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

(Positive)
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Citius Pharmaceuticals (Nasdaq: CTXR) reported fiscal Q3 2026 results, highlighting initial commercial traction for LYMPHIR, launched by majority-owned subsidiary Citius Oncology (Nasdaq: CTOR). For the three months ended June 30, 2026, Citius recorded $1.5 million in revenue and gross profit of $1.0 million, a ~67% gross margin. Nine-month revenue reached $7.1 million with a ~77% gross margin. Cash and cash equivalents were $17.0 million at June 30, 2026.

LYMPHIR availability expanded to 44 institutions, institutional vial orders rose 31%, and new ordering institutions increased 80%. Citius Oncology completed nationwide deployment of 29 commercial and medical affairs professionals. Citius reported a Q3 2026 net loss applicable to common stockholders of $8.9 million and a nine‑month net loss of $38.3 million.

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Positive

  • $7.1 million LYMPHIR revenue in nine months of fiscal 2026, from zero in 2025
  • Q3 2026 revenue of $1.5 million with ~67% gross margin
  • Nine‑month 2026 gross profit of $5.5 million and ~77% gross margin
  • R&D expenses reduced to $4.3 million for nine months 2026 from $7.5 million
  • Cash and cash equivalents increased to $17.0 million from $4.3 million at Sept 30, 2025
  • Financing inflows: ~$4.5 million direct offering, $9.7 million warrant exercises, $10.0 million term loan tranche
  • LYMPHIR available at 44 institutions; July institutional orders reached 383 vials, highest month to date
  • Phase 1 DLBCL study reported 86% ORR and 57% CR with no dose‑limiting toxicities

Negative

  • Net loss applicable to common stockholders of $8.9 million in Q3 2026
  • Nine‑month 2026 net loss applicable to common stockholders of $38.3 million
  • Nine‑month 2026 operating cash outflow of $23.0 million
  • General and administrative expenses rose to $38.3 million for nine months 2026 from $14.6 million
  • Includes non‑recurring $19.7 million contract cancellation charge recognized in March 2026
  • Common shares outstanding increased to 27.45 million from 18.07 million at Sept 30, 2025
  • New notes payable of $6.4 million and related interest expense of $0.4 million for nine months 2026

News Explained

The financing added cash but also debt and shares; $10.0 million of a facility of up to $25.0 million was funded by June 30, 2026.

Citius Pharmaceuticals reported fiscal third-quarter results; its financing update records a closed offering, exercised warrants, and a funded loan tranche, bringing in cash while changing the capital structure through debt and issued shares.

Common shares issued and outstanding were 27,452,570 at June 30, 2026, versus 18,067,744 at September 30, 2025; issuing additional shares increases the total share count and reduces an existing holder's percentage ownership absent offsetting changes.

The April 2026 transaction was a registered direct offering, meaning a negotiated sale of registered securities to selected investors; the company reported approximately $4.5 million of net proceeds from it.

The loan facility is described as up to $25.0 million, while the funded first tranche was $10.0 million.

Market reaction after 3Q26 earnings report: CTOR -19.76%

-19.76% $0.73 4.9x vol
15m delay
-19.76% Vs previous close
$0.73 Last Price
$0.72 $0.93 Day Range
$66.62M Market Cap
4.9x Rel. Volume

Following this news, CTOR has declined 19.76%, 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 $0.73. Trading volume is very high at 4.9x the average, suggesting heavy selling pressure.

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Market Context

CTOR's earnings record includes -13.95% and -9.84% reactions alongside a 5.92% gain. The effective S...
Analysis

CTOR's earnings record includes -13.95% and -9.84% reactions alongside a 5.92% gain. The effective S-3 resale registration adds share-registration context, while low short positioning remains a volatility risk lens.

Key Figures

Nine-month revenue: $7.1 million Cash and equivalents: $17 million LYMPHIR availability: 44 institutions +5 more
8 metrics
Nine-month revenue $7.1 million first nine months of fiscal 2026
Cash and equivalents $17 million as of June 30, 2026
LYMPHIR availability 44 institutions academic oncology centers, NCCN institutions and community infusion centers
Quarterly revenue $1.5 million three months ended June 30, 2026
New institutional accounts 80% increase in new institutions ordering LYMPHIR
Objective response rate 86% Phase 1 LYMPHIR before CAR-T therapy in high-risk relapsed or refractory DLBCL
Complete response 57% Phase 1 LYMPHIR before CAR-T therapy in high-risk relapsed or refractory DLBCL
Net loss $8.9 million applicable to common stockholders for fiscal third quarter 2026

Previous Earnings Reports

5 past events · Latest: May 15 (Negative)
Same Type Pattern 5 events
Date Event Sentiment 24h Move Catalyst
May 15 2Q26 earnings report Negative -13.9% Quarterly loss increased alongside a non-recurring contract cancellation charge.
May 15 2Q26 earnings report Negative -13.9% Parent company reported higher losses and additional financing requirements.
Dec 23 FY25 earnings report Negative -9.8% Commercial launch progress accompanied substantial financing and an annual net loss.
Dec 23 FY25 earnings report Negative -9.8% Launch milestones were accompanied by a $39.7 million net loss.
Aug 12 3Q25 earnings report Negative +5.9% Pre-launch results showed limited cash and a higher quarterly net loss.

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 included negative reactions of -13.95% and -9.84%, alongside one positive reaction of 5.92%, indicating predominantly negative but non-uniform responses.

Key Terms

objective response rate, complete response, dose-limiting toxicities, senior secured term loan
4 terms
objective response rate medical
"showed an 86% objective response rate, including 57% complete response"
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.
complete response medical
"including 57% complete response, with no dose-limiting toxicities observed"
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.
dose-limiting toxicities medical
"with no dose-limiting toxicities observed"
Dose-limiting toxicities are the harmful side effects seen in early clinical trials that are severe enough to stop researchers from raising a drug’s dose. Like a car’s speed limiter marking the safe top speed, DLTs define the maximum tolerable dose, and they matter to investors because they determine whether a medicine can reach effective levels, influence development timelines, costs, and regulatory chances, and thus affect a drug’s commercial prospects.
senior secured term loan financial
"funded $10.0 million under the first tranche of a Citius Oncology senior secured term loan"
A senior secured term loan is a type of borrowing where a company borrows money and promises to pay it back over a fixed period, with the loan secured by the company's assets as collateral. Because it is "senior," it has priority over other debts if the company faces financial trouble, and being "secured" means lenders have a claim on specific assets. For investors, this makes the loan a safer and more predictable investment compared to unsecured or subordinate debts.

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 from commercial sales of LYMPHIR ®

$17 million in cash and cash equivalents as of June 30, 2026

Expanded LYMPHIR commercial and medical affairs organizations deployed nationwide

CRANFORD, N.J., Aug. 14, 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 financial results for the fiscal third quarter ended June 30, 2026, and provided a business update, including progress at its majority-owned subsidiary, Citius Oncology, Inc. (Nasdaq: CTOR).

"The LYMPHIR launch continued to build momentum in our fiscal third quarter and remains the primary driver of our business. The number of institutional vial orders increased, new institutions placed orders, and LYMPHIR became available at 44 leading academic oncology centers, NCCN institutions and community infusion centers. These indicators demonstrate meaningful progress in formulary access and treatment-driven demand as physicians gain familiarity with LYMPHIR's differentiated clinical profile," said Leonard Mazur, Chairman and Chief Executive Officer of Citius Pharma and Citius Oncology.

"Following the quarter end, we completed the nationwide deployment of Citius Oncology's expanded commercial and medical affairs teams, which now total 29 professionals. These teams are positioned to leverage the existing platform established to support LYMPHIR's success, including patient hub services, marketing, reimbursement support, and market access. We believe our expanded organization will facilitate increased engagement with priority treatment centers, support formulary adoption and broaden access for eligible patients as the launch matures," added Mazur.

"We also continued to advance LYMPHIR's longer-term value proposition. Phase 1 investigator-initiated data presented at ASCO demonstrated encouraging clinical activity and durable responses for LYMPHIR in combination with pembrolizumab in heavily pre-treated gynecologic malignancies. Additionally, Phase 1 data of LYMPHIR administered prior to CAR-T therapy in high-risk relapsed or refractory DLBCL, presented at the 2026 ASTCT® & CIBMTR® Tandem Meetings, showed an 86% objective response rate, including 57% complete response, with no dose-limiting toxicities observed. These positive signals point to LYMPHIR's potential beyond cutaneous T-cell lymphoma. As we scale, we remain focused on disciplined execution and building the long-term sustainable value of LYMPHIR," concluded Mazur.

Fiscal Third Quarter 2026 Business Highlights and Subsequent Developments

  • Continued commercial momentum for LYMPHIR, with availability in 44 institutions, including academic oncology centers, leading National Comprehensive Cancer Network (NCCN) institutions and community infusion centers;
  • Increased the number of new institutions ordering LYMPHIR by 80% and grew institutional vial orders from wholesalers by 31%;
  • Drove continued institutional demand growth in July, with 383 vials ordered by institutions from wholesalers, the largest vial order month to date;
  • Secured near universal payer coverage, with no reimbursement denials or preauthorization barriers reported to date;
  • Expanded Citius Oncology's commercial organization by 21 commercial field-based professionals and added eight medical science liaisons, with nationwide deployment completed in August 2026 through EVERSANA, the Company's exclusive commercialization partner;
  • Advanced Phase 1 investigator-initiated trials:
    • Data were presented at the 2026 American Society of Clinical Oncology (ASCO) Annual Meeting evaluating LYMPHIR in combination with pembrolizumab in recurrent or refractory gynecologic malignancies:
      • 24% overall response rate (ORR) and a 48% clinical benefit rate, and
      • median progression-free survival of 20.5 months among patients achieving clinical benefit;
    • Data were presented at the 2026 ASTCT® & CIBMTR® Tandem Meetings evaluating LYMPHIR administered prior to CAR-T therapy in high-risk relapsed or refractory diffuse large B-cell lymphoma (DLBCL):
      • 86% ORR, including 57% complete response (CR) and 29% partial response (PR),
      • LYMPHIR was well-tolerated with no dose-limiting toxicities observed;
  • Closed a registered direct offering in April 2026 for net proceeds of approximately $4.5 million;
  • 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 Citius Oncology senior secured term loan facility of up to $25.0 million; and,
  • Citius Oncology appointed Jonathan Peri, Ph.D., J.D., as an independent director, effective August 10, 2026, expanding the board to nine members.

Fiscal Third Quarter 2026 Financial Highlights and Subsequent Developments

  • Cash and cash equivalents of $17.0 million as of June 30, 2026;
  • Revenues of $1.5 million for the three months ended June 30, 2026, compared with no revenue for the three months ended June 30, 2025; and $7.1 million for the nine months ended June 30, 2026, compared with no revenue for the nine months ended June 30, 2025;
  • Gross profit of $1.0 million for the three months ended June 30, 2026, representing a gross margin of approximately 67%, and $5.5 million for the nine months ended June 30, 2026, representing a gross margin of approximately 77%;
  • Research and development expenses of $1.1 million for the three months ended June 30, 2026, compared with $1.6 million for the three months ended June 30, 2025; and $4.3 million for the nine months ended June 30, 2026, compared with $7.5 million for the nine months ended June 30, 2025;
  • General and administrative expenses of $6.1 million for the three months ended June 30, 2026, compared with $4.4 million for the three months ended June 30, 2025. General and administrative expenses were $38.3 million for the nine months ended June 30, 2026, compared with $14.6 million for the nine months ended June 30, 2025. The nine-month increase primarily reflects a non-recurring $19.7 million contract cancellation charge recognized in March 2026 and increased expenses related to the commercial launch of LYMPHIR;
  • Stock-based compensation expense of $3.8 million for the three months ended June 30, 2026, compared with $2.7 million for the three months ended June 30, 2025; and $11.9 million for the nine months ended June 30, 2026, compared with $7.9 million for the nine months ended June 30, 2025; and,
  • Net loss applicable to common stockholders of $8.9 million, or $(0.34) per share, for the three months ended June 30, 2026, compared with $8.8 million, or $(0.80) per share, for the three months ended June 30, 2025; and $38.3 million, or $(1.64) per share, for the nine months ended June 30, 2026, compared with $29.5 million, or $(3.27) per share, for the nine months ended June 30, 2025.

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.

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.

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 Pharma. 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 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 obtain, perform under and maintain financing, strategic and third party agreements and relationships, including obtaining a new bulk drug substance supplier; 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 ability to obtain regulatory approval for and commercialize or enter into strategic partnerships with respect to Mino-Lok and Halo-Lido; 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. 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 Pharma'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)






June 30,



September 30,




2026



2025


ASSETS







Current Assets:







Cash and cash equivalents


$

17,007,523



$

4,252,290


Accounts receivable, net of allowances



686,235




-


Inventory



22,625,945




22,286,693


Prepaid expenses



3,011,660




1,395,490


Total Current Assets



43,331,363




27,934,473











Operating lease right-of-use asset, net



753,039




818,694











Deposits



38,062




38,062


In-process research and development, net of accumulated amortization



88,785,938




92,800,000


Goodwill



9,346,796




9,346,796


Total Other Assets



98,170,796




102,184,858











Total Assets


$

142,255,198



$

130,938,025











LIABILITIES AND STOCKHOLDERS' EQUITY









Current Liabilities:









Accounts payable


$

8,037,899



$

13,693,692


License payable



15,650,000




22,650,000


Accrued expenses



25,913,962




4,190,253


Accrued compensation



1,871,320




3,292,447


Note payable



-




1,000,000


Operating lease liability



176,170




88,348


Total Current Liabilities



51,649,351




44,914,740











Deferred tax liability



7,696,443




7,770,760


Notes payable, net of deferred financing fees



6,410,161




-


Operating lease liability – noncurrent



590,787




724,925


Total Liabilities



66,346,742




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; 27,452,570 and
18,067,744 shares issued and outstanding at June 30, 2026 and September 30, 2025,
respectively



27,452




18,068


Additional paid-in capital



343,704,577




306,336,239


Accumulated deficit



(277,118,897)




(238,804,129)


Total Citius Pharmaceuticals, Inc. Stockholders' Equity



66,613,132




67,550,178


Non-controlling interest



9,295,324




9,977,422


Total Equity



75,908,456




77,527,600











Total Liabilities and Equity


$

142,255,198



$

130,938,025


 

CITIUS PHARMACEUTICALS, 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



1,053,869




1,621,325




4,287,106




7,514,888


Amortization of in-process research and development



1,720,312







4,014,062





General and administrative



6,149,173




4,447,008




38,261,001




14,626,882


Stock-based compensation – general and administrative



3,810,665




2,719,674




11,879,167




7,946,529


Total Operating Expenses



12,734,019




8,788,007




58,441,336




30,088,299



















Operating Loss



(11,732,074)




(8,788,007)




(52,946,068)




(30,088,299)



















Other Income (Expense)

















Interest income



116,691




20,637




215,372




56,658


Gain on sale of New Jersey net operating losses









3,833,277





Amortization of deferred financing costs



(179,492)







(179,492)





Interest expense



(231,732)




(172,262)




(420,301)




(172,262)


Total Other Income (Expense), Net



(294,533)




(151,625)




3,448,856




(115,604)



















Loss before Income Taxes



(12,026,607)




(8,939,632)




(49,497,212)




(30,203,903)


Income tax expense (benefit)



(107,347)




264,240




(74,317)




792,720



















Net Loss



(11,919,260)




(9,203,872)




(49,422,895)




(30,996,623)


Net loss attributable to non-controlling interest



3,056,417




414,000




11,108,127




1,522,000



















Net loss applicable to common stockholders


$

(8,862,843)



$

(8,789,872)



$

(38,314,768)



$

(29,474,623)



















Net Loss Per Share - Basic and Diluted


$

(0.34)



$

(0.80)



$

(1.64)



$

(3.27)



















Weighted Average Common Shares Outstanding

















Basic and diluted (includes pre-funded warrants)



26,169,589




11,006,896




23,343,869




9,020,356


 

CITIUS PHARMACEUTICALS, 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


$

(49,422,895)



$

(30,996,623)


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









Stock-based compensation expense



11,879,167




7,946,529


Issuance of common stock for services



107,510





Issuance of common stock warrant



68,597





Amortization of in-process research and development



4,014,062





Amortization of operating lease right-of-use asset



65,655




152,212


Amortization of deferred financing costs



179,492





Deferred income tax expense (benefit)



(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



(1,616,170)




1,386,824


Accounts payable



(5,655,793)




5,166,831


Accrued expenses



19,961,209




8,506,648


Accrued compensation



(1,421,127)




1,481,023


Operating lease liability



(46,316)




(167,911)


Net Cash Used In Operating Activities



(22,986,413)




(14,671,948)











Cash Flows From Investing Activities:









License fee payments



(7,000,000)





Net Cash Used in Investing Activities



(7,000,000)














Cash Flows From Financing Activities:









Proceeds from (repayment of) note payable and advance from employee



(1,000,000)




1,300,000


Repayment of advance from employee







(300,000)


Net proceeds from loan agreement



9,635,000





Proceeds from exercise of warrants



9,731,103





Deferred Financing Costs



(892,551)





Proceeds from sale of Series A preferred stock






100


Redemption of Series A preferred stock






(100)


Net proceeds from common stock offerings



25,268,094




16,509,194


Net Cash Provided By Financing Activities



42,741,646




17,509,194











Net Change in Cash and Cash Equivalents



12,755,233




2,837,246


Cash and Cash Equivalents - Beginning of Period



4,252,290




3,251,880


Cash and Cash Equivalents - End of Period


$

17,007,523



$

6,089,126


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









Interest paid


$

303,644



$


Operating lease right-of-use asset and liability recorded


$



$

786,697


Warrants issued for loan agreement included in deferred financing costs


$

749,280



$


Deferred financing costs included in accrued expenses


$

1,762,500



$


 

Citius Pharmaceuticals, a late-stage biopharmaceutical company

Cision View original content to download multimedia:https://www.prnewswire.com/news-releases/citius-pharmaceuticals-inc-reports-fiscal-third-quarter-2026-financial-results-and-provides-business-update-302852124.html

SOURCE Citius Pharmaceuticals, Inc.

FAQ

How much revenue did Citius Pharmaceuticals (CTXR) generate from LYMPHIR in fiscal Q3 2026?

Citius Pharmaceuticals reported $1.5 million in revenue for the quarter ended June 30, 2026, all from LYMPHIR commercial sales. According to the company, nine‑month fiscal 2026 revenue totaled $7.1 million, compared with no revenue in the same period of 2025.

What were Citius Pharmaceuticals’ (CTXR) profits and margins in fiscal Q3 2026?

Citius Pharmaceuticals recorded gross profit of $1.0 million in Q3 2026, representing a gross margin of about 67%. For the nine months ended June 30, 2026, gross profit was $5.5 million with an approximately 77% gross margin, according to the company’s financial results.

What net loss did Citius Pharmaceuticals (CTXR) report for fiscal Q3 2026 and year-to-date?

Citius Pharmaceuticals reported a net loss applicable to common stockholders of $8.9 million in Q3 2026. For the nine months ended June 30, 2026, the net loss applicable to common stockholders was $38.3 million, or $(1.64) per share, according to the company.

How strong is Citius Pharmaceuticals’ (CTXR) cash position as of June 30, 2026?

Citius Pharmaceuticals held $17.0 million in cash and cash equivalents as of June 30, 2026. According to the company, cash increased from $4.3 million at September 30, 2025, supported by equity offerings, warrant exercises, and the first tranche of a senior secured term loan.

How widely is LYMPHIR from Citius Oncology (CTOR) available and reimbursed in 2026?

According to Citius Oncology, LYMPHIR was available at 44 institutions, including academic centers, NCCN institutions, and community infusion centers. The company reported near universal payer coverage, with no reimbursement denials or preauthorization barriers reported to date for eligible patients.

What clinical data did Citius Oncology (CTOR) report for LYMPHIR in 2026?

Citius Oncology highlighted Phase 1 data in high‑risk relapsed or refractory DLBCL showing an 86% objective response rate and 57% complete response. According to the company, no dose‑limiting toxicities were observed, and separate gynecologic malignancy data showed a 24% overall response rate.

How have operating expenses changed for Citius Pharmaceuticals (CTXR) in fiscal 2026?

For the nine months ended June 30, 2026, total operating expenses were $58.4 million, up from $30.1 million in 2025. According to Citius, the increase mainly reflects a non‑recurring $19.7 million contract cancellation charge and higher commercialization expenses for LYMPHIR.