A Phase 3 Study of HRS-8080 Versus Treatment Chosen by Physicians in Locally Advanced and Metastatic Breast Cancer
Interventionsstudie
Phase 3
Sun Yat-sen University Cancer Center
Sponsor: Shandong Suncadia Medicine
Zuletzt aktualisiert: 26. Januar 2026 Hinweis - Die Informationen stammen aus öffentlichen Registern und spiegeln möglicherweise nicht die Echtzeitänderungen am lokalen Studienzentrum wider.
This study is a multicenter, open-label, randomized controlled Phase 3 clinical trial. It is planned to enroll 240 female patients with locally advanced or metastatic breast cancer followed by disease progression after previous endocrine therapy.
Behandlungskategorie
Andere Medikamente, Hormontherapie, Zielgerichtete Therapie
1. Women aged 18 to 75 years old (including both values).
2. ECOG Physical Strength Status (PS) : 0 to 1 point.
3. Patients with locally advanced or metastatic breast cancer confirmed by histology.
4. Patients previously received 1-2 lines of endocrine therapy.
5. Expected survival > 6 months.
6. The functional level of the organs must meet the requirements.
7. Subjects that voluntarily participate in this clinical trial, be willing and able to abide by the procedures related to clinical visits and research, understand the research procedures and have signed the informed consent.
Ausschlusskriterien
1. Patients with rapid disease progress and investigators determine that endocrine therapy is not suitable or tolerant.
2. A history of severe clinical cardiovascular diseases.
3. Patients with uncontrollable tumor-related pain as judged by investigators.
4. Severe infection exists within 4 weeks before the first study administration.
5. Patients with clinically significant endometrial abnormalities.
6. Untreated active hepatitis.
7. Patients known to be allergic to HRS-8080 components.
8. Pregnant and lactating women, or those planning to become pregnant during the study period.
Glauben Sie, dass diese klinische Studie fälschlicherweise angezeigt wird?
Design-Details
ZuteilungRandomized
InterventionsmodellParallel Assignment
MaskierungNone (Open Label)
Anzahl der Teilnehmer240
Arme & Interventionen
Arme
Interventionen
Typ: Experimental
Beschreibung:
Interventionen:
HRS-8080 Tablet
Fulvestrant injection
Exemestane tablets
Everolimus Tablets
Anastrozole Tablets
Letrozole Tablets
Ergebnismessungen
Primäre Ergebnismessungen
Progression free survival (PFS) evaluated by the blinded independent central review (BICR).Approximately 2 years.
Sekundäre Ergebnismessungen
Overall response rate (ORR).Approximately 2 years.
Clinical benefit rate (CBR).Approximately 2 years.
Duration of response (DOR).Approximately 2 years.
Overall survival (OS).Approximately 3 years.
Adverse events (AEs).Approximately 2 years.
Serious adverse events (SAEs).Approximately 2 years.
Progression free survival (PFS) evaluated by investigators.Approximately 2 years.
Studie vormerken
Studie teilen
Studie herunterladen
Glauben Sie, dass diese klinische Studie fälschlicherweise angezeigt wird?