Efficacy and Safety of Precision Therapy in Refractory Tumor

NCT03239015 · Status: UNKNOWN · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 300

Last updated 2022-03-04

No results posted yet for this study

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

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

Olaparib is an FDA/CFDA approved targeted drugs used for BRCA1/2 mutation based on NGS results.

DRUG

Everolimus

Everolimus is an FDA/CFDA approved targeted drugs used for mTOR or PI3KCA mutation based on NGS results.

DRUG

Cabozantinib

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

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

More Related Trials

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 NCT03239015 on ClinicalTrials.gov