Citius Pharmaceuticals, Inc. Reports Fiscal Full Year 2021 Financial Results and Provides Business Update
Citius Pharmaceuticals (Nasdaq: CTXR) reported its fiscal year 2021 results, highlighting significant advancements and financial activities. The company completed the subject treatment in the pivotal Phase 3 trial of I/ONTAK and expects topline results in the first half of 2022, with a BLA submission set for the second half. They raised $120.6 million in financing, boosting cash reserves to $70.1 million. However, the net loss increased to $23.1 million, primarily due to rising R&D and G&A expenses. Citius is positioned for growth with a robust pipeline and anticipates multiple milestones in 2022.
- Raised $120.6 million in financing activities, enhancing liquidity.
- Positioned to advance multiple clinical programs and submit BLA for I/ONTAK in 2022.
- Received positive recommendation for Mino-Lok® trial from independent Data Monitoring Committee.
- Net loss increased to $23.1 million from $17.5 million year-over-year.
- Research and Development expenses rose to $12.2 million, impacting financial performance.
- General and Administrative expenses increased by $1.7 million, affecting overall profitability.
CRANFORD, N.J., Dec. 15, 2021 /PRNewswire/ -- Citius Pharmaceuticals, Inc. ("Citius" or the "Company") (Nasdaq: CTXR), a late-stage biopharmaceutical company dedicated to the development and commercialization of first-in-class critical care products with a focus on oncology, anti-infective products in adjunct cancer care, unique prescription products, and stem cell therapies, today reported business and financial results for the fiscal full year ended September 30, 2021.
Fiscal Full Year 2021 Business Highlights and Subsequent Developments
- Completed subject treatment in December 2021 in Pivotal Phase 3 trial of I/ONTAK (E7777) with topline results anticipated in the first half of 2022 and a biologics license application (BLA) submission in the second half of 2022;
- Acquired Dr. Reddy's Laboratories' license for late-Phase 3 oncology immunotherapy I/ONTAK for the treatment of cutaneous T-cell lymphoma (CTCL) and other cancer indications;
- Received third positive recommendation from independent Data Monitoring Committee to continue the Mino-Lok® Phase 3 clinical superiority trial as planned without modifications; no safety concerns identified;
- Completed dose-ranging proof-of-concept sheep study of iPSC-derived novel induced-mesenchymal stem cells (i-MSCs) for the treatment of acute respiratory distress syndrome (ARDS); analysis and documentation underway for peer-reviewed publication submission;
- Expanded clinical, manufacturing and commercial capabilities with the addition of seasoned pharmaceutical executives;
- Citius added to the Russell 3000® and 2000® indexes; and,
- Raised net proceeds of
$120.6 million in financing activities during the year.
Financial Highlights
- Cash and cash equivalents of
$70.1 million as of September 30, 2021; - R&D expenses were
$12.2 million for the full year ended September 30, 2021, compared to$8.8 million for the full year ended September 30, 2020; - G&A expenses were
$9.8 million for the full year ended September 30, 2021, compared to$8.1 million for the full year ended September 30, 2020; - Stock-based compensation expense was
$1.5 million for the full year ended September 30, 2021, compared to$0.8 million for the full year ended September 30, 2020; and, - Net loss was
$23.1 million , or ($0.23) per share for the full year ended September 30, compared to a net loss of$17.5 million , or ($0.45) per share for the full year ended September 30, 2020.
"2021 was a transformative year for Citius as we positioned the company financially and strategically to drive growth. We raised more than
"As we move into 2022, we anticipate multiple positive milestones. These include: accelerated enrollment and completion of the Mino-Lok® trial during the year, topline results in the first half of 2022 for the recently completed I/ONTAK Pivotal Phase 3 trial followed by a BLA submission in the second half of the year, initiation of the Halo-Lido study in early 2022 and completion of the study by the end of the year, and continued progress on Mino-Wrap and our iPSC-derived mesenchymal stem cells for the treatment of acute respiratory distress syndrome (ARDS). With the addition of key personnel to our clinical, manufacturing and commercial teams, we are aligning our resources to ensure continued progress across each of our development programs, and the successful launch of potentially two commercial products in 2023. We believe our strong balance sheet will allow us to execute our development programs as planned in 2022 and we do not anticipate a need to raise additional capital in the coming year," concluded Mr. Holubiak.
Full Year 2021 Financial Results:
Liquidity
As of September 30, 2021, the Company had
In January 2021, the Company closed a private placement for common stock and warrants totaling gross proceeds of approximately
On June 21, 2021, stockholders approved an amendment to the Company's Articles of Incorporation to increase the authorized number of shares from 210,000,000 to 410,000,000 and the authorized number of common shares from 200,000,000 to 400,000,000. As of September 30, 2021, the Company had 145,979,429 common shares issued and outstanding.
In 2021, the Company raised a total of
Research and Development (R&D) Expenses
R&D expenses were
We expect that research and development expenses will increase in fiscal 2022 as we continue to focus on our Phase 3 trial for Mino-Lok®, progress the Halo-Lido product candidate, and continue our research and development efforts related to ARDS, Mino-Wrap and I/ONTAK (E7777).
General and Administrative (G&A) Expenses
G&A expenses were
Stock-based Compensation Expense
For the full year ended September 30, 2021, stock-based compensation expense was
Net loss
Net loss was
About Citius Pharmaceuticals, Inc.
Citius is a late-stage biopharmaceutical company dedicated to the development and commercialization of first-in-class critical care products, with a focus on oncology, anti-infectives in adjunct cancer care, unique prescription products, and stem cell therapies. The Company has two late-stage product candidates, Mino-Lok®, an antibiotic lock solution for the treatment of patients with catheter-related bloodstream infections (CRBSIs), which is currently enrolling patients in a Phase 3 Pivotal superiority trial, and I/ONTAK (E7777), a novel IL-2R immunotherapy for an initial indication in cutaneous T-cell lymphoma (CTCL), which has completed subject treatment in its Pivotal Phase 3 trial. Mino-Lok® was granted Fast Track designation by the U.S. Food and Drug Administration (FDA). I/ONTAK has received orphan drug designation by the FDA for the treatment of CTCL and peripheral T-cell lymphoma (PTCL). Through its subsidiary, NoveCite, Inc., Citius is developing a novel proprietary mesenchymal stem cell treatment derived from induced pluripotent stem cells (iPSCs) for acute respiratory conditions, with a near-term focus on acute respiratory distress syndrome (ARDS). For more information, please visit www.citiuspharma.com.
Safe Harbor
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: risks relating to the results of research and development activities, including those from existing and new pipeline assets; uncertainties relating to preclinical and clinical testing; the early stage of products under development; our ability to successfully undertake and complete clinical trials and the results from those trials for our product candidates; our need for substantial additional funds; our dependence on third-party suppliers; 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 commercialize our products if approved by the FDA; 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 attract, integrate, and retain key personnel; our ability to obtain, perform under and maintain financing and strategic agreements and relationships; our ability to identify, acquire, close and integrate product candidates and companies successfully and on a timely basis; our ability to procure cGMP commercial-scale supply; 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. 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, 2021, filed with the SEC on December 15, 2021 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:
Ilanit Allen
Vice President, Corporate Communications and Investor Relations
T: 908-967-6677 x113
E: iallen@citiuspharma.com
-- Financial Tables Follow –
CITIUS PHARMACEUTICALS, INC. CONSOLIDATED BALANCE SHEETS SEPTEMBER 30, 2021 AND 2020 | ||||||||
2021 | 2020 | |||||||
ASSETS | ||||||||
Current Assets: | ||||||||
Cash and cash equivalents | $ | 70,072,946 | $ | 13,859,748 | ||||
Prepaid expenses | 2,741,404 | 122,237 | ||||||
Total Current Assets | 72,814,350 | 13,981,985 | ||||||
Property and equipment, net | 7,023 | 1,577 | ||||||
Operating lease right-of-use asset, net | 822,828 | 986,204 | ||||||
Other Assets: | ||||||||
Deposits | 38,062 | 57,093 | ||||||
In-process research and development | 59,400,000 | 19,400,000 | ||||||
Goodwill | 9,346,796 | 9,346,796 | ||||||
Total Other Assets | 68,784,858 | 28,803,889 | ||||||
Total Assets | $ | 142,429,059 | $ | 43,773,655 | ||||
LIABILITIES AND STOCKHOLDERS' EQUITY | ||||||||
Current Liabilities: | ||||||||
Accounts payable | $ | 1,277,095 | $ | 1,856,235 | ||||
Accrued expenses | 621,960 | 164,040 | ||||||
Accrued compensation | 1,906,000 | 1,654,919 | ||||||
Accrued interest | — | 89,970 | ||||||
Notes payable – related parties | — | 172,970 | ||||||
Operating lease liability | 177,237 | 158,999 | ||||||
Total Current Liabilities | 3,982,292 | 4,097,133 | ||||||
Note payable – paycheck protection program | — | 164,583 | ||||||
Deferred tax liability | 4,985,800 | 4,985,800 | ||||||
Operating lease liability – non current | 678,234 | 855,471 | ||||||
Total Liabilities | 9,646,326 | 10,102,987 | ||||||
Commitments and Contingencies | ||||||||
Stockholders' Equity: | ||||||||
Preferred stock - | — | — | ||||||
Common stock - | 145,979 | 55,577 | ||||||
Additional paid-in capital | 228,084,195 | 104,208,958 | ||||||
Accumulated deficit | (96,047,821) | (70,593,867) | ||||||
Total Citius Pharmaceuticals, Inc. Stockholders' Equity | 132,182,353 | 33,670,668 | ||||||
Non-controlling interest | 600,380 | — | ||||||
Total Equity | 132,782,733 | 33,670,668 | ||||||
Total Liabilities and Equity | $ | 142,429,059142,587,832 | $ | 43,773,655 | ||||
See accompanying report of independent registered public accounting firm and notes to the consolidated financial statements. | ||||||||
CITIUS PHARMACEUTICALS, INC. CONSOLIDATED STATEMENTS OF OPERATIONS FOR THE YEARS ENDED SEPTEMBER 30, 2021 AND 2020 | ||||||||
2021 | 2020 | |||||||
Revenues | $ | — | $ | — | ||||
Operating Expenses: | ||||||||
Research and development | 12,240,503 | 8,812,810 | ||||||
General and administrative | 9,836,412 | 8,094,614 | ||||||
Stock-based compensation – general and administrative | 1,454,979 | 803,261 | ||||||
Total Operating Expenses | 23,531,894 | 17,710,685 | ||||||
Operating Loss | (23,531,894) | (17,710,685) | ||||||
Other Income (Expense): | ||||||||
Interest income | 261,825 | 68,066 | ||||||
Gain on forgiveness of note payable - Paycheck Protection Program and accrued | 166,557 | |||||||
Other income | 59,917 | 110,207 | ||||||
Interest expense | (10,839) | (15,673) | ||||||
Total Other Income, Net | 477,460 | 162,600 | ||||||
Net Loss | (23,054,434) | (17,548,085) | ||||||
Deemed dividend on warrant extension | 1,450,876 | — | ||||||
Net Loss Applicable to Common Stockholders | $ | (24,505,310) | $ | (17,548,085) | ||||
Net Loss Per Share Applicable to Common Stockholders - Basic and Diluted | $ | (0.23) | $ | (0.45) | ||||
Weighted Average Common Shares Outstanding | ||||||||
Basic and diluted | 108,599,080 | 39,165,248 | ||||||
See accompanying report of independent registered public accounting firm and notes to the consolidated financial statements. | ||||||||
CITIUS PHARMACEUTICALS, INC. CONSOLIDATED STATEMENTS OF CASH FLOWS FOR THE YEARS ENDED SEPTEMBER 30, 2021 AND 2020 | ||||||||
2021 | 2020 | |||||||
Cash Flows From Operating Activities: | ||||||||
Net loss | $ | (23,054,434) | $ | (17,548,085) | ||||
Adjustments to reconcile net loss to net cash used in operating | ||||||||
Stock-based compensation | 1,454,979 | 803,261 | ||||||
Issuance of common stock for services | 68,000 | 528,770 | ||||||
Amortization of operating lease right-of-use asset | 163,376 | 151,520 | ||||||
Depreciation | 1,492 | 844 | ||||||
Gain from forgiveness of notes payable – paycheck protection | (166,557) | — | ||||||
Changes in operating assets and liabilities: | ||||||||
Prepaid expenses | (2,619,167) | (74,126) | ||||||
Deposits | 19,031 | — | ||||||
Accounts payable | (579,140) | (857,307) | ||||||
Accrued expenses | 457,920 | (82,185) | ||||||
Accrued compensation | 251,081 | 254,231 | ||||||
Accrued interest | (87,996) | 15,673 | ||||||
Operating lease liability | (158,999) | (123,254) | ||||||
Net Cash Used In Operating Activities | (24,250,414) | (16,930,658) | ||||||
Cash Flows From Investing Activities: | ||||||||
Purchase of property and equipment | (6,938) | (1,831) | ||||||
Purchase of in-process research and development | (40,000,000) | — | ||||||
Net Cash Used In Investing Activities | (40,006,938) | (1,831) | ||||||
Cash Flows From Financing Activities: | ||||||||
Proceeds from notes payable – paycheck protection program | — | 164,583 | ||||||
Principal paid on notes payable – related parties | (172,970) | — | ||||||
Proceeds from sale of NoveCite, Inc. common stock | 500 | — | ||||||
Proceeds from common stock warrant exercises | 31,130,134 | 7,156,549 | ||||||
Proceeds from common stock option exercises | 82,634 | — | ||||||
Net proceeds from underwritten offerings | — | 8,700,201 | ||||||
Net proceeds from private placement | 18,450,410 | — | ||||||
Net proceeds from registered direct offerings | 70,979,842 | 6,877,100 | ||||||
Net Cash Provided By Financing Activities | 120,470,550 | 22,898,433 | ||||||
Net Change in Cash and Cash Equivalents | 56,213,198 | 5,965,944 | ||||||
Cash and Cash Equivalents – Beginning of Year | 13,859,748 | 7,893,804 | ||||||
Cash and Cash Equivalents – End of Year | $ | 70,072,946 | $ | 13,859,748 | ||||
Supplemental Disclosures of Cash Flow Information and | ||||||||
Operating lease right-of-use asset and liability recorded upon | $ | — | $ | 1,137,724 | ||||
See accompanying report of independent registered public accounting firm and notes to the consolidated financial statements. | ||||||||
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SOURCE Citius Pharmaceuticals, Inc.
FAQ
What financial results did Citius Pharmaceuticals report for the fiscal year ended September 30, 2021?
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