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NCT00381654 · ClinicalTrials.gov registry record · Phase 1

Safety/Tolerability Study of AV-412 in Subjects With Refractory or Relapsed Solid Tumor Malignancies

A Phase 1 study, sponsored by AVEO Pharmaceuticals.

Terminated
Registry status
Phase 1
Development phase
27
Enrollment target

NCT00381654: Clinical Trial Phase 1 study, sponsored by AVEO Pharmaceuticals.

NCT00381654 is a Phase 1 study that was terminated before completion, run by AVEO Pharmaceuticals. The registered enrollment target is 27 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (55% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00381654, a Phase 1 study, was terminated before completion, sponsored by AVEO Pharmaceuticals.

TERMINATED
Registry status
Phase 1
Development phase
27 participants
Enrollment target

Study Summary

AV-412 is a new oral therapy developed to inhibit the growth of solid tumors in patients who have not responded to standard therapy or surgical interventions, or who have experienced relapse. This study will test the safety of AV-412 and determine the maximum tolerated dose for the treatment of solid tumors.

Interventions

  • DRUG AV-412

Trial Details

FieldValue
Enrollment Target 27 participants
Start Date 2006-10
Est. Completion 2010-02
Phase Phase 1
AVEO Pharmaceuticals

27 total trials

Why NCT00381654 stopped before completion

NCT00381654 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 27 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (55% lower).

The record links to 0 conditions, and to 1 intervention - of which AV-412 is the first listed.

NCT00381654 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00381654 about?

NCT00381654 is a clinical study titled "Safety/Tolerability Study of AV-412 in Subjects With Refractory or Relapsed Solid Tumor Malignancies". AV-412 is a new oral therapy developed to inhibit the growth of solid tumors in patients who have not responded to standard therapy or surgical interventions, or who have experienced relapse. This study will test the safety of AV-412 and determine the maximum tolerated dose for the treatment of soli...

What is the current status of trial NCT00381654?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 27 participants. The study started on 2006-10. Estimated completion is 2010-02.

What interventions are being tested in trial NCT00381654?

The interventions under investigation include: AV-412 (DRUG).

Who is sponsoring clinical trial NCT00381654?

This trial is sponsored by AVEO Pharmaceuticals, which has 27 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00381654's enrollment target sits among peer trials

27 1463rd of 2000 higher than 519 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 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 NCT00381654, the US trial registry maintained by the National Library of Medicine. NCT00381654 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.