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

NCT00588900 · ClinicalTrials.gov registry record · Phase 2

Irinotecan and Cediranib in Treating Patients With Metastatic Colorectal Cancer That Did Not Respond to Previous Oxaliplatin, Fluoropyrimidine, and Bevacizumab

A Phase 2 study, sponsored by Alliance for Clinical Trials in Oncology.

Terminated
Registry status
Phase 2
Development phase
5
Enrollment target

NCT00588900: Clinical Trial Phase 2 study, sponsored by Alliance for Clinical Trials in Oncology.

NCT00588900 is a Phase 2 study that was terminated before completion, run by Alliance for Clinical Trials in Oncology. The registered enrollment target is 5 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (96% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00588900, a Phase 2 study, was terminated before completion, sponsored by Alliance for Clinical Trials in Oncology.

TERMINATED
Registry status
Phase 2
Development phase
5 participants
Enrollment target

Study Summary

RATIONALE: Drugs used in chemotherapy, such as irinotecan, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Cediranib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Giving irinotecan together with cediranib may kill more tumor cells. PURPOSE: This phase II clinical trial is studying how well giving irinotecan together with cediranib works in treating patients with metastatic colorectal cancer that did not respond to previous oxaliplatin, fluoropyrimidine, and bevacizumab.

Primary Outcome

The 12 week progression-free rate was defined as the percentage of patients that were alive and progression-free 12 weeks after start of second-line therapy. Disease progression was assessed per modified RECIST criteria, and defined as at least a 20% increase in the sum of the longest diameters of target lesions, in either primary or nodal lesions, taking as reference the smallest sum longest diameter recorded since the baseline measurements, or the appearance of new lesions.

Interventions

  • DRUG irinotecan hydrochloride
  • DRUG cediranib maleate

Trial Details

FieldValue
Enrollment Target 5 participants
Start Date 2008-03
Est. Completion 2011-11
Phase Phase 2

Why NCT00588900 stopped before completion

NCT00588900 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 5 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (96% lower).

The record links to 0 conditions, and to 2 interventions - of which irinotecan hydrochloride is the first listed.

NCT00588900 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00588900 about?

NCT00588900 is a clinical study titled "Irinotecan and Cediranib in Treating Patients With Metastatic Colorectal Cancer That Did Not Respond to Previous Oxaliplatin, Fluoropyrimidine, and Bevacizumab". RATIONALE: Drugs used in chemotherapy, such as irinotecan, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Cediranib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Giving irinotecan t...

What is the current status of trial NCT00588900?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 5 participants. The study started on 2008-03. Estimated completion is 2011-11.

What interventions are being tested in trial NCT00588900?

The interventions under investigation include: irinotecan hydrochloride (DRUG), cediranib maleate (DRUG).

Who is sponsoring clinical trial NCT00588900?

This trial is sponsored by Alliance for Clinical Trials in Oncology, which has 446 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00588900's enrollment target sits among peer trials

5 2000th of 2000 the lowest 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 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 NCT00588900, the US trial registry maintained by the National Library of Medicine. NCT00588900 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.