The overall aim of this project is to help improve the Health Related Quality of Life (HRQOL) of metastatic breast cancer (MBC) patients. There is currently an urgent and unmet need for specific tools to aid in the evaluation of HRQOL in MBC and this project aims to address these needs by developing a comprehensive EORTC questionnaire for assessing the HRQOL of this group. The new module will be used in conjunction with EORTC QLQ-C30 and will provide better measurement of the quality of life issues experienced by women with MBC. Interviews will be conducted with patients from several centres across Europe, guiding the development process in a patient centred way.
A Study of Chidamide Plus Endocrine in Maintenance Treatment of HR+/HER2- Breast Cancer After First-line Chemotherapy
This is not medical advice. AI-assisted translation — inaccuracies may occur. Always verify the original and consult your oncologist before taking any steps.
This trial is no longer recruiting — here are similar active trials
Matched by cancer type/biomarker, currently recruiting.
This is a Phase III, multicenter, randomized, open-label, global study designed to evaluate the efficacy and safety of inavolisib plus fulvestrant compared with alpelisib plus fulvestrant in patients with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2) -negative, PIK3CA-mutated, locally advanced (LA) or metastatic breast cancer (mBC), who progressed during or after cyclin dependent kinase 4/6i (CDK4/6i)-based therapy. Enrollment for the main study is now complete.
Open label, multi-centre, Phase Ia/b adaptive design study with an initial 2-stage Dose Escalation Phase followed by a Dose Expansion Phase.
The purpose of this study is to investigate the efficacy, safety, and tolerability of camizestrant in combination with ribociclib in patients with ER+ HER2- BC who have not received any other systemic treatment for advanced disease. Participants will be treated within the trial until they discontinue the study treatment for any reason.
About the trial
To explore the efficacy and safety of Chidamide combined with endocrine for maintenance therapy after first-line chemotherapy for HR+/HER2- breast cancer
Original English text from ClinicalTrials.gov
Who can (and can't) join
✓ Qualifies
- •Kobieta w wieku 18-70 lat (przed lub po menopauzie)
- •Potwierdzony rakiem piersi dodatnim na receptory hormonalne (HR+) i ujemnym na HER2
- •Zaawansowany, miejscowo zaawansowany lub przerzutowy rak piersi potwierdzony badaniem histologicznym
- •Rak nie leczony wcześniej lub pacjent po poprzedniej terapii endokrynnej z inhibitorami CDK4/6
- •Co najmniej jedno mierzalne ognisko choroby (według standardu RECIST v1.1)
- •Stan ogólny pacjenta 0-2 w skali ECOG
- •Prawidłowe wyniki morfologii krwi: neutrocyty ≥1,5 x 10⁹/L, płytki ≥100 x 10⁹/L, hemoglobina ≥90 g/L
- •Dobra funkcja wątroby i nerek: bilirubina ≤1,5 x norma, transaminazy ≤2,5 x norma, kreatynina ≤1,5 x norma
✗ Disqualifies
- •Niemożność połykania, przewlekła biegunka lub niedrożność jelit wpływające na wchłanianie leków
- •Uczulenie na składniki badanego leku
- •Inny nowotwór w ciągu ostatnich 5 lat (z wyjątkiem leczonych raków skóry czy tarczycy)
- •Uczestnictwo w innym badaniu klinicznym w ciągu ostatnich 4 tygodni
- •Historia zakażenia HIV, niedoboru odporności lub przeszczepienia narządu
- •Niekontrolowana choroba serca: znaczące wydłużenie QT, QTc >450 ms, niewydolność serca, zawał w ostatnich 6 miesięcy
- •Ciąża, karmienie piersią lub dodatni test ciążowy u kobiety w wieku rozrodczym
- •Wcześniejsze leczenie inhibitorami HDAC
Simplified criteria — AI translation
Trial details
- Minimum age
- 18 Years
- Maximum age
- 75 Years
- Last updated (source)
- June 6, 2023
- Sex
- Female only
Therapies / drugs in trial
Locations (1)
天津市肿瘤医院
Tianjin, China
Trial contact
Li Zhang
Contact information from ClinicalTrials.gov. Contact in English.
Share this trial
Data from ClinicalTrials.gov. AI-assisted translation, last sync: 7/1/2026.
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