STOCK TITAN

ORIC Pharmaceuticals (Nasdaq: ORIC) starts Phase 3 cancer trial with $387.6M cash

(Moderate)
(Neutral)
Form Type
8-K

Rhea-AI Filing Summary

ORIC Pharmaceuticals, Inc. reported financial results and pipeline progress for the quarter ended June 30, 2026. Cash, cash equivalents and investments totaled $387.6 million, including $59.9 million in net proceeds raised under an at-the-market program, which are expected to fund the operating plan into 2H 2028.

For Q2 2026, research and development expenses were $36.3 million versus $30.5 million a year earlier, and general and administrative expenses were $9.0 million versus $8.5 million. Net loss was $41,492 thousand, with net loss per share of $0.38 compared with $0.47 in Q2 2025.

Operationally, ORIC initiated Himalayas-1, a global Phase 3 registrational trial of rinzimetostat in mCRPC, targeting about 600 patients across 25 countries, and entered a collaboration with Bayer, which will supply NUBEQA (darolutamide) at no cost while ORIC retains full rights to rinzimetostat. Enozertinib continues in Phase 1b NSCLC studies, with multiple data readouts anticipated in 2H 2026 and October 2026.

Positive

  • None.

Negative

  • None.
Item 2.02 Results of Operations and Financial Condition Financial
Disclosure of earnings results, typically an earnings press release or preliminary financials.
Item 9.01 Financial Statements and Exhibits Exhibits
Financial statements, pro forma financial information, and exhibit attachments filed with this report.
Cash, cash equivalents and investments $387.6 million As of June 30, 2026
ATM net proceeds $59.9 million Raised from healthcare specialist funds in Q1 2026 under the ATM program
R&D expenses Q2 2026 $36.3 million Three months ended June 30, 2026; $5.7 million increase from Q2 2025
G&A expenses Q2 2026 $9.0 million Three months ended June 30, 2026; $0.5 million increase from Q2 2025
Net loss Q2 2026 $41,492 thousand Three months ended June 30, 2026 (in thousands)
Net loss per share Q2 2026 $0.38 Basic and diluted net loss per share for the quarter ended June 30, 2026
Weighted-average shares outstanding Q2 2026 108,012,388 shares Basic and diluted for the three months ended June 30, 2026
mCRPC medical
"Himalayas-1 global Phase 3 trial in patients with mCRPC previously treated"
mCRPC stands for metastatic castration‑resistant prostate cancer, a form of prostate cancer that has spread beyond the prostate and keeps progressing despite treatments that lower male hormones. It matters to investors because this stage is harder to treat, drives demand for new therapies, and often involves large, expensive clinical trials and regulatory decisions that can strongly influence a drug maker’s future revenue and stock value—think of it as a stubborn problem that creates both medical need and commercial opportunity.
Phase 3 registrational trial regulatory
"initiation of Himalayas-1, a global Phase 3 registrational trial, brings us closer"
A phase 3 registrational trial is a large, late-stage clinical study designed to produce the definitive safety and effectiveness data regulators need to decide whether to approve a new medical product. For investors, its results are critical because positive findings greatly increase the chance of market authorization and future sales, while negative or ambiguous results can sharply reduce expected value—think of it as the product’s final exam before getting a license to sell.
radiographic progression-free survival medical
"The primary endpoint is radiographic progression-free survival and the key secondary"
The length of time during which a patient’s cancer does not get worse on medical imaging scans; it is measured from the start of treatment until scans show tumor growth or new lesions. Investors care because it’s a common measure used in clinical trials to signal whether a therapy is working — like a stopwatch showing how long a treatment keeps disease stable — and strong results can influence regulatory approval, sales potential and stock value.
allosteric inhibitor medical
"rinzimetostat: a potent and selective allosteric inhibitor of PRC2"
An allosteric inhibitor is a molecule, often a drug, that attaches to a spot on a protein away from its main active site and changes the protein’s shape so it works less effectively or stops working. For investors, these compounds matter because they can offer greater selectivity and fewer side effects than drugs that block the active site directly, potentially improving clinical success, reducing safety risks, and extending the commercial value of a therapy.
EGFR exon 20 insertion mutations medical
"a brain-penetrant, selective inhibitor targeting EGFR exon 20 insertion mutations"
EGFR exon 20 insertion mutations are a specific type of genetic change where extra DNA pieces are inserted into exon 20 of the EGFR gene, altering the protein that helps regulate cell growth. For investors, they matter because these mutations define a distinct patient group and can determine whether a drug, test, or clinical trial will work, similar to how a unique lock requires a matching key in drug development and diagnostics.
at-the-market (ATM) program financial
"net proceeds raised from healthcare specialist funds during the first quarter under the ATM"
An at-the-market (ATM) program is a way for a company to sell newly issued shares directly into the open market at the current trading price over time, rather than all at once. For investors it matters because it provides a flexible, ongoing source of capital but can dilute existing ownership and put steady selling pressure on a stock’s price—similar to a store quietly adding more items for sale at the posted price.
R&D expenses Q2 2026 $36.3 million $5.7 million increase from Q2 2025
G&A expenses Q2 2026 $9.0 million $0.5 million increase from Q2 2025
Net loss per share Q2 2026 $0.38 Compared with $0.47 in Q2 2025
Guidance

The company expects its existing cash and investments to fund its current operating plan into the second half of 2028.

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

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FAQ

What were ORIC (ORIC) cash and investment balances as of June 30, 2026?

ORIC reported $387.6 million in cash, cash equivalents and investments as of June 30, 2026, including $59.9 million raised under an ATM program, and expects this to fund its operating plan into 2H 2028.

What loss did ORIC (ORIC) report for the second quarter of 2026?

For Q2 2026, ORIC reported a net loss of $41,492 thousand, with net loss per share of $0.38 basic and diluted, compared with $36,355 thousand and $0.47 per share in the same quarter of 2025.

How did ORIC (ORIC) research and development expenses change in Q2 2026?

Research and development expenses were $36.3 million for the three months ended June 30, 2026, up from $30.5 million a year earlier, an increase of $5.7 million, primarily driven by higher external costs for rinzimetostat.

What major clinical trial did ORIC (ORIC) initiate in Q2 2026?

ORIC initiated Himalayas-1, a global Phase 3 registrational trial of rinzimetostat in mCRPC, targeting about 600 patients across more than 250 sites in 25 countries, with radiographic progression-free survival as the primary endpoint.

What collaboration did ORIC (ORIC) enter regarding the Himalayas-1 trial?

ORIC entered a clinical trial collaboration and supply agreement with Bayer, under which Bayer will provide NUBEQA (darolutamide) at no cost for Himalayas-1, while ORIC sponsors the trial and retains full global rights to rinzimetostat.

What upcoming clinical milestones has ORIC (ORIC) highlighted for 2026?

ORIC expects a rinzimetostat program update in 2H 2026 and multiple enozertinib data readouts, including first-line EGFR atypical monotherapy data at the ESMO Congress 2026 in October and additional first-line exon 20 and combination data in 2H 2026.
false000179628000017962802026-08-032026-08-03

 

 

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 3, 2026

 

ORIC Pharmaceuticals, Inc.

(Exact name of registrant as specified in its charter)

 

 

 

 

 

 

 

Delaware

001-39269

47-1787157

(State or other jurisdiction

of incorporation)

(Commission

File Number)

(IRS Employer
Identification No.)

 

240 E. Grand Ave, 2nd Floor

South San Francisco, CA 94080

(Address of principal executive offices, including zip code)

 

(650) 388-5600

(Registrant’s telephone number, including area code)

 

Not Applicable

(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

 

ORIC

 

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 3, 2026, ORIC Pharmaceuticals, Inc. (the “Company”), issued a press release announcing its financial results for the fiscal quarter ended June 30, 2026. A copy of the press release is attached hereto as Exhibit 99.1 and is incorporated herein by reference.

All of the information furnished in this Item 2.02 and Item 9.01 (including Exhibit 99.1) shall not be deemed to be “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 into any filing under the Securities Act of 1933, as amended (the “Securities Act”), or the Exchange Act, except as shall be expressly set forth by specific reference in such a filing.

Item 9.01 Financial Statements and Exhibits.

 

(d) Exhibits

Exhibit No.

 

Description

 

 

 

99.1

 

Press Release dated August 3, 2026

104

 

Cover Page Interactive Data File (embedded with 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.

 

 

 

 

 

 

 

 

 

 

ORIC PHARMACEUTICALS, INC.

 

 

 

 

    Date: August 3, 2026

 

By:

/s/ Dominic Piscitelli

 

 

 

Dominic Piscitelli

Chief Financial Officer

 


img48504584_0.gif

Exhibit 99.1

 

ORIC® Pharmaceuticals Reports Second Quarter 2026 Financial Results and Operational Updates

 

Initiated Himalayas-1 global Phase 3 trial in patients with mCRPC previously treated with abiraterone

 

Entered into a clinical trial collaboration and supply agreement with Bayer to provide darolutamide for Himalayas-1

 

Anticipate rinzimetostat program update in 2H 2026 and enozertinib clinical updates in 2H 2026 ahead of potential initiation of a registrational trial

 

Cash and investments of approximately $388 million expected to provide runway into 2H 2028 and beyond anticipated primary endpoint readout from first Phase 3 trial for rinzimetostat

 

SOUTH SAN FRANCISCO and SAN DIEGO, CA – August 3, 2026 – ORIC Pharmaceuticals, Inc. (Nasdaq: ORIC), a clinical stage oncology company focused on developing and commercializing treatments that address mechanisms of therapeutic resistance, today reported financial results and provided operational updates for the quarter ended June 30, 2026.

 

“The recent initiation of Himalayas-1, a global Phase 3 registrational trial, brings us closer to delivering a potentially practice-changing therapy for patients with prostate cancer,” said Jacob M. Chacko, M.D., president and chief executive officer. “With rinzimetostat now in Phase 3 and enozertinib approaching a key clinical update in the second half of the year, ORIC has become a diversified, late-stage oncology company with multiple opportunities to create meaningful value for patients while advancing our mission of Overcoming Resistance In Cancer.”

 

Second Quarter 2026 and Other Recent Highlights

 

Rinzimetostat: a potent and selective allosteric inhibitor of PRC2

 

Finalized the trial protocol and initiated the Himalayas-1 global Phase 3 registrational trial following End-of-Phase 1 interactions with the FDA and other global health authorities. The Himalayas-1 trial is expected to enroll approximately 600 patients from over 250 sites in 25 countries, randomized 1:1 to receive 400 mg once daily rinzimetostat (with or without food) in combination with darolutamide versus physician’s choice of an androgen receptor (AR) inhibitor or docetaxel. The primary endpoint is radiographic progression-free survival and the key secondary endpoint is overall survival.
Entered into a clinical trial collaboration and supply agreement with Bayer to provide darolutamide for Himalayas-1. Under the terms of the agreement, the company will conduct and sponsor the Himalayas-1 trial and Bayer will provide their AR inhibitor, NUBEQA® (darolutamide), at no cost for use in the trial in combination with rinzimetostat. This agreement does not grant Bayer any license, option, or other rights to

 


 

 

 

rinzimetostat and ORIC retains full global development and commercial rights to rinzimetostat.
Presented preclinical data at AACR showing PRC2 inhibition reduces prostate tumor adaptability and sustains the benefit derived from AR inhibition, with potential advantages of EED over EZH2 inhibition.

 

Enozertinib: a brain-penetrant, selective inhibitor targeting EGFR exon 20 insertion mutations and EGFR atypical mutations

Enozertinib is currently being evaluated in Phase 1b trials across the following first-line patient populations with advanced NSCLC:

As a single-agent in patients with EGFR atypical mutations.
As a single-agent in patients with EGFR exon 20 insertion mutations.
In combination with subcutaneous (SC) amivantamab and in combination with chemotherapy in patients with EGFR exon 20 insertion mutations.

 

Anticipated Program Milestones:

 

ORIC anticipates the following upcoming milestones:

Rinzimetostat in mCRPC:
2H 2026: Program update
Enozertinib in NSCLC:
October 2026: 1L EGFR atypical monotherapy data to be presented at ESMO Congress 2026
2H 2026: 1L EGFR exon 20 insertion monotherapy data and combination data with SC amivantamab

 

Second Quarter 2026 Financial Results

Cash, Cash Equivalents and Investments: Cash, cash equivalents and investments totaled $387.6 million as of June 30, 2026, which includes $59.9 million in net proceeds raised from healthcare specialist funds during the first quarter under the ATM (at-the-market) program. The company expects its cash and investments to fund the operating plan into 2H 2028.

 

R&D Expenses: Research and development (R&D) expenses were $36.3 million for the three months ended June 30, 2026, compared to $30.5 million for the three months ended June 30, 2025, an increase of $5.7 million. For the six months ended June 30, 2026, R&D expenses were $67.7 million, compared to $55.2 million for the six months ended June 30, 2025, an increase of $12.5 million. The increases were primarily due to an increase in external expenses related to the advancement of rinzimetostat, offset by lower enozertinib costs due to timing of manufacturing and clinical costs as well as lower preclinical costs.

 

G&A Expenses: General and administrative (G&A) expenses were $9.0 million for the three months ended June 30, 2026, compared to $8.5 million for the three months ended

 

 

 

 


 

 

 

June 30, 2025, an increase of $0.5 million. For the six months ended June 30, 2026, G&A expenses were $17.2 million, compared to $16.6 million for the six months ended June 30, 2025, an increase of $0.6 million. The increases were primarily due to higher personnel costs and professional services.

 

About ORIC Pharmaceuticals, Inc.

ORIC Pharmaceuticals is a clinical stage biopharmaceutical company dedicated to improving patients’ lives by Overcoming Resistance In Cancer. ORIC’s clinical stage product candidates include (1) rinzimetostat, an allosteric inhibitor of the polycomb repressive complex 2 (PRC2) via the EED subunit, being developed for prostate cancer, and (2) enozertinib, a brain-penetrant inhibitor targeting EGFR exon 20 insertion and EGFR atypical mutations, being developed for NSCLC. ORIC has offices in South San Francisco and San Diego, California. For more information, please go to www.oricpharma.com, and follow us on X or LinkedIn.

 

Cautionary Note Regarding Forward-Looking Statements

This press release contains forward-looking statements as that term is defined in Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934. Statements in this press release that are not purely historical are forward-looking statements. Such forward-looking statements include, among other things, the continued clinical development of rinzimetostat and enozertinib; the potential advantages of rinzimetostat and enozertinib; the development plans and timelines for rinzimetostat and enozertinib; plans underlying ORIC’s clinical trials and development; anticipated program milestones, including timing of program and data updates; the period over which ORIC estimates its existing cash and investments will be sufficient to fund its current operating plan; and statements by the company’s chief executive officer. Words such as “believes,” “anticipates,” “plans,” “expects,” “intends,” “will,” “goal,” “potential” and similar expressions are intended to identify forward-looking statements. The forward-looking statements contained herein are based upon ORIC’s current expectations and involve assumptions that may never materialize or may prove to be incorrect. Actual results could differ materially from those projected in any forward-looking statements due to numerous risks and uncertainties, including but not limited to: risks associated with the process of discovering, developing and commercializing drugs that are safe and effective for use as human therapeutics and ORIC’s limited operating history; ORIC’s ability to develop, initiate or complete preclinical studies and clinical trials for, obtain approvals for and commercialize any of its product candidates; changes in ORIC’s plans to develop and commercialize its product candidates; the potential for clinical trials of rinzimetostat, enozertinib or any other product candidates to differ from preclinical, initial, interim, preliminary, expected or prior clinical trial results; negative impacts of health emergencies, economic instability or international conflicts on ORIC’s operations, including clinical trials; the risk of the occurrence of any event, change or other circumstance that could give rise to the termination of ORIC’s license and collaboration agreements or its clinical trial collaboration and supply agreements; the potential market for ORIC’s product candidates, and the progress and success of competing therapeutics currently available or in development; ORIC’s ability to raise any additional funding it will need to continue to pursue its business and product development plans; regulatory developments in the United States and foreign countries; ORIC’s

 

 

 

 


 

 

 

reliance on third parties, including contract manufacturers and contract research organizations; ORIC’s ability to obtain and maintain intellectual property protection for its product candidates; the loss of key scientific or management personnel; competition in the industry in which ORIC operates; general economic and market conditions; and other risks. Information regarding the foregoing and additional risks may be found in the section entitled “Risk Factors” in ORIC’s Quarterly Report on Form 10-Q filed with the Securities and Exchange Commission (the SEC) on August 3, 2026, and ORIC’s future reports to be filed with the SEC. These forward-looking statements are made as of the date of this press release, and ORIC assumes no obligation to update the forward-looking statements, or to update the reasons why actual results could differ from those projected in the forward-looking statements, except as required by law.

 

Contact:

Dominic Piscitelli, Chief Financial Officer

dominic.piscitelli@oricpharma.com

info@oricpharma.com

 

All registered trademarks are the property of their respective owners.

 

 

 

 


 

 

 

ORIC PHARMACEUTICALS, INC.

CONDENSED BALANCE SHEETS

(in thousands)

 

 

June 30, 2026

 

 

December 31, 2025

 

 

(unaudited)

 

 

 

 

Assets

 

Current assets:

 

 

 

 

 

Cash, cash equivalents and short-term investments

$

264,761

 

 

$

281,488

 

Prepaid expenses and other current assets

 

8,934

 

 

 

6,978

 

Total current assets

 

273,695

 

 

 

288,466

 

 

 

 

 

 

Long-term investments

 

122,799

 

 

 

110,762

 

Property and equipment, net

 

2,242

 

 

 

2,415

 

Other assets

 

5,949

 

 

 

7,247

 

Total assets

$

404,685

 

 

$

408,890

 

 

 

 

 

Liabilities and Stockholders' Equity

 

Current liabilities:

 

 

 

 

 

Accounts payable

$

3,873

 

 

$

3,824

 

Accrued liabilities

 

16,883

 

 

 

16,593

 

Total current liabilities

 

20,756

 

 

 

20,417

 

 

 

 

 

 

Other long-term liabilities

 

2,673

 

 

 

4,111

 

Total liabilities

 

23,429

 

 

 

24,528

 

 

 

 

 

 

Total stockholders' equity

 

381,256

 

 

 

384,362

 

Total liabilities and stockholders' equity

$

404,685

 

 

$

408,890

 

 

 

 

 

 

 

 


 

 

 

ORIC PHARMACEUTICALS, INC.

STATEMENTS OF OPERATIONS AND COMPREHENSIVE LOSS

(Unaudited)

(in thousands, except share and per share amounts)

 

 

Three Months Ended
June 30,

 

 

Six Months Ended
June 30,

 

 

2026

 

 

2025

 

 

2026

 

 

2025

 

Operating expenses:

 

 

 

 

 

 

 

 

 

 

 

Research and development

$

36,296

 

 

$

30,549

 

 

$

67,733

 

 

$

55,189

 

General and administrative

 

9,000

 

 

 

8,515

 

 

 

17,182

 

 

 

16,593

 

Total operating expenses

 

45,296

 

 

 

39,064

 

 

 

84,915

 

 

 

71,782

 

Loss from operations

 

(45,296

)

 

 

(39,064

)

 

 

(84,915

)

 

 

(71,782

)

 

 

 

 

 

 

 

 

 

 

 

Other income, net

 

3,804

 

 

 

2,709

 

 

 

7,656

 

 

 

5,406

 

Net loss

$

(41,492

)

 

$

(36,355

)

 

$

(77,259

)

 

$

(66,376

)

Other comprehensive loss:

 

 

 

 

 

 

 

 

 

 

 

 Unrealized loss on investments

 

(728

)

 

 

(22

)

 

 

(1,804

)

 

 

(192

)

Comprehensive loss

$

(42,220

)

 

$

(36,377

)

 

$

(79,063

)

 

$

(66,568

)

Net loss per share, basic and diluted

$

(0.38

)

 

$

(0.47

)

 

$

(0.72

)

 

$

(0.89

)

Weighted-average shares outstanding, basic and diluted

 

108,012,388

 

 

 

78,126,257

 

 

 

106,749,594

 

 

 

74,602,994

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 


Filing Exhibits & Attachments

2 documents