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Olema Oncology's KAT6 Inhibitor OP-3136 Receives FDA IND Clearance, Phase 1 Trial Planned for 2025

7 months ago2 min read
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Key Insights

  • Olema Oncology has received FDA clearance for its Investigational New Drug (IND) application for OP-3136, a novel KAT6 inhibitor, marking a key regulatory milestone.

  • OP-3136, a small molecule, has demonstrated compelling preclinical activity as a monotherapy and in combination with palazestrant for breast cancer.

  • A Phase 1 clinical trial is scheduled to begin in early 2025 to assess the safety and initial efficacy of OP-3136 in patients with breast and other cancers.

Olema Oncology, a biopharmaceutical company specializing in targeted therapies for breast cancer, announced that the U.S. Food and Drug Administration (FDA) has cleared the Investigational New Drug (IND) application for OP-3136, a novel and selective KAT6 inhibitor. This clearance paves the way for a Phase 1 clinical trial, slated to begin in early 2025, to evaluate OP-3136's safety and potential efficacy in patients with breast cancer and other cancers where KAT6 is dysregulated.

OP-3136: Targeting KAT6 in Cancer

OP-3136 is a small molecule designed to potently and selectively inhibit KAT6 (Lysine Acetyltransferase 6), a validated epigenetic target. KAT6 plays a crucial role in gene regulation, and its dysregulation has been implicated in the development and progression of various cancers, including breast cancer. By inhibiting KAT6, OP-3136 aims to restore normal gene expression patterns and inhibit cancer cell growth.

Preclinical Evidence and Investigator Interest

According to David C. Myles, Ph.D., Chief Discovery and Non-Clinical Development Officer of Olema Oncology, preclinical studies have demonstrated compelling activity of OP-3136, both as a single agent and in combination with palazestrant, Olema's lead product candidate. Palazestrant (OP-1250) is an orally available complete estrogen receptor (ER) antagonist (CERAN) and a selective ER degrader (SERD) currently in Phase 3 clinical trials. The promising preclinical data has generated significant interest from investigators, fueling enthusiasm for the upcoming Phase 1 trial.

Phase 1 Trial Design and Objectives

The Phase 1 clinical trial will be a first-in-human study designed to assess the safety, tolerability, and pharmacokinetics of OP-3136. The trial will also explore preliminary efficacy signals in a select patient population with breast and other cancers characterized by KAT6 dysregulation. Details regarding the trial design, including specific inclusion/exclusion criteria and dosing regimens, will be disclosed closer to the trial's initiation in early 2025.

Olema Oncology's Broader Pipeline

Beyond OP-3136, Olema Oncology is actively advancing palazestrant (OP-1250), a complete estrogen receptor antagonist (CERAN) and selective ER degrader (SERD), in a Phase 3 clinical trial (OPERA-01) for breast cancer. The company's strategy focuses on developing targeted therapies that address endocrine-driven cancers and mechanisms of acquired resistance. The advancement of OP-3136 into clinical development diversifies Olema's pipeline and reinforces its commitment to transforming the standard of care for patients with breast cancer and other cancers.
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