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Olema Oncology Reports First Quarter 2023 Financial Results and Provides Corporate Update Initiation of first pivotal Phase 3 monotherapy clinical trial of OP-1250 in second- and third-line metastatic breast cancer plann

Key Takeaway: Olema Oncology reported its financial results for the first quarter of 2023 and announced significant progress in its clinical development pipeline. The company is on track to initiate its first pivotal Phase 3 trial of OP-1250, targeting ER+/HER2- metastatic breast cancer, in the latter half of the year. Olema's cash reserves of $186 million are expected to fund operations until 2025. However, the company experienced an increase in net losses, primarily due to rising R&D costs and restructuring expenditures.
Price reaction · baseline $6.8 (2023-05-11 close) · hit after-hours · clean, no other OLMA news in the window
day 0 close · peak
+2.5%

Market Sentiment Analysis

POSITIVE FACTORS

  • Initiation of pivotal Phase 3 trial of OP-1250 is on track.
  • Anticipated milestones demonstrate strong progress in clinical trials.
  • Significant financial resources available to support operations until 2025.

CONCERNS & RISKS

  • Net loss increased to $28.3 million in Q1 2023 compared to $23.0 million last year.
  • Continued high R&D expenditures indicate financial challenges ahead.

BiopharmaWatch Analysis

From our catalyst data and publicly available data · not financial advice
Best trade, last catalyst
+73%
120-day peak, hindsight
Typical move
8%
average across 7 past catalysts
Cash runway
~30 mo
Minimal dilution risk
Lead asset
Palazestrant
Phase 3 · Breast Cancer

Full Press Release Details

Olema Oncology Reports First Quarter 2023 Financial Results and Provides Corporate Update
SAN FRANCISCO, May 9, 2023 - Olema Pharmaceuticals, Inc. ("Olema", "Olema Oncology", Nasdaq: OLMA), a clinical-stage biopharmaceutical company focused on the discovery, development and commercialization of targeted therapies for women's cancers, today reported financial results for the first quarter ended March 31, 2023, and provided a corporate update.
"We are on track for the initiation of our first pivotal Phase 3 clinical trial in the second half of this year," said Sean P. Bohen, M.D., Ph.D., President and Chief Executive Officer of Olema Oncology. "Our ongoing Phase 2 studies continue to generate data in support of our underlying thesis that OP-1250 has the potential to become a best-in-class complete estrogen receptor antagonist and improve upon the current standard of care in the treatment of ER+/HER2- metastatic breast cancer. We look forward to presenting our next clinical update at the 2023 ESMO Breast Cancer Annual Congress in mid-May, and we believe we are well-positioned to achieve our goal to significantly improve endocrine therapy for women living with breast cancer."
Anticipated Upcoming Milestones
First Quarter 2023 Financial Results
Cash, cash equivalents and marketable securities as of March 31, 2023, were $186.0 million. Olema anticipates that this balance will be sufficient to fund operations into 2025.
Net loss for the quarter ended March 31, 2023, was $28.3 million, as compared to $23.0 million for same period of the prior year. The increase in net loss related primarily to Olema's continued investment in OP-1250, increased spending on research and development (R&D) activities, and personnel-related costs, including a one-time restructuring charge of $2.8 million. The increase in R&D spending was partially offset by a decrease in general and administrative (G&A) costs.
GAAP R&D expenses were $22.8 million for the quarter ended March 31, 2023, as compared to $16.0 million for the quarter ended March 31, 2022. The increase in R&D expenses was primarily related to increases in advancing ongoing clinical studies of OP-1250 and associated manufacturing costs, nonclinical research and discovery program activities, and personnel-related expenses, including a one-time restructuring charge of $1.8 million.
Non-GAAP R&D expenses were $19.7 million for the quarter ended March 31, 2023, excluding $3.1 million non-cash stock-based compensation expense. Non-GAAP R&D expenses were $12.9 million for the quarter ended March 31, 2022, respectively, excluding $3.1 million non-cash stock-based compensation expense, respectively. A reconciliation of GAAP to non-GAAP financial measures used in this press release can be found at the end of this press release.
GAAP G&A expenses were $6.8 million for the quarter ended March 31, 2023, as compared to $7.2 million for the quarter ended March 31, 2022. The decrease in G&A expenses was primarily due to lower corporate costs, and personnel-related expenses, including non-cash stock-based compensation expense. The decrease in spending was partially offset by a one-time restructuring charge of $1.0 million.
Non-GAAP G&A expenses were $5.2 million for the quarter ended March 31, 2023, excluding $1.5 million non-cash stock-based compensation expense. Non-GAAP G&A expenses were $5.3 million for the quarter ended March 31, 2022, excluding $1.9 million non-cash stock-based compensation expense. A reconciliation of GAAP to non-GAAP financial measures used in this press release can be found at the end of this press release.
About Olema Oncology
Olema Oncology is a clinical-stage biopharmaceutical company focused on the discovery, development and commercialization of targeted therapies for women's cancers. Olema's lead product candidate, OP-1250, is a proprietary, orally-available small molecule with dual activity as both a complete estrogen receptor (ER) antagonist (CERAN) and a selective ER degrader (SERD). It is currently being evaluated both as a single agent in an ongoing Phase 2 clinical trial, and in combination with CDK4/6 inhibitors (palbociclib and ribociclib) and a PI3Ka inhibitor (alpelisib), in patients with recurrent, locally advanced or metastatic ER-positive (ER+), human epidermal growth factor receptor 2-negative (HER2-) breast cancer. OP-1250 has been granted 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. Olema is headquartered in San Francisco and has operations in Cambridge, Massachusetts.
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 non-cash 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," "expect," "will," "may," "goal," "potential" 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 the company's financial condition, results of operations, cash position, the sufficiency of the company's financial resources, potential beneficial characteristics, safety, tolerability, efficacy and therapeutic effects of OP-1250, the potential of OP-1250 to become a best-in-class treatment option for ER+/HER2- metastatic breast cancer or significantly improve endocrine therapy for women living with ER+/HER2- metastatic breast cancer, OP-1250's combinability with other drugs, and the timelines for potential clinical study results and clinical trials of OP-1250 as a monotherapy and in combination trials. 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-Q for the quarter ended March 31, 2023, 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 or to update the reasons if actual results differ materially from those anticipated in the forward-looking statements.
Olema Pharmaceuticals, Inc.
Condensed Consolidated Balance Sheets Data
March 31, December 31,
2023 2022
Cash, cash equivalents and marketable securities $ 185,954 $ 204,421
Total assets 195,768 215,645
Total current liabilities 19,410 16,549
Total liabilities 20,793 18,099
Total stockholders' equity 174,975 197,546
Total liabilities and stockholders' equity $ 195,768 $ 215,645
Olema Pharmaceuticals, Inc.
Condensed Consolidated Statements of Operations
(In thousands, except share and per share data)
Three Months Ended March 31,
2023 2022
Operating expenses:
Research and development (1) $ 22,826 $ 16,009
General and administrative (2) 6,776 7,245
Total operating expenses 29,602 23,254
Loss from operations (29,602) (23,254)
Other income:
Interest income 1,305 218
Other income 11 6
Total other income 1,316 224
Net loss attributable to common stockholders $ (28,286) $ (23,030)
Net loss per share attributable to common stockholders , basic and diluted $ (0.70) $ (0.58)
Weighted average shares used to compute net loss per share attributable to common stockholders , basic and diluted 40,354,493 39,834,619
Reconciliation of GAAP to Non-GAAP Information
Three Months Ended March 31,
2023 2022
(1) Research and development reconciliation
GAAP research and development $ 22,826 $ 16,009
Less: share-based compensation expense 3,088 3,067
Non-GAAP research and development $ 19,738 $ 12,942
(2) General and administrative reconciliation
GAAP general and administrative $ 6,776 $ 7,245
Less: share-based compensation expense 1,542 1,898
Non-GAAP general and administrative $ 5,234 $ 5,347
Shane Kovacs, Chief Operating and Financial Officer
Ignacio Guerrero-Ros, Ph.D., Russo Partners

Frequently Asked Questions

What is Olema Oncology's financial status as of March 31, 2023?

As of March 31, 2023, Olema had $186.0 million in cash and securities, expected to cover operations into 2025.

What are OP-1250's anticipated benefits in breast cancer treatment?

OP-1250 may become a best-in-class treatment for ER+/HER2- metastatic breast cancer, improving current therapy standards.

What was Olema's net loss for Q1 2023?

Olema's net loss for the first quarter of 2023 was $28.3 million, up from $23.0 million the previous year.

What is Olema's lead product candidate?

Olema's lead candidate, OP-1250, is an orally-available dual-action estrogen receptor antagonist.

What clinical trials are being conducted for OP-1250?

OP-1250 is in Phase 2 trials as a single agent and with CDK4/6 inhibitors for advanced breast cancer.

Last updated: May 12, 2023