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NCT00072475 · ClinicalTrials.gov registry record · Phase 2

Vatalanib in Treating Patients With Primary or Secondary Myelodysplastic Syndromes

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

Completed
Registry status
Phase 2
Development phase
155
Enrollment target

NCT00072475: Completed Phase 2 study, sponsored by Alliance for Clinical Trials in Oncology.

NCT00072475 is a Phase 2 study that has completed, run by Alliance for Clinical Trials in Oncology. The registered enrollment target is 155 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (17% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00072475, a Phase 2 study, has completed, sponsored by Alliance for Clinical Trials in Oncology.

COMPLETED
Registry status
Phase 2
Development phase
155 participants
Enrollment target

Study Summary

RATIONALE: Vatalanib may be effective in preventing the development of leukemia in patients who have myelodysplastic syndromes. PURPOSE: This phase II trial is studying vatalanib to see how well it works in treating patients with primary or secondary myelodysplastic syndromes.

Primary Outcome

Response was measured by International Standardized Response Criteria for MDS * Complete Response: Bone marrow showing \< 5% myeloblasts with normal maturation of all cell lines; Hgb \> 11 g/dL (untransfused), ANC ≥1.5 K/L, PLT ≥ 100 K/L, No blasts, no dysplasia * Partial remission: All of the CR criteria (if abnormal at baseline), except BM evaluation. Blasts decreased by ≥ 50% over baseline. Cellularity and morphology are not relevant. Hematologic improvement: * Erythroid (HI-E): For partic

Interventions

  • DRUG vatalanib

Trial Details

FieldValue
Enrollment Target 155 participants
Start Date 2003-12
Est. Completion 2014-06
Phase Phase 2

What the finished NCT00072475 record still lists

NCT00072475 is an interventional study that assigns participants to a tested intervention. The registered 155 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (17% higher).

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

NCT00072475 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00072475 about?

NCT00072475 is a clinical study titled "Vatalanib in Treating Patients With Primary or Secondary Myelodysplastic Syndromes". RATIONALE: Vatalanib may be effective in preventing the development of leukemia in patients who have myelodysplastic syndromes. PURPOSE: This phase II trial is studying vatalanib to see how well it works in treating patients with primary or secondary myelodysplastic syndromes.

What is the current status of trial NCT00072475?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 155 participants. The study started on 2003-12. Estimated completion is 2014-06.

What interventions are being tested in trial NCT00072475?

The interventions under investigation include: vatalanib (DRUG).

Who is sponsoring clinical trial NCT00072475?

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 NCT00072475's enrollment target sits among peer trials

155 448th of 2000 higher than 1,553 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 NCT00072475, the US trial registry maintained by the National Library of Medicine. NCT00072475 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.