, or ($0.06) per share for Q1 2024 compared to $3.6 million, or ($0.02) per share for Q1 2023.
- None.
Insights
The resubmission of LYMPHIR™ BLA and the completion of Mino-Lok® Phase 3 trial enrollment are pivotal developments for Citius Pharmaceuticals. These advancements are likely to be closely monitored by investors as they can significantly influence the company's revenue prospects and market position upon successful approval and commercialization. The financial health of Citius, as indicated by the cash runway through August 2024, is a critical parameter for assessing the company's ability to sustain operations without the immediate need for additional funding. However, the projected need for future capital raises to support operations beyond this period suggests a potential dilution risk for current shareholders.
Furthermore, the decrease in R&D expenses aligns with the completion of certain trial stages, which is typically viewed positively as it indicates progression toward potential product commercialization. On the other hand, the substantial increase in G&A expenses and stock-based compensation raises questions about the company's cost management and compensation strategies, especially in light of the wider net loss compared to the previous year. The financial results, combined with the strategic developments, will likely influence investor sentiment and could impact the stock's performance in the short to medium term.
The resubmission of the LYMPHIR™ BLA marks a significant step in Citius Pharmaceuticals' pipeline progression. LYMPHIR™, being a biologic for critical care, represents a high-value proposition in the biopharmaceutical sector. The anticipation of the PDUFA date is a key event, as it will provide a timeline for potential FDA approval. The successful completion of enrollment in the Mino-Lok® Phase 3 trial indicates that Citius is moving closer to having conclusive data on the efficacy and safety of this treatment for infected catheters. The outcome of this trial is crucial as it may offer a new standard of care for catheter-related bloodstream infections, which are a major healthcare concern.
Additionally, the upcoming meeting with the FDA to discuss the development of Halo-Lido for hemorrhoids treatment is another important milestone that could shape the drug's regulatory pathway. These developments not only have the potential to improve patient care but also to significantly increase Citius's market presence in the critical care space. The implications of these trials' outcomes are far-reaching, potentially affecting prescribing habits, healthcare costs and the competitive landscape.
The definitive agreement to merge Citius's oncology subsidiary with TenX to form Citius Oncology, Inc. indicates a strategic move to enhance the company's market position and financial flexibility. This merger could facilitate resource pooling and potentially expedite the development and commercialization of oncology products. The nomination of Robert Smith to the Citius Board of Directors could also bring fresh perspectives and strategic insights, possibly affecting governance and decision-making processes.
From a market analysis standpoint, the financial and operational updates provided by Citius Pharmaceuticals serve as indicators of the company's trajectory and strategic priorities. The focus on maximizing the value of the pipeline while maintaining financial stewardship is a common theme in biopharmaceutical companies at this stage. Investors and market analysts will be evaluating the potential market size for LYMPHIR™, Mino-Lok® and Halo-Lido, as well as the competitive advantages these products may offer. The outcomes of these evaluations will be critical in shaping investor expectations and the company's valuation in the stock market.
Resubmitted LYMPHIR™ Biologics License Application; awaiting PDUFA date
Completed enrollment in the Mino-Lok® Pivotal Phase 3 trial
First Quarter 2024 Business Highlights and Subsequent Developments
- Resubmitted LYMPHIR™ (denileukin diftitox) biologics license application (BLA) to the
U.S. Food and Drug Administration (FDA); awaiting Prescription Drug User Fee Act (PDUFA) target date; - Completed enrollment in the Mino-Lok® Pivotal Phase 3 trial; topline results anticipated in calendar 2Q 2024;
- Scheduled end of Phase 2b trial meeting with FDA in calendar 2Q 2024 to discuss next steps in development of Halo-Lido for the treatment of hemorrhoids;
- Executed definitive agreement to merge our wholly owned subsidiary with TenX Keane Acquisition (Nasdaq: TENK) to form publicly listed Citius Oncology, Inc.; transaction is expected to be completed in the first half of 2024; and,
- Nominated Robert Smith to be elected to the Citius Board of Directors at the upcoming Annual Meeting of Stockholders.
Financial Highlights
- Cash and cash equivalents of
$20.3 million - R&D expenses were
$2.6 million $3.4 million - G&A expenses were
$3.7 million $2.6 million - Stock-based compensation expense was
$3.1 million $1.2 million - Net loss was
$9.2 million $0.06 $3.6 million $0.02
"We had a strong first quarter of fiscal 2024 during which we achieved multiple mission critical goals. We are hopeful that topline results from our completed Mino-Lok pivotal Phase 3 trial, which we expect to be available in the second quarter of 2024, support the benefit of using Mino-Lok to clear infected catheters. The data will clarify the path forward for Mino-Lok and our opportunities to monetize the asset. Likewise, our upcoming end of Phase 2 meeting with the FDA should provide valuable input on the development plan for Halo-Lido," stated Leonard Mazur, Chairman and CEO of Citius.
"Importantly, we believe we have addressed the items noted by the FDA in our BLA submission for LYMPHIR and have resubmitted the application. We look forward to receiving a PDUFA date shortly and potential approval later this year. In parallel, we executed an agreement to merge our oncology subsidiary with TenX to form a publicly listed company. With unanimous board of directors' approval, we believe the transaction will ultimately provide greater financial flexibility and drive sustained value for all stakeholders. The transaction is expected to be completed in the first half of 2024," added Mazur.
"For the balance of 2024, our focus will remain on financial stewardship and execution to maximize the value of our pipeline," concluded Mazur.
FIRST QUARTER 2024 Financial Results:
Liquidity
As of December 31, 2023, the Company had
As of December 31, 2023, the Company had 158,966,576 common shares outstanding.
The Company estimates that its available cash resources will be sufficient to fund its operations through August 2024. We expect to need to raise additional capital in the future to support our operations beyond August 2024.
Research and Development (R&D) Expenses
R&D expenses were
We expect that research and development expenses will stabilize in fiscal 2024 as we focus on the commercialization of LYMPHIR, complete our Phase 3 trial for Mino-Lok, and analyze the data from our Phase 2b trial and begin planning our Phase 3 trial for Halo-Lido.
General and Administrative (G&A) Expenses
G&A expenses were
Stock-based Compensation Expense
For the first quarter ended December 31, 2023, stock-based compensation expense was
Net loss
Net loss was
About Citius Pharmaceuticals, Inc.
Citius Pharma is a late-stage biopharmaceutical company dedicated to the development and commercialization of first-in-class critical care products. The Company's diversified pipeline includes two late-stage product candidates. At the end of 2023, Citius completed enrollment in a Phase 3 Pivotal superiority trial of Mino-Lok®, an antibiotic lock solution to salvage catheters in patients with catheter-related bloodstream infections. Citius resubmitted the Biologics License Application for LYMPHIR, a novel IL-2R immunotherapy for an initial indication in cutaneous T-cell lymphoma, in early 2024, and announced plans to form Citius Oncology, a standalone publicly traded company with LYMPHIR as its primary asset. LYMPHIR received orphan drug designation by the FDA for the treatment of CTCL and PTCL. In addition, Citius completed enrollment in its Phase 2b trial of CITI-002 (Halo-Lido), a topical formulation for the relief of hemorrhoids. For more information, please visit www.citiuspharma.com.
Forward-Looking Statements
This press release may contain "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 are made based on our expectations and beliefs concerning future events impacting Citius. You can identify these statements by the fact that they use words such as "will," "anticipate," "estimate," "expect," "plan," "should," and "may" and other words and terms of similar meaning or use of future dates. Forward-looking statements are based on management's current expectations and are subject to risks and uncertainties that could negatively affect our business, operating results, financial condition and stock price. Factors that could cause actual results to differ materially from those currently anticipated are: the FDA may not approve LYMPHIR; risks relating to the results of research and development activities, including those from the resubmission of the BLA for LYMPHIR, the Mino-Lok Phase 3 trial and other existing and new pipeline assets; our need for substantial additional funds; our ability to commercialize our products if approved by the FDA; our dependence on third-party suppliers; our ability to procure cGMP commercial-scale supply; the estimated markets for our product candidates and the acceptance thereof by any market; the ability of our product candidates to impact the quality of life of our target patient populations; our ability to obtain, perform under and maintain financing and strategic agreements and relationships; uncertainties relating to preclinical and clinical testing; the early stage of products under development; market and other conditions; our ability to attract, integrate, and retain key personnel; risks related to our growth strategy; patent and intellectual property matters; our ability to identify, acquire, close and integrate product candidates and companies successfully and on a timely basis; government regulation; competition; as well as other risks described in our SEC filings. These risks have been and may be further impacted by Covid-19 and could be impacted by any future public health risks. Accordingly, these forward-looking statements do not constitute guarantees of future performance, and you are cautioned not to place undue reliance on these forward-looking statements. Risks regarding our business are described in detail in our Securities and Exchange Commission ("SEC") filings which are available on the SEC's website at www.sec.gov, including in our Annual Report on Form 10-K for the year ended September 30, 2023, filed with the SEC on December 29, 2023, and updated by our subsequent filings with the Securities and Exchange Commission. These forward-looking statements speak only as of the date hereof, and we expressly disclaim any obligation or undertaking to release publicly any updates or revisions to any forward-looking statements contained herein to reflect any change in our expectations or any changes in events, conditions or circumstances on which any such statement is based, except as required by law.
Investor Relations for Citius Pharmaceuticals:
Investor Contact:
Ilanit Allen
ir@citiuspharma.com
908-967-6677 x113
Media Contact:
STiR-communications
Greg Salsburg
Greg@STiR-communications.com
-- Financial Tables Follow –
CITIUS PHARMACEUTICALS, INC. CONDENSED CONSOLIDATED BALANCE SHEETS (Unaudited) | ||||||||
December 31, | September 30, | |||||||
2023 | 2023 | |||||||
ASSETS | ||||||||
Current Assets: | ||||||||
Cash and cash equivalents | $ | 20,345,618 | $ | 26,480,928 | ||||
Prepaid expenses | 7,864,496 | 7,889,506 | ||||||
Total Current Assets | 28,210,114 | 34,370,434 | ||||||
Property and equipment, net | 854 | 1,432 | ||||||
Operating lease right-of-use asset, net | 403,996 | 454,426 | ||||||
Other Assets: | ||||||||
Deposits | 38,062 | 38,062 | ||||||
In-process research and development | 59,400,000 | 59,400,000 | ||||||
Goodwill | 9,346,796 | 9,346,796 | ||||||
Total Other Assets | 68,784,858 | 68,784,858 | ||||||
Total Assets | $ | 97,399,822 | $ | 103,611,150 | ||||
LIABILITIES AND STOCKHOLDERS' EQUITY | ||||||||
Current Liabilities: | ||||||||
Accounts payable | $ | 2,647,251 | $ | 2,927,334 | ||||
Accrued expenses | 276,897 | 476,300 | ||||||
Accrued compensation | 2,430,671 | 2,156,983 | ||||||
Operating lease liability | 224,000 | 218,380 | ||||||
Total Current Liabilities | 5,578,819 | 5,778,997 | ||||||
Deferred tax liability | 6,281,800 | 6,137,800 | ||||||
Operating lease liability – noncurrent | 204,569 | 262,865 | ||||||
Total Liabilities | 12,065,188 | 12,179,662 | ||||||
Commitments and Contingencies | ||||||||
Stockholders' Equity: | ||||||||
Preferred stock – | — | — | ||||||
Common stock – | 158,967 | 158,858 | ||||||
Additional paid-in capital | 256,037,851 | 252,903,629 | ||||||
Accumulated deficit | (171,462,564) | (162,231,379) | ||||||
Total Citius Pharmaceuticals, Inc. Stockholders' Equity | 84,734,254 | 90,831,108 | ||||||
Non-controlling interest | 600,380 | 600,380 | ||||||
Total Equity | 85,334,634 | 91,431,488 | ||||||
Total Liabilities and Equity | $ | 97,399,822 | $ | 103,611,150 | ||||
CITIUS PHARMACEUTICALS, INC. CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS FOR THE THREE MONTHS ENDED DECEMBER 31, 2023 AND 2022 (Unaudited) | ||||||||
Three Months Ended | ||||||||
December 31, | December 31, | |||||||
2023 | 2022 | |||||||
Revenues | $ | — | $ | — | ||||
Operating Expenses | ||||||||
Research and development | 2,621,910 | 3,445,515 | ||||||
General and administrative | 3,660,728 | 2,603,287 | ||||||
Stock-based compensation – general and administrative | 3,058,185 | 1,201,081 | ||||||
Total Operating Expenses | 9,340,823 | 7,249,883 | ||||||
Operating Loss | (9,340,823) | (7,249,883) | ||||||
Other Income | ||||||||
Interest income | 253,638 | 214,549 | ||||||
Gain on sale of | — | 3,585,689 | ||||||
Total Other Income | 253,638 | 3,800,238 | ||||||
Loss before Income Taxes | (9,087,185) | (3,449,645) | ||||||
Income tax expense | 144,000 | 144,000 | ||||||
Net Loss | $ | (9,231,185) | $ | (3,593,645) | ||||
Net Loss Per Share - Basic and Diluted | $ | (0.06) | $ | (0.02) | ||||
Weighted Average Common Shares Outstanding | ||||||||
Basic and diluted | 158,955,935 | 146,211,130 | ||||||
CITIUS PHARMACEUTICALS, INC. CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS FOR THE THREE MONTHS ENDED DECEMBER 31, 2023 AND 2022 (Unaudited) | ||||||||
2023 | 2022 | |||||||
Cash Flows From Operating Activities: | ||||||||
Net loss | $ | (9,231,185) | $ | (3,593,645) | ||||
Adjustments to reconcile net loss to net cash used in operating activities: | ||||||||
Stock-based compensation expense | 3,058,185 | 1,201,081 | ||||||
Issuance of common stock for services | 76,146 | — | ||||||
Amortization of operating lease right-of-use asset | 50,430 | 46,457 | ||||||
Depreciation | 578 | 730 | ||||||
Deferred income tax expense | 144,000 | 144,000 | ||||||
Changes in operating assets and liabilities: | ||||||||
Prepaid expenses | 25,010 | (2,577,545) | ||||||
Accounts payable | (280,083) | 372,200 | ||||||
Accrued expenses | (199,403) | (714,992) | ||||||
Accrued compensation | 273,688 | 344,763 | ||||||
Operating lease liability | (52,676) | (47,488) | ||||||
Net Cash Used In Operating Activities | (6,135,310) | (4,824,439) | ||||||
Net Change in Cash and Cash Equivalents | (6,135,310) | (4,824,439) | ||||||
Cash and Cash Equivalents - Beginning of Period | 26,480,928 | 41,711,690 | ||||||
Cash and Cash Equivalents - End of Period | $ | 20,345,618 | $ | 36,887,251 | ||||
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SOURCE Citius Pharmaceuticals, Inc.
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