Molecularly Targeted Umbrella Study in Luminal Advanced Breast Cancer

NCT04355858 · Status: UNKNOWN · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 319

Last updated 2022-07-26

No results posted yet for this study

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

Capecitabine

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

Everolimus

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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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04355858 on ClinicalTrials.gov