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Citius Pharmaceuticals, Inc. Reports Fiscal Second Quarter 2026 Financial Results and Provides Business Update

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Citius Pharmaceuticals (Nasdaq: CTXR) reported fiscal Q2 2026 results and a business update for majority-owned Citius Oncology (Nasdaq: CTOR). LYMPHIR generated $1.7M Q2 and $5.6M H1 2026 net revenue at ~80% gross margin, with payer coverage near 100% and 83% of target accounts on or in formulary review.

Citius Pharma held $4.6M cash on March 31, 2026, then raised $5M via a registered direct offering. Citius Oncology arranged up to $36.5M in combined warrant and debt financing. Management expects combined funds to support operations through November 2026. Net loss to common stockholders was $21.2M in Q2 2026, including a $19.7M one-time CMO contract cancellation charge.

The company highlighted initial LYMPHIR shipments to Europe via Uniphar, near-term completion of the U.S. commercial field force, and positive preliminary topline Phase 1 data from two investigator-initiated LYMPHIR combination studies. Engagement with the FDA continues for Mino-Lok and Halo-Lido.

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Positive

  • LYMPHIR H1 2026 net revenue reached $5.6 million at ~80% margin
  • Q2 2026 net product revenue of $1.7 million versus zero a year earlier
  • Near 100% payer coverage and 83% of target accounts on or in formulary review
  • Citius Oncology secured up to $36.5 million in debt and equity financing
  • Citius Pharma raised $5 million in a registered direct offering
  • Management expects funding to support operations through November 2026
  • Positive preliminary topline data from two investigator-initiated Phase 1 LYMPHIR studies
  • Initial shipment of LYMPHIR to Europe across 19 markets via Uniphar
  • R&D expenses declined to $1.6 million in Q2 2026 from $3.8 million year prior
  • Recognized a $3.8 million gain from sale of New Jersey NOLs

Negative

  • Q2 2026 net loss to common stockholders widened to $21.2 million
  • G&A expenses rose to $26.4 million in Q2 2026, including $19.7 million CMO cancellation charge
  • Cash and cash equivalents were $4.6 million as of March 31, 2026
  • Funding runway currently expected only through November 2026
  • Quarter-over-quarter revenue declined due to larger initial distributor orders in Q1 2026
  • Stock-based compensation increased to $3.8 million in Q2 2026 from $2.7 million

News Market Reaction – CTOR

-13.95%
6 alerts
-13.95% News Effect
-4.0% Trough in 9 hr 19 min
-$14M Valuation Impact
$85.04M Market Cap
0.1x Rel. Volume

On the day this news was published, CTOR declined 13.95%, reflecting a significant negative market reaction. Argus tracked a trough of -4.0% from its starting point during tracking. Our momentum scanner triggered 6 alerts that day, indicating moderate trading interest and price volatility. This price movement removed approximately $14M from the company's valuation, bringing the market cap to $85.04M at that time.

Data tracked by StockTitan Argus on the day of publication.

Market Context

The stock dropped -13.9% in the session following this news. A negative reaction despite early LYMPH...
Analysis

The stock dropped -13.9% in the session following this news. A negative reaction despite early LYMPHIR revenue could fit prior earnings patterns, which averaged a -3.99% move and often focused on losses and funding needs. Today’s update combines $1.7 million in quarterly product revenue and $4.6 million in cash with sizeable G&A of $26.4 million and a net loss of $21.2 million. Recent financings, including up to $36.5 million for CTOR, may also raise dilution and leverage concerns.

Key Figures

LYMPHIR net revenue: $5.6 million CTXR offering: $5 million CTOR financing capacity: Up to $36.5 million +5 more
8 metrics
LYMPHIR net revenue $5.6 million First half fiscal 2026 from LYMPHIR launch
CTXR offering $5 million Registered direct offering in April 2026
CTOR financing capacity Up to $36.5 million Combined debt and equity financing for Citius Oncology
Cash balance $4.6 million Cash and cash equivalents as of March 31, 2026
Q2 product revenue $1.7 million Net product revenues for quarter ended March 31, 2026
Q2 gross profit $1.3 million Three months ended March 31, 2026; ~80% gross margin
Q2 R&D expense $1.6 million Three months ended March 31, 2026, down from $3.8M prior year
Q2 G&A expense $26.4 million Three months ended March 31, 2026; includes $19.7M one‑time charge

Previous Earnings Reports

5 past events · Latest: Dec 23 (Negative)
Same Type Pattern 5 events
Date Event Sentiment 24h Move Catalyst
Dec 23 FY25 CTOR results Negative -9.8% Reported FY25 net loss with modest cash and prior strategic financings post‑launch.
Dec 23 FY25 CTXR results Negative -9.8% Parent company reported FY25 net loss despite $61M in financings and LYMPHIR launch.
Aug 12 Q3 2025 earnings Positive +5.9% Q3 2025 results plus new financing to support upcoming LYMPHIR commercial launch.
May 14 Q2 2025 earnings Negative -0.6% Q2 2025 loss, rising R&D and G&A, and disclosure of limited cash needing more capital.
Feb 14 Q1 2025 earnings Negative -5.6% Q1 2025 net loss with low cash while preparing for LYMPHIR launch and raising funds.

24h Move is the share-price change in the day after each event; other market factors may also have contributed.

Pattern Detected

Earnings and financial updates have often been followed by negative price reactions, especially when capital needs and losses were emphasized.

Recent Company History

Over the past year, CTOR’s earnings and financial updates have focused on financing LYMPHIR’s launch and managing losses. In Q2 2025, results highlighted rising R&D and G&A and a need for additional capital. Subsequent quarters, including Q3 2025 and full‑year 2025, showed continued net losses but also incremental financings. Historically, these earnings‑type announcements have averaged a -3.99% move, framing today’s fiscal Q2 2026 update on early LYMPHIR revenues and higher G&A.

Key Terms

registered direct offering, senior secured credit facility, Phase 1, pembrolizumab, +4 more
8 terms
registered direct offering financial
"Citius Pharma raised $5 million in a registered direct offering;"
A registered direct offering is a way for a company to sell new shares of its stock directly to select investors with regulatory approval. This method allows the company to raise funds quickly and efficiently without needing a public auction, similar to offering exclusive access to a limited number of buyers. For investors, it often provides an opportunity to purchase shares at a favorable price, while giving the company immediate access to capital.
senior secured credit facility financial
"financing through its senior secured credit facility with Avenue Capital"
A senior secured credit facility is a loan or revolving line of credit where lenders have first legal claim on specific company assets (collateral) and the debt ranks above other obligations for repayment. For investors it signals where a lender sits in the repayment pecking order and how much protection creditors have if the company struggles, affecting credit costs, the company’s ability to borrow more, and potential recoveries in a default — like a mortgage taking priority over other claims on a house.
Phase 1 medical
"positive preliminary topline Phase 1 data from two investigator-initiated combination studies"
Phase 1 is the first stage of testing a new drug or medical treatment in people, focused primarily on safety, how the body handles the product, and finding a tolerated dose. Think of it as a short, tightly controlled experiment with a small group to check for dangerous side effects before wider testing; for investors it is an early milestone that reduces some uncertainty but still carries high risk and potential for both big value changes and setbacks.
pembrolizumab medical
"combination studies, with pembrolizumab and prior to CAR-T therapy, which reinforce"
A cancer immunotherapy drug that helps the body’s immune system recognize and attack tumor cells by blocking a molecular “brake” that tumors use to hide. Investors watch it because regulatory approvals, clinical trial results, dosing rules, and competition directly affect potential sales, profit forecasts, and the valuation of companies that sell or license the drug—think of trial outcomes as checkpoint signs that can open or close a revenue road.
CAR-T therapy medical
"LYMPHIR administered prior to commercial CD19-directed CAR-T therapy in patients"
CAR-T therapy is a type of medical treatment that uses a patient's own immune cells, specially modified to better recognize and attack cancer cells. For investors, it represents a significant advancement in cancer care, with the potential to transform treatment options and generate substantial demand, making companies involved in its development and production potentially valuable in the healthcare industry.
diffuse large B-cell lymphoma medical
"high-risk relapsed or refractory diffuse large B-cell lymphoma (DLBCL), with positive"
A fast-growing form of blood cancer that starts in white blood cells within the lymphatic system and can spread quickly to other organs. Investors watch it because the need for effective treatments, the size of the patient population, and results from clinical trials or regulatory approvals can significantly affect pharmaceutical and biotech company revenues—think of it like a large, urgent market for new medicines where trial results or approvals can move stock prices.
Named Patient Programs (NPPs) regulatory
"available to eligible patients through Named Patient Programs (NPPs) in accordance"
Named patient programs (NPPs) let doctors obtain medicines that are not yet approved or broadly available for individual patients with urgent or unmet medical needs. Think of it like a doctor getting a special, limited-use supply of a new tool for one patient before it’s sold in stores. For investors, NPPs can reveal early clinical demand and real-world safety experience, but they usually produce limited, irregular revenue and carry regulatory and reputational risks.
formulary regulatory
"83% of LYMPHIR target accounts on formulary or in review"
A formulary is a list of prescription drugs that a health insurer, hospital system, or government program has approved for coverage and payment. Think of it like an approved menu or shopping list that determines which medicines patients can get with financial help. For investors, formulary placement affects a drug maker’s potential sales, pricing power and market access, so being included—or excluded—can materially change a company’s revenue outlook.

AI-generated analysis. How Rhea-AI works. Not financial advice.

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$5.6 Million in net revenue for the first half of fiscal 2026 from ongoing launch of LYMPHIR®

Citius Pharma raised $5 million in a registered direct offering; Citius Oncology secured up to $36.5 million in debt and equity financing

Advanced patient access with payer coverage near 100% of commercial lives and 83% of LYMPHIR target accounts on formulary or in review

CRANFORD, N.J., May 15, 2026 /PRNewswire/ -- Citius Pharmaceuticals, Inc. ("Citius Pharma" or the "Company") (Nasdaq: CTXR), a biopharmaceutical company dedicated to the development and commercialization of first-in-class critical care products, today reported business and financial results for the fiscal second quarter ended March 31, 2026, and provided a business update, including progress at its majority-owned subsidiary, Citius Oncology, Inc. (Nasdaq: CTOR).

"The first half of fiscal 2026 demonstrated meaningful commercial progress at our majority-owned subsidiary Citius Oncology. In the four months of commercial sales since the December 2025 launch of LYMPHIR, Citius Oncology generated $5.6 million in net revenue at approximately 80% gross margins, advanced 83% of target accounts to formulary inclusion or active review, and secured payer coverage representing near 100% of covered commercial lives with no reimbursement denials reported to date. Importantly, major academic centers have begun to transition patients to local community infusion centers for treatment, a critical next phase of commercial scaling. These results reflect our efforts to build a durable patient access foundation upon which to drive growth," said Leonard Mazur, Chairman and Chief Executive Officer of Citius Pharma and Citius Oncology.

"Subsequent to quarter end, Citius Oncology secured up to $36.5 million in combined debt and equity financing through its senior secured credit facility with Avenue Capital and the exercise of outstanding warrants, complemented by Citius Pharma's $5 million registered direct offering. Together, these proceeds are expected to fund Citius Pharma's activities as well as the completion of the LYMPHIR commercial field force buildout by mid-summer. This will support expanded physician engagement and broader market penetration, positioning Citius Oncology to accelerate growth as the launch matures. We believe Citius Oncology maintains sufficient inventory to support anticipated commercial demand, as well as additional demand outside the U.S., as we begin to see orders for product through our global distribution partners."

"Moreover, we are encouraged by positive preliminary topline Phase 1 data from two investigator-initiated combination studies, with pembrolizumab and prior to CAR-T therapy, which reinforce LYMPHIR's potential as a platform asset in combination regimens. At the Citius Pharma level, we also remain focused on advancing Mino-Lok and Halo-Lido with the FDA and on disciplined execution of our mission to bring first-in-class therapies to patients," concluded Mazur.

Fiscal Second Quarter 2026 Business Highlights and Subsequent Developments

  • Reported key commercial metrics of LYMPHIR launch:
    • 83% of target accounts had added or were actively progressing LYMPHIR through formulary review;
    • Secured near 100% of covered commercial lives; no reimbursement denials or prior authorization barriers reported;
    • Initial accounts placing repeat orders;
    • Patients beginning to transition from larger academic cancer centers to community infusion centers;
  • Announced initial shipment of LYMPHIR to Europe on April 29, 2026 through Uniphar, a leading international healthcare services company, with LYMPHIR being made available to eligible patients through Named Patient Programs (NPPs) in accordance with local regulations across 19 markets in Southern Europe, the Middle East, and additional European territories;
  • Announced positive topline results from two investigator-initiated Phase 1 studies, including:
    • LYMPHIR in combination with pembrolizumab in patients with recurrent or refractory gynecologic cancers, including ovarian and endometrial malignancies;
    • LYMPHIR administered prior to commercial CD19-directed CAR-T therapy in patients with high-risk relapsed or refractory diffuse large B-cell lymphoma (DLBCL), with positive topline safety and efficacy results; and,
  • Continued FDA engagement on Mino-Lok®, an antibiotic lock solution to salvage catheters in patients with catheter-related bloodstream infections, and on Halo-Lido (CITI-002), a topical formulation for hemorrhoids.

Fiscal Second Quarter 2026 Financial Highlights and Subsequent Events

  • Cash and cash equivalents of $4.6 million as of March 31, 2026;
  • Citius Pharma closed a $5 million registered direct offering in April 2026;
  • Citius Oncology secured up to $36.5 million in financing subsequent to quarter end, consisting of:
    • $11.5 million in gross proceeds received May 5, 2026 from the exercise of certain outstanding warrants;
    • a loan agreement of up to $25 million from Avenue Capital Group, with $10 million in gross proceeds funded at close on May 6, 2026, and up to $15 million available in subsequent tranches pending certain revenue and liquidity milestones; and,
  • Citius Pharma and Citius Oncology collectively expect to have sufficient funds to continue operations through November 2026;
  • Net product revenues of $1.7 million for the three months ended March 31, 2026, compared to no revenue in the three months ended March 31, 2025, and $5.6 million for the six months ended March 31, 2026, compared to no revenue in the six months ended March 31, 2025; quarter over quarter decline reflects larger initial orders from specialty distributors at launch in the first quarter;
  • Gross profit of $1.3 million for the three months ended March 31, 2026, and $4.5 million for the six months ended March 31, 2026; approximately 80% in both periods, reflecting continued commercial progress since the December 2025 launch of LYMPHIR;
  • R&D expenses of $1.6 million for the three months ended March 31, 2026, compared to $3.8 million for the three months ended March 31, 2025; and $3.2 million for the six months ended March 31, 2026, compared to $5.9 million for the six months ended March 31, 2025. The decrease in both periods primarily reflects reduced clinical development activity, as the prior-year periods included costs for a pre-license inspection batch of LYMPHIR previously manufactured;
  • G&A expenses of $26.4 million for the three months ended March 31, 2026, compared to $4.8 million for the three months ended March 31, 2025, primarily driven by a $19.7 million one-time CMO contract cancellation charge. G&A expenses were $32.1 million for the six months ended March 31, 2026, compared to $10.2 million for the six months ended March 31, 2025;
  • Stock-based compensation expense was $3.8 million for the three months ended March 31, 2026, compared to $2.7 million for the three months ended March 31, 2025. For the six months ended March 31, 2026, stock-based compensation was $8.1 million, compared to $5.2 million for the six months ended March 31, 2025;
  • Recognized a gain of $3.8 million from the sale of New Jersey state net operating losses under the New Jersey Technology Business Tax Certificate Transfer Program; and,
  • Net loss applicable to common stockholders of $21.2 million, or $(0.95) per share, for the three months ended March 31, 2026, compared to $10.9 million, or $(1.27) per share, for the three months ended March 31, 2025; and $29.5 million, or $(1.34) per share, for the six months ended March 31, 2026, compared to $20.7 million, or $(2.58) per share, for the six months ended March 31, 2025.

About Citius Oncology, Inc.

Citius Oncology, Inc. (Nasdaq: CTOR) is a platform to develop and commercialize novel targeted oncology therapies. In December 2025, Citius Oncology launched LYMPHIR, approved by the FDA for the treatment of adults with relapsed or refractory Stage I–III CTCL who had had at least one prior systemic therapy. Management estimates the initial market for LYMPHIR currently exceeds $400 million, is growing, and is underserved by existing therapies. Robust intellectual property protections that span orphan drug designation, complex technology, trade secrets and pending patents for immuno-oncology use as a combination therapy with checkpoint inhibitors would further support Citius Oncology's competitive positioning. For more information, please visit www.citiusonc.com.

About Citius Pharmaceuticals, Inc.

Citius Pharmaceuticals, Inc. (Nasdaq: CTXR) is a biopharmaceutical company dedicated to the development and commercialization of first-in-class critical care products. Citius Pharma owns approximately 71% of Citius Oncology. In December 2025, Citius Oncology launched LYMPHIR, a targeted immunotherapy for the treatment of adults with relapsed or refractory Stage I–III CTCL who had had at least one prior systemic therapy. Citius Pharma's late-stage pipeline also includes Mino-Lok®, a catheter 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 Pharma 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 Pharmaceuticals. 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: our need for substantial additional funds and our ability to raise additional money to fund our operations for at least the next 12 months as a going concern; our ability to obtain, perform under and maintain financing, strategic and third party agreements and relationships, including obtaining a new bulk drug substance supplier; our ability to regain compliance with Nasdaq's continued listing standards; our ability to successfully commercialize LYMPHIR and establish a sustainable revenue stream; the estimated markets for LYMPHIR and our product candidates and the acceptance thereof by any market; our ability to secure strategic partnerships and expand international access to LYMPHIR; our ability to use the latest technology to support our commercialization efforts for LYMPHIR; physician and patient acceptance of LYMPHIR in a competitive treatment landscape; our reliance on third-party logistics providers, distributors, and specialty pharmacies to support commercial operations; our ability to educate providers and payers, secure adequate reimbursement, and maintain uninterrupted product supply; post-marketing requirements and ongoing regulatory compliance related to LYMPHIR; the ability of LYMPHIR and our product candidates to impact the quality of life of our target patient populations; risks relating to the results of research and development activities, including those from any new pipeline assets; our ability to procure cGMP commercial-scale supply; market and other conditions; risks related to our growth strategy; patent and intellectual property matters; government regulation; as well as other risks described in our Securities and Exchange Commission ("SEC") filings. These risks have been and may be further 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 SEC filings which are available on the SEC's website at www.sec.gov, including in Citius Oncology's Annual Report on Form 10-K for the year ended September 30, 2025, filed with the SEC on December 23, 2025 and as amended on January 28, 2026. 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 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)




March 31,



September 30,




2026



2025


ASSETS







Current Assets:







Cash and cash equivalents


$

4,590,174



$

4,252,290


Accounts receivable, net of allowances



1,079,055




-


Inventory



22,659,590




22,286,693


Prepaid expenses



3,356,882




1,395,490


Total Current Assets



31,685,701




27,934,473











Operating lease right-of-use asset, net



794,518




818,694











Deposits



38,062




38,062


In-process research and development, net of accumulated amortization



90,506,250




92,800,000


Deferred financing costs



169,252




-


Goodwill



9,346,796




9,346,796


Total Other Assets



100,060,360




102,184,858











Total Assets


$

132,540,579



$

130,938,025











LIABILITIES AND STOCKHOLDERS' EQUITY









Current Liabilities:









Accounts payable


$

9,453,803



$

13,693,692


License payable



17,650,000




22,650,000


Accrued expenses



24,138,264




4,190,253


Accrued compensation



3,602,007




3,292,447


Note payable



-




1,000,000


Operating lease liability



171,495




88,348


Total Current Liabilities



55,015,569




44,914,740











Deferred tax liability



7,803,790




7,770,760


Operating lease liability – noncurrent



636,667




724,925


Total Liabilities



63,456,026




53,410,425











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; 250,000,000 shares authorized; 22,376,427 and
18,067,744 shares issued and outstanding at March 31, 2026 and September 30,
2025, respectively



22,376




18,068


Additional paid-in capital



329,775,214




306,336,239


Accumulated deficit



(268,256,054)




(238,804,129)


Total Citius Pharmaceuticals, Inc. Stockholders' Equity



61,541,536




67,550,178


Non-controlling interest



7,543,017




9,977,422


Total Equity



69,084,553




77,527,600











Total Liabilities and Equity


$

132,540,579



$

130,938,025


 

CITIUS PHARMACEUTICALS, INC.

CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS

FOR THE THREE AND SIX MONTHS ENDED MARCH 31, 2026 AND 2025

(Unaudited)




Three Months Ended



Six Months Ended




March 31,



March 31,



March 31,



March 31,




2026



2025



2026



2025


Revenues


$

1,667,298



$



$

5,611,409



$


Cost of revenues



(328,878)







(1,118,086)





Gross Profit



1,338,420







4,493,323






















Operating Expenses

















Research and development



1,633,518




3,766,525




3,233,237




5,893,563


Amortization of in-process research and development



1,720,312







2,293,750





General and administrative



26,391,101




4,792,122




32,111,828




10,179,874


Stock-based compensation – general and administrative



3,788,275




2,702,031




8,068,502




5,226,855


Total Operating Expenses



33,533,206




11,260.678




45,707,317




21,300,292



















Operating Loss



(32,194,786)




(11,260,678)




(41,213,994)




(21,300,292)



















Other Income (Expense)

















Interest income



53,584




13,413




98,681




36,021


Gain on sale of New Jersey net operating losses



3,833,277







3,833,277





Interest expense



(33,031)







(188,569)





Total Other Income, Net



3,853,830




13,413




3,743,389




36,021



















Loss before Income Taxes



(28,340,956)




(11,247,265)




(37,470,605)




(21,264,271)


Income tax expense (benefit)



(231,210)




264,240




33,030




528,480



















Net Loss



(28,109,746)




(11,511,505)




(37,503,635)




(21,792,751)


Net loss attributable to non-controlling interest



6,878,606




595,000




8,051,710




1,108,000



















Net loss applicable to common stockholders


$

(21,231,140)



$

(10,916,505)



$

(29,451,925)



$

(20,684,751)



















Net Loss Per Share - Basic and Diluted


$

(0.95)



$

(1.27)



$

(1.34)



$

(2.58)



















Weighted Average Common Shares Outstanding

















Basic and diluted (includes pre-funded warrants from the
October 2025 offering)



22,376,427




8,581,207




21,931,009




8,029,834


 

CITIUS PHARMACEUTICALS, INC.

CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS

FOR THE SIX MONTHS ENDED MARCH 31, 2026 AND 2025

(Unaudited)




2026



2025


Cash Flows From Operating Activities:







Net loss


$

(37,503,635)



$

(21,792,751)


Adjustments to reconcile net loss to net cash used in operating activities:









Stock-based compensation expense



8,068,502




5,226,855


Issuance of common stock for services



107,510




-


Issuance of common stock warrant



68,597




-


Amortization of in-process research and development



2,293,750




-


Amortization (accretion) of operating lease right-of-use asset



24,176




110,845


Deferred income tax expense



33,030




528,480


Changes in operating assets and liabilities:









Accounts receivable, net of allowances



(1,079,055)




-


Inventory



(372,897)




(7,070,487)


Prepaid expenses



(1,961,392)




(308,791)


Accounts payable



(4,239,889)




4,441,023


Accrued expenses



19,948,011




8,762,217


Accrued compensation



309,560




955,048


Operating lease liability



(5,111)




(117,767)


Net Cash Used In Operating Activities



(14,308,843)




(9,265,328)











Cash Flows From Investing Activities:









License fee payments



(5,000,000)





Net Cash Used in Investing Activities



(5,000,000)














Cash Flows From Financing Activities:









Repayment of note payable



(1,000,000)





Deferred financing costs



(169,252)





Proceeds from exercise of Citius Oncology pre-funded warrants



818





Net proceeds from common stock offerings



20,815,161




6,039,858


Net Cash Provided By Financing Activities



19,646,727




6,039,858











Net Change in Cash and Cash Equivalents



337,884




(3,225,470)


Cash and Cash Equivalents - Beginning of Period



4,252,290




3,251,880


Cash and Cash Equivalents - End of Period


$

4,590,174



$

26,410


Supplemental Disclosures of Cash Flow Information and Non-cash Transactions:









Interest paid


$

105,310



$


Operating lease right-of-use asset and liability recorded


$



$

786,697


 

Citius Pharmaceuticals, a late-stage biopharmaceutical company (PRNewsfoto/Citius Pharmaceuticals, Inc.)

Cision View original content to download multimedia:https://www.prnewswire.com/news-releases/citius-pharmaceuticals-inc-reports-fiscal-second-quarter-2026-financial-results-and-provides-business-update-302773890.html

SOURCE Citius Pharmaceuticals, Inc.

FAQ

How much revenue did Citius Oncology (NASDAQ: CTOR) generate from LYMPHIR in fiscal Q2 2026?

Citius Oncology reported $1.7 million in net product revenue for LYMPHIR in fiscal Q2 2026. For the six months ended March 31, 2026, net product revenue totaled $5.6 million, compared with no revenue in the prior-year periods, according to the company.

What were the key LYMPHIR launch metrics for Citius Oncology (CTOR) as of March 31, 2026?

LYMPHIR achieved 83% of target accounts added or in formulary review and near 100% covered commercial lives. According to Citius, no reimbursement denials or prior authorization barriers were reported, and initial accounts were already placing repeat orders for the product.

What financing did Citius Oncology (CTOR) secure in 2026 and how does it affect liquidity?

Citius Oncology secured up to $36.5 million in combined warrant and debt financing in May 2026. This includes $11.5 million from warrant exercises and a loan facility of up to $25 million, which, along with other capital, is expected to fund operations through November 2026.

What was Citius Pharmaceuticals’ net loss and cash position in fiscal Q2 2026?

Citius reported a net loss to common stockholders of $21.2 million in Q2 2026. Cash and cash equivalents were $4.6 million on March 31, 2026, before a subsequent $5 million registered direct offering and Citius Oncology’s additional financings, according to the company.

How is Citius Oncology (CTOR) expanding LYMPHIR internationally in 2026?

Citius announced the first LYMPHIR shipment to Europe on April 29, 2026 through Uniphar. According to the company, LYMPHIR will be available via Named Patient Programs in 19 markets across Southern Europe, the Middle East, and other European territories, subject to local regulations.

What clinical data updates did Citius provide for LYMPHIR in 2026?

Citius reported positive preliminary topline Phase 1 results from two investigator-initiated LYMPHIR combination studies. According to the company, these involved LYMPHIR with pembrolizumab in gynecologic cancers and LYMPHIR before CD19-directed CAR-T therapy in high-risk relapsed or refractory DLBCL.

What is the status of Mino-Lok and Halo-Lido in Citius Pharmaceuticals’ 2026 pipeline?

Citius indicated it is continuing FDA engagement for both Mino-Lok and Halo-Lido during 2026. According to the company, Mino-Lok targets catheter-related bloodstream infections and Halo-Lido is being developed as a topical formulation for hemorrhoids, complementing the LYMPHIR commercial effort.