Efficacy and Safety of Precision Therapy in Refractory Tumor
NCT03239015 · Status: UNKNOWN · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 300
Last updated 2022-03-04
Summary
This study is intended to evaluate efficacy and safety of targeted precision therapy in patients with refractory tumor, including rare tumor without standard recommended treatment and common tumor after multiple line of therapy.
Conditions
- Rare Tumor
- Refractory Tumor
Interventions
- DRUG
-
Gefitinib
Gefitinib is an FDA/CFDA approved targeted drugs used for EGFR mutation based on NGS results.
- DRUG
-
Erlotinib
Erlotinib is an FDA/CFDA approved targeted drugs used for EGFR mutation based on NGS results.
- DRUG
-
Afatinib
Afatinib is an FDA/CFDA approved targeted drugs used for EGFR mutation based on NGS results.
- DRUG
-
Trastuzumab is an FDA/CFDA approved targeted drugs used for Her2 amplification based on NGS results.
- DRUG
-
Oxazolidine
Oxazolidine is an FDA/CFDA approved targeted drugs used for ALK or ROS-1 or MET fusion based on NGS results.
- DRUG
-
Olaparib is an FDA/CFDA approved targeted drugs used for BRCA1/2 mutation based on NGS results.
- DRUG
-
Everolimus is an FDA/CFDA approved targeted drugs used for mTOR or PI3KCA mutation based on NGS results.
- DRUG
-
Cabozantinib is an FDA/CFDA approved targeted drugs used for RET mutation based on NGS results.
- DRUG
-
Vemurafenib
Vemurafenib is an FDA/CFDA approved targeted drugs used for BRAF mutation based on NGS results.
- DRUG
-
Dabrafenib
Dabrafenib is an FDA/CFDA approved targeted drugs used for BRAF mutation based on NGS results.
- DRUG
-
Palbociclib is an FDA/CFDA approved targeted drugs used for CDK4/6 mutation or amplification based on NGS results.
- DRUG
-
PD-1/L1 inhibitor plus anti-angiogenic agent
PD-1/L1 inhibitor plus anti-angiogenic agent is a regimen used for refractory tumor without druggable target
Sponsors & Collaborators
-
Baodong Qin
lead OTHER
Principal Investigators
-
Yuan-Sheng Zang, MD.PHD · Shanghai Changzheng Hospital
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Max Age
- 75 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2017-01-01
- Primary Completion
- 2023-06-30
- Completion
- 2023-12-31
Countries
- China
Study Locations
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