STOCK TITAN

CG Oncology (NASDAQ: CGON) widens Q2 loss, adds $500M stock sale capacity

(Moderate)
(Neutral)
Form Type
8-K

Rhea-AI Filing Summary

CG Oncology, Inc. reported second quarter 2026 results and expanded its equity financing capacity. For the quarter ended June 30, 2026, total revenues were $1,157 thousand and net loss was $79,056 thousand, or $0.90 per share, driven mainly by higher research and development and general and administrative expenses.

Cash, cash equivalents and marketable securities totaled approximately $1.0 billion as of June 30, 2026, which the company expects will fund operations through 2029. CG Oncology continues late‑stage development of cretostimogene grenadenorepvec, with Phase 3 PIVOT‑006 topline data anticipated in the near term and completion of a BLA for high‑risk BCG‑unresponsive NMIBC targeted for the fourth quarter of 2026. Phase 3 BOND‑003 Cohort C results were published in The Lancet Oncology, and a Delaware court denied ANI’s post‑trial motions, leaving in place a prior jury verdict favorable to CG Oncology.

Separately, CG Oncology filed Amendment No. 2 to its prospectus under an Open Market Sale Agreement with Jefferies, increasing the amount of common stock that may be sold under the at‑the‑market program by up to $500.0 million, after previously registering and selling approximately $550.0 million of shares.

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Filing Explained

The August 6 8-K records an amendment adding up to $500.0 million of common-stock capacity under CG Oncology’s existing Open Market Sale Agreement; this is registration capacity rather than a completed sale or issuance, so the filing alone does not establish new dilution for existing holders.

Item 2.02 Results of Operations and Financial Condition Financial
Disclosure of earnings results, typically an earnings press release or preliminary financials.
Item 8.01 Other Events Other
Voluntary disclosure of events the company deems important to shareholders but not covered by other items.
Item 9.01 Financial Statements and Exhibits Exhibits
Financial statements, pro forma financial information, and exhibit attachments filed with this report.
Total revenues Q2 2026 $1,157 (in thousands) Three months ended June 30, 2026
Net loss Q2 2026 $79,056 (in thousands) Three months ended June 30, 2026
Net loss per share Q2 2026 $(0.90) Basic and diluted, three months ended June 30, 2026
R&D expenses Q2 2026 $54,657 (in thousands) Three months ended June 30, 2026
G&A expenses Q2 2026 $28,976 (in thousands) Three months ended June 30, 2026
Cash, cash equivalents and marketable securities $1,028,278 (in thousands) As of June 30, 2026
Additional ATM capacity $500.0 million Increase in shares available under Open Market Sale Agreement
Prior ATM sales Approximately $550.0 million Previously registered and sold under the Sale Agreement
Open Market Sale Agreement financial
"pursuant to that certain Open Market Sale Agreement, dated March 28, 2025"
A contract that lets a shareholder or issuer authorize a broker to sell stock into the public market over time rather than to one specific buyer. Think of it like hiring a salesperson to quietly sell items from your garage in small batches so you don’t crash the price; for investors it matters because it increases supply and liquidity, can put downward pressure on the share price, and signals an upcoming flow of shares into the market.
Registration Statement on Form S-3ASR regulatory
"filed with the SEC as part of the Company’s Registration Statement on Form S-3ASR"
A registration statement on Form S-3ASR is a pre-approved filing used by well-established public companies to register securities they may sell over time, with the paperwork becoming effective automatically so offerings can begin quickly. For investors, it matters because it lets a company raise money or issue stock or debt on short notice — like a company keeping a ready-to-use credit line — which can dilute existing shares or change the company’s cash position rapidly.
BLA regulatory
"BLA completion for HR BCG-unresponsive NMIBC expected fourth quarter 2026"
oncolytic immunotherapy medical
"intravesical cretostimogene grenadenorepvec oncolytic immunotherapy in high-risk, BCG-unresponsive"
A type of cancer treatment that uses specially engineered viruses to infect and destroy tumor cells while also stimulating the patient’s immune system to recognize and attack cancer elsewhere—think of the virus as a guided seed that both blows up weeds and trains a gardening robot to find the rest. For investors, progress or setbacks in trials and approvals can sharply change a company’s value because outcomes tend to be binary (successful approval or failure) and can open large, high-value markets if effective.
non-muscle invasive bladder cancer (NMIBC) medical
"more than 600 patients with Non-Muscle Invasive Bladder Cancer (NMIBC)"
Non-muscle invasive bladder cancer (NMIBC) is a form of bladder cancer that is confined to the inner lining of the bladder and has not grown into the deeper muscle layer; think of it as a superficial patch on wallpaper rather than a stain that has soaked through the wall. It matters to investors because NMIBC often requires repeated treatments and monitoring, drives demand for outpatient therapies and diagnostics, and creates a sizable, ongoing market for drugs, devices, and procedures due to high recurrence and long-term care costs.
BCG-unresponsive medical
"high-risk, BCG-unresponsive, non-muscle invasive bladder cancer with carcinoma in situ"
BCG-unresponsive describes a situation in which a patient’s bladder cancer does not shrink or returns despite receiving an adequate course of BCG, a common vaccine-based intravesical treatment used to stimulate the immune system in the bladder. For investors this matters because it defines a group of patients who need alternative therapies or procedures, shaping clinical trial eligibility, regulatory pathways, and the potential market for new drugs; think of it like weeds that resist the usual weed killer and require a different product.
Total revenues $1,157 (in thousands) Compared with $0 (in thousands) in the quarter ended June 30, 2025.
Net loss $79,056 (in thousands) Compared with $41,426 (in thousands) in the quarter ended June 30, 2025.
Net loss per share, basic and diluted $(0.90) Compared with $(0.54) in the quarter ended June 30, 2025.
Cash, cash equivalents and marketable securities $1,028,278 (in thousands) as of June 30, 2026 Up from $742,155 (in thousands) as of December 31, 2025.
Guidance

The company states its existing cash, cash equivalents and marketable securities as of June 30, 2026 will be sufficient to fund operations through 2029.

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FAQ

What were CGON’s key financial results for the quarter ended June 30, 2026?

CG Oncology reported Q2 2026 revenues of $1,157 thousand and a net loss of $79,056 thousand, or $0.90 per share. Higher research and development and general and administrative expenses were the primary drivers of the larger loss versus the prior-year period.

What is CGON’s cash position and runway after Q2 2026?

As of June 30, 2026, CG Oncology held approximately $1.0 billion in cash, cash equivalents and marketable securities. The company states this balance is expected to be sufficient to fund operations through 2029, supporting its late-stage clinical and regulatory programs.

How did CGON change its at-the-market stock sale program?

CG Oncology filed Amendment No. 2 to its prospectus, increasing shares available under its Open Market Sale Agreement with Jefferies by an additional $500.0 million. The company had previously registered and sold approximately $550.0 million of common stock under the same agreement.

What are the key clinical milestones CGON highlighted for cretostimogene?

CG Oncology expects PIVOT-006 Phase 3 topline data in intermediate-risk NMIBC in the near term and plans to complete its BLA submission for high-risk BCG-unresponsive NMIBC in the fourth quarter of 2026, alongside additional durability data from multiple ongoing cohorts.

What recent data publications support CGON’s cretostimogene program?

Phase 3 BOND-003 Cohort C results in high-risk, BCG-unresponsive NMIBC with carcinoma in situ were published in The Lancet Oncology. The company states this publication further validates the strength of the clinical evidence supporting its oncolytic immunotherapy cretostimogene grenadenorepvec.
false000199179200019917922026-08-062026-08-06

 

UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
WASHINGTON, D.C. 20549

 

FORM 8-K

 

CURRENT REPORT

Pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934

Date of Report (Date of earliest event reported): August 06, 2026

 

 

CG Oncology, Inc.

(Exact name of Registrant as Specified in Its Charter)

 

 

Delaware

001-41925

37-1611499

(State or Other Jurisdiction
of Incorporation)

(Commission File Number)

(IRS Employer
Identification No.)

 

 

 

 

 

3000 Pegasus Park Drive

Suite 1640

 

Dallas, Texas

 

75247

(Address of Principal Executive Offices)

 

(Zip Code)

 

Registrant’s Telephone Number, Including Area Code: (949) 409-3700

 

N/A

(Former Name or Former Address, if Changed Since Last Report)

 

Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions:

Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)
Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)
Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))
Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))

Securities registered pursuant to Section 12(b) of the Act:


Title of each class

 

Trading
Symbol(s)

 


Name of each exchange on which registered

Common Stock, par value $0.0001 per share

 

CGON

 

The Nasdaq Global Select Market

Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§ 230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§ 240.12b-2 of this chapter).

Emerging growth company

If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act.

 


 

Item 2.02 Results of Operations and Financial Condition.

 

On August 6, 2026, CG Oncology, Inc. issued a press release announcing its financial results for the quarter ended June 30, 2026. A copy of the press release is attached hereto as Exhibit 99.1 and is incorporated herein by reference.

In accordance with General Instruction B.2 of Form 8-K, the information in this Current Report on Form 8-K, including Exhibit 99.1, shall not be deemed “filed” for purposes of Section 18 of the Securities Exchange Act of 1934, as amended (the "Exchange Act"), or otherwise subject to the liabilities of that section, nor shall it be deemed incorporated by reference in any filing under the Securities Act of 1933, as amended, or the Exchange Act, whether made before or after the date hereof, except as expressly set forth by specific reference in such filing.

 

Item 8.01 Other Events.

On August 6, 2026, the Company filed Amendment No. 2 to Prospectus (the “Amendment No. 2”) with the Securities and Exchange Commission (the “SEC”) for the offer and sale of shares of its common stock, par value $0.0001 per share (the “Shares”), pursuant to that certain Open Market Sale Agreement, dated March 28, 2025, by and between the Company and Jefferies LLC (the “Sale Agreement”), to increase the Shares available to be sold pursuant to the terms of the Sale Agreement by an additional $500.0 million (the “Additional Shares”). The Amendment amends and supplements the information in the prospectus dated March 28, 2025 (the “Prospectus”) filed with the SEC as part of the Company’s Registration Statement on Form S-3ASR (File No. 333-286230) and Amendment No. 1 to Prospectus dated January 13, 2026 (the “Amendment No. 1”), pursuant to which the Company previously registered and sold approximately $550.0 million of shares of the Company’s common stock pursuant to the Sale Agreement.

The Amendment should be read in conjunction with the Prospectus and Amendment No. 1, and is qualified by reference thereto, except to the extent that the information therein amends or supersedes the information contained in the Prospectus and Amendment No. 1. The Amendment is not complete without, and may only be delivered or utilized in connection with, the Prospectus, Amendment No. 1 to Prospectus and any future amendments or supplements thereto.

A copy of the opinion of Cooley LLP relating to the validity of the Additional Shares is attached as Exhibit 5.1 hereto.

 

 


 

Item 9.01 Financial Statements and Exhibits.

(d)

Exhibits

 

 

 

Exhibit No.

Description

 

 

5.1

 

Opinion of Cooley LLP

23.1

 

Consent of Cooley LLP (included in Exhibit 5.1)

99.1

Press release, dated August 6, 2026

104

 

Cover Page Interactive Data File (embedded within the Inline XBRL document).

 

 


 

SIGNATURES

 

Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.

 

 

CG Oncology, Inc.

 

 

Date: August 6, 2026

By: /s/ Josh Patterson

 

Name: Josh Patterson

 

Title: General Counsel and Chief Compliance Officer

 

 


Exhibit 99.1

img89521117_0.jpg

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

 

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, August 6, 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.

 

 

 

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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
o
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.

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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.

 

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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.

 

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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
 

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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

 

 

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Filing Exhibits & Attachments

3 documents