Olema Oncology Reports Fourth Quarter and Full Year 2025 Financial and Operating Results
Rhea-AI Summary
Olema Oncology (Nasdaq: OLMA) reported Q4 and full-year 2025 results, highlighting late-stage progress for palazestrant and early data plans for OP-3136. The company raised approximately $218.5 million in a follow-on offering and ended 2025 with $505.4 million in cash, cash equivalents, and marketable securities.
Operationally, OPERA-01 top-line data are expected in fall 2026, OPERA-02 enrollment is advanced, a Phase 1b/2 study with Pfizer began, and OP-3136 initial clinical data are anticipated in Q2 2026.
Positive
- $505.4M cash, cash equivalents, and marketable securities at year-end 2025
- Follow-on public offering generated $218.5M gross proceeds
- OPERA-01 top-line data expected in fall 2026
- Advanced enrollment in OPERA-02 pivotal Phase 3 trial
- Initiated Phase 1b/2 palazestrant + atirmociclib study with Pfizer
- OP-3136 initial clinical data anticipated in Q2 2026
Negative
- Net loss of $162.5M for full-year 2025, up from $129.5M
- GAAP R&D expenses of $157.7M in 2025, up year-over-year
- GAAP G&A expenses increased to $21.0M for 2025
Market Reaction – OLMA
Following this news, OLMA has gained 5.37%, reflecting a notable positive market reaction. Our momentum scanner has triggered 2 alerts so far, indicating moderate trading interest and price volatility. The stock is currently trading at $15.50. This price movement has added approximately $59M to the company's valuation.
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Key Figures
Market Reality Check
Peers on Argus
OLMA slipped 1.34% with mixed peer action: ARVN, SAGE, BCAX, VSTM were negative while ORKA gained 21.8%. The mixed directions and lack of momentum flags suggest the move was stock‑specific rather than a broad biotech rotation.
Previous Earnings Reports
| Date | Event | Sentiment | Move | Catalyst |
|---|---|---|---|---|
| Nov 10 | Q3 2025 earnings | Positive | +4.2% | Higher cash balance and advancing palazestrant programs with Pfizer collaboration. |
| Aug 11 | Q2 2025 earnings | Positive | +16.2% | Dose selection for Phase 3 trials and strong cash with defined milestones. |
| May 13 | Q1 2025 earnings | Positive | -3.9% | Promising palazestrant PFS data and OP-3136 preclinical results despite higher losses. |
| Mar 18 | FY 2024 earnings | Positive | -0.7% | Capital raise and advancement of OPERA-01 and OPERA-02 to pivotal stages. |
| Nov 12 | Q3 2024 earnings | Negative | -0.5% | Net loss increase tied to higher R&D spend despite solid cash position. |
Earnings updates often led to modest positive moves, but there are instances where clinically and financially constructive releases were met with flat or negative reactions.
Over the past five earnings cycles, Olema has consistently highlighted progress for palazestrant and OP-3136 while operating with sizable cash balances. Cash rose from $214.8M in Q3 2024 to $434.1M at 2024 year-end and then to $392.7M, $361.9M, and $329.0M across 2025 quarters, alongside growing R&D spend and net losses. Price moves around these updates were mixed, with both double‑digit gains and mild declines, indicating varied investor response to similar clinical and financial messages.
Historical Comparison
In the last five earnings releases, OLMA’s average 1-day move was 3.06%, with both sizeable rallies and mild declines following similar cash and pipeline updates.
Earnings updates have traced a steady build-out of palazestrant from early data into pivotal OPERA-01 and OPERA-02 trials, while OP-3136 advanced from preclinical data and IND plans into ongoing Phase 1 studies, supported by a strengthening but actively utilized cash position.
Market Pulse Summary
The stock is up +5.4% following this news. A strong positive reaction aligns with Olema’s pattern of occasional sizable gains around earnings updates, where prior reports saw moves averaging 3.06%. The combination of a bolstered cash position of $505.4M, progress of pivotal OPERA trials, and early OP-3136 timeline may have reinforced confidence. However, rising annual net loss of $162.5M and elevated R&D commitments suggest that any sharp upside could remain sensitive to future data readouts and financing needs.
Key Terms
phase 3 medical
phase 1b/2 medical
metastatic breast cancer medical
pharmacokinetics medical
pharmacodynamics medical
non-gaap financial
underwritten public offering financial
marketable securities financial
AI-generated analysis. Not financial advice.
- On-track to report top-line data in the fall of 2026 from the pivotal Phase 3 OPERA-01 trial of palazestrant as a monotherapy in patients with 2/3L ER+/HER2- metastatic breast cancer
- Advanced enrollment in the OPERA-02 pivotal Phase 3 trial of palazestrant in combination with ribociclib in patients with frontline ER+/HER2- metastatic breast cancer
- Initiated the Phase 1b/2 study of palazestrant in combination with Pfizer’s novel CDK4 inhibitor, atirmociclib, in patients with ER+/HER2- metastatic breast cancer
- Continued enrollment in the Phase 1 clinical study of OP-3136 in breast cancer and other solid tumors, with initial clinical data expected in Q2 2026
- Generated
$218.5 million in gross proceeds from a follow-on public offering, further strengthening the Company’s balance sheet; ended 2025 with$505.4 million in cash, cash equivalents, and marketable securities - Transformation into a fully-integrated oncology company underway in preparation for the Company’s first potential commercial launch in late 2027
SAN FRANCISCO, March 16, 2026 (GLOBE NEWSWIRE) -- Olema Pharmaceuticals, Inc. (“Olema” or “Olema Oncology”, Nasdaq: OLMA), a clinical-stage biopharmaceutical company focused on the discovery, development, and commercialization of targeted therapies for breast cancer and beyond, today reported financial and operating results for the fourth quarter and full year ended December 31, 2025.
“2025 was a year of strong execution across the business as we advanced palazestrant as a differentiated endocrine therapy across multiple regimens, highlighted by continued enrollment and strong investigator interest in our OPERA-01 and OPERA-02 trials,” said Sean P. Bohen, M.D., Ph.D., President and Chief Executive Officer of Olema Oncology. “Our earlier-phase combination studies with palazestrant continue to advance and we are pleased to have initiated a Phase 1b/2 study with atirmociclib in collaboration with Pfizer, further demonstrating palazestrant’s potential as the combination endocrine therapy of choice in the metastatic setting.”
Bohen continued, “In November, we strengthened our balance sheet through a public offering that generated gross proceeds of approximately
Recent Progress
- Initiated the Phase 1b/2 study evaluating palazestrant in combination with atirmociclib in estrogen receptor-positive, human epidermal growth factor receptor 2-negative (ER+/HER2-) metastatic breast cancer in collaboration with Pfizer.
- Presented a trial-in-progress poster for the pivotal Phase 3 OPERA-02 trial evaluating palazestrant in combination with ribociclib in frontline ER+/HER2- advanced or metastatic breast cancer at the San Antonio Breast Cancer Symposium (SABCS) 2025.
- Continued enrollment in the Phase 1 study evaluating the safety, tolerability, pharmacokinetics, pharmacodynamics, and preliminary efficacy of OP-3136, as a monotherapy and in combination with fulvestrant and palazestrant, in participants with advanced solid tumors.
- Completed an underwritten public offering of an aggregate of 11,500,000 shares of common stock, including the full exercise of the underwriters’ option to purchase additional shares, resulting in gross proceeds of approximately
$218.5 million , before deducting underwriting discounts and commissions and estimated offering expenses.
Anticipated Upcoming Events
- Report initial clinical results for OP-3136 in Q2 2026 at a major medical conference.
- Report top-line data from the pivotal Phase 3 OPERA-01 trial of palazestrant as a monotherapy in second- and third-line (2/3L) ER+/HER2- metastatic breast cancer in the fall of 2026.
Fourth Quarter and Full Year 2025 Financial Results
Cash, cash equivalents, and marketable securities as of December 31, 2025, were
Net loss for the quarter and year ended December 31, 2025 was
GAAP research and development (R&D) expenses were
Non-GAAP R&D expenses were
GAAP G&A expenses were
Non-GAAP G&A expenses were
About Olema Oncology
Olema Oncology is a clinical-stage biopharmaceutical company committed to transforming the standard of care and improving outcomes for patients living with breast cancer and beyond. Olema is advancing a pipeline of novel therapies by leveraging our deep understanding of endocrine-driven cancers, nuclear receptors, and mechanisms of acquired resistance. Our lead product candidate, palazestrant (OP-1250), is a proprietary, orally available complete estrogen receptor (ER) antagonist (CERAN) and a selective estrogen receptor degrader (SERD), currently in two Phase 3 clinical trials. In addition, Olema is developing OP-3136, a potent lysine acetyltransferase 6 (KAT6) inhibitor, now in a Phase 1 clinical study. Olema is headquartered in San Francisco and has operations in Cambridge, Massachusetts. For more information, please visit www.olema.com.
About Palazestrant (OP-1250)
Palazestrant (OP-1250) is a novel, orally available small molecule with dual activity as both a complete estrogen receptor antagonist (CERAN) and selective estrogen receptor degrader (SERD). It is currently being investigated in patients with recurrent, locally advanced or metastatic ER-positive (ER+), human epidermal growth factor receptor 2-negative (HER2-) breast cancer. In clinical studies, palazestrant completely blocks ER-driven transcriptional activity in both wild-type and mutant forms of metastatic ER+ breast cancer and has demonstrated anti-tumor efficacy along with attractive pharmacokinetics and exposure, favorable tolerability, central nervous system penetration, and combinability with cyclin-dependent kinase 4/6 (CDK4/6) inhibitors. Palazestrant has been granted U.S. Food and Drug Administration (FDA) Fast Track designation for the treatment of ER+/HER2- metastatic breast cancer that has progressed following one or more lines of endocrine therapy with at least one line given in combination with a CDK4/6 inhibitor. It is being evaluated as a single agent in the ongoing pivotal Phase 3 clinical trial, OPERA-01, and in combination with ribociclib in the ongoing pivotal Phase 3 clinical trial, OPERA-02. Palazestrant is also being evaluated in multiple Phase 1/2 studies in combination with ribociclib, palbociclib, alpelisib, everolimus, and atirmociclib.
About OP-3136
OP-3136 is a novel, orally available small molecule that potently and selectively inhibits lysine acetyltransferase 6 (KAT6), an epigenetic target that is dysregulated in breast and other cancers. In preclinical studies, OP-3136 has demonstrated significant anti-proliferative activity in ER+ breast cancer models and is combinable and synergistic with endocrine therapies including palazestrant and cyclin-dependent kinase 4/6 (CDK4/6) inhibitors. The Investigational New Drug (IND) application for OP-3136 was cleared by the U.S. Food and Drug Administration (FDA) in December 2024 and patients are currently enrolling in the Phase 1 clinical study.
Non-GAAP Financial Information
The results presented in this press release include both GAAP information and non-GAAP information. As used in this release, non-GAAP R&D expense is defined by Olema as GAAP R&D expense excluding stock-based compensation expense, and non-GAAP G&A expense is defined by Olema as GAAP G&A expense excluding stock-based compensation expense. We use these non-GAAP financial measures to evaluate our ongoing operations and for internal planning and forecasting purposes. We believe that non-GAAP financial information, when taken collectively, may be helpful to investors because it provides consistency and comparability with past financial performance. However, non-GAAP financial information is presented for supplemental informational purposes only, has limitations as an analytical tool, and should not be considered in isolation or as a substitute for financial information presented in accordance with GAAP. Other companies, including companies in our industry, may calculate similarly titled non-GAAP measures differently or may use other measures to evaluate their performance, all of which could reduce the usefulness of our non-GAAP financial measures as tools for comparison. Investors are encouraged to review the related GAAP financial measures and the reconciliation of these non-GAAP financial measures to their most directly comparable GAAP financial measures and not rely on any single financial measure to evaluate our business.
Forward Looking Statements
Statements contained in this press release regarding matters that are not historical facts are “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. Words such as “anticipate,” “believe,” “could,” “expect,” “goal,” “intend,” “may,” “on track,” “potential,” “upcoming,” “will” and similar expressions (as well as other words or expressions referencing future events, conditions or circumstances) are intended to identify forward-looking statements. These statements include those related to timelines for enrollment for current clinical studies and for the receipt and presentation of results of clinical trials of palazestrant and OP-3136 each as a monotherapy and in combination trials, the timeline for potential approval and related commercial launch preparations, Olema’s financial condition and resources, results of operations, cash position, cash runway, and balance sheet strength, Olema’s potential commercial capabilities and timelines, the potential for palazestrant to become a differentiated endocrine therapy across multiple regimens, the potential for palazestrant to become a combination agent of choice in the metastatic setting, Olema’s ability to transform the breast cancer paradigm and ability to deliver meaningful new treatment options to patients living with breast cancer and beyond, Olema’s transformation into a fully-integrated oncology company, and the potential beneficial characteristics including but not limited to safety, tolerability, activity, efficacy and therapeutic effects of palazestrant or OP-3136, the combinability of palazestrant or OP-3136 with other drugs, including in the metastatic setting. Because such statements deal with future events and are based on Olema’s current expectations, they are subject to various risks and uncertainties, and actual results, performance, or achievements of Olema could differ materially from those described in or implied by the statements in this press release. These forward-looking statements are subject to risks and uncertainties, including, without limitation, those discussed in the section titled “Risk Factors” in Olema’s Annual Report on Form 10-K for the year ended December 31, 2025, and future filings and reports that Olema makes from time to time with the U.S. Securities and Exchange Commission. Except as required by law, Olema assumes no obligation to update these forward-looking statements, including in the event that actual results differ materially from those anticipated in the forward-looking statements.
Media and Investor Relations Contact
Courtney O’Konek
Vice President, Corporate Communications
Olema Oncology
media@olema.com
| Olema Pharmaceuticals, Inc. | |||||||
| Condensed Consolidated Balance Sheets Data | |||||||
| (In thousands) | |||||||
| December 31, | December 31, | ||||||
| 2025 | 2024 | ||||||
| Cash, cash equivalents and marketable securities | $ | 505,437 | $ | 434,086 | |||
| Total assets | 533,430 | 450,979 | |||||
| Total current liabilities | 51,802 | 41,758 | |||||
| Total liabilities | 54,871 | 42,015 | |||||
| Total stockholders’ equity | 478,559 | 408,964 | |||||
| Total liabilities and stockholders’ equity | $ | 533,430 | $ | 450,979 | |||
| Olema Pharmaceuticals, Inc. | |||||||||||||
| Condensed Consolidated Statements of Operations | |||||||||||||
| (In thousands, except for share and per share data) | |||||||||||||
| Three Months Ended December 31, | Years Ended December 31, | ||||||||||||
| 2025 | 2024 | 2025 | 2024 | ||||||||||
| Operating expenses: | |||||||||||||
| Research and development (1) | $ | 43,220 | $ | 32,299 | $ | 157,697 | $ | 124,517 | |||||
| General and administrative (2) | 6,864 | 4,469 | 21,001 | 17,741 | |||||||||
| Total operating expenses | 50,084 | 36,768 | 178,698 | 142,258 | |||||||||
| Loss from operations | (50,084 | ) | (36,768 | ) | (178,698 | ) | (142,258 | ) | |||||
| Other income: | |||||||||||||
| Interest income | 4,010 | 3,294 | 16,224 | 12,682 | |||||||||
| Other income (expense) | 13 | (93 | ) | 23 | 102 | ||||||||
| Total other income | 4,023 | 3,201 | 16,247 | 12,784 | |||||||||
| Net loss | $ | (46,061 | ) | $ | (33,567 | ) | $ | (162,451 | ) | $ | (129,474 | ) | |
| Net loss per share, basic and diluted | $ | (0.50 | ) | $ | (0.51 | ) | $ | (1.87 | ) | $ | (2.20 | ) | |
| Weighted average shares used to compute net loss per share, basic and diluted (3) | 91,317,496 | 65,793,359 | 87,006,027 | 58,743,522 | |||||||||
(1) Research and development expenses for the year ended December 31, 2025 include a
Research and development expenses for the year ended December 31, 2024 include a
(1) and (2) Used to reference to the table below.
(3) The weighted average shares used to compute net loss per share, basic and diluted include the effect from the pre-funded warrants.
| Reconciliation of GAAP to Non-GAAP Information | |||||||||||||
| (In thousands) | |||||||||||||
| Three Months Ended December 31, | Years Ended December 31, | ||||||||||||
| 2025 | 2024 | 2025 | 2024 | ||||||||||
| (1) Research and development reconciliation | |||||||||||||
| GAAP research and development | $ | 43,220 | $ | 32,299 | $ | 157,697 | $ | 124,517 | |||||
| Less: stock-based compensation expense | 2,572 | 4,618 | 12,164 | 16,543 | |||||||||
| Non-GAAP research and development | $ | 40,648 | $ | 27,681 | $ | 145,533 | $ | 107,974 | |||||
| (2) General and administrative reconciliation | |||||||||||||
| GAAP general and administrative | $ | 6,864 | $ | 4,469 | $ | 21,001 | $ | 17,741 | |||||
| Less: stock-based compensation expense | 1,694 | 1,705 | 5,422 | 6,039 | |||||||||
| Non-GAAP general and administrative | $ | 5,170 | $ | 2,764 | $ | 15,579 | $ | 11,702 | |||||
FAQ
When will Olema (OLMA) report top-line data from the OPERA-01 Phase 3 trial?
How much cash did Olema (OLMA) have at year-end 2025 and what funded it?
What is the status of the OPERA-02 Phase 3 trial for palazestrant + ribociclib (OLMA)?
When will Olema (OLMA) report initial clinical data for OP-3136 and what is expected?
How did Olema's (OLMA) 2025 operating results affect expenses and net loss?
