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OnKure Therapeutics Reports Second Quarter 2026 Financial Results and Provides Business Highlights                                               

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OnKure Therapeutics (Nasdaq: OKUR) reported second quarter 2026 results and progress on its next-generation PI3Kα pan-mutant selective inhibitor programs. Lead candidates OKI-355 for vascular anomalies and OKI-345 for breast cancer are in IND-enabling studies, with IND submissions planned for 1H 2027.

According to the company, cash, cash equivalents and marketable securities totaled $176.4 million at June 30, 2026, extending estimated operating runway into 2029. Second quarter 2026 R&D expenses were $12.6 million, flat year over year, while G&A expenses rose to $4.3 million from $3.7 million. Net loss for the quarter was $15.3 million, or $0.31 per share, compared with $15.4 million, or $1.14 per share, a year earlier, reflecting higher interest income and a larger share count. OnKure also highlighted scientific engagement through a PI3Kα-focused Key Opinion Leader event and sponsorship of the ISSVA World Congress 2026.

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Positive

  • Cash and securities $176.4M at 6/30/26, runway into 2029
  • Net loss slightly improved to $15.3M from $15.4M year over year
  • Q2 R&D stable at $12.6M vs prior-year quarter while advancing two IND-enabling programs
  • Six-month operating expenses down to $32.5M from $33.3M year over year
  • Stockholders’ equity increased to $172.1M from $56.2M at 12/31/25

Negative

  • Q2 net loss $15.3M and six-month net loss $30.5M
  • Q2 operating expenses $16.9M, up from $16.3M year over year
  • G&A rose to $4.3M from $3.7M in Q2 2025, driven by personnel and consulting
  • Ongoing operating losses with no reported product revenue in the period

Market Context

Across five tag-specific earnings events, the average move was -0.14%. The report’s cash position an...
Analysis

Across five tag-specific earnings events, the average move was -0.14%. The report’s cash position and pipeline timing are read alongside Net Selling insider activity and low short positioning, which add context and leave funding and execution as risks to watch.

Key Figures

Cash and securities: $176.4 million Cash runway: Into 2029 R&D expenses: $12.6 million +4 more
7 metrics
Cash and securities $176.4 million As of June 30, 2026
Cash runway Into 2029 Expected funding period
R&D expenses $12.6 million Q2 2026 and Q2 2025
G&A expenses $4.3 million Q2 2026 vs. $3.7 million in Q2 2025
Net loss $15.3 million Q2 2026 vs. $15.4 million in Q2 2025
Net loss per share $0.31 per share Q2 2026 vs. $1.14 per share in Q2 2025
IND submissions 1H 2027 Planned for OKI-355 and OKI-345

Previous Earnings Reports

5 past events · Latest: May 05 (Positive)
Same Type Pattern 5 events
Date Event Sentiment 24h Move Catalyst
May 05 Q1 earnings results Positive -10.0% Strategic pipeline updates and private placement accompanied quarterly financial results.
Mar 12 Q4/FY earnings results Positive +7.4% Cash position, enrollment milestones, and next-generation candidate update supported the release.
Nov 06 Q3 earnings update Positive -7.0% Clinical enrollment progress and expansion arms were reported alongside expected data milestones.
Aug 12 Q2 earnings update Positive +20.0% Trial enrollment completion and new combination arms were reported with financial results.
May 06 Q1 earnings results Positive -11.2% Preliminary clinical results and development milestones accompanied quarterly financial disclosures.

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 showed three divergences and two alignments, with an average move of -0.14%.

Key Terms

therapeutic index, wildtype, allosteric inhibition
3 terms
therapeutic index medical
"potentially enabling a wider therapeutic index"
The therapeutic index is a measure of a drug’s safety margin—the gap between the dose that produces a desired effect and the dose that causes harmful effects. For investors, a larger therapeutic index means a wider safety cushion, lower risk of dangerous side effects, smoother regulatory review and broader market acceptance, all of which can reduce clinical and commercial risk and affect a drug developer’s valuation.
wildtype medical
"while sparing wildtype PI3Kα"
The naturally occurring or standard form of a gene, organism, or virus used as the baseline in laboratory and clinical work. Investors see “wildtype” when companies compare a new drug, diagnostic, or engineered strain against the original version; it’s like the “original recipe” that scientists measure changes from, helping regulators and researchers judge how much a treatment or mutation alters behavior or response.
allosteric inhibition medical
"Pan-Mutant Allosteric Inhibition Delivers"
A form of drug action where a molecule binds to a site on a protein (often an enzyme or receptor) that is different from the main active site, causing the protein's shape and activity to change. Like pressing a side button that alters how a machine works, this can fine-tune or block biological signals; for investors, allosteric inhibitors matter because they can offer unique efficacy, safety profiles, resistance patterns and intellectual property advantages that affect a drug candidate's development, regulatory review and commercial value.

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

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-- Executing IND-enabling activities for next-generation PI3Kα pan-mutant selective candidates OKI-345 in breast cancer and OKI-355 in vascular anomalies, with IND submissions planned for 1H 2027

-- Hosted a Key Opinion Leader event highlighting the evolving PI3Kα treatment landscape and the scientific rationale supporting OnKure's next-generation PI3Kα pan-mutant inhibitor programs

-- Participated as an exhibitor and sponsor at the ISSVA World Congress 2026 in Philadelphia, supporting engagement with leading vascular anomalies clinicians and researchers

-- $176 million of cash, cash equivalents and marketable securities expected to fund operations into 2029

BOULDER, Colo., Aug. 04, 2026 (GLOBE NEWSWIRE) -- OnKure Therapeutics, Inc. (Nasdaq: OKUR), a clinical-stage biopharmaceutical company focused on developing novel precision medicines, today reported financial results for the second quarter ended June 30, 2026, and provided recent business highlights.

“Following our strategic transformation earlier this year, we continue to advance our next-generation PI3Kα pan-mutant selective inhibitor pipeline, which we believe represents the most compelling opportunity to deliver differentiated therapies across PI3Kα-driven diseases,” said Nicholas Saccomano, Ph.D., President and Chief Executive Officer of OnKure. “Both OKI-355 and OKI-345 continue to advance through IND-enabling activities and remain on track for planned IND submissions in the first half of 2027. We believe the combination of our chemistry platform and deep understanding of PI3Kα biology positions us to develop differentiated therapies with the potential to meaningfully improve outcomes for patients. Our recent Key Opinion Leader event reinforced the scientific rationale underpinning our strategy and highlighted the significant opportunity for next-generation PI3Kα pan-mutant selective inhibitors to overcome the limitations of current therapies across multiple disease settings.”

Vascular Anomalies

OnKure continues to advance OKI-355, a next-generation PI3Kα pan-mutant-selective inhibitor candidate announced in March 2026 to lead its development pipeline in vascular anomalies. OKI-355 has been designed to selectively inhibit mutant PI3Kα while sparing wildtype PI3Kα, potentially enabling a wider therapeutic index and avoidance of class-limiting toxicities. High and sustained target coverage across all hotspot PI3Kα mutations can support the potential for deep and durable responses in vascular anomalies. OnKure plans to submit an Investigational New Drug (IND) application to the U.S. Food and Drug Administration (FDA) for OKI-355 in the first half of 2027.

Additionally, earlier this year, OnKure initiated a discovery research program to expand its vascular anomalies pipeline beyond targeting PI3Kα.

Breast Cancer

In breast cancer, OnKure continues to advance OKI-345, a next-generation PI3Kα pan-mutant-selective inhibitor candidate selected in March 2026. OKI-345 has been designed to selectively inhibit mutant PI3Kα while sparing wildtype PI3Kα, potentially enabling a wider therapeutic index and avoidance of class-limiting toxicities. High and sustained target coverage across all hotspot PI3Kα mutations can support the potential for deep and durable responses in breast cancer, both as monotherapy and in combination. OnKure plans to submit an IND application to the FDA for OKI-345 in the first half of 2027.

Scientific Engagement

OnKure recently hosted a virtual Key Opinion Leader event titled "Selectivity Matters and Pan-Mutant Allosteric Inhibition Delivers," featuring Benjamin F. Cravatt, Ph.D., of Scripps Research, and Robert Abraham, Ph.D., Chief Scientific Officer of Engine Biosciences. The discussion explored the scientific rationale supporting next-generation PI3Kα pan-mutant selective inhibitors, including the importance of PI3Kα selectivity, the potential to overcome limitations of current therapies, and the Company's structure-based drug design approach.

OnKure also participated as an exhibitor and sponsor at the International Society for the Study of Vascular Anomalies (ISSVA) World Congress 2026 in Philadelphia, held in May.

Financial Results

Cash position: As of June 30, 2026, the Company reported cash, cash equivalents, and marketable securities of $176.4 million, which is expected to provide cash runway into 2029.

Research and development (R&D) expenses: R&D expenses were $12.6 million for both the second quarter of 2026 and the second quarter of 2025. During the second quarter of 2026, an increase in clinical trial and outsourced manufacturing expenses was offset by a decrease in outsourced preclinical R&D expenses.

General and Administrative (G&A) expenses: G&A expenses were $4.3 million for the second quarter of 2026, compared to $3.7 million for the second quarter of 2025. The increase of $0.6 million was primarily driven by increases in personnel-related and consulting costs.

Net loss and net loss per share were $15.3 million, or $0.31 per share, for the second quarter of 2026, compared to $15.4 million, or $1.14 per share, for the second quarter of 2025.

About OnKure Therapeutics

OnKure Therapeutics (Nasdaq: OKUR) is a clinical-stage biopharmaceutical company focused on the discovery and development of best-in-class precision medicines that target biologically validated drivers of vascular anomalies and cancers that are underserved by available therapies. Using a structure and computational chemistry-driven drug design platform, OnKure is committed to improving clinical outcomes for patients by building a pipeline of small molecule drugs designed to selectively target specific mutations thought to be key drivers of vascular anomalies and cancer. OnKure aims to become a leader in targeting PI3Kα and has multiple programs designed to enable best-in-class targeting of this important molecular target.

For more information about OnKure, visit us at www.onkure.com and follow us on LinkedIn.

Cautionary Note Regarding Forward-Looking Statements

This press release contains forward-looking statements that involve substantial risks and uncertainties. All statements other than statements of historical facts contained in this press release are forward-looking statements. Such forward-looking statements include, among other things, statements regarding the potential of, and expectations regarding, OnKure’s product candidates and programs, including OKI-355 and OKI-345; OnKure’s ability to discover, develop and advance additional programs; expected milestones and the timing of such milestones, including the submission of IND applications for OKI-355 and OKI-345; OnKure’s expected cash runway; and statements by OnKure’s President and Chief Executive Officer. In some cases, you can identify forward-looking statements by terminology such as “believe,” “expect,” “estimate,” “intend,” “may,” “plan,” “potentially,” “will” or the negative of these terms or other similar expressions.

These forward-looking statements are based largely on OnKure’s current expectations and projections about future events and trends that OnKure believes may affect its financial condition, results of operations, business strategy and financial needs. These forward-looking statements are subject to a number of risks, uncertainties and assumptions, including, among other things: OnKure’s limited operating history; the significant net losses incurred since inception; the ability to raise additional capital to finance operations; the risk that actual uses of cash and cash equivalents differ from the assumptions underlying OnKure’s expected cash runway; the ability to advance product candidates through preclinical and clinical development; the ability to obtain regulatory approval for, and ultimately commercialize, OnKure’s product candidates; the outcome of preclinical testing and early clinical trials for OnKure’s product candidates, including the ability of those trials to satisfy relevant governmental or regulatory requirements and the potential that the outcome of preclinical testing and early clinical trials may not be predictive of the success of later clinical trials; OnKure’s limited resources; the risk of adverse events, toxicities or other undesirable side effects; potential delays or difficulties in the enrollment or maintenance of patients in clinical trials; the decision to develop or seek strategic collaborations to develop OnKure’s current or future product candidates in combination with other therapies and the cost of combination therapies; OnKure’s limited experience in designing clinical trials and lack of experience in conducting clinical trials; the substantial competition OnKure faces in discovering, developing, or commercializing products; OnKure’s ability to protect its intellectual property and proprietary technologies; developments relating to OnKure’s competitors and its industry, including competing product candidates and therapies; reliance on third parties, contract manufacturers, and contract research organizations; legislative, regulatory, political and economic developments and general market conditions; and those risks described in the section entitled “Risk Factors” in documents that OnKure files from time to time with the SEC, including its Annual Report on Form 10-K filed with the SEC on March 12, 2026, its Quarterly Report on Form 10-Q for the quarter ended June 30, 2026 filed with the SEC on August 4, 2026, and any subsequent filings with the SEC. These risks are not exhaustive. New risk factors emerge from time to time, and it is not possible for OnKure’s management to predict all risk factors, nor can OnKure assess the impact of all factors on OnKure’s business or the extent to which any factor, or combination of factors, may cause actual results to differ materially from those contained in, or implied by, any forward-looking statements. You should not rely upon forward-looking statements as predictions of future events. Although OnKure believes that the expectations reflected in the forward-looking statements are reasonable, OnKure cannot guarantee future results, levels of activity, performance or achievements. Except as required by law, OnKure undertakes no obligation to update publicly any forward-looking statements for any reason after the date of this press release.

Contact:

Dan Ferry
LifeSci Advisors
daniel@lifesciadvisors.com


ONKURE THERAPEUTICS, INC.
Condensed Consolidated Balance Sheets
(In thousands, unaudited)
 
  
  June 30,
2026
  December 31,
2025
 
       
Assets      
Current assets:      
Cash, cash equivalents and marketable securities $176,386  $59,050 
Prepaid expenses and other current assets  1,291   1,789 
Total current assets  177,677   60,839 
Property and equipment, net  435   618 
Operating lease, right-of-use asset  840   387 
Other assets  401   273 
Total assets $179,353  $62,117 
Liabilities and Stockholders’ Equity      
Current liabilities:      
Accounts payable, accrued expenses, and other current liabilities $6,307  $5,372 
Operating lease liabilities, current portion  336   549 
Total current liabilities  6,643   5,921 
Long-term liabilities  602   12 
Total liabilities  7,245   5,933 
Stockholders’ equity  172,108   56,184 
Total liabilities and stockholders’ equity $179,353  $62,117 


ONKURE THERAPEUTICS, INC.
Condensed Consolidated Statements of Operations
(In thousands, except share and per share data, unaudited)

 
  
 Three Months Ended  Six Months Ended 
 June 30,  June 30, 
 2026  2025  2026  2025 
Operating expenses:           
Research and development$12,611  $12,613  $24,318  $25,625 
General and administrative 4,288   3,711   8,196   7,699 
Total operating expenses 16,899   16,324   32,514   33,324 
Loss from operations (16,899)  (16,324)  (32,514)  (33,324)
Other income:           
Interest income 1,553   934   2,011   2,009 
Total other income 1,553   934   2,011   2,009 
Net loss$(15,346) $(15,390) $(30,503) $(31,315)
            
Net loss per share attributable to common stockholders:           
Basic and diluted$(0.31) $(1.14) $(0.96) $(2.33)
Weighted average shares outstanding:           
Basic and diluted 49,869,177   13,509,080   31,871,862   13,466,942 



FAQ

What were OnKure Therapeutics (OKUR) second quarter 2026 financial results?

OnKure reported a Q2 2026 net loss of $15.3 million, or $0.31 per share. According to OnKure, research and development expenses were $12.6 million and general and administrative expenses were $4.3 million, leading to total operating expenses of $16.9 million for the quarter.

How much cash does OnKure Therapeutics (OKUR) have and what is its runway?

OnKure reported $176.4 million in cash, cash equivalents and marketable securities as of June 30, 2026. According to OnKure, this balance is expected to fund operations into 2029, supporting ongoing IND-enabling work for its PI3Kα pan-mutant inhibitor programs.

What are the timelines for OnKure Therapeutics’ PI3Kα programs OKI-345 and OKI-355?

OnKure plans to submit IND applications in the first half of 2027 for both OKI-345 and OKI-355. According to OnKure, OKI-345 targets breast cancer and OKI-355 targets vascular anomalies, with current work focused on IND-enabling activities.

How did OnKure Therapeutics’ expenses change in Q2 2026 versus Q2 2025?

OnKure’s R&D expenses were flat at $12.6 million, while G&A expenses increased to $4.3 million from $3.7 million. According to OnKure, higher personnel-related and consulting costs drove the G&A increase, lifting total operating expenses to $16.9 million.

What progress is OnKure Therapeutics (OKUR) making in vascular anomalies?

OnKure is advancing OKI-355, a next-generation PI3Kα pan-mutant-selective inhibitor for vascular anomalies, through IND-enabling studies. According to OnKure, an IND filing with the FDA is planned for the first half of 2027, and a broader vascular anomalies research program has begun.

How is OnKure Therapeutics targeting breast cancer with its PI3Kα program?

OnKure is developing OKI-345, a PI3Kα pan-mutant-selective inhibitor designed for breast cancer treatment. According to OnKure, OKI-345 aims to selectively inhibit mutant PI3Kα, support deep and durable responses, and is on track for a 1H 2027 IND submission.

Did OnKure Therapeutics (OKUR) report any revenue in its Q2 2026 results?

OnKure’s Q2 2026 statement highlights operating expenses, other income and net loss, with no product revenue reported. According to OnKure, the company remains in the clinical-stage development phase, focused on advancing its PI3Kα-targeted precision medicine pipeline.