Clinical Trials Directory

Trials / Unknown

UnknownNCT03355612

XELOX Plus Apatinib vs XELOX as Post-operative Chemotherapy in Locally Advanced Gastric Signet Ring Carcinoma

A Randomized, Multicenter, Controlled Study of XELOX (Oxaliplatin With Capecitabine) Combined With Apatinib Versus XELOX as Post-operative Chemotherapy in Locally Advanced Gastric Signet Ring Carcinoma With D2 Dissection.

Status
Unknown
Phase
Phase 3
Study type
Interventional
Enrollment
456 (estimated)
Sponsor
Tianjin Medical University Cancer Institute and Hospital · Academic / Other
Sex
All
Age
18 Years – 70 Years
Healthy volunteers
Not accepted

Summary

This is a randomized, multicenter, controlled study to compared the Efficacy and Safety of XELOX combined with Apatinib versus XELOX as post-operative chemotherapy in locally advanced gastric signet ring carcinoma with D2 dissection.

Detailed description

The purpose of this study is to prove that as for disease free survival time, and safety, Apatinib with XELOX(Oxaliplatin with Capecitabine) has a better effect over that of XELOX adjunct therapy group for postoperative chemotherapy of locally advanced gastric signet ring carcinoma with D2 dissection.

Conditions

Interventions

TypeNameDescription
DRUGApatinibApatinib: 500 mg, qd, po, last 180 days
DRUGXELOXCapecitabine:1000 mg/m2 bid d1-14 q3w, Oxaliplatin:130 mg/m2 d1 q3w

Timeline

Start date
2017-12-20
Primary completion
2020-12-20
Completion
2025-12-20
First posted
2017-11-28
Last updated
2017-11-28

Source: ClinicalTrials.gov record NCT03355612. Inclusion in this directory is not an endorsement.