Feasibility Study of SOL (S-1,Oral Leucovorin,and Oxaliplatin) for Colorectal Cancer in China

NCT01110941 · Status: COMPLETED · Phase: PHASE1/PHASE2 · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2015-05-19

No results posted yet for this study

Summary

S-1 is an oral fluoropyrimidine with demonstrated efficacy on gastric cancer and colorectal cancer. The new regimen with Oxaliplatin and leucovorin is expected to achieve more encouraging efficacy on colorectal cancer. This study is to explore the feasibility of the SOL regimen on efficacy and tolerability on Chinese colorectal cancer patients.

Conditions

Interventions

DRUG

S-1, leucovorin, oxaliplatin

S-1(20mg、25mg), capsule, 40\~60mg, Bid,p.o., day1\~7; LV (25 mg), tablet, 25mg,Bid,p.o., day1\~7; L-OHP (50 mg),injection 85mg/m2, day1. repeated at every 2 weeks cycle till disease progression.

Sponsors & Collaborators

  • 307 Hospital of PLA

    collaborator OTHER
  • Beijing Union Hosptial

    collaborator UNKNOWN
  • Tianjin Medical University Cancer Institute and Hospital

    collaborator OTHER
  • Hebei Provincial Cancer Hospital

    collaborator UNKNOWN
  • Shen Lin

    lead OTHER

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
20 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-09-30
Primary Completion
2010-03-31
Completion
2010-10-31

Countries

  • China

Study Locations

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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 NCT01110941 on ClinicalTrials.gov