Clin2
NCT06254066Possibly a fitNot yet recruiting

Immunotherapy plus PARP inhibitor for HR+ HER2- advanced breast cancer

Female Breast Cancer PatientsHistopathologically Confirmed Advanced HR +/HER2-invasive Breast CancerHRD Positive Advanced Breast Cancer

Part of Cancer, Women’s health & pregnancy clinical trials.

This trial tests a combination of an immunotherapy (adebrelimab) and a PARP inhibitor (fluzoparib) for women with HR+, HER2- advanced breast cancer that has a specific genetic feature called HRD positivity. It may offer a new option if standard hormone therapy and limited chemotherapy haven't worked.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 2
Enrollment
40 people
Ages
1.5 years to 75 years
Study type
Interventional

Who can take part

  • You are a woman aged 18 to 75.
  • Your breast cancer is HR+ (hormone receptor positive) and HER2- (negative).
  • Your tumor has a high level of genomic instability (HRD positive) or a BRCA mutation.
  • Your cancer has spread or cannot be cured by surgery.
  • You have had at least one prior endocrine therapy (like a CDK4/6 inhibitor) and no more than one prior chemotherapy for advanced disease.
  • You have not had prior treatment with a PD-1/PD-L1 inhibitor.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

Similar studies

Other trials that look related to this one.

NCT06561022Not yet recruiting· Phase 2
Precision treatment for HR+ HER2- advanced breast cancer

This trial tests a personalized treatment plan for people with advanced HR+ HER2- breast cancer whose cancer has progressed on a CDK4/6 inhibitor. It uses a special molecular test to match you to the targeted therapy most likely to work.

Shanghai
NCT05759546Recruiting· Phase 2
Test a PARP and CDK4/6 medicine plus hormone therapy

This Phase 2 study tests whether combining a PARP inhibitor with a CDK4/6 inhibitor and hormone (endocrine) therapy can help people with advanced HR-positive, HER2-negative breast cancer. It’s for certain patients who have not yet had chemotherapy or targeted therapy for metastatic disease.

Shanghai, Shanghai Municipality
NCT05576389Recruiting· Phase 2
Fluzoparib plus camrelizumab before surgery for BRCA-related HER2-negative breast cancer

This study tests a combination of two drugs – fluzoparib (a PARP inhibitor) and camrelizumab (an immunotherapy) – given before surgery for early-stage or locally advanced HER2-negative breast cancer in people with an inherited BRCA mutation. The goal is to see if this treatment can shrink the tumor and improve outcomes.

Beijing, Beijing Municipality
NCT06255392Recruiting· Phase 3
Fluzoparib with apatinib vs chemo for advanced breast cancer

This trial tests a combination of two oral targeted drugs (fluzoparib and apatinib) against standard chemotherapy for women with advanced, HRD-positive, HER2-negative breast cancer. It may be an option if you have already received some treatments but not too many.

Guangzhou, Guangdong
NCT06954584Recruiting· Phase 3
Fluzoparib with or without bevacizumab or diet for advanced ovarian cancer

This trial tests if adding bevacizumab (a drug that blocks blood vessel growth) or a special diet to fluzoparib (a PARP inhibitor) works better than fluzoparib alone for women with advanced ovarian cancer whose tumors have specific genetic features (HRD-positive or HRD-negative). It is for patients who have already responded well to initial chemotherapy.

Wuhan, Hubei
NCT07113964Not yet recruiting· Phase 2
QL1706 with olaparib for advanced HER2-negative breast cancer with HRD

This trial tests a combination of two drugs (QL1706 and olaparib) for people with advanced breast cancer that is HER2-negative and has a specific DNA repair problem called HRD. It's for those who have already tried 2 to 4 previous treatments.

Nanjing, Jiangsu

Hear when a new Female Breast Cancer Patients trial opens

We’ll email you when one opens — at most once a week, no account needed, unsubscribe anytime.