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Olema Oncology Announces Clinical Trial Collaboration and Supply Agreement with Bayer to Evaluate OP-3136 in Combination with NUBEQA® (darolutamide) in Metastatic Castration-Resistant Prostate Cancer

(Moderate)
(Very Positive)

Olema Oncology (Nasdaq: OLMA) announced a clinical trial collaboration and supply agreement with Bayer to evaluate KAT6 inhibitor OP-3136 plus NUBEQA (darolutamide) in metastatic castration-resistant prostate cancer.

The Phase 1b/2 trial will enroll about 36 patients, start in H2 2026, and assess safety, tolerability, and preliminary anti-tumor activity. Bayer supplies darolutamide; Olema leads the study, with combined-use data and inventions jointly owned. Olema retains full global commercial and marketing rights to OP-3136 and is also running ongoing OP-3136 studies in solid tumors and ER+/HER2- metastatic breast cancer.

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Positive

  • First clinical collaboration for OP-3136 with Bayer in mCRPC
  • Planned Phase 1b/2 combo trial in ~36 mCRPC patients starting H2 2026
  • Bayer to supply darolutamide, reducing Olema’s sourcing burden
  • Combined-use clinical data and inventions to be jointly owned
  • Olema retains full global commercial and marketing rights to OP-3136
  • OP-3136 already in ongoing Phase 1/2 studies in multiple solid tumors

Negative

  • None.

News Market Reaction – OLMA

-0.95%
4 alerts
-0.95% Session close to close
+4.7% Peak Tracked
-17.2% Trough Tracked
$1.19B Market Cap
0.0x Rel. Volume

In the May 26 session, OLMA declined 0.95%, reflecting a mild negative market reaction. Argus tracked a peak move of +4.7% during that session. Argus tracked a trough of -17.2% from its starting point during tracking. Our momentum scanner triggered 4 alerts that day, indicating moderate trading interest and price volatility.

Data tracked by StockTitan Argus on the day of publication.

Market Context

This announcement extends Olema’s OP-3136 strategy into metastatic castration-resistant prostate can...
Analysis

This announcement extends Olema’s OP-3136 strategy into metastatic castration-resistant prostate cancer via a Phase 1b/2 collaboration with Bayer’s darolutamide in about 36 patients, with trial start expected in H2 2026. It builds on prior OP-3136 preclinical and early clinical data and follows other combination collaborations. Investors may track upcoming ASCO data on May 30, 2026, progress of the new study, and how this program complements Olema’s ongoing late-stage palazestrant trials.

Key Figures

Planned enrollment: approximately 36 patients Study phase: Phase 1b/2 Study start timing: H2 2026 +1 more
4 metrics
Planned enrollment approximately 36 patients Phase 1b/2 OP-3136 + darolutamide mCRPC study
Study phase Phase 1b/2 Combination trial design for OP-3136 and darolutamide
Study start timing H2 2026 Expected initiation of the Phase 1b/2 mCRPC trial
ASCO poster date May 30, 2026 Initial OP-3136 Phase 1 data presentation at ASCO

Previous Clinical trial Reports

5 past events · Latest: May 21 (Positive)
Same Type Pattern 5 events
Date Event Sentiment 24h Move Catalyst
May 21 Phase 1 data update Positive -2.7% Initial Phase 1 data for OP-3136 showed tolerability and early anti-tumor activity.
Apr 21 ASCO presentation plans Positive -0.6% Announcement of upcoming ASCO data for OP-3136 and OPERA-02 trial-in-progress.
Sep 02 Pfizer trial collaboration Positive +18.5% New Phase 1b/2 collaboration with Pfizer combining palazestrant and atirmociclib.
Apr 25 OP-3136 preclinical data Positive -3.7% Preclinical OP-3136 data showed anti-tumor activity across multiple solid tumor models.
Dec 10 Palazestrant combo results Positive +2.1% Updated palazestrant plus ribociclib data with favorable PFS and response metrics.

24h Move is the share-price change in the day after each event; other market factors may also have contributed.

Pattern Detected

Clinical trial updates have produced mixed reactions: some strong gains on partnership news but several instances where positive data coincided with share price declines.

Recent Company History

Over the past 18 months, Olema has steadily built a clinical narrative around palazestrant and OP-3136, with multiple Phase 1b/2 and Phase 3 programs and preclinical data across solid tumors. Prior clinical trial news, including a Pfizer collaboration in September 2025 and OP-3136 data and presentations through 2025–2026, drew varied market responses. Today’s Bayer collaboration for OP-3136 in metastatic prostate cancer extends this combination-focused strategy within the same clinical-development arc.

Key Terms

lysine acetyltransferase 6 (kat6), kat6 inhibitor, metastatic castration-resistant prostate cancer, mcrpc, +4 more
8 terms
lysine acetyltransferase 6 (kat6) medical
"OP-3136, Olema’s investigational lysine acetyltransferase 6 (KAT6) inhibitor, in combination"
Lysine acetyltransferase 6 (KAT6) is an enzyme that adds a small chemical tag to proteins that help control whether genes are turned on or off, acting like a dimmer switch for cellular activity. Investors care because KAT6 is often implicated in diseases such as certain cancers and developmental disorders, so drugs or tests that target or measure KAT6 can drive the value of biotech companies, influence clinical trial outcomes, and affect regulatory and market expectations.
kat6 inhibitor medical
"OP-3136, Olema’s novel KAT6 inhibitor, in combination with darolutamide"
A KAT6 inhibitor is a type of drug that blocks the activity of the KAT6 enzyme, which helps turn certain genes on by adding chemical tags; think of it as dimming a light switch that controls gene programs. Investors care because these inhibitors are being tested as treatments for cancers and other diseases, and clinical progress, safety results, or regulatory decisions can materially affect a company’s future revenue prospects and stock value.
metastatic castration-resistant prostate cancer medical
"darolutamide), Bayer’s androgen receptor inhibitor, in patients with metastatic castration-resistant prostate cancer"
An advanced form of prostate cancer that has spread beyond the prostate to other parts of the body (metastatic) and no longer responds to treatments that lower male hormones designed to starve the tumor (castration-resistant). It matters to investors because it defines a high unmet medical need with limited treatment options, so clinical trial results, new drug approvals, or safety setbacks can sharply change the valuation and prospects of companies working in this area; think of it as a weed that has spread and become resistant to the usual weedkiller.
mcrpc medical
"in combination with darolutamide in patients with metastatic castration-resistant prostate cancer (mCRPC)"
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.
androgen receptor inhibitor medical
"NUBEQA® (darolutamide), Bayer’s androgen receptor inhibitor, in patients with"
An androgen receptor inhibitor is a drug that blocks the cellular “locks” where male hormones (androgens) normally fit, preventing those hormones from turning on growth signals in certain tissues such as prostate cancer cells. Investors watch these drugs because they can form the basis of new treatments, create recurring revenue if approved, and carry clinical and regulatory risks or milestones that can sharply change a company’s value—think of it as stopping a key from opening a keyhole to halt unwanted activity.
monotherapy medical
"ongoing Phase 1/2 study of this novel KAT6 inhibitor as a monotherapy in multiple solid tumor types"
Monotherapy is a treatment approach that uses only one type of medicine or therapy to address a condition, instead of combining multiple options. For investors, understanding monotherapy matters because it can influence a company's development strategy, risk profile, and potential market size, especially if the single-treatment approach proves effective or faces limitations compared to combination therapies.
anti-tumor activity medical
"study is designed to assess the safety, tolerability, and preliminary anti-tumor activity of OP-3136"
Anti-tumor activity describes evidence that a drug or treatment can reduce tumor size, slow or stop tumor growth, or prevent new tumors from forming in lab, animal, or human studies. For investors this signals the treatment’s potential to succeed in clinical development and reach the market; like early road-test results for a new car, stronger anti-tumor activity generally raises the odds of regulatory approval, commercial value and return on investment.
phase 1b/2 medical
"The Phase 1b/2 study is designed to assess the safety, tolerability"
Phase 1b/2 is a combined early-stage human study that first checks a drug’s safety and side effects in a small group and then expands to test whether it shows signs of working in patients. Think of it as a product test that first confirms it’s safe to use, then looks for early evidence of benefit; positive results can significantly reduce clinical risk and increase a company’s value, while negative results raise the opposite.

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

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  • Study to evaluate OP-3136, Olema’s novel KAT6 inhibitor, in combination with darolutamide in approximately 36 patients; expected to initiate in H2 2026
  • First clinical collaboration for OP-3136; results to inform combination strategy in metastatic prostate cancer setting

SAN FRANCISCO, May 26, 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 announced a clinical trial collaboration and supply agreement with Bayer AG (“Bayer”) to evaluate OP-3136, Olema’s investigational lysine acetyltransferase 6 (KAT6) inhibitor, in combination with NUBEQA® (darolutamide), Bayer’s androgen receptor inhibitor, in patients with metastatic castration-resistant prostate cancer (mCRPC). The Phase 1b/2 study is designed to assess the safety, tolerability, and preliminary anti-tumor activity of OP-3136 in combination with darolutamide in approximately 36 patients with mCRPC.

“We are very pleased to partner with Bayer to explore the combination of OP-3136 with darolutamide in metastatic castration-resistant prostate cancer, which is an aggressive disease characterized by poor clinical outcomes,” said Sean P. Bohen, M.D., Ph.D., President and Chief Executive Officer of Olema Oncology. “This agreement represents the first clinical collaboration for OP-3136 and builds upon our ongoing Phase 1/2 study of this novel KAT6 inhibitor as a monotherapy in multiple solid tumor types and in combination with fulvestrant and palazestrant in ER+/HER2- metastatic breast cancer. We look forward to advancing OP-3136 in combination with darolutamide in the clinic as we work to bring better medicines to patients living with cancer.”

Under the terms of the agreement, Bayer will supply darolutamide for use in the Phase 1b/2 study and Olema will lead the conduct of the study. All clinical data and inventions related to the combined use of OP-3136 and darolutamide will be jointly owned. Olema will maintain full global commercial and marketing rights to OP-3136.

As previously announced, Olema will present initial clinical data from the Phase 1 study of OP-3136 in a poster presentation on May 30, 2026 at the American Society of Clinical Oncology (ASCO) Annual Meeting in Chicago, Illinois.

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 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.

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 potential benefits of the collaboration between Olema and Bayer, including the evaluation of OP-3136 in combination with darolutamide for the treatment of metastatic castration-resistant prostate cancer; the initiation, progress, design, and timing of the planned Phase 1b/2 clinical study; the potential of OP-3136 as a novel KAT6 inhibitor, including as a monotherapy and in combination with other therapies; the potential therapeutic effects and clinical benefits of OP-3136, alone or in combination, in multiple solid tumor types; Olema’s ability to successfully conduct the clinical study and advance OP-3136 in the clinic; and the potential for OP-3136, alone or in combination, to provide improved treatment options or outcomes for patients living with cancer. 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


FAQ

What did Olema Oncology (NASDAQ: OLMA) announce on May 26, 2026 about OP-3136 and NUBEQA?

Olema Oncology announced a clinical trial collaboration with Bayer to test OP-3136 plus NUBEQA (darolutamide) in metastatic castration-resistant prostate cancer. According to Olema, this Phase 1b/2 study will evaluate safety, tolerability, and preliminary anti-tumor activity in approximately 36 patients.

What is the design of Olema Oncology’s OP-3136 and NUBEQA (darolutamide) Phase 1b/2 trial in mCRPC (OLMA)?

The OP-3136 and NUBEQA Phase 1b/2 trial is designed to assess safety, tolerability, and preliminary anti-tumor activity in metastatic castration-resistant prostate cancer. According to Olema, the study will enroll around 36 patients treated with the combination regimen.

When will the OP-3136 plus NUBEQA metastatic castration-resistant prostate cancer trial start and how many patients will enroll?

The OP-3136 plus NUBEQA Phase 1b/2 trial is expected to start in the second half of 2026 and enroll about 36 patients. According to Olema, the goal is to characterize safety and early anti-tumor activity in mCRPC.

Who will conduct the OP-3136 and NUBEQA (darolutamide) study and who supplies the drugs in the Olema-Bayer collaboration?

Olema will lead the conduct of the OP-3136 and NUBEQA Phase 1b/2 study, while Bayer will supply darolutamide. According to Olema, all clinical data and inventions related to the combined use will be jointly owned by both companies.

What commercial rights does Olema Oncology retain for OP-3136 under the Bayer collaboration (NASDAQ: OLMA)?

Olema retains full global commercial and marketing rights to OP-3136 under the collaboration with Bayer. According to Olema, only the clinical data and inventions related to the combined use of OP-3136 and darolutamide will be jointly owned.

How does the Bayer collaboration fit with Olema’s broader OP-3136 development strategy?

The Bayer collaboration is the first clinical partnership for OP-3136 and extends its development into metastatic prostate cancer. According to Olema, OP-3136 is already being studied as monotherapy and in combinations in multiple solid tumors, including ER+/HER2- metastatic breast cancer.

When and where will initial clinical data from Olema’s Phase 1 OP-3136 study be presented?

Initial clinical data from the Phase 1 OP-3136 study will be presented on May 30, 2026, at the American Society of Clinical Oncology Annual Meeting in Chicago. According to Olema, this poster presentation will share early results from the ongoing trial.