🇮🇪Ireland
16°C Partly Cloudy · Dublin
Live Updates
--:--:-- IST
Contributor sign in
Latest
Clinical Trials in Germany / NCT07085767
Recruiting Phase 3

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

NCT07085767 · tracked via the Priya Life Science Germany tracker
Phase
Phase 3
Started
2025-11-03
Last updated
2026-09-23

Condition(s) studied

Breast CancerLocally Advanced Breast CancerMetastatic Breast CancerER Positive Breast CancerHER2 Negative Breast Carcinoma

Investigational drug(s) / intervention(s)

Palazestrant →Letrozole-matching placeboRibociclib →Letrozole →Palazestrant matching-placebo

Palazestrant: Participants will be treated with palazestrant 90 mg once daily on a 4-week (28-day) cycle.

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

Ribociclib: Participants will be treated with ribociclib 600 mg once daily on Days 1-21 of a 4-week (28 day) cycle.

Letrozole: Participants will be treated with letrozole 2.5 mg once daily on a 4-week (28-day) cycle

Palazestrant matching-placebo: Participants will be treated with palazestrant-matching placebo once daily on a 4-week (28-day) cycle

Study summary

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.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
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.

Primary outcome measure(s)

Trial sites (200)

FacilityCityRegionStatus
Clinical Trial Site Hot Springs Arkansas Recruiting
Clinical Trial Site Beverly Hills California Recruiting
Clinical Trial Site La Jolla California Recruiting
Clinical Trial Site Los Alamitos California Recruiting
Clinical Trial Site Oakland California Recruiting
Clinical Trial Site Roseville California Recruiting
Clinical Trial Site San Francisco California Recruiting
Clinical Trial Site San Francisco California Recruiting
Clinical Trial Site Santa Barbara California Recruiting
Clinical Trial Site Santa Clara California Recruiting
Clinical Trial Site Vallejo California Recruiting
Clinical Trial Site Walnut Creek California Recruiting
Clinical Trial Site Aurora Colorado Recruiting
Clinical Trial Site Denver Colorado Recruiting
Clinical Trial Site New Haven Connecticut Recruiting
Clinical Trial Site Tampa Florida Recruiting
Clinical Trial Site Marietta Georgia Recruiting
Clinical Trial Site Honolulu Hawaii Recruiting
Clinical Trial Site Peoria Illinois Recruiting
Clinical Trial Site Urbana Illinois Recruiting
Clinical Trial Site Ames Iowa Withdrawn
Clinical Trial Site Scarborough Maine Recruiting
Clinical Trial Site Annapolis Maryland Recruiting
Clinical Trial Site Baltimore Maryland Recruiting
Clinical Trial Site Baltimore Maryland Recruiting
Clinical Trial Site Catonsville Maryland Recruiting
Clinical Trial Site Burlington Massachusetts Recruiting
Clinical Trial Site Ann Arbor Michigan Recruiting
Clinical Trial Site Minneapolis Minnesota Recruiting
Clinical Trial Site Jackson Mississippi Recruiting
Clinical Trial Site Kansas City Missouri Recruiting
Clinical Trial Site Lebanon New Hampshire Recruiting
Clinical Trial Site Santa Fe New Mexico Recruiting
Clinical Trial Site New York New York Recruiting
Clinical Trial Site New York New York Recruiting
Clinical Trial Site Charlotte North Carolina Recruiting
Clinical Trial Site Durham North Carolina Recruiting
Clinical Trial Site Cincinnati Ohio Recruiting
Clinical Trial Site Columbus Ohio Recruiting
Clinical Trial Site Columbus Ohio Recruiting

+ 160 more sites — see the full list on the official registry below.

On this site

📄 Kisqali (ribociclib) drug profile →

More Olema Pharmaceuticals, Inc. trials in Germany

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 NCT07085767 on ClinicalTrials.gov ↗ ← All trials in Germany