Study of TKI 258 in Combination With Xeloda and Oxaliplatin in Advanced Colorectal and Gastric Cancer

NCT02720926 · Status: TERMINATED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 3

Last updated 2016-03-28

No results posted yet for this study

Summary

Standard "3+3" dose escalation design of TKI258/XELOX in advanced gastric/gastro-oesophageal and colorectal cancer.

Conditions

Interventions

DRUG

Xeloda,

Capecitabine (xeloda): 2000mg/m2, twice a day on Day 1-14;

DRUG

Oxaliplatin

Oxaliplatin: 130mg/m2 day 1 every 21days

DRUG

TKI258

4 dose levels of TKI258: 200mg, 300mg, 400mg, 500mg once daily, 5days on and 2 days off;

Sponsors & Collaborators

  • Novartis

    collaborator INDUSTRY
  • National Cancer Centre, Singapore

    lead OTHER

Principal Investigators

  • Iain BH Tan, Dr · National Cancer Centre, Singapore

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-09-30
Primary Completion
2012-01-31
Completion
2012-01-31

Countries

  • Singapore

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 NCT02720926 on ClinicalTrials.gov