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Olema Oncology Nominates OP-3136, an Orally Bioavailable KAT6 Inhibitor, as a Development Candidate

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Olema Pharmaceuticals, Inc. (OLMA) announced the selection of a development candidate, OP-3136, for the Company’s program targeting KAT6, an epigenetic target dysregulated in breast cancer and other cancers. The compound has demonstrated potent anti-tumor activity and is set to advance into clinical development by the end of 2024. OP-3136 is an orally bioavailable, potent KAT6A/B-selective inhibitor developed in collaboration with Aurigene Oncology. The company presented promising data at the 2023 AACR-NCI-EORTC International Conference on Molecular Targets and Cancer Therapeutics, showing highly selective and potent activity against KAT6A and KAT6B in ER+ breast cancer cell lines. Olema is initiating non-clinical Investigational New Drug (IND) enabling studies to support a potential IND submission to the FDA for OP-3136 by the end of 2024.
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The development of OP-3136 by Olema Pharmaceuticals represents a significant advancement in the field of oncology, particularly for the treatment of ER+ breast cancer. KAT6, the epigenetic target of OP-3136, plays a crucial role in the regulation of gene expression and its dysregulation has been implicated in various cancers. The selection of OP-3136 as a development candidate based on its potent anti-tumor activity and selectivity for KAT6A/B over other KAT family members indicates a promising therapeutic strategy.

From a clinical perspective, the potency and oral bioavailability of OP-3136 suggest that it could offer a more convenient and potentially efficacious treatment option compared to current therapies. Its demonstrated synergy with existing treatments like CDK4/6 inhibitors and palazestrant also opens up the possibility of combination therapies that could enhance patient outcomes. As the compound moves towards IND-enabling studies, the oncology community will be keen to observe its progression into clinical trials and subsequent patient response data.

Olema's strategic focus on targeted therapies for women's cancers and specifically the development of OP-3136, aligns with the broader industry trend towards personalized medicine. The preclinical data showing dose-dependent tumor growth inhibition and the potential for tumor regression set OP-3136 apart as a highly promising candidate in the competitive landscape of cancer therapeutics.

The upcoming IND-enabling studies are critical for assessing the safety profile of OP-3136 and determining the appropriate dosing for human trials. The successful transition into clinical development could have a substantial impact on Olema's valuation and partnerships, particularly given the collaboration with Aurigene Oncology. Investors will likely monitor the IND submission closely, as it will be a pivotal milestone for the company's pipeline and future prospects.

The announcement regarding OP-3136's advancement to IND-enabling studies is a significant development for stakeholders in Olema Pharmaceuticals. The breast cancer therapeutics market is highly competitive and novel treatments that offer improved efficacy and safety profiles are well-positioned for market penetration. OP-3136's potential to serve as a new targeted therapy for ER+ breast cancer, a subtype with a substantial patient population, could represent a considerable market opportunity for Olema.

Given the compound's promising preclinical results, there is potential for OP-3136 to capture market share from existing treatments if it demonstrates superior clinical outcomes. The collaboration with Aurigene Oncology could also provide strategic advantages in terms of development expertise and potential access to new markets. Investors should consider the long-term implications of Olema's pipeline development on the company's growth trajectory and the broader oncology market.

OP-3136 demonstrated potent anti-tumor activity alone and in combination with both palazestrant and CDK4/6 inhibitors in preclinical ER+ breast cancer models

Initiating IND-enabling studies with goal to advance into clinical development by end of 2024

SAN FRANCISCO, Jan. 08, 2024 (GLOBE NEWSWIRE) -- 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 announced the selection of a development candidate for the Company’s program targeting KAT6, an epigenetic target that is dysregulated in breast cancer and other cancers. The compound, named OP-3136, is an orally bioavailable, potent KAT6A/B-selective inhibitor developed by Olema in collaboration with Aurigene Oncology.

“We are excited to advance our KAT6 program with the nomination of OP-3136 as a development candidate. OP-3136 has the potential to become a new targeted therapy for breast cancer and other cancers,” said Dr. David C. Myles, Ph.D., Chief Discovery and Non-Clinical Development Officer of Olema Oncology. “Our KAT6 program supports our commitment to discovering and developing new treatment options for women living with cancer and is a natural complement to Olema’s ongoing development of palazestrant in ER+/HER2- breast cancer. We look forward to providing future updates on our progress with OP-3136 development.”

Olema presented data regarding the discovery and pre-clinical development of its KAT6 program in a poster session at the 2023 AACR-NCI-EORTC International Conference on Molecular Targets and Cancer Therapeutics (ANE 2023) in Boston, Massachusetts. OP-3136 is orally bioavailable in multiple non-clinical species with desirable pharmacokinetics and has demonstrated highly selective and potent activity against KAT6A and KAT6B versus other KAT family members. In KAT6-amplified and overexpressing estrogen receptor-positive (ER+) breast cancer cell lines, OP-3136 strongly inhibited cell proliferation whereas KAT6-low cell lines were insensitive to the compounds. In a non-clinical xenograft model, OP-3136 caused dose-dependent tumor growth inhibition and tumor regression comparable to or better than a positive-control patented KAT6 inhibitor and demonstrated synergy in combination with CDK4/6 inhibitors or palazestrant (OP-1250).

Olema is initiating non-clinical Investigational New Drug (IND) enabling studies in order to support a potential IND submission to the U.S. Food and Drug Administration (FDA) for OP-3136 by the end of 2024.

About Olema Oncology
Olema Oncology is a biopharmaceutical company committed to transforming the standard of care and improving outcomes for women living with cancer. Olema is advancing a pipeline of novel therapies by leveraging our deep understanding of endocrine-driven cancers, nuclear receptors, and mechanisms of acquired resistance. In addition to our lead product candidate, palazestrant (OP-1250), a proprietary, orally-available complete estrogen receptor (ER) antagonist (CERAN) and a selective ER degrader (SERD), Olema is developing a potent KAT6 inhibitor. Olema is headquartered in San Francisco and has operations in Cambridge, Massachusetts. For more information, please visit us at www.olema.com.

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 Olema’s preclinical program, including the potential beneficial characteristics and potency of its KAT6 inhibitor compound and its applicability to breast and other cancers, the potential synergistic activity of Olema’s KAT6 inhibitor compounds with CDK4/6 inhibitors or palazestrant (OP-1250), anticipated timing of an IND submission and development of OP-3136. 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 Quarterly Report on Form 10-Q for the quarter ended September 30, 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, including in the event that actual results differ materially from those anticipated in the forward-looking statements.

Contact:
Geoffrey Mogilner, Vice President, Investor Relations and Communications
ir@olema.com


FAQ

What did Olema Pharmaceuticals announce?

Olema Pharmaceuticals, Inc. (OLMA) announced the selection of a development candidate, OP-3136, for the Company’s program targeting KAT6, an epigenetic target dysregulated in breast cancer and other cancers.

What is the potential of OP-3136?

OP-3136 has demonstrated potent anti-tumor activity and is set to advance into clinical development by the end of 2024.

What is OP-3136?

OP-3136 is an orally bioavailable, potent KAT6A/B-selective inhibitor developed in collaboration with Aurigene Oncology.

What studies is Olema initiating for OP-3136?

Olema is initiating non-clinical Investigational New Drug (IND) enabling studies to support a potential IND submission to the FDA for OP-3136 by the end of 2024.

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About OLMA

olema oncology is a biopharmaceutical company developing innovative targeted therapies for women’s cancers. our lead program, op-1250, a potential best-in-class complete estrogen receptor antagonist (ceran), is in development to treat estrogen receptor-positive (er+), human epidermal growth factor receptor 2-negative (her2-) breast cancer. olema recently initiated a phase 1/2 dose-escalation and expansion clinical trial of op-1250. we are supported in our mission by experienced and accomplished scientists and board members, leading healthcare investors and some of the most innovative pharma companies. for more information about the company please visit www.olema.com.