Clinical Trials Directory

Trials / Unknown

UnknownNCT02852798

Apatinib Combined With Docetaxel Monotherapy as Second-line Therapy of Advanced EGFR WT, Non-squamous NSCLC

Clinical Study of Apatinib Mesylate Tablets Combined With Docetaxel Monotherapy as Second-line Therapy of Advanced EGFR Wild-type, Non-squamous, Non-small-cell Lung Cancer

Status
Unknown
Phase
Study type
Observational
Enrollment
60 (estimated)
Sponsor
Jiangsu ShengDiYa Medicine Co., Ltd. · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This is a clinical study of Apatinib Mesylate Tablets combined with docetaxel monotherapy as second-line therapy of advanced EGFR wild-type, non-squamous, non-small-cell lung cancer.

Detailed description

In order to seek high-efficiency, low-toxicity anti-angiogenic drugs, Jiangsu Hengrui Medical Co., Ltd has developed an efficient VEGFR2 tyrosine kinase inhibitor (TKI) - Apatinib. This drug works mainly by inhibiting VEGFR2 to produce the anti-angiogenic effects and treat malignant tumors. Apatinib was shown to have good tumor growth-inhibiting activity against lung cancer in both in vivo and in vitro experiments. This study aims to further validate the efficacy and safety of Apatinib combined with chemotherapeutics in the treatment of advanced EGFR wild-type non-squamous, non-small-cell lung cancer.

Conditions

Interventions

TypeNameDescription
DRUGApatinib Combined With DocetaxelDocetaxel 75 mg/ (m2.d)IV gtt 1h d1 q3w Apatinib Mesylate Tablets : 500 mg qd, 4 weeks as one cycle for continuous drug administration

Timeline

Start date
2016-08-01
Primary completion
2017-08-01
Completion
2018-08-01
First posted
2016-08-02
Last updated
2016-08-03

Source: ClinicalTrials.gov record NCT02852798. Inclusion in this directory is not an endorsement.