STOCK TITAN

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

(Positive)
Tags

Citius Oncology (Nasdaq: CTOR) reported fiscal Q3 2026 results highlighted by initial LYMPHIR® commercialization. Revenue reached $1.5 million for the quarter and $7.1 million for the nine months ended June 30, 2026, versus no revenue a year earlier, generating gross profit of $1.0 million and $5.5 million, respectively.

Institutional demand for LYMPHIR continued to build, with vial orders from prescribing centers up 31% sequentially (926 vs. 708) and 44 institutions having ordered since launch. The company reported near-universal payer coverage and expanded its commercial and medical affairs field force to 29 professionals. Cash and equivalents totaled $16.6 million, supported by $9.7 million in warrant exercises and funding of $10.0 million from the first tranche of a $25.0 million term loan. CTOR recorded a Q3 net loss of $8.9 million and a nine‑month net loss of $41.1 million, driven largely by commercial build‑out and a one‑time $19.7 million CMO contract cancellation charge.

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Positive

  • Q3 2026 revenue $1.5M; nine‑month revenue $7.1M versus zero in 2025
  • Institutional LYMPHIR demand up 31% QoQ to 926 vials; 44 institutions ordered
  • Near‑universal LYMPHIR payer coverage with no reported reimbursement denials
  • Cash and equivalents at June 30, 2026 of $16.6 million
  • $9.7 million net proceeds from warrant exercises plus $10.0 million term loan funding
  • R&D expenses reduced to $2.3 million for nine months from $5.3 million prior year

Negative

  • Net loss of $8.9 million in Q3 and $41.1 million for nine months
  • Nine‑month G&A of $30.7 million, including $19.7 million one‑time CMO contract cancellation
  • Net cash used in operating activities of $13.9 million for nine months ended June 30, 2026
  • Total liabilities increased to $71.7 million from $56.1 million at September 30, 2025
  • License payments used $7.0 million of cash in investing activities

News Explained

As of June 30, 2026, reported common shares outstanding were 105,758,982, versus 83,513,442 at September 30, 2025; under the supplied dilution definition, additional shares reduce existing holders’ percentage ownership absent offsetting changes.

Market reaction after 3Q26 earnings report: CTOR -17.58%

-17.58% $0.75 5.2x vol
15m delay
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$0.75 Last Price
$0.72 $0.93 Day Range
$68.44M Market Cap
5.2x Rel. Volume

Following this news, CTOR has declined 17.58%, reflecting a significant negative market reaction. Our momentum scanner has triggered 14 alerts so far, indicating notable trading interest and price volatility. The stock is currently trading at $0.75. Trading volume is exceptionally heavy at 5.2x the average, suggesting significant selling pressure.

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Market Context

The active S-3 resale registration covers up to 32,931,482 shares for selling stockholders. The plat...
Analysis

The active S-3 resale registration covers up to 32,931,482 shares for selling stockholders. The platform record adds a capital-structure consideration to improving LYMPHIR demand, while quarterly losses remain a reported risk.

Key Figures

Nine-month revenue: $7.1 million Quarterly revenue: $1.5 million Cash and equivalents: $16.6 million +5 more
8 metrics
Nine-month revenue $7.1 million first nine months of fiscal 2026
Quarterly revenue $1.5 million three months ended June 30, 2026
Cash and equivalents $16.6 million as of June 30, 2026
Quarterly net loss $8.9 million three months ended June 30, 2026
Institutional vial-order growth 31% sequentially, quarter ended June 30, 2026 versus March 31, 2026
Ordering institutions 44 institutions since LYMPHIR launch
Objective response rate 86% ORR Phase 1 LYMPHIR study before CAR-T therapy in DLBCL
Complete response rate 57% CR Phase 1 LYMPHIR study before CAR-T therapy in DLBCL

Previous Earnings Reports

5 past events · Latest: May 15 (Negative)
Same Type Pattern 5 events
Date Event Sentiment 24h Move Catalyst
May 15 Q2 earnings report Negative -13.9% Quarterly loss and one-time CMO cancellation charge outweighed launch and financing updates.
May 15 Parent earnings report Negative -13.9% Parent-company loss and financing disclosures accompanied LYMPHIR commercialization progress.
Dec 23 FY25 earnings report Negative -9.8% Fiscal loss and financing disclosures accompanied LYMPHIR's commercial launch.
Dec 23 Parent earnings report Negative -9.8% Parent-company loss and financing disclosures accompanied FDA approval and launch.
Aug 12 Q3 earnings report Negative +5.9% Pre-launch loss and financing updates preceded a positive price reaction.

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

Pattern Detected

Tag-specific earnings history was mostly negative, with four of five selected events aligned with negative price reactions and an average move of -8.33%.

Key Terms

objective response rate, progression-free survival, complete response, partial response, +1 more
5 terms
objective response rate medical
"including a 24% objective response rate (ORR) overall"
The objective response rate (ORR) is the percentage of patients in a clinical trial whose tumors measurably shrink or disappear according to preset rules. Investors use it as a quick, objective signal of a drug’s ability to produce a clear treatment effect—like counting how many plants visibly respond after applying a new fertilizer—and higher ORR can improve odds of regulatory approval, commercial success, and company valuation.
progression-free survival medical
"20.5 months of median progression-free survival among 48%"
Progression-free survival is the length of time during and after a treatment that a patient's disease does not get worse, measured from the start of treatment until the disease shows measurable signs of progression or the patient dies. Investors care because longer progression-free survival in clinical trials often signals that a drug is effective, improving chances of regulatory approval, market adoption, and revenue potential—think of it as a stopwatch showing how long a therapy can keep the illness at bay.
complete response medical
"86% ORR, including 57% complete response (CR)"
A complete response is a positive outcome in which a company’s efforts to address issues or questions fully resolve the problem, often meaning that no further action or investigation is needed. For investors, it signals that concerns have been thoroughly addressed, which can boost confidence in the company's stability or decision-making. Think of it like a doctor fully treating an illness, leaving no remaining symptoms.
partial response medical
"including 57% complete response (CR) and 29% partial response (PR)"
A partial response is a clinical outcome where a treatment produces a clear, measurable improvement in a disease — for example a substantial shrinkage of a tumor or reduction in symptom measures — but does not eliminate the disease entirely. For investors it signals meaningful efficacy that can support regulatory progress, further trials, or commercial potential, like seeing a product gain market traction even though it hasn’t achieved a complete cure.
senior secured term loan facility financial
"funded $10.0 million under the first tranche of a senior secured term loan facility"
A senior secured term loan facility is a type of borrowed money that a company takes out, which is backed by its valuable assets like property or equipment. Because it is secured by these assets and ranks higher in repayment priority, it is considered safer for lenders and typically offers lower interest rates. For investors, it provides a relatively stable and priority claim on the company's assets if it encounters financial difficulties.

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

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$7.1 million in revenue for the first nine months of fiscal 2026 as the LYMPHIR® launch progresses

Strong institutional demand drives growth in total vials ordered and number of institutions ordering

LYMPHIR ordered by 44 institutions since launch

CRANFORD, N.J., Aug. 14, 2026 /PRNewswire/ -- Citius Oncology, Inc. ("Citius Oncology" or the "Company") (Nasdaq: CTOR), an oncology-focused biopharmaceutical company and majority-owned subsidiary of Citius Pharmaceuticals, Inc. ("Citius Pharma") (Nasdaq: CTXR), today reported financial results for the fiscal third quarter ended June 30, 2026, and provided a business update.

Citius Oncology logo

"Institutional demand (LYMPHIR vials ordered by prescribing centers from wholesalers) is accelerating. Institutional vial orders grew 31% sequentially, from 708 in the quarter ended March 31, 2026 to 926 in the quarter ended June 30, 2026. In July, institutions ordered 383 vials from wholesalers, the largest order month to date, reflecting a 25% increase over the prior quarter's monthly average order. Currently, 44 institutions have prescribed and ordered LYMPHIR," said Leonard Mazur, Chairman and Chief Executive Officer of Citius Oncology.

"We expect continued institutional demand to drive new wholesaler orders. The Company recognizes revenue when wholesaler orders are fulfilled. Consequently, net revenue for any period reflects actual wholesaler orders fulfilled. In July, we began to see growth in institutional demand translate into increased wholesale orders and associated revenue. The positive trajectory of formulary approvals, institutional adoption, and unit demand gives us confidence in a robust remainder of the fiscal year," added Mazur.

"We generated initial momentum with a lean internal team, maintaining healthy product margins and securing broad market access. In August, our full 29-person-strong commercial and medical affairs organizations expanded to nationwide coverage. The teams are now positioned to accelerate commercial execution and support broader adoption by leveraging the comprehensive, scalable infrastructure already established for LYMPHIR, including patient hub services, marketing and reimbursement support. Citius Oncology is now well positioned to broaden engagement with treatment centers, targeting formulary inclusion at 100 priority institutions by year-end and first-in-class support for health care providers. At the same time, we continue to advance LYMPHIR's longer-term value proposition through investigator-initiated studies exploring its potential in combination regimens beyond CTCL," added Mazur.

"Overall, the launch is moving in the right direction: more institutions are ordering LYMPHIR, vial demand is increasing, and our commercial footprint is expanding. We believe the underlying increasing demand trends provide a strong basis for the remainder of fiscal 2026," concluded Mazur.

Fiscal Third Quarter 2026 Business Highlights and Subsequent Developments

  • Secured prescriptions and orders from 44 institutions for LYMPHIR® (denileukin diftitox-cxdl), including academic oncology centers, leading National Comprehensive Cancer Network (NCCN) institutions, and community infusion centers;
  • Increased the number of new ordering institutions by 80% in the quarter ended June 30, 2026, compared to the quarter ended March 31, 2026;
  • Grew the number of vials ordered by institutions from wholesalers by 31% in the quarter ended June 30, 2026, compared to the quarter ended March 31, 2026, with 383 institutional vials ordered in July 2026, the largest vial order month to date;
  • Secured near-universal payer coverage, with no reimbursement denials or prior authorization barriers reported to date;
  • Expanded the commercial organization by 21 additional field-based professionals and added eight medical science liaisons, executed by the Company's exclusive commercialization partner, EVERSANA;
  • Engaged U.S. and international CTCL key opinion leaders at the Sixth World Congress of Cutaneous Lymphomas in Montreal through scientific exchange and educational initiatives;
  • Advanced two investigator-initiated Phase 1 studies of LYMPHIR in combination settings:
    • Phase 1 data for LYMPHIR with pembrolizumab in recurrent or refractory gynecologic cancers presented at the 2026 American Society of Clinical Oncology (ASCO) Annual Meeting, demonstrating:
      • 20.5 months of median progression-free survival among 48% of efficacy-evaluable patients achieving clinical benefit (10 of 21),
      • Responses observed in patients previously treated with immune checkpoint inhibitors, including a 24% objective response rate (ORR) overall, and 33% ORR in patients with relapsed or refractory endometrial cancer; and,
    • Phase 1 data for LYMPHIR administered prior to CAR-T therapy in high-risk relapsed or refractory diffuse large B-cell lymphoma (DLBCL) presented at 2026 ASTCT® & CIBMTR® Tandem Meetings, demonstrating:
      • 86% ORR, including 57% complete response (CR) and 29% partial response (PR),
      • LYMPHIR was well-tolerated with no dose-limiting toxicities observed; and,
  • Appointed Jonathan Peri, Ph.D., J.D., as an independent director on August 10, 2026, bringing three decades of leadership experience across law, financial services and corporate governance.

Fiscal Third Quarter 2026 Financial Highlights and Subsequent Developments

  • Cash and cash equivalents of $16.6 million as of June 30, 2026;
  • Received approximately $9.7 million in net proceeds from the exercise of certain warrants and funded $10.0 million under the first tranche of a senior secured term loan facility of up to $25.0 million;
  • Revenues of $1.5 million for the three months ended June 30, 2026, compared to no revenue for the three months ended June 30, 2025; and $7.1 million for the nine months ended June 30, 2026, compared to no revenue for the nine months ended June 30, 2025;
  • Gross profit of $1.0 million for the three months ended June 30, 2026, and $5.5 million for the nine months ended June 30, 2026;
  • Research and development (R&D) expenses of $0.2 million for the three months ended June 30, 2026, compared to $0.9 million for the prior-year quarter; and $2.3 million for the nine months ended June 30, 2026, compared to $5.3 million for the prior-year period;
  • General and administrative (G&A) expenses of $4.2 million for the three months ended June 30, 2026, compared to $1.9 million for the prior-year quarter, reflecting the expansion of the commercial organization; nine-month G&A of $30.7 million included a $19.7 million one-time CMO contract cancellation charge recognized in the second fiscal quarter in connection with a notice of termination; and,
  • Net loss of $8.9 million, or $(0.08) per share, for the three months ended June 30, 2026, compared to $5.4 million, or $(0.08) per share, for the prior-year quarter; and $41.1 million, or $(0.42) per share, for the nine months ended June 30, 2026, compared to $19.8 million, or $(0.28) per share, for the prior-year period.

About LYMPHIR™ (denileukin diftitox-cxdl)
LYMPHIR is a targeted immune therapy for relapsed or refractory cutaneous T-cell lymphoma (CTCL) indicated for use in Stage I-III disease after at least one prior systemic therapy. It is a recombinant fusion protein that combines the IL-2 receptor binding domain with diphtheria toxin (DT) fragments. The agent specifically binds to IL-2 receptors on the cell surface, causing diphtheria toxin fragments that have entered cells to inhibit protein synthesis, resulting in cell death. Denileukin diftitox-cxdl has demonstrated the ability to deplete immunosuppressive regulatory T lymphocytes (Tregs) and antitumor activity through a direct cytocidal action on IL-2R-expressing tumors. LYMPHIR was approved by the FDA and subsequently launched in the U.S. in December 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 CTCL 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 62% 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 include: 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 successfully commercialize LYMPHIR and establish a sustainable revenue stream; our ability to regain compliance with Nasdaq's continued listing standards; the estimated markets for LYMPHIR and our product candidates and the acceptance thereof by any market; physician and patient acceptance of LYMPHIR in a competitive treatment landscape; our ability to obtain, perform under, and maintain third party agreements and relationships, including obtaining a new bulk drug substance supplier; 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; our ability to secure and maintain strategic partnerships and expand international access to LYMPHIR; risks relating to the results of research and development activities; our ability to procure cGMP commercial-scale supply; 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. 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, except as required by law.

Contacts
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)




June 30,
2026



September 30,
2025


Current Assets:







Cash and cash equivalents


$

16,563,705



$

3,924,908


Accounts receivable, net of allowances



686,235





Inventory



22,625,945




22,286,693


Prepaid expenses



2,831,280




1,331,280


Total Current Assets



42,707,165




27,542,881











Other Assets:









In-process research and development, net of accumulated amortization



69,385,938




73,400,000











Total Assets


$

112,093,103



$

100,942,881


LIABILITIES AND STOCKHOLDERS' EQUITY









Current Liabilities:









Accounts payable


$

7,315,516



$

13,234,684


License payable



15,650,000




22,650,000


Accrued expenses



25,836,120




4,093,124


Due to related party



9,985,558




9,513,771


Total Current Liabilities



58,787,194




49,491,579











Notes payable, net of deferred financing costs



6,410,161





Deferred tax liability



2,710,643




2,784,960


Note payable to related party



3,800,111




3,800,111


Total Liabilities



71,708,109




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 June 30, 2026 and
     September 30, 2025; 105,758,982 and 83,513,442 shares issued and outstanding at June
     30, 2026 and September 30, 2025, respectively



10,576




8,351


Additional paid-in capital



145,481,984




108,897,836


Accumulated deficit



(105,107,566)




(64,039,956)


Total Stockholders' Equity



40,384,994




44,866,231


Total Liabilities and Stockholders' Equity


$

112,093,103



$

100,942,881


 

CITIUS ONCOLOGY, INC.

CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS

FOR THE THREE AND NINE MONTHS ENDED JUNE 30, 2026 AND 2025 (Unaudited)




Three Months Ended



Nine Months Ended




June 30,



June 30,



June 30,



June 30,




2026



2025



2026



2025


Revenues


$

1,493,788



$



$

7,105,197



$


Cost of revenues



(491,843)







(1,609,929)





Gross Profit



1,001,945







5,495,268






















Operating Expenses

















Research and development



218,496




938,277




2,316,202




5,342,198


Amortization of in-process research and development



1,720,312







4,014,062





General and administrative



4,219,163




1,881,447




30,704,141




7,446,753


Stock-based compensation – general and administrative



3,560,791




2,125,237




11,043,551




6,022,287


Total Operating Expenses



9,718,762




4,944,961




48,077,956




18,811,238



















Operating Loss



(8,716,817)




(4,944,961)




(42,582,688)




(18,811,238)



















Other Income (Expense)

















Interest income



96,848







168,857





Gain on sale of New Jersey net operating losses









1,762,000





Amortization of deferred financing costs



(179,492)







(179,492)





Interest expense



(231,732)




(160,755)




(310,604)




(160,755)


Total Other Income (Expense), Net



(314,376)




(160,755)




1,440,761




(160,755)



















Loss before Income Taxes



(9,031,193)




(5,105,716)




(41,141,927)




(18,971,993)


Income tax expense (benefit)



(107,347)




264,240




(74,317)




792,720



















Net Loss


$

(8,923,846)



$

(5,369,956)



$

(41,067,610)



$

(19,764,713)



















Net Loss Per Share - Basic and Diluted


$

(0.08)



$

(0.08)



$

(0.42)



$

(0.28)



















Weighted Average Common Shares Outstanding

















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



107,890,452




71,552,402




98,413,989




71,552,402


 

CITIUS ONCOLOGY, INC.

CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS

FOR THE NINE MONTHS ENDED JUNE 30, 2026 AND 2025

(Unaudited)




2026



2025


Cash Flows From Operating Activities:









Net loss


$

(41,067,610)



$

(19,764,713)


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









Stock-based compensation expense



11,043,551




6,022,287


Amortization of in-process research and development



4,014,062




-


Amortization of deferred financing costs



179,492




-


Deferred income tax expense



(74,317)




792,720


Changes in operating assets and liabilities:









Accounts receivable, net of allowances



(686,235)




-


Inventory



(339,252)




(8,940,201)


Prepaid expenses



(1,500,000)




1,600,000


Accounts payable



(5,919,168)




4,955,797


Accrued expenses



19,980,496




8,458,554


Due to related party



471,787




6,875,556


Net Cash (Used In) Provided By Operating Activities



(13,897,194)




-


Cash Flows From Investing Activities









    License payments



(7,000,000)




-


Net Cash Used In Investing Activities



(7,000,000)




-


Cash Flows From Financing Activities









    Net proceeds from notes payable



9,635,000




-


    Net proceeds from exercise of warrants and pre-funded warrants



9,730,818




-


    Deferred Financing Costs



(892,551)






    Net proceeds from issuance of common stock



15,062,724




-


Net Cash Provided by Financing Activities



33,535,991




-


Net Change in Cash and Cash Equivalents



12,638,797




-


Cash and Cash Equivalents – Beginning of Period



3,924,908




112


Cash and Cash Equivalents – End of Period


$

16,563,705



$

112


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









Interest Paid


$

212,794



$

-


Warrants issued for loan agreement included in deferred financing costs


$

749,280



$

-


Deferred financing costs included in accrued expenses


$

1,762,500



$

-


 

Cision View original content to download multimedia:https://www.prnewswire.com/news-releases/citius-oncology-inc-reports-fiscal-third-quarter-2026-financial-results-and-provides-business-update-302852117.html

SOURCE Citius Oncology, Inc.

FAQ

How much revenue did Citius Oncology (CTOR) report for Q3 and the first nine months of fiscal 2026?

Citius Oncology reported $1.5 million in Q3 2026 revenue and $7.1 million for the nine months ended June 30, 2026. According to Citius Oncology, this compares to no revenue in the same periods of 2025, reflecting LYMPHIR’s first commercial sales.

What were Citius Oncology’s (CTOR) net loss and cash position as of June 30, 2026?

Citius Oncology posted a Q3 2026 net loss of $8.9 million and a nine‑month net loss of $41.1 million. According to Citius Oncology, cash and cash equivalents totaled $16.6 million at June 30, 2026, following warrant exercises and funding of a senior secured term loan.

How is Citius Oncology (CTOR) funding the LYMPHIR commercial launch in fiscal 2026?

Citius Oncology is funding the launch through equity-linked and debt financing plus operating cash. According to Citius Oncology, it received about $9.7 million from warrant exercises and $10.0 million under the first tranche of a $25.0 million senior secured term loan facility.

What did Citius Oncology (CTOR) disclose about operating expenses and the CMO contract cancellation in 2026?

Citius Oncology reported nine‑month G&A expenses of $30.7 million, including a $19.7 million one‑time CMO contract cancellation charge. According to Citius Oncology, this charge was recognized in the second fiscal quarter following a notice of termination, contributing significantly to the year‑to‑date net loss.

What clinical data involving LYMPHIR were presented in 2026, according to Citius Oncology (CTOR)?

Citius Oncology highlighted Phase 1 data combining LYMPHIR with pembrolizumab in gynecologic cancers and LYMPHIR before CAR‑T in DLBCL. According to Citius Oncology, reported outcomes included a 24% ORR overall in one study and an 86% ORR in the CAR‑T setting, with no dose‑limiting toxicities observed.