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Набира участници Фаза 3 NCT07085767

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

Фаза 3 – широко изпитване преди одобрение
Заболявания: Breast Cancer Locally Advanced Breast Cancer Metastatic Breast Cancer ER Positive Breast Cancer HER2 Negative Breast Carcinoma

Спонсор: Olema Pharmaceuticals, Inc.

Налично на: БГ
Обобщение
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.
Описание
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.
Кой може да участва
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.
Места на провеждане 16
Австралия (1)
Clinical Trial Site
Sydney , New South Wales
Канада (1)
Clinical Trial Site
Toronto , Ontario
Франция (1)
Clinical Trial Site
Bobigny
ACTIVE_NOT_RECRUITING
Гърция (1)
Clinical Trial Site
Athens , Pireas
ACTIVE_NOT_RECRUITING
Hong Kong (1)
Clinical Trial Site
Hong Kong , Hong Kong
ACTIVE_NOT_RECRUITING
Италия (1)
Clinical Trial Site
Milan , Milano
ACTIVE_NOT_RECRUITING
Malaysia (1)
Clinical Trial Site
Ipoh , Ipoh Perak
ACTIVE_NOT_RECRUITING
Нидерландия (1)
Clinical Trial Site
Apeldoorn , Gelderland
ACTIVE_NOT_RECRUITING
Полша (1)
Clinical Trial Site
Rzeszów , Podkarpackie Voivodeship
ACTIVE_NOT_RECRUITING
Румъния (1)
Clinical Trial Site
Cluj-Napoca , Cluj
Южна Корея (1)
Clinical Trial Site
Busan , Busan Metropolitan City
ACTIVE_NOT_RECRUITING
Испания (1)
Clinical Trial Site
Alicante , Alicante
ACTIVE_NOT_RECRUITING
Taiwan (1)
Clinical Trial Site
Chang-hua , Chang Hua
ACTIVE_NOT_RECRUITING
Тайланд (1)
Clinical Trial Site
Bangkok , Bangkok
Великобритания (1)
Clinical Trial Site
Brighton , England
САЩ (1)
Clinical Trial Site
Hot Springs , Arkansas
ACTIVE_NOT_RECRUITING
Технически детайли
Статус
Набира участници
Фаза
Фаза 3
Вид изследване
INTERVENTIONAL
Пол
Мъже и жени
Минимална възраст
18 Years
Здрави доброволци
Не
Начална дата
03.11.2025
Крайна дата
01.01.2032
Регистрационен номер
NCT07085767
Източник
anzctr
Запитване за медицински туризъм

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