CClinicalTrials.gg
Status unknownNCT00506571TIROX2Updated Jul 25, 2007

Phase II Study of Irinotecan,Oxaliplatin Plus TS-1 in Untreated Metastatic Colorectal Cancer

A Phase 2 interventional study of S-1, irinotecan, oxaliplatin in Colorecal Neoplasms and Secondary, sponsored by National Cancer Center, Korea. Status unknown at 1 site in Korea, Republic of. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2007-07-25.

Sponsored by National Cancer Center, Korea · Phase 2, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Apr 2007), so the status shown — last known as Recruiting — may be out of date.
Phase
Phase 2
Study type
Interventional
Enrollment
42
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study summary

Patients will be treated with irinotecan (150 mg/m2) followed by oxaliplatin (85 mg/m2) on day 1 and S-1 (80 mg/m2/day) from day 1 to 14 every 3 weeks. Patients will receive up to a planned treatment of maximum 12 cycles of chemotherapy. Response assessment will be performed every 2 cycles of chemotherapy.

02

Conditions studied

  • Colorecal Neoplasms
  • Secondary

Keywords

  • colorectal neoplasms
  • secondary
  • Combination chemotherapy
  • S-1
  • irinotecan
  • oxaliplatin
03

In context

Neoplasms

9,365 studies on the registry are indexed under Neoplasms; 2,489 are open to participants now.

This study's planned enrollment of 42 is below the median of 50 across 7,253 interventional studies indexed under Neoplasms.

Browse Neoplasms studies →

Lead sponsor

National Cancer Center, Korea is the lead sponsor of 193 studies on the registry; 34 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Histologically confirmed unresectable or metastatic colorectal cancer, not amenable to surgery or radiation treatment for curative intent
  • At least one unidimensional measurable lesion
  • ECOG performance status 0-2.
  • No prior chemotherapy in metastatic settings, but adjuvant or neo-adjuvant treatment for non-metastatic (M0) disease is allowed if completed at least 6 months prior to initiation of study treatment
  • Adequate major organ functions
  • Give written informed consent

Exclusion criteria

Exclusion Criteria:

  • Prior systemic chemotherapy for metastatic disease
  • Prior treatment with oxaliplatin or irinotecan
  • Prior radiotherapy is permitted if it was not administered to target lesions selected for this study and provided it has been completed at least 4 weeks before registration
  • Prior surgical treatment of stage IV disease is permitted
  • CNS metastases
  • Prior history of peripheral neuropathy ≥ NCI CTC grade 1
  • Uncontrolled or severe cardiovascular disease
  • Serious concurrent infection or nonmalignant illness
  • Other malignancy within the past 3 years except cured non-melanomatous skin cancer or carcinoma in situ of the cervix
  • Organ allografts requiring immunosuppressive therapy
  • Psychiatric disorder or uncontrolled seizure that would preclude compliance
  • Pregnant, nursing women or patients with reproductive potential without contraception
  • Patients receiving a concomitant treatment with drugs interacting with S-1 such as flucytosine, phenytoin, or warfarin et al.
  • Prior unanticipated severe reaction to fluoropyrimidine therapy, or known dihydropyrimidine dehydrogenase (DPD) deficiency
  • Known hypersensitivity to platinum compounds or any of the components of the study medications
  • Major surgery within 3 weeks prior to study treatment starts, or lack of complete recovery from the effects of major surgery
  • Received any investigational drug or agent/procedure, i.e. participation in another trial within 4 weeks before beginning treatment with study drug
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
42 participants (estimated)

Interventions

  • DrugS-1, irinotecan, oxaliplatin
06

What researchers measure

Primary outcomes

  1. Maximal overall response rate

    Time frame: During chemotherapy

Secondary outcomes

  1. Progression-free survival, Overall survival, Toxicity assessment, & Pharmacokinetic characteristics and association with genetic polymorphism

07

Study locations

1 of 1 sites recruiting
  • National Cancer Center Korea
    Goyang, Gyeonggi 410-769, Korea, Republic of
    • Kyung Hae Jung, M.D.Ph.D · Contact · khjung@ncc.re.kr · +82-31-920-1611
    • Hwa Jeong Kim · Contact · ncccoloonco@hanmail.net · +82-31-920-1145
    • Yong Sang Hong, M.D. · Sub investigator
    • Sun Young Kim, M.D. · Sub investigator
    • Hye Suk Han, M.D. · Sub investigator
    • Seung-Yong Jeong, M.D.Ph.D · Sub investigator
    • Hyo Seong Choi, M.D. · Sub investigator
    • Seok-Byung Lim, M.D. · Sub investigator
    • Hee Jin Chang, M.D.Ph.D. · Sub investigator
    • Jun Yong Jeong, M.D. · Sub investigator
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 25, 2007, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00506571
Lead sponsor
National Cancer Center, Korea
First posted
Jul 25, 2007
Start date
Jul 2007
Completion
Jun 2010 (estimated)
Last update
Jul 25, 2007

Study contacts

Kyung Hae Jung, M.D.Ph.D
Contact
khjung@ncc.re.kr
+82-31-920-1611
Hwa Jung Kim
Contact
ncccoloonco@hanmail.net
+82-31-920-1145
Kyung Hae Jung, M.D.Ph.D.
principal investigator · not affiliated

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Apr 2007. You cannot join it, but the record below documents what was studied.

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