Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00338039 · ClinicalTrials.gov registry record · Phase 2

Induction Cetuximab (IM-C225), Gemcitabine, and Oxaliplatin in Pancreatic Cancer Patients

A Phase 2 study, sponsored by M.D. Anderson Cancer Center.

Completed
Registry status
Phase 2
Development phase
69
Enrollment target

NCT00338039: Completed Phase 2 study, sponsored by M.D. Anderson Cancer Center.

NCT00338039 is a Phase 2 study that has completed, run by M.D. Anderson Cancer Center. The registered enrollment target is 69 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (48% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist → Add completion date to calendar (.ics) →

The verdict

NCT00338039, a Phase 2 study, has completed, sponsored by M.D. Anderson Cancer Center.

COMPLETED
Registry status
Phase 2
Development phase
69 participants
Enrollment target

Study Summary

The primary objective is to evaluate the efficacy of a combination of cetuximab with systemic chemotherapy followed by chemoradiation in locally advanced pancreatic cancer. The primary endpoint is actuarial one-year survival. The secondary objectives are: * To evaluate the local tumor response in patients treated with the above regimen. * To characterize the safety of the above regimen.

Primary Outcome

1-year, 2-year, and 4-year actuarial overall survival (OS) rates defined as number of participants out of total participants alive at 1, 2 or 4 years post baseline treatment.

Interventions

  • DRUG Capecitabine
  • DRUG Oxaliplatin
  • RADIATION Radiotherapy
  • DRUG Cetuximab
  • DRUG Gemcitabine

Trial Details

FieldValue
Enrollment Target 69 participants
Start Date 2005-09
Est. Completion 2011-06
Phase Phase 2
M.D. Anderson Cancer Center

2,692 total trials

What the finished NCT00338039 record still lists

NCT00338039 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 69 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (48% lower).

The record links to 0 conditions, and to 5 interventions - of which Capecitabine is the first listed.

NCT00338039 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00338039 about?

NCT00338039 is a clinical study titled "Induction Cetuximab (IM-C225), Gemcitabine, and Oxaliplatin in Pancreatic Cancer Patients". The primary objective is to evaluate the efficacy of a combination of cetuximab with systemic chemotherapy followed by chemoradiation in locally advanced pancreatic cancer. The primary endpoint is actuarial one-year survival. The secondary objectives are: * To evaluate the local tumor response in ...

What is the current status of trial NCT00338039?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 69 participants. The study started on 2005-09. Estimated completion is 2011-06.

What interventions are being tested in trial NCT00338039?

The interventions under investigation include: Capecitabine (DRUG), Oxaliplatin (DRUG), Radiotherapy (RADIATION), Cetuximab (DRUG), Gemcitabine (DRUG).

Who is sponsoring clinical trial NCT00338039?

This trial is sponsored by M.D. Anderson Cancer Center, which has 2,692 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00338039's enrollment target sits among peer trials

69 965th of 2000 higher than 1,034 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT04020575 · 69 participants · Phase 1

    Autologous huMNC2-CAR44 or huMNC2-CAR22 T Cells for Breast Cancer Targeting Cleaved Form of MUC1 (MUC1*)

  • NCT04163614 · 69 participants · NA

    Blood Pressure Slopes and Ultrafiltration in Hemodialysis Patients

  • NCT04164641 · 69 participants · NA

    Noraxon myoRESEARCH™ Software Gait Analysis Evaluation and Orthotic Gait Correction in Reducing Diabetic Foot Ulceration Or Subsequent Amputation in Patients With a History of a Diabetic Foot Ulceration

  • NCT04493372 · 69 participants · NA

    Deciphering Preserved Autonomic Function After Spinal Cord Injury

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00338039, the US trial registry maintained by the National Library of Medicine. NCT00338039 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.