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CG Oncology Reports Second Quarter 2026 Financial Results and Provides Business Updates

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CG Oncology (NASDAQ: CGON) reported second quarter 2026 results and clinical, regulatory and legal updates. For the quarter ended June 30, 2026, total revenue was $1.2 million, driven by commercial and development revenue, while the company recorded a net loss of $79.1 million or $(0.90) per share.

R&D expenses rose to $54.7 million and G&A to $29.0 million, reflecting higher clinical, CMC and personnel costs. Cash, cash equivalents and marketable securities were about $1.0 billion, which CG Oncology expects will fund operations through 2029. Phase 3 PIVOT-006 topline data in intermediate-risk NMIBC are anticipated near term, and completion of a BLA for high-risk BCG-unresponsive NMIBC is expected in 4Q 2026. Phase 3 BOND-003 Cohort C results were published in The Lancet Oncology, and a Delaware court ruling upheld a prior jury verdict maintaining the company’s agreement with ANI.

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Positive

  • Cash and securities $1.03 billion as of June 30, 2026
  • Expected cash runway to fund operations through 2029
  • Q2 2026 total revenue $1.2 million versus none prior year
  • Phase 3 PIVOT-006 topline data expected in near term
  • BOND-003 Cohort C Phase 3 results published in The Lancet Oncology
  • Delaware court ruling upholds agreement with ANI after jury verdict

Negative

  • Q2 2026 net loss $79.1 million, $(0.90) per share
  • R&D expenses increased to $54.7 million from $31.3 million
  • G&A expenses increased to $29.0 million from $17.4 million
  • Q2 2026 cost of sales $3.9 million exceeds reported revenues

News Explained

Cretostimogene remains an investigational candidate: the company states that its safety and efficacy have not been established by the FDA or any other health authority.

Market Context

Tag-specific earnings history averaged a 2.44% 24-hour move across five events. That record places t...
Analysis

Tag-specific earnings history averaged a 2.44% 24-hour move across five events. That record places this update within a variable response pattern; moderate short positioning and Net Buying were additional platform risk and context signals.

Key Figures

Cash position: $1,028,278 thousand Operating runway: 2029 R&D expenses: $54.7 million vs. $31.3 million +4 more
7 metrics
Cash position $1,028,278 thousand June 30, 2026
Operating runway 2029 Existing cash expected to fund operations through 2029
R&D expenses $54.7 million vs. $31.3 million Second quarter 2026 vs. prior-year period
G&A expenses $29.0 million vs. $17.4 million Second quarter 2026 vs. prior-year period
Net loss $79.1 million vs. $41.4 million Second quarter 2026 vs. prior-year period
Net loss per share $(0.90) vs. $(0.54) Second quarter 2026 vs. prior-year period
BLA completion Fourth quarter 2026 Initial indication of HR BCG-unresponsive NMIBC

Previous Earnings Reports

5 past events · Latest: May 08 (Positive)
Same Type Pattern 5 events
Date Event Sentiment 24h Move Catalyst
May 08 First-quarter earnings Positive +0.6% Cash runway and clinical milestones accompanied a modest positive 24-hour reaction.
Feb 27 Year-end earnings Positive +4.8% Cash runway and clinical milestones accompanied a strong positive 24-hour reaction.
Nov 14 Third-quarter earnings Positive +8.6% BLA progress, clinical response data, and cash runway preceded the strongest positive earnings reaction.
Aug 08 Second-quarter earnings Positive +2.0% Clinical efficacy, cash runway, and legal progress accompanied a positive quarterly reaction.
May 13 First-quarter earnings Positive -3.9% Clinical results and cash runway were followed by a negative 24-hour 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 events produced aligned positive reactions in four of five cases, with one divergence.

Key Terms

nmibc, cmc, single-arm
3 terms
nmibc medical
"PIVOT-006 Phase 3 topline data evaluating cretostimogene monotherapy"
A common form of bladder cancer that stays confined to the bladder’s inner lining or the layer just below it and has not grown into the deeper muscle wall. It matters to investors because it often requires repeated procedures, ongoing surveillance and long-term treatments, creating a sizable and stable market for diagnostics, drugs and medical devices; think of it like a surface-level problem that needs frequent check-ups and follow-up care rather than a one-time fix.
cmc technical
"including CMC costs"
Chemistry, Manufacturing, and Controls (CMC) describes the technical documentation and processes that show how a drug or medical product is made, tested for consistent quality, and kept stable from batch to batch. Investors care because strong CMC means a product can be manufactured reliably at scale and meet regulatory standards—similar to proving a recipe can be cooked the same way in any kitchen before restaurants expand—affecting approval, production costs, and potential revenue.
single-arm medical
"a single-arm, phase 3 trial"
A single-arm study is a clinical trial that gives all participants the same treatment and does not include a separate comparison group or placebo. Think of it like testing a new recipe by serving it to diners without offering a control dish — you can see how people respond, but you can’t directly compare results to another option. For investors, single-arm trials can speed development and reduce cost but leave more uncertainty about how a treatment stacks up against existing therapies and how regulators will view the evidence.

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

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  • PIVOT-006 Phase 3 topline data evaluating cretostimogene monotherapy as an adjuvant therapy in intermediate-risk NMIBC anticipated in the near-term
  • BLA completion for HR BCG-unresponsive NMIBC expected fourth quarter 2026
  • Phase 3 BOND-003 Cohort C Study Results published in The Lancet Oncology, further validating the strength of the clinical evidence supporting cretostimogene
  • Well-positioned to deliver on key milestones with approximately $1.0 billion cash, cash equivalents and marketable securities sufficient to fund operations through 2029

DALLAS, Texas, Aug. 06, 2026 (GLOBE NEWSWIRE) -- CG Oncology, Inc. (NASDAQ: CGON) today reported financial results for the second quarter ended June 30, 2026, and provided business updates.

“This quarter we have made significant progress across our clinical, regulatory, manufacturing and commercial-readiness initiatives, positioning the Company for long-term success.  PIVOT-006 has accrued the vast majority of the target events, and we look forward to sharing topline results soon. We are confident in the potential of cretostimogene and are committed to delivering what we believe will be a backbone therapy for patients,” stated Arthur Kuan, Chairman & Chief Executive Officer at CG Oncology.

Corporate Highlights

  • In July, BOND-003 Cohort C Study Results were published in The Lancet Oncology validating the strength of the clinical evidence supporting cretostimogene
    • Title: Intravesical cretostimogene grenadenorepvec oncolytic immunotherapy in high-risk, BCG-unresponsive, non-muscle invasive bladder cancer with carcinoma in situ (BOND-003 Cohort C): a single-arm, phase 3 trial
  • In July, the Superior Court of the State of Delaware denied ANI’s post-trial motion for a new trial and judgment as a matter of law, upholding the jury’s verdict in favor of CG Oncology that the invalidated royalty provision was properly severed and that the remainder of the agreement with ANI remains in force, while rejecting ANI’s challenges to the verdict and related claims
  • In May, CORE-008 Cohort CX data were presented at the Society of Urologic Oncology (SUO) session at the American Urological Association (AUA) 2026 Annual Meeting

Anticipated 2026 Milestones

  • PIVOT-006 (intermediate-risk NMIBC): Phase 3 topline data
  • Completion of BLA submission in initial indication of HR BCG-unresponsive NMIBC with CIS with or without Ta/T1 disease in 4Q’26
  • BOND-003 Cohort C (HR BCG-unresponsive NMIBC with CIS with or without Ta/T1 disease), BOND-003 Cohort P (HR BCG-unresponsive NMIBC in Ta/T1 disease without CIS), CORE-008 Cohort CX (HR BCG-exposed and BCG-unresponsive NMIBC) and CORE-008 Cohort A (HR BCG-naïve NMIBC with CIS +/- Ta/T1), durability data

Second Quarter Financial Highlights

  • Cash Position: Cash, cash equivalents and marketable securities as of June 30, 2026 were $1.0 billion, compared with $1.1 billion as of March 31, 2026.  The Company anticipates its existing cash, cash equivalents and marketable securities as of this date will be sufficient to fund operations through 2029.
  • Research and Development (R&D) Expenses: R&D expenses were $54.7 million for the second quarter of 2026, as compared to $31.3 million for the prior year period. The increase was primarily due to an increase in clinical trial expenses, including CMC costs, and an increase in compensation costs due to increased headcount.
  • General and Administrative (G&A) Expenses: G&A expenses were $29.0 million for the second quarter of 2026, as compared to $17.4 million for the prior year period. The increase was primarily attributed to an increase in personnel-related expenses, including compensation costs from increased headcount.
  • Net Loss: Net loss was $79.1 million, or $(0.90) per share, for the second quarter of 2026, as compared to a net loss of $41.4 million, or $(0.54) per share, for the prior year period.

About Cretostimogene Grenadenorepvec
Cretostimogene is an investigational, intravesically delivered oncolytic immunotherapy that has been studied in a clinical development program, which includes more than 600 patients with Non-Muscle Invasive Bladder Cancer (NMIBC). This program includes two Phase 3 clinical trials: BOND-003 for high-risk BCG-unresponsive NMIBC and PIVOT-006 for intermediate-risk NMIBC. CG Oncology also has a multi-cohort Phase 2 trial, CORE-008, evaluating the safety and efficacy of cretostimogene in high-risk NMIBC. Additionally, we have initiated an Expanded Access Program for cretostimogene in North America for patients who are unresponsive to BCG and meet certain program eligibility requirements. Cretostimogene is an investigational candidate, and its safety and efficacy have not been established by the FDA or any other health authority.

About CG Oncology
CG Oncology is a late-stage clinical biopharmaceutical company focused on developing and commercializing a potential backbone bladder-sparing therapeutic for patients afflicted with bladder cancer. CG Oncology sees a world where urologic cancer patients may benefit from our innovative immunotherapies to live with dignity and have an enhanced quality of life. To learn more, please visit: www.cgoncology.com.

Forward-Looking Statements
CG Oncology cautions you that statements contained in this press release regarding matters that are not historical facts are forward-looking statements. The forward-looking statements are based on our current beliefs and expectations and include, but are not limited to, statements regarding our anticipated cash runway, future results of operations and financial position; the anticipated timing and conduct of our ongoing and planned clinical trials and preclinical studies for cretostimogene, including anticipated next milestones in our development pipeline; the timing and likelihood of regulatory filings and approvals for cretostimogene; the potential therapeutic benefits of cretostimogene for high-risk and intermediate-risk NMIBC patients; and that cretostimogene has a best-in-disease product profile. Actual results may differ from those set forth in this press release due to the risks and uncertainties inherent in our business, including, without limitation: interim results of a clinical trial are not necessarily indicative of final results and one or more of the clinical outcomes may materially change as patient enrollment continues, following more comprehensive reviews of the data, and as more patient data becomes available; potential delays in the commencement, enrollment and completion of clinical trials, including the BOND-003 and PIVOT-006 trials; we may use our capital resources sooner than expected and they may be insufficient to allow us to achieve our anticipated milestones; our dependence on third parties in connection with manufacturing, shipping and clinical and preclinical testing; results from earlier clinical trials and preclinical studies not necessarily being predictive of future results; unexpected adverse side effects or inadequate efficacy of cretostimogene that may limit its development, regulatory approval, and/or commercialization; and other risks described in our filings with the Securities and Exchange Commission (SEC), including under the heading “Risk Factors” in our annual report on Form 10-K and other filings that we make with the SEC from time to time (which are available at http://www.sec.gov). You are cautioned not to place undue reliance on these forward-looking statements, which speak only as of the date hereof, and we undertake no obligation to update such statements to reflect events that occur or circumstances that exist after the date hereof. All forward-looking statements are qualified in their entirety by this cautionary statement, which is made under the safe harbor provisions of the Private Securities Litigation Reform Act of 1995.

Contacts:
Media
Sarah Connors
Vice President, Communications and Patient Advocacy, CG Oncology
sarah.connors@cgoncology.com

Investor Relations
Megan Knight
Vice President, Investor Relations, CG Oncology
megan.knight@cgoncology.com

CG ONCOLOGY, INC.

Condensed Consolidated Statements of Operations and Comprehensive Loss
(In thousands, except share and per share amounts)
(unaudited)
 
  Three Months Ended June 30,  Six Months Ended June 30, 
  2026  2025  2026  2025 
Revenues            
Commercial and development revenue $1,147  $  $2,216  $ 
License and collaboration revenue  10      24   52 
Total revenues  1,157      2,240   52 
Operating costs and expenses            
Cost of sales  3,925      6,887    
Research and development  54,657   31,331   98,387   58,799 
General and administrative  28,976   17,410   49,756   32,198 
Total operating costs and expenses  87,558   48,741   155,030   90,997 
Loss from operations  (86,401)  (48,741)  (152,790)  (90,945)
Other income (expense), net:            
Interest income, net  7,329   7,319   13,617   15,066 
Other income (expense), net  16   (4)  (85)  1 
Total other income, net  7,345   7,315   13,532   15,067 
Net loss and comprehensive loss $(79,056) $(41,426) $(139,258) $(75,878)
Net loss per share, basic and diluted $(0.90) $(0.54) $(1.61) $(1.00)
Weighted average shares of common stock outstanding, basic and diluted  88,200,023   76,226,829   86,369,437   76,207,333 


CG ONCOLOGY, INC.

Consolidated Balance Sheet Data
(In thousands)
 
  June 30,  December 31,
  2026  2025
  (unaudited)   
Cash, cash equivalents, and marketable securities $1,028,278  $742,155
Total assets  1,085,655   791,592
Total liabilities  56,537   38,990
Total stockholders' equity  1,029,118   752,602

FAQ

How did CG Oncology (NASDAQ: CGON) perform financially in Q2 2026?

CG Oncology reported Q2 2026 revenue of about $1.2 million and a net loss of $79.1 million. According to CG Oncology, higher R&D and G&A spending drove the loss, with increased clinical trial, CMC and personnel costs supporting its cretostimogene program.

What is CG Oncology's cash position and runway after the Q2 2026 results?

CG Oncology ended June 30, 2026 with approximately $1.0 billion in cash, cash equivalents and marketable securities. According to CG Oncology, this capital is expected to fund operations through 2029, supporting late-stage trials, regulatory activities and commercial-readiness efforts for cretostimogene.

What key clinical milestones did CG Oncology (CGON) highlight for 2026?

Key 2026 milestones include Phase 3 PIVOT-006 topline data and completion of a BLA in high-risk BCG-unresponsive NMIBC in 4Q 2026. According to CG Oncology, durability data updates from multiple BOND-003 and CORE-008 cohorts are also anticipated.

What is the significance of the PIVOT-006 Phase 3 trial for CG Oncology?

PIVOT-006 evaluates cretostimogene monotherapy as adjuvant therapy in intermediate-risk NMIBC, with topline Phase 3 data expected near term. According to CG Oncology, the trial has accrued the vast majority of target events and is a major component of its clinical strategy.

When does CG Oncology plan to complete the BLA for BCG-unresponsive NMIBC?

CG Oncology expects to complete its Biologics License Application for high-risk BCG-unresponsive NMIBC with CIS with or without Ta/T1 disease in fourth quarter 2026. According to CG Oncology, this represents the initial regulatory filing for cretostimogene in this indication.

How is cretostimogene being evaluated across CG Oncology's clinical trials?

Cretostimogene is being studied in Phase 3 trials BOND-003 and PIVOT-006 and the multi-cohort Phase 2 CORE-008 in high-risk and intermediate-risk NMIBC. According to CG Oncology, more than 600 NMIBC patients have been enrolled across this development program to date.