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NCT00309946 · ClinicalTrials.gov registry record · Phase 2

Cediranib Maleate in Treating Patients With Malignant Mesothelioma That Cannot Be Removed By Surgery

A Phase 2 study, sponsored by National Cancer Institute (NCI).

Completed
Registry status
Phase 2
Development phase
51
Enrollment target

NCT00309946: Completed Phase 2 study, sponsored by National Cancer Institute (NCI).

NCT00309946 is a Phase 2 study that has completed, run by National Cancer Institute (NCI). The registered enrollment target is 51 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (62% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

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The verdict

NCT00309946, a Phase 2 study, has completed, sponsored by National Cancer Institute (NCI).

COMPLETED
Registry status
Phase 2
Development phase
51 participants
Enrollment target

Study Summary

This phase II trial is studying how well cediranib maleate works in treating patients with malignant mesothelioma that cannot be removed by surgery. Cediranib maleate may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth and by blocking blood flow to the tumor

Primary Outcome

Evaluated in this study using the new international criteria proposed by the Response Evaluation Criteria in Solid Tumors (RECIST) Committee. To be assigned a status of PR or CR, changes in tumor measurements must be confirmed by repeat assessments that should be performed no less than 4 weeks after the criteria for response are first met.

Interventions

  • DRUG cediranib maleate

Trial Details

FieldValue
Enrollment Target 51 participants
Start Date 2005-12
Est. Completion 2010-09
Phase Phase 2
National Cancer Institute (NCI)

3,257 total trials

What the finished NCT00309946 record still lists

NCT00309946 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 51 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (62% lower).

The record links to 0 conditions, and to 1 intervention - of which cediranib maleate is the first listed.

NCT00309946 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00309946 about?

NCT00309946 is a clinical study titled "Cediranib Maleate in Treating Patients With Malignant Mesothelioma That Cannot Be Removed By Surgery". This phase II trial is studying how well cediranib maleate works in treating patients with malignant mesothelioma that cannot be removed by surgery. Cediranib maleate may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth and by blocking blood flow to the tumor

What is the current status of trial NCT00309946?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 51 participants. The study started on 2005-12. Estimated completion is 2010-09.

What interventions are being tested in trial NCT00309946?

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

Who is sponsoring clinical trial NCT00309946?

This trial is sponsored by National Cancer Institute (NCI), which has 3,257 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00309946's enrollment target sits among peer trials

51 1190th of 2000 higher than 806 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

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Source: ClinicalTrials.gov NCT00309946, the US trial registry maintained by the National Library of Medicine. NCT00309946 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.