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NCT00551850 · ClinicalTrials.gov registry record · Phase 1

A Safety Study of an Oral EGFR Inhibitor, AV-412, Administered Three Times Weekly in Advanced Solid Tumor Patients

A Phase 1 study, sponsored by AVEO Pharmaceuticals.

Completed
Registry status
Phase 1
Development phase
37
Enrollment target

NCT00551850: Completed Phase 1 study, sponsored by AVEO Pharmaceuticals.

NCT00551850 is a Phase 1 study that has completed, run by AVEO Pharmaceuticals. The registered enrollment target is 37 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (38% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00551850, a Phase 1 study, has completed, sponsored by AVEO Pharmaceuticals.

COMPLETED
Registry status
Phase 1
Development phase
37 participants
Enrollment target

Study Summary

The Epidermal Growth Factor Receptor (EGFR) is a validated target for the treatment of cancer, and agents targeting EGFR such as erlotinib (Tarceva®) are approved by the FDA for treatment of various solid tumors. AV-412 is a novel inhibitor of the EGFR-tyrosine kinase, with added activity against Her2 and other oncogenic kinases. Based on evidence of preclinical activity in various solid tumors, AV-412 is being developed as a possible novel treatment for cancer in humans. PURPOSE: The purpose of this study is to test the safety and tolerability of AV-412, and determine the maximum tolerated dose of AV-412 when administered orally three times weekly.

Interventions

  • DRUG AV-412

Trial Details

FieldValue
Enrollment Target 37 participants
Start Date 2007-10
Est. Completion 2010-05
Phase Phase 1
AVEO Pharmaceuticals

27 total trials

What the finished NCT00551850 record still lists

NCT00551850 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 37 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (38% lower).

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

NCT00551850 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00551850 about?

NCT00551850 is a clinical study titled "A Safety Study of an Oral EGFR Inhibitor, AV-412, Administered Three Times Weekly in Advanced Solid Tumor Patients". The Epidermal Growth Factor Receptor (EGFR) is a validated target for the treatment of cancer, and agents targeting EGFR such as erlotinib (Tarceva®) are approved by the FDA for treatment of various solid tumors. AV-412 is a novel inhibitor of the EGFR-tyrosine kinase, with added activity against He...

What is the current status of trial NCT00551850?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 37 participants. The study started on 2007-10. Estimated completion is 2010-05.

What interventions are being tested in trial NCT00551850?

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

Who is sponsoring clinical trial NCT00551850?

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 NCT00551850's enrollment target sits among peer trials

37 1204th of 2000 higher than 791 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 NCT00551850, the US trial registry maintained by the National Library of Medicine. NCT00551850 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.