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Clinical Trials in the UK / NCT06016738
Active, not recruiting Phase 3

OP-1250 (Palazestrant) vs. Standard of Care for the Treatment of ER+/HER2- Advanced Breast Cancer

NCT06016738 · tracked via the Priya Life Science UK tracker
Sponsor
Olema Pharmaceuticals, Inc.
Phase
Phase 3
Started
2023-11-16
Last updated
2026-08-13

Condition(s) studied

Breast CancerAdvanced Breast CancerMetastatic Breast CancerER Positive Breast CancerHER2 Negative Breast Carcinoma

Investigational drug(s) / intervention(s)

PalazestrantFulvestrantAnastrozoleLetrozoleExemestane

Palazestrant: Participants will be treated with palazestrant once daily on a 4 week (28 day) cycle. Doses evaluated in the dose-selection part will be 120 mg once daily and 90 mg once daily.

Fulvestrant: Participants will be treated with fulvestrant on C1D1, C1D15, and then on Day 1 of every subsequent 4 week (28 day) cycle

Anastrozole: Participants will be treated with anastrozole once daily on a 4 week (28 day) cycle

Letrozole: Participants will be treated with letrozole once daily on a 4 week (28 day) cycle

Exemestane: Participants will be treated with exemestane once daily on a 4 week (28 day) cycle

Study summary

This phase 3 clinical trial compares the safety and efficacy of palazestrant (OP-1250) to the standard-of-care options of fulvestrant or an aromatase inhibitor in women and men with breast cancer whose disease has advanced on one endocrine therapy in combination with a CDK4/6 inhibitor.

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
Key inclusion criteria: * Adult female or male participants. * ER+, HER2- locally advanced or metastatic breast cancer that is not amenable to curative therapy. * Evaluable disease (measurable disease or bone-only disease). * Previously received a CDK4/6 inhibitor in combination with an endocrine therapy in the advanced setting. One additional line of ET as a monotherapy is allowed. Duration of the most recent prior ET must be at least 6 months. * Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1. * Adequate hematologic, hepatic, and renal functions. * Female participants can be pre-, peri- or postmenopausal. * Male and pre- or peri-menopausal female participants must be willing to take a GnRH (or LHRH) agonist. Key exclusion criteria: * Symptomatic visceral disease, imminent organ failure, or any other reason that makes the participant ineligible for endocrine monotherapy. * Previously received chemotherapy in the advanced/metastatic setting. * Previously received treatment with elacestrant or an investigational estrogen receptor-directed therapy. * History of allergic reactions to study treatment. * Any contraindications to the selected standard-of-care endocrine therapy in the local prescribing information. * Symptomatic central nervous system metastases, carcinomatous meningitis, leptomeningeal disease, or a spinal cord compression that require immediate treatment. * Clinically significant comorbidities such as significant cardiac or cerebrovascular disease, gastrointestinal disorders that could affect absorption of study treatment.

Primary outcome measure(s)

Trial sites (233)

FacilityCityRegionStatus
Clinical Trial Site Tucson Arizona
Clinical Trial Site Fountain Valley California
Clinical Trial Site Glendale California
Clinical Trial Site La Jolla California
Clinical Trial Site Los Alamitos California
Clinical Trial Site Los Angeles California
Clinical Trial Site Whittier California
Clinical Trial Site Aurora Colorado
Clinical Trial Site Denver Colorado
Clinical Trial Site Golden Colorado
Clinical Trial Site Grand Junction Colorado
Clinical Trial Site Danbury Connecticut
Clinical Trial Site Newark Delaware
Clinical Trials Site Jacksonville Florida
Clinical Trial Site Margate Florida
Clinical Trial Site Orlando Florida
Clinical Trial Site Plantation Florida
Clinical Trial Site Tamarac Florida
Clinical Trial Site Atlanta Georgia
Clinical Trial Site Chicago Illinois
Clinical Trial Site Chicago Illinois
Clinical Trial Site Urbana Illinois
Clinical Trial Site Baton Rouge Louisiana
Clinical Trial Site New Orleans Louisiana
Clinical Trial Site Baltimore Maryland
Clinical Trial Site Boston Massachusetts
Clinical Trial Site Detroit Michigan
Clinical Trial Site Saint Louis Park Minnesota
Clinical Trial Site Woodbury Minnesota
Clinical Trial Site Lincoln Nebraska
Clinical Trial Site Farmington New Mexico
Clinical Trial Site New York New York
Clinical Trial Site Port Jefferson Station New York
Clinical Trial Site Dayton Ohio
Clinical Trial Site Toledo Ohio
Clinical Trial Site Portland Oregon
Clinical Trial Site Sayre Pennsylvania
Clinical Trial Site Nashville Tennessee
Clinical Trial Site Nashville Tennessee
Clinical Trial Site Nashville Tennessee

+ 193 more sites — see the full list on the official registry below.

More Olema Pharmaceuticals, Inc. trials in the UK

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06016738 on ClinicalTrials.gov ↗ ← All trials in the UK