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

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Citius Oncology (Nasdaq: CTOR) reported fiscal Q2 2026 results and a business update. LYMPHIR® generated $1.7 million in quarterly and $5.6 million in first-half 2026 net revenue at ~80% gross margins. About 83% of target accounts have LYMPHIR on formulary or in review, with near 100% commercial payer coverage and no reimbursement denials.

The company held $2.6 million in cash at March 31, 2026, then secured up to $36.5 million in combined debt and equity in May. A one-time $19.7 million CMO contract cancellation drove G&A higher and contributed to a $26.6 million quarterly net loss.

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Positive

  • First-half 2026 LYMPHIR net revenue of $5.6 million at ~80% margin
  • Q2 2026 LYMPHIR net revenue of $1.7 million versus no revenue year-ago
  • Up to $36.5 million in new debt and equity financing in May 2026
  • Near 100% commercial payer coverage and no LYMPHIR reimbursement denials
  • 83% of target accounts have LYMPHIR on formulary or in review
  • $22.7 million of LYMPHIR inventory to support anticipated demand
  • Net operating loss sale generated a $1.76 million gain

Negative

  • Q2 2026 net loss of $26.6 million, up from $7.7 million
  • Six-month 2026 net loss of $32.1 million, up from $14.4 million
  • G&A expenses rose to $23.6 million on $19.7 million CMO cancellation
  • Cash and equivalents only $2.6 million at March 31, 2026 pre-financing
  • Company expects combined funds support operations only through November 2026

News Market Reaction – CTOR

-13.95%
6 alerts
-13.95% Session close to close
-4.0% Trough in 9 hr 19 min
$85.04M Market Cap
0.1x Rel. Volume

In the May 18 session, 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.

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 commercial ...
Analysis

The stock dropped -13.9% in the session following this news. A negative reaction despite commercial progress would fit CTOR’s history of earnings updates coinciding with downside moves, averaging -3.99%. The quarter combined early LYMPHIR revenue and strong 80% margins with a $26.6 million net loss and low quarter-end cash before May financings. That mix of growth and funding needs, plus a large CMO cancellation charge, has previously weighed on sentiment following financial disclosures.

Key Figures

Net product revenue: $5.6 million Quarterly revenue: $1.7 million Gross margin: 80% +5 more
8 metrics
Net product revenue $5.6 million First six months of fiscal 2026 since LYMPHIR launch
Quarterly revenue $1.7 million Net product revenues for three months ended March 31, 2026
Gross margin 80% Gross margins on LYMPHIR net revenue in first half fiscal 2026
Cash & equivalents $2.6 million Balance as of March 31, 2026 before May financings
Debt & equity financing Up to $36.5 million Combined capital secured in early May 2026
Term loan facility Up to $25 million Senior secured term loan capacity from Avenue Capital Group
Net loss $26.6 million Three months ended March 31, 2026
Inventory $22.7 million Finished goods and WIP as of March 31, 2026

Previous Earnings Reports

5 past events · Latest: Dec 23 (Negative)
Same Type Pattern 5 events
Date Event Sentiment 24h Move Catalyst
Dec 23 FY25 results Negative -9.8% Reported FY25 loss and low cash alongside LYMPHIR launch update.
Dec 23 Parent FY25 results Negative -9.8% Parent company FY25 loss despite LYMPHIR launch and prior financings.
Aug 12 Q3 2025 earnings Positive +5.9% Quarterly loss but additional financing to support upcoming LYMPHIR launch.
May 14 Q2 2025 earnings Negative -0.6% Higher net loss and disclosure of need for additional capital post-approval.
Feb 14 Q1 2025 earnings Negative -5.6% Ongoing losses with low cash while preparing LYMPHIR commercial launch.

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

Pattern Detected

Earnings-related releases have often coincided with downside moves, with an average same-day move of about -3.99% and multiple prior fiscal updates trading lower shortly after publication.

Recent Company History

Over the past year, CTOR’s key events have centered on LYMPHIR’s path from pre-launch to commercialization and the financing needed to support it. Prior earnings updates in 2025 highlighted low cash balances, recurring net losses, and repeated capital raises, with share reactions often negative (e.g., -9.84% after FY25 results). Some quarters, like fiscal Q3 2025, paired higher losses with new funding and saw a modest gain. Today’s earnings fit into this pattern of balancing commercial progress with continued operating losses and financing needs.

Key Terms

t-regulatory cell (treg), car-t therapy, diffuse large b-cell lymphoma (dlbcl), named patient programs (npps), +3 more
7 terms
t-regulatory cell (treg) medical
"including its T-regulatory cell (Treg) depletion mechanism"
A T-regulatory cell (Treg) is a type of white blood cell that acts like the immune system’s brakes, damping down other immune cells to prevent excessive or misdirected attacks. For investors, Tregs matter because drugs that increase or suppress their activity can treat conditions where the immune system is too aggressive (the body attacking itself), help prevent transplant rejection, or affect cancer immunotherapies—outsized outcomes that can shift biotech valuations.
car-t therapy medical
"LYMPHIR administered prior to CAR-T therapy in patients with high-risk"
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 (dlbcl) medical
"relapsed or refractory diffuse large B-cell lymphoma (DLBCL)"
Diffuse large B‑cell lymphoma (DLBCL) is an aggressive cancer of the immune system in which a type of white blood cell grows quickly and forms tumors in lymph nodes and other tissues; think of it like a fast‑spreading weed in the body’s infection‑fighting system. It matters to investors because the disease’s incidence, treatment options, clinical trial results, and regulatory approvals can directly affect the revenues and valuations of drugmakers, hospitals, and diagnostic companies tied to cancer therapies.
named patient programs (npps) regulatory
"available through Named Patient Programs (NPPs) per local regulations"
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.
ai-powered machine learning platform technical
"deployment of a proprietary AI-powered machine learning platform"
An ai-powered machine learning platform is a software system that uses automated learning algorithms to find patterns in large volumes of data, make predictions, and improve over time without explicit reprogramming. For investors, it matters because such platforms can speed up decision-making, reduce costly manual analysis, and create scalable advantages—think of it as a smart assistant that gets better with use and can increase a company’s efficiency, product value, or competitive edge.
bulk drug substance (bds) technical
"evaluation of new bulk drug substance (BDS) suppliers"
Bulk drug substance (BDS) is the raw active ingredient that gives a medicine its therapeutic effect, produced in large quantities before it is mixed with fillers and packaged as a finished drug. For investors, BDS matters because its cost, quality control, manufacturing capacity and regulatory approval directly affect a drug maker’s ability to supply products, generate revenue and face risks from shortages or compliance problems—like a factory’s central component for a final consumer good.
contract manufacturing organization (cmo) technical
"letter of intent with a new contract manufacturing organization (CMO)"
An outside company hired to manufacture, package and often test pharmaceutical drugs or medical products for another company, handling the physical production instead of the product owner. For investors, CMOs matter because they determine whether a product can be made at the right quality, scale and cost—think of them as a hired factory whose reliability and efficiency can directly affect timing, expenses and the commercial success of a medical product.

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 as LYMPHIR® launch progresses
Up to $36.5 million in debt and equity capital secured
Broad payer coverage established with no reimbursement denials
83% of target accounts on formulary or in review

CRANFORD, N.J., May 15, 2026 /PRNewswire/ -- Citius Oncology, Inc. ("Citius Oncology" or the "Company") (Nasdaq: CTOR), the oncology-focused subsidiary of Citius Pharmaceuticals, Inc. ("Citius Pharma") (Nasdaq: CTXR), today reported financial results for the fiscal second quarter ended March 31, 2026, and provided a business update.

"LYMPHIR's commercial launch gives us confidence in the trajectory ahead. In the first six months of fiscal 2026, which includes only four months of commercial sales since LYMPHIR's December 2025 launch, we generated $5.6 million in net revenue at gross margins of approximately 80%. This reflects initial orders by distributors during the first quarter, and subsequent reorders during the second quarter as we begin to see increased institutional demand for the therapy. As leading medical centers continue to add LYMPHIR to formulary and we build out our sales force, we believe we are moving through the expected transition from initial channel fill to sustained treatment-driven demand. We have achieved strong institutional penetration for a newly launched specialty therapy, with 83% of our target accounts having added LYMPHIR or actively progressing it through formulary review. Payer coverage has expanded to near 100% of covered commercial lives, with no reimbursement denials reported to date," said Leonard Mazur, Chairman and Chief Executive Officer of Citius Oncology and Citius Pharma.

"With market access efforts underway, our focus is on establishing LYMPHIR's position in the CTCL treatment journey. The financing we secured, subsequent to quarter end, is the catalyst that provides us with resources to complete the buildout of our commercial field force. We expect to have the full commercial team deployed by mid-summer. We have ample finished goods and work-in-process inventory on hand to support anticipated commercial demand for the foreseeable future. A fully staffed sales organization, reinforced by broad market access and sufficient inventory to support anticipated demand, is how we plan to drive continued momentum. The fundamentals of a successful specialty pharmaceutical launch, which include strong formulary and payer access, a funded commercial buildout, and healthy margins, are all moving in the right direction," added Mazur.

"Building on the commercial foundation we are establishing in the U.S., we have initiated our first European shipment as part of the international distribution agreements we have in place across 19 markets in Southern Europe, the Middle East, and additional Western and Eastern European territories. At the same time, we continue to strengthen LYMPHIR's long-term value proposition through our support of clinical evidence generation. Recent preliminary topline Phase 1 investigator-initiated trial data reinforce the immuno-oncology rationale for LYMPHIR in combination settings, including its T-regulatory cell (Treg) depletion mechanism, and we look forward to additional data readouts in the future. Together, these execution milestones and data-driven catalysts reinforce our view that LYMPHIR can be developed beyond U.S. CTCL as a platform asset in combination regimens. We look forward to sharing continued positive momentum as LYMPHIR establishes itself as a meaningful new option in the treatment of relapsed or refractory CTCL, and we remain confident in its broader long-term commercial potential," concluded Mazur.

Fiscal Second Quarter 2026 Business Highlights and Subsequent Developments

  • Advanced formularly inclusion with 83% of target accounts having added or actively progressing LYMPHIR through formulary review;
  • Secured near 100% of covered commercial lives; no reimbursement denials or prior authorization barriers reported;
  • Initiated community infusion center penetration, with patients beginning to transition from larger academic cancer centers, a critical next phase of commercial scaling;
  • Initiated shipment of LYMPHIR to Europe, with LYMPHIR being made available through Named Patient Programs (NPPs) per local regulations;
  • Continued deployment of a proprietary AI-powered machine learning platform to support targeted physician engagement and efficient penetration of the highly concentrated CTCL prescriber base;
  • Recruited and trained initial field sales team, with expanded field force recruitment underway;
  • Announced positive topline results from two investigator-initiated Phase 1 studies evaluating LYMPHIR in combination settings, including:
    • Phase 1 trial of LYMPHIR in combination with pembrolizumab (KEYTRUDA®) in patients with recurrent or refractory gynecologic cancers, including ovarian and endometrial malignancies;
    • Phase 1 trial of LYMPHIR administered prior to 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,
  • Initiated evaluation of new bulk drug substance (BDS) suppliers with letter of intent with a new contract manufacturing organization (CMO) expected by the end of June 2026; $22.7 million of finished goods and work-in-process inventory as of March 31, 2026 to support anticipated commercial demand during the transition;

Fiscal Second Quarter 2026 Financial Highlights and Subsequent Developments

  • Cash and cash equivalents of $2.6 million as of March 31, 2026, prior to the up to $36.5 million concurrent debt and equity financings that closed in early May 2026;
  • Secured up to $36.5 million in combined financing subsequent to quarter end, consisting of:
    • a senior secured term loan facility of up to $25 million from Avenue Venture Opportunities Fund II, L.P. (Avenue Capital Group), with $10 million funded at close on May 6, 2026, up to $7 million available beginning October 1, 2026 subject to revenue and liquidity milestones, and up to $8 million available beginning January 1, 2027 subject to additional revenue milestones; and,
    • approximately $11.5 million in gross proceeds received May 5, 2026 from the exercise of certain outstanding warrants; and,
  • Net product revenues of $1.7 million for the three months ended March 31, 2026, compared to no revenue for the three months ended March 31, 2025; and $5.6 million for the six months ended March 31, 2026, compared to no revenue for the six months ended March 31, 2025;
  • Gross profit of $1.3 million (80% margin) for the three months ended March 31, 2026, and $4.5 million (80% margin) for the six months ended March 31, 2026;
  • R&D expenses of $1.1 million for the three months ended March 31, 2026, compared to $3.1 million for the three months ended March 31, 2025; and $2.1 million for the six months ended March 31, 2026, compared to $4.4 million for the six months ended March 31, 2025;
  • G&A expenses of $23.6 million for the three months ended March 31, 2026, compared to $2.2 million for the three months ended March 31, 2025, primarily driven by the $19.7 million one-time CMO contract cancellation charge. G&A expenses were $26.5 million for the six months ended March 31, 2026, compared to $5.6 million for the six months ended March 31, 2025;
  • Stock-based compensation expense of $3.5 million for the three months ended March 31, 2026, compared to $2.1 million for the three months ended March 31, 2025; and $7.5 million for the six months ended March 31, 2026, compared to $3.9 million for the six months ended March 31, 2025;
  • Recognized a gain of $1.76 million from the sale of New Jersey state net operating losses under the New Jersey Technology Business Tax Certificate Transfer Program; and,
  • Net loss of $26.6 million for the three months ended March 31, 2026, compared to a net loss of $7.7 million for the three months ended March 31, 2025; and a net loss of $32.1 million for the six months ended March 31, 2026, compared to a net loss of $14.4 million for the six months ended March 31, 2025.

Fiscal Second Quarter 2026 Financial Results:

Liquidity

As of March 31, 2026, the Company had $2.6 million in cash and cash equivalents.

Subsequent to quarter end, on May 5, 2026, the Company received approximately $11.5 million in gross proceeds from the exercise of certain outstanding warrants, and on May 6, 2026, the Company funded $10 million in gross proceeds under the first tranche of a senior secured term loan facility with Avenue Capital Group providing access to up to $25 million in total gross proceeds.

We plan to continue to partially rely on funding from Citius Pharma, to raise capital through equity and debt financings, and to generate revenue from sales of LYMPHIR. We also have retained Jefferies LLC as our exclusive financial advisor in evaluating strategic alternatives aimed at maximizing shareholder value.

After giving effect to the May 2026 equity and debt financings, we expect that Citius Oncology and Citius Pharma collectively will have sufficient funds to continue operations through November 2026.   

Net Revenue

Net product revenues were $1.7 million for the three months ended March 31, 2026, compared to no revenue for the three months ended March 31, 2025. For the six months ended March 31, 2026, net product revenues were $5.6 million, compared to no revenue for the six months ended March 31, 2025.

The Company launched LYMPHIR in December 2025. The quarterly decrease in product revenues is primarily attributable to larger initial orders in the quarter ended December 31, 2025, as US distributors established their initial inventories. We believe that revenues will increase in the future as LYMPHIR gains market acceptance and initial accounts continue placing repeat orders. At the end of April 2026, we announced an initial shipment of LYMPHIR to Europe.

Research and Development (R&D) Expenses

R&D expenses were $1.1 million for the three months ended March 31, 2026, compared to $3.1 million for the three months ended March 31, 2025, a decrease of $2.0 million. For the six months ended March 31, 2026, R&D expenses were $2.1 million, compared to $4.4 million for the six months ended March 31, 2025, a decrease of $2.3 million. 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.

General and Administrative (G&A) Expenses

G&A expenses were $23.6 million for the three months ended March 31, 2026, compared to $2.2 million for the three months ended March 31, 2025, an increase of $21.4 million. For the six months ended March 31, 2026, G&A expenses were $26.5 million, compared to $5.5 million for the six months ended March 31, 2025, an increase of $21.9 million. The increase in both periods was primarily driven by a $19.7 million one-time contract cancellation charge related to the CMO termination recognized in March 2026.

Stock-based Compensation Expense

Stock-based compensation expense was $3.5 million for the three months ended March 31, 2026, compared to $2.1 million for the three months ended March 31, 2025. For the six months ended March 31, 2026, stock-based compensation was $7.5 million, compared to $3.9 million for the six months ended March 31, 2025.

Net Loss

Net loss was $26.6 million for the three months ended March 31, 2026, compared to $7.7 million for the three months ended March 31, 2025, an increase of $18.9 million. For the six months ended March 31, 2026, net loss was $32.1 million, compared to $14.4 million for the six months ended March 31, 2025, an increase of $17.7 million. The increase in net loss for the three-month period was primarily attributable to the $19.7 million CMO contract cancellation charge, partially offset by $1.7 million in LYMPHIR revenues and the $1.76 million gain on the sale of New Jersey net operating losses.

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 Oncology. 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. 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 ONCOLOGY, INC.

CONDENSED CONSOLIDATED BALANCE SHEETS

(Unaudited)




March 31,
2026



September 30,
2025


Current Assets:







Cash and cash equivalents


$

2,632,634



$

3,924,908


Accounts receivable, net of allowances



1,079,055





Inventory



22,659,590




22,286,693


Prepaid expenses



3,052,387




1,331,280


Total Current Assets



29,423,666




27,542,881











Other Assets:









In-process research and development, net of accumulated amortization



71,106,250




73,400,000


Deferred financing costs



169,252





Total Other Assets



71,275,502




73,400,000











Total Assets


$

100,699,168



$

100,942,881


LIABILITIES AND STOCKHOLDERS' EQUITY









Current Liabilities:









Accounts payable


$

8,883,239



$

13,234,684


License payable



17,650,000




22,650,000


Accrued expenses



24,057,573




4,093,124


Due to related party



8,221,486




9,513,771


Total Current Liabilities



58,812,298




49,491,579











Deferred tax liability



2,817,990




2,784,960


Note payable to related party



3,800,111




3,800,111


Total Liabilities



65,430,399




56,076,650


Stockholders' Equity:









Preferred stock - $0.0001 par value; 10,000,000 shares authorized: no shares issued
     and outstanding







Common stock - $0.0001 par value; 400,000,000 shares authorized at March 31,
     2026 and September 30, 2025; 92,981,204 and 83,513,442 shares issued and
     outstanding at March 31, 2026 and September 30, 2025, respectively



9,298




8,351


Additional paid-in capital



131,443,191




108,897,836


Accumulated deficit



(96,183,720)




(64,039,956)


Total Stockholders' Equity



35,268,769




44,866,231


Total Liabilities and Stockholders' Equity


$

100,699,168



$

100,942,881


 

CITIUS ONCOLOGY, 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



1,079,354




3,139,413




2,097,706




4,403,921


Amortization of in-process research and development



1,720,312







2,293,750





General and administrative



23,625,639




2,243,327




26,484,978




5,565,306


Stock-based compensation – general and administrative



3,526,710




2,088,572




7,482,760




3,897,050


Total Operating Expenses



29,952,015




7,471,312




38,359,194




13,866,277



















Operating Loss



(28,613,595)




(7,471,312)




(33,865,871)




(13,866,277)



















Other Income (Expense)

















Interest income



43,721







72,009





Gain on sale of New Jersey net operating losses



1,762,000







1,762,000





Interest expense



(33,031)







(78,872)





Total Other Income



1,772,690







1,755,137






















Loss before Income Taxes



(26,840,905)




(7,471,312)




(32,110,734)




(13,866,277)


Income tax expense (benefit)



(231,210)




264,240




33,030




528,480



















Net Loss


$

(26,609,695)



$

(7,735,552)



$

(32,143,764)



$

(14,394,757)



















Net Loss Per Share - Basic and Diluted


$

(0.27)



$

(0.11)



$

(0.34)



$

(0.20)



















Weighted Average Common Shares Outstanding

















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



100,027,204




71,552,402




93,657,757




71,552,402


 

CITIUS ONCOLOGY, 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


$

(32,143,764)



$

(14,394,757)


Adjustments to reconcile net loss to net cash provided by operating activities:









Stock-based compensation expense



7,482,760




3,897,050


Amortization of in-process research and development



2,293,750




-


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



(1,721,107)




-


Accounts payable



(4,351,445)




3,964,688


Accrued expenses



19,964,449




8,722,168


Due to related party



(1,292,285)




4,352,858


Net Cash (Used In) Provided By Operating Activities



(11,186,564)




-


Cash Flows From Investing Activities









    License payments



(5,000,000)




-


Net Cash Used In Investing Activities



(5,000,000)




-


Cash Flows From Financing Activities









    Deferred financing costs



(169,252)




-


    Net proceeds from issuance of common stock



15,063,542




-


Net Cash Provided by Financing Activities



14,894,290




-


Net Change in Cash and Cash Equivalents



(1,292,274)




-


Cash and Cash Equivalents – Beginning of Period



3,924,908




112


Cash and Cash Equivalents – End of Period


$

2,632,634



$

112


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









Interest Paid


$

14,460



$

-


 

Cision View original content to download multimedia:https://www.prnewswire.com/news-releases/citius-oncology-inc-reports-fiscal-second-quarter-2026-financial-results-and-provides-business-update-302773892.html

SOURCE Citius Oncology, Inc.

FAQ

How did Citius Oncology (CTOR) perform financially in Q2 2026?

Citius Oncology reported a Q2 2026 net loss of $26.6 million. According to Citius Oncology, net product revenue was $1.7 million, gross profit was $1.3 million at an 80% margin, and higher G&A expenses were driven by a $19.7 million CMO cancellation charge.

What LYMPHIR revenue did Citius Oncology (CTOR) report for the first half of fiscal 2026?

Citius Oncology generated $5.6 million in net product revenue for the first half of fiscal 2026. According to Citius Oncology, this reflects about four months of commercial LYMPHIR sales since its December 2025 launch, with approximately 80% gross margins supported by distributor orders and reorders.

What financing did Citius Oncology (CTOR) secure in May 2026 and how much capital is available?

Citius Oncology secured up to $36.5 million in combined debt and equity financing in May 2026. According to Citius Oncology, this includes a senior secured term loan facility of up to $25 million and approximately $11.5 million in gross proceeds from warrant exercises completed on May 5, 2026.

What is Citius Oncology’s (CTOR) cash runway after the Q2 2026 financings?

Citius Oncology expects sufficient funds to operate through November 2026 when combined with Citius Pharma. According to Citius Oncology, this outlook reflects March 31, 2026 cash of $2.6 million, May 2026 equity and debt financings, and continued reliance on LYMPHIR revenues and Citius Pharma funding.

How advanced is LYMPHIR market access and formulary coverage for Citius Oncology (CTOR)?

LYMPHIR has achieved broad market access and strong institutional penetration. According to Citius Oncology, about 83% of target accounts have added or are reviewing LYMPHIR for formulary inclusion, and commercial payer coverage has expanded to near 100% of covered lives with no reimbursement denials reported.

What were the key drivers of higher expenses for Citius Oncology (CTOR) in Q2 2026?

Higher Q2 2026 expenses were mainly due to a one-time contract charge. According to Citius Oncology, G&A expenses rose to $23.6 million, primarily from a $19.7 million CMO contract cancellation recognized in March 2026, alongside increased stock-based compensation versus the prior-year period.

What clinical and international expansion updates did Citius Oncology (CTOR) provide for LYMPHIR?

Citius Oncology reported initial European LYMPHIR shipments and positive Phase 1 combination data. According to Citius Oncology, LYMPHIR is being supplied through Named Patient Programs in multiple markets and showed positive topline results in investigator-initiated trials in gynecologic cancers and high-risk relapsed or refractory DLBCL.