Clinical Trials Directory

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UnknownNCT03376191

Apatinib in Advanced Non-squamous,NSCLC

Prospective, Multicenter, Non-intervention Clinical Trial of Apatinib in the Treatment of Advanced Non-squamous,Non-small Cell Lung Cancer

Status
Unknown
Phase
Study type
Observational
Enrollment
100 (estimated)
Sponsor
Jian Fang · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

To explore the efficacy and safety of apatinib in non-squamous non-small cell lung cancer in the real-world.

Detailed description

This is a multi-center, non-interventional clinical study. The number of patients that planned to be recruited is: from May 2017 to April 2019, the actual number of cases recruited into this study. If the clinicians thought the patient is suitable to take apatinib treatment, and give the patient apatinib treatment, the patient can be recruited into this study. Clinicians chose the initial dose of apatinib according to the patient's physical condition. Besides the clinicians adjusted the dose according to the patient's tolerance during the medication. The dosage was demanded not higher than 750 milligram (mg) per day. The patients received apatinib continuously, 28 days for a period, until intolerance, no longer getting benefits or patient wanted stop. During the course of the study, the researchers will not intervene the treatment of the patients, but only record the efficacy and adverse reactions. Main evaluation criteria: PFS Secondary evaluation criteria: OS,DCR and ORR (according to RECIST1.1). Main safety indicators:AE, SAE (according to NCI CTCAE V4.0) and QOL scores (Quality of Life Questionnaire-lung cancer).

Conditions

Interventions

TypeNameDescription
DRUGapatinibClinicians chose the initial dose of apatinib according to the patient's physical condition. Besides the clinicians adjusted the dose according to the patient's tolerance during the medication.The dosage was demanded not higher than 750 milligram (mg) per day. The patients received apatinib continuously, 28 days for a period, until intolerance, no longer getting benefits or patient wanted stop.

Timeline

Start date
2017-05-01
Primary completion
2019-04-01
Completion
2019-10-01
First posted
2017-12-18
Last updated
2017-12-18

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT03376191. Inclusion in this directory is not an endorsement.