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ACTIVE_NOT_RECRUITING • Phasen II, III • Stufe III, IV • ER positiv • PR positiv • HER2 negativ • CDK4/6 inhibitor absent • mTOR absent • Somatic PIK3CA present • Medical Oncology • Post-Menopausal • Interventionell

Folgendes wird aus ClinicalTrials.gov importiert:

A Study Evaluating the Efficacy and Safety of Inavolisib + Palbociclib + Fulvestrant vs Placebo + Palbociclib + Fulvestrant in Patients With PIK3CA-Mutant, Hormone Receptor-Positive, HER2-Negative, Locally Advanced or Metastatic Breast Cancer

This study will evaluate the efficacy, safety, and pharmacokinetics of inavolisib in combination with palbociclib and fulvestrant compared with placebo plus palbociclib and fulvestrant in participants with PIK3CA-mutant, hormone receptor (HR)-positive, HER2-negative locally advanced or metastatic breast cancer whose disease progressed during treatment or within 12 months of completing adjuvant endocrine therapy and who have not received prior systemic therapy for metastatic disease.

Breast Cancer

Studiendesign
Studientyp:

INTERVENTIONAL

Geschätzte Einschreibung:

325 Teilnehmer

Aktueller Studienbeginn:

29. Januar 2020

Zulassungskriterien
Alter für die Studie berechtigt:

18 - 999

Geschlechter für die Studie berechtigt:

all


Arms and Intervention
  • Inavolisib

  • Placebo

  • Palbociclib

  • Fulvestrant

Trial Information at Site
Last Updated:
Studieninformationen
ClinicalTrial.gov ID:

ACTIVE_NOT_RECRUITING

Estimated Enrollment:

325

Last Updated:

04/26/2025


Hauptermittler

Clinical Trials


Studiensponsor

Hoffmann-La Roche

Outcomes4Me

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