Molecularly Targeted Umbrella Study in Luminal Advanced Breast Cancer
NCT04355858 · Status: UNKNOWN · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 319
Last updated 2022-07-26
Summary
This study is a prospective, single-center, open-label, umbrella-shaped phase II clinical study for patients with HR+/HER2- endocrine-resistant advanced breast cancer.
Conditions
Interventions
- DRUG
-
SHR7390
MEK1/2 inhibitor
- DRUG
-
Famitinib
Multi-target tyrosine kinase inhibitor
- DRUG
-
SHR3162
PARP inhibitor
- DRUG
-
Pyrotinib
HER1 / HER2 receptor tyrosine kinase inhibitor
- DRUG
-
In Arm III, if the patient had not previously used capecitabine,she would receive pyrotinib and capecitabine, if the patients have previously used capecitabine, she would only used pyrotinib as a single agent.
- DRUG
-
SHR1210
PD-1 antibody
- DRUG
-
mTOR inhibitor
- DRUG
-
Nab paclitaxel
Albumin bound paclitaxel
- DRUG
-
SHR2554
EZH2 inhibitor
- DRUG
-
SHR3680
AR inhibitor
- DRUG
-
SHR6390
CDK4/6 inhibitor
- DRUG
-
SHR1701
anti-PD-L1/TGF-βRII bifunctional fusion protein
- DRUG
-
SERD
Fulvestrant
- DRUG
-
AI
aromatase inhibitor
- DRUG
-
VEGFi
Bevacizumab
Sponsors & Collaborators
-
Fudan University
lead OTHER
Principal Investigators
-
Zhi-Ming Shao · Fudan University
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 75 Years
- Sex
- FEMALE
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2020-05-01
- Primary Completion
- 2023-05-01
- Completion
- 2025-04-01
Countries
- China
Study Locations
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