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Recruiting Phase 3 NCT07085767

Palazestrant in Combination With Ribociclib for the First-line Treatment of ER+/HER2- Advanced Breast Cancer

Phase 3 – large-scale trial before approval
Conditions: Breast Cancer Locally Advanced Breast Cancer Metastatic Breast Cancer ER Positive Breast Cancer HER2 Negative Breast Carcinoma

Sponsor: Olema Pharmaceuticals, Inc.

trial.available_in: БГ
Overview
This phase 3 clinical trial compares the efficacy and safety of palazestrant with ribociclib to letrozole and ribociclib in women and men who have not received prior systemic anti-cancer treatment for advanced breast cancer.
Description
This is an international, multicenter, randomized, double-blind, active-controlled, phase 3 clinical trial. The purpose of this trial is to compare the efficacy and safety of palazestrant in combination with ribociclib +letrozole -matching placebo (Arm A: investigational arm) with letrozole in combination with ribociclib + palazestrant-matching placebo (Arm B: control arm). This trial is seeking adult participants with ER+, HER2- advanced breast cancer who have not received prior systemic anti-cancer treatment for advanced disease. Approximately 1,000 participants will be randomized in a 1:1 ratio to one of the two study arms.
Who can participate
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 per RECIST 1.1 or bone-only disease). * De novo advanced breast cancer or with disease recurrence occurring after 12 months of completing adjuvant endocrine therapy (with or without CDK4/6 inhibitors) * 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. Exclusion Criteria: * Disease recurrence during adjuvant endocrine therapy * Currently receiving or previously received systemic anti-cancer therapy for ER+, HER2- advanced breast cancer. * Previously received treatment with fulvestrant, elacestrant or an investigational endocrine therapy in any setting. * History of allergic reactions to study treatment. * Any contraindications to letrozole and ribociclib. * Symptomatic central nervous system metastases, carcinomatous meningitis, leptomeningeal disease, or a spinal cord compression that require immediate treatment.
Locations 16
Australia (1)
Clinical Trial Site
Sydney , New South Wales
Canada (1)
Clinical Trial Site
Toronto , Ontario
France (1)
Clinical Trial Site
Bobigny
ACTIVE_NOT_RECRUITING
Greece (1)
Clinical Trial Site
Athens , Pireas
ACTIVE_NOT_RECRUITING
Hong Kong (1)
Clinical Trial Site
Hong Kong , Hong Kong
ACTIVE_NOT_RECRUITING
Italy (1)
Clinical Trial Site
Milan , Milano
ACTIVE_NOT_RECRUITING
Malaysia (1)
Clinical Trial Site
Ipoh , Ipoh Perak
ACTIVE_NOT_RECRUITING
Netherlands (1)
Clinical Trial Site
Apeldoorn , Gelderland
ACTIVE_NOT_RECRUITING
Poland (1)
Clinical Trial Site
Rzeszów , Podkarpackie Voivodeship
ACTIVE_NOT_RECRUITING
Romania (1)
Clinical Trial Site
Cluj-Napoca , Cluj
South Korea (1)
Clinical Trial Site
Busan , Busan Metropolitan City
ACTIVE_NOT_RECRUITING
Spain (1)
Clinical Trial Site
Alicante , Alicante
ACTIVE_NOT_RECRUITING
Taiwan (1)
Clinical Trial Site
Chang-hua , Chang Hua
ACTIVE_NOT_RECRUITING
Thailand (1)
Clinical Trial Site
Bangkok , Bangkok
United Kingdom (1)
Clinical Trial Site
Brighton , England
United States (1)
Clinical Trial Site
Hot Springs , Arkansas
ACTIVE_NOT_RECRUITING
Technical details
Status
Recruiting
Phase
Phase 3
Study type
INTERVENTIONAL
Sex
Male and female
Minimum age
18 Years
Healthy volunteers
No
Start date
03.11.2025
Completion date
01.01.2032
Registry ID
NCT07085767
Source
anzctr
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Information is automatically extracted from ClinicalTrials.gov. Consult your doctor before taking action.