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UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
FORM 8-K
CURRENT REPORT
Pursuant to Section 13 or 15(d) of
the Securities Exchange Act of 1934
Date of Report (Date of earliest event reported)
August 12, 2024
Citius Pharmaceuticals, Inc.
(Exact name of registrant as specified in its charter)
Nevada
(State or other jurisdiction of incorporation)
001-38174 |
|
27-3425913 |
(Commission File Number) |
|
(IRS Employer Identification No.) |
11 Commerce Drive, 1st Floor, Cranford, NJ |
|
07016 |
(Address of principal executive offices) |
|
(Zip Code) |
Registrant's telephone number, including area
code (908) 967-6677
Check the appropriate box below if the Form 8-K filing is
intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions:
| ☐ | Written
communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425) |
| ☐ | Soliciting
material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12) |
| ☐ | Pre-commencement communications pursuant to
Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b)) |
| ☐ | Pre-commencement communications pursuant to
Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c)) |
Securities registered pursuant to Section 12(b) of the Act:
Title of each class |
|
Trading Symbol(s) |
|
Name
of each exchange on which registered |
Common stock, $0.001 par value |
|
CTXR |
|
The Nasdaq Capital Market |
Indicate by check mark whether the registrant is an
emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§230.405 of this chapter) or Rule 12b-2 of the Securities
Exchange Act of 1934 (§240.12b-2 of this chapter).
Emerging growth company ☐
If an emerging growth company, indicate by check mark
if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards
provided pursuant to Section 13(a) of the Exchange Act. ☐
Item 2.02 Results of Operations and Financial Condition.
On August 12, 2024, we issued a press release
announcing our results of operations for the second quarter of fiscal 2024. A copy of the press release is furnished as Exhibit 99.1 to
this report and is incorporated herein by reference.
The
information in this Item 2.02 (including Exhibit 99.1) shall not be deemed “filed” for purposes of Section 18 of the Securities
Exchange Act of 1934 (the “Exchange Act”) or otherwise subject to the liabilities of that section, nor shall it be deemed
incorporated by reference in any filing under the Securities Act of 1933 or the Exchange Act, except as expressly set forth by specific
reference in such a filing.
Item 9.01. Financial Statements and Exhibits.
(d) Exhibits
104 |
| Cover Page Interactive Date File (embedded within the Inline XBRL document). |
SIGNATURE
Pursuant to the requirements of the Securities
Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.
|
CITIUS PHARMACEUTICALS, INC. |
|
|
Date: August 12, 2024 |
/s/ Leonard Mazur |
|
Leonard Mazur |
|
Chairman and Chief Executive Officer |
2
Exhibit 99.1
Citius Pharmaceuticals, Inc. Reports Fiscal
Third Quarter 2024 Financial Results and Provides Business Update
Granted FDA approval of LYMPHIR™ in treatment
of cutaneous T-cell lymphoma
Completed merger of oncology subsidiary with TenX
Keane; Citius Oncology expected to begin trading on Nasdaq on August 13, 2024 under ticker CTOR
Achieved primary and secondary endpoints of Mino-Lok®
Phase 3 Trial
CRANFORD, N.J., August 12, 2024 -- Citius
Pharmaceuticals, Inc. (“Citius Pharma” or the “Company”) (Nasdaq: CTXR), a late-stage
biopharmaceutical company dedicated to the development and commercialization of first-in-class critical care products today reported
business and financial results for the fiscal third quarter 2024 ended June 30, 2024.
Third Quarter 2024 Business Highlights and
Subsequent Developments
| - | Announced FDA Approval of LYMPHIR™ (denileukin
diftitox-cxdl), an immunotherapy for the treatment of cutaneous T-cell lymphoma (CTCL); |
| - | Completed the merger of our wholly owned subsidiary
with TenX Keane to form publicly listed Citius Oncology, Inc. on August 12, 2024; trading of Citius Oncology, Inc. (Nasdaq: CTOR) stock
expected to begin on August 13, 2024; |
| - | Achieved primary and secondary endpoints in Phase
3 Pivotal Trial of Mino-Lok®, designed to salvage central venous catheters in patients with catheter-related bloodstream
infections; |
| - | Onboarded National Sales Director to recruit
and lead the sales organization in preparation for the anticipated launch of LYMPHIR; |
| - | Continued engagement with the FDA following end
of Phase 2b meeting to determine next steps in the development of Halo-Lido for the treatment of hemorrhoids; and, |
| - | Completed $15 million registered direct offering
in April 2024, extending the Company’s cash runway. |
Financial Highlights
| - | Cash and cash equivalents of $17.9 million as
of June 30, 2024; |
| - | $15 million in gross proceeds from a registered
direct offering on April 30, 2024, extends the Company’s cash runway through December 2024; |
| - | R&D expenses were $2.8 million and $9.0 million
for the three and nine months ended June 30, 2024, respectively, compared to $3.8 million and $11.9 million for the three and nine months
ended June 30, 2023, respectively; |
| - | G&A expenses were $4.8 million and $12.8
million for the three and nine months ended June 30, 2024, respectively, compared to $3.7 million and $11.1 million for the three and
nine months ended June 30, 2023, respectively; |
| - | Stock-based compensation expense was $3.1 million
and $9.2 million for the three and nine months ended June 30, 2024, respectively, compared to $1.2 million and $3.5 million for the three
and nine months ended June 30, 2023, respectively; and, |
| - | Net loss was $10.6 million and $28.7 million,
or ($0.06) and ($0.17) per share for the three and nine months ended June 30, 2024, respectively, compared to a net loss of $8.5 million
and $22.6 million, or ($0.06) and ($0.15) per share for the three and nine months ended June 30, 2023, respectively. |
“We continued to achieve multiple value-driving
milestones during and since the end of the quarter. Last week, LYMPHIR was approved by the FDA for the treatment of a rare and incurable
cancer. This the first FDA-approved product in our portfolio and paves the way for Citius Oncology to transition from a development stage
company to a commercial biopharmaceutical organization,” stated Leonard Mazur, CEO of Citius Pharma and Citius Oncology.
“The completion of our Phase 3 Pivotal Trial
for Mino-Lok, followed by highly statistically significant topline results that met primary and secondary endpoints, further underscores
our commitment to developing life-saving treatments. Operationally, we secured $15 million in additional funding to extend our runway,
continued expanding our organizational resources to support the planned launch of LYMPHIR, and completed the spin-off of this asset into
our majority-owned standalone, publicly traded oncology company. This should provide us with access to a broader investment community
and enable both companies to begin to focus on their respective development and commercialization paths. In addition to the spin-off,
Citius is evaluating opportunities to optimize the Company’s capital allocation, current cash runway, future cash needs, and potential
non-dilutive sources of capital. We believe Citius is poised for a transformative second half of 2024,” concluded Mazur.
THIRD
QUARTER 2024 Financial Results:
Liquidity
As of June 30, 2024, the Company had $17.9 million
in cash and cash equivalents.
As of June 30, 2024, the Company had 158,857,798
common shares outstanding.
Based on our cash and cash equivalents as of June
30, 2024, and after giving effect to a capital raising that closed on April 30, 2024, we expect to have sufficient funds to continue our
operations through December 2024. We expect to identify additional sources of capital in the future to support our operations beyond December
2024.
Research and Development (R&D) Expenses
R&D expenses were $2.8 million for the quarter
ended June 30, 2024, compared to $3.8 million for the quarter ended June 30, 2023. For the nine months ended June 30, 2024, R&D expenses
were $9.0 million as compared to $11.9 million during the nine months ended June 30, 2023, a decrease of $2.9 million. The decrease primarily
reflects incremental costs related to the completion of the Mino-Lok Phase 3 trial and remediation activities for the LYMPHIR BLA resubmission,
offset by lower costs in the current period due to the completion of the Halo-Lido Phase 2b trial.
We expect that research and development expenses
will stabilize at current levels in fiscal 2024 as we focus on the commercialization of LYMPHIR, prepare a submission to the FDA and schedule
a Type B meeting 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 $4.8 million for the quarter
ended June 30, 2024, compared to $3.7 million for the quarter ended June 30, 2023. The increase was primarily due to lower costs for pre-launch
and market research activities associated with LYMPHIR during the period.
For the nine months ended June 30, 2024, G&A
expenses were $12.8 million as compared to $11.1 million during the nine months ended June 30, 2023. The primary reason for the increase
was higher costs for pre-launch and market research activities associated with LYMPHIR.
General and administrative expenses consist primarily
of compensation costs, professional fees for legal, regulatory, accounting, and corporate development services, and investor relations
expenses.
Stock-based Compensation Expense
For the quarter ended June 30, 2024, stock-based
compensation expense was $3.1 million as compared to $1.2 million for the quarter ended June 30, 2023. For the nine months ended June
30, 2024, stock-based compensation expense was $9.2 million as compared to $3.5 million for the nine months ended June 30, 2023. The increase
is primarily due to the Citius Oncology stock plan.
Net loss
Net loss was $10.6 million, or ($0.06) per share for the quarter ended
June 30, 2024, compared to a net loss of $8.5 million, or ($0.06) per share for the quarter ended June 30, 2023. The $2.1 million increase
in the net loss was primarily due to increases of $1.0 million in general and administrative expenses and $1.9 million in stock-based
compensation expense, partially offset by the $1.0 million decrease in research and development expenses.
Net loss was $28.3 million, or ($0.17) per share
for the nine months ended June 30, 2024, compared to a net loss of $22.6 million, or ($0.15) per share for the nine months ended June
30, 2023. The increase in the net loss was primarily due to the increase in stock-based compensation expense.
About Citius Pharmaceuticals, Inc.
Citius Pharmaceuticals, Inc. is a biopharmaceutical
company dedicated to the development and commercialization of first-in-class critical care products. In August 2024, the FDA approved
LYMPHIR, a targeted immunotherapy for an initial indication in the treatment of cutaneous T-cell lymphoma. Citius Pharma’s late-stage
pipeline also includes Mino-Lok®, an antibiotic lock solution to salvage catheters in patients with catheter-related bloodstream infections,
and CITI-002 (Halo-Lido), a topical formulation for the relief of hemorrhoids. A Pivotal Phase 3 Trial for Mino-Lok and a Phase 2b trial
for Halo-Lido were completed in 2023. Mino-Lok met primary and secondary endpoints of its Phase 3 Trial. Citius is actively engaged with
the FDA to outline next steps for both programs. 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, and that apply to Citius Pharma and Citius Oncology as our majority owned subsidiary,
are: the anticipated benefits of the transaction between TenX Keane Acquisition
and Citius Pharma to form Citius Oncology may not be realized fully, if at all, or may take longer to realize than expected; Citius Oncology’s
ability to commercialize LYMPHIR; our need for substantial additional funds; 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; our ability to commercialize our other product candidates 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; 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;
our ongoing businesses which may be adversely affected and subject to certain risks and consequences as a result of the anticipated spinoff
transaction; 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
may be further impacted by any future public health risks or geopolitical events. 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 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 SEC. 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)
| |
June 30, | | |
September 30, | |
| |
2024 | | |
2023 | |
ASSETS | |
| | |
| |
Current Assets: | |
| | |
| |
Cash and cash equivalents | |
$ | 17,911,192 | | |
$ | 26,480,928 | |
Prepaid expenses | |
| 10,094,597 | | |
| 7,889,506 | |
Total Current Assets | |
| 28,005,789 | | |
| 34,370,434 | |
| |
| | | |
| | |
Property and equipment, net | |
| — | | |
| 1,432 | |
Operating lease right-of-use asset, net | |
| 299,932 | | |
| 454,426 | |
Deposits | |
| 38,062 | | |
| 38,062 | |
In-process research and development | |
| 59,400,000 | | |
| 59,400,000 | |
Goodwill | |
| 9,346,796 | | |
| 9,346,796 | |
Total Assets | |
$ | 97,090,579 | | |
$ | 103,611,150 | |
| |
| | | |
| | |
LIABILITIES AND STOCKHOLDERS’ EQUITY | |
| | | |
| | |
Current Liabilities: | |
| | | |
| | |
Accounts payable | |
$ | 1,663,336 | | |
$ | 2,927,334 | |
Accrued expenses | |
| 550,485 | | |
| 476,300 | |
Accrued compensation | |
| 1,702,668 | | |
| 2,156,983 | |
Operating lease liability | |
| 235,581 | | |
| 218,380 | |
Total Current Liabilities | |
| 4,152,070 | | |
| 5,778,997 | |
| |
| | | |
| | |
Deferred tax liability | |
| 6,569,800 | | |
| 6,137,800 | |
Operating lease liability – noncurrent | |
| 84,430 | | |
| 262,865 | |
Total Liabilities | |
| 10,806,300 | | |
| 12,179,662 | |
| |
| | | |
| | |
Commitments and Contingencies | |
| | | |
| | |
| |
| | | |
| | |
Stockholders’ Equity: | |
| | | |
| | |
Preferred stock – $0.001 par value; 10,000,000 shares authorized; no shares issued and outstanding | |
| — | | |
| — | |
Common stock – $0.001 par value; 400,000,000 shares authorized; 180,725,407 and 158,857,798 shares issued and outstanding at June 30, 2024 and September 30, 2023, respectively | |
| 180,725 | | |
| 158,858 | |
Additional paid-in capital | |
| 276,083,228 | | |
| 252,903,629 | |
Accumulated deficit | |
| (190,580,054 | ) | |
| (162,231,379 | ) |
Total Citius Pharmaceuticals, Inc. Stockholders’ Equity | |
| 85,683,899 | | |
| 90,831,108 | |
Non-controlling interest | |
| 600,380 | | |
| 600,380 | |
Total Equity | |
| 86,284,279 | | |
| 91,431,488 | |
Total Liabilities and Equity | |
$ | 97,090,579 | | |
$ | 103,611,150 | |
CITIUS PHARMACEUTICALS, INC.
CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS
FOR THE THREE AND NINE MONTHS ENDED JUNE 30,
2024 AND 2023
(Unaudited)
| |
Three Months Ended | | |
Nine Months Ended | |
| |
June 30, | | |
June 30, | | |
June 30, | | |
June 30, | |
| |
2024 | | |
2023 | | |
2024 | | |
2023 | |
Revenues | |
$ | — | | |
$ | — | | |
$ | — | | |
$ | — | |
| |
| | | |
| | | |
| | | |
| | |
Operating Expenses | |
| | | |
| | | |
| | | |
| | |
Research and development | |
| 2,763,865 | | |
| 3,764,675 | | |
| 8,991,673 | | |
| 11,937,045 | |
General and administrative | |
| 4,808,551 | | |
| 3,733,326 | | |
| 12,755,190 | | |
| 11,129,463 | |
Stock-based compensation – general and administrative | |
| 3,061,763 | | |
| 1,174,111 | | |
| 9,198,340 | | |
| 3,540,787 | |
Total Operating Expenses | |
| 10,634,179 | | |
| 8,672,112 | | |
| 30,945,203 | | |
| 26,607,295 | |
| |
| | | |
| | | |
| | | |
| | |
Operating Loss | |
| (10,634,179 | ) | |
| (8,672,112 | ) | |
| (30,945,203 | ) | |
| (26,607,295 | ) |
| |
| | | |
| | | |
| | | |
| | |
Other Income | |
| | | |
| | | |
| | | |
| | |
Interest income | |
| 204,843 | | |
| 336,780 | | |
| 640,686 | | |
| 854,604 | |
Gain on sale of New Jersey net operating losses | |
| — | | |
| — | | |
| 2,387,842 | | |
| 3,585,689 | |
Total Other Income | |
| 204,843 | | |
| 336,780 | | |
| 3,028,528 | | |
| 4,440,293 | |
| |
| | | |
| | | |
| | | |
| | |
Loss before Income Taxes | |
| (10,429,336 | ) | |
| (8,335,332 | ) | |
| (27,916,675 | ) | |
| (22,167,002 | ) |
Income tax expense | |
| 144,000 | | |
| 144,000 | | |
| 432,000 | | |
| 432,000 | |
| |
| | | |
| | | |
| | | |
| | |
Net Loss | |
| (10,573,336 | ) | |
| (8,479,332 | ) | |
| (28,348,675 | ) | |
| (22,599,002 | ) |
Deemed dividend on warrant extension | |
| 321,559 | | |
| — | | |
| 321,559 | | |
| — | |
| |
| | | |
| | | |
| | | |
| | |
Net Loss Applicable to Common Stockholders | |
$ | (10,894,895 | ) | |
$ | (8,479,332 | ) | |
$ | (28,670,234 | ) | |
$ | (22,599,002 | ) |
| |
| | | |
| | | |
| | | |
| | |
Net Loss Per Share - Basic and Diluted | |
$ | (0.06 | ) | |
$ | (0.06 | ) | |
$ | (0.17 | ) | |
$ | (0.15 | ) |
| |
| | | |
| | | |
| | | |
| | |
Weighted Average Common Shares Outstanding | |
| | | |
| | | |
| | | |
| | |
Basic and diluted | |
| 173,856,960 | | |
| 153,775,380 | | |
| 163,947,311 | | |
| 148,746,002 | |
CITIUS PHARMACEUTICALS, INC.
CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS
FOR THE NINE MONTHS ENDED JUNE 30, 2024 AND
2023
(Unaudited)
| |
2024 | | |
2023 | |
Cash Flows From Operating Activities: | |
| | |
| |
Net loss | |
$ | (28,348,675 | ) | |
$ | (22,599,002 | ) |
Adjustments to reconcile net loss to net cash used in operating activities: | |
| | | |
| | |
Stock-based compensation expense | |
| 9,198,340 | | |
| 3,540,787 | |
Issuance of common stock for services | |
| 284,175 | | |
| 102,000 | |
Amortization of operating lease right-of-use asset | |
| 154,494 | | |
| 142,257 | |
Depreciation | |
| 1,432 | | |
| 2,090 | |
Deferred income tax expense | |
| 432,000 | | |
| 432,000 | |
Changes in operating assets and liabilities: | |
| | | |
| | |
Prepaid expenses | |
| (2,205,091 | ) | |
| (4,979,740 | ) |
Accounts payable | |
| (1,263,998 | ) | |
| 1,914,289 | |
Accrued expenses | |
| 74,185 | | |
| (512,520 | ) |
Accrued compensation | |
| (454,315 | ) | |
| (156,806 | ) |
Operating lease liability | |
| (161,234 | ) | |
| (145,352 | ) |
Net Cash Used In Operating Activities | |
| (22,288,687 | ) | |
| (22,259,997 | ) |
| |
| | | |
| | |
Cash Flows From Financing Activities: | |
| | | |
| | |
Net proceeds from registered direct offering | |
| 13,718,951 | | |
| 13,798,870 | |
Proceeds from common stock option exercise | |
| — | | |
| 31,267 | |
Net Cash Provided By Financing Activities | |
| 13,718,951 | | |
| 13,830,137 | |
| |
| | | |
| | |
Net Change in Cash and Cash Equivalents | |
| (8,569,736 | ) | |
| (8,429,860 | ) |
Cash and Cash Equivalents - Beginning of Period | |
| 26,480,928 | | |
| 41,711,690 | |
Cash and Cash Equivalents - End of Period | |
$ | 17,911,192 | | |
$ | 33,281,830 | |
v3.24.2.u1
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Aug. 12, 2024 |
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Citius Pharmaceuticals, Inc.
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0001506251
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NV
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11 Commerce Drive
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