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NCT00826878 · ClinicalTrials.gov registry record · Phase 1

An Open-Label Study of QD Oral Administration of Tivozanib (AV-951) in Subjects With Non-Small Cell Lung Cancer (NSCLC)

A Phase 1 study, sponsored by AVEO Pharmaceuticals.

Completed
Registry status
Phase 1
Development phase
17
Enrollment target

NCT00826878: Completed Phase 1 study, sponsored by AVEO Pharmaceuticals.

NCT00826878 is a Phase 1 study that has completed, run by AVEO Pharmaceuticals. The registered enrollment target is 17 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (72% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00826878, a Phase 1 study, has completed, sponsored by AVEO Pharmaceuticals.

COMPLETED
Registry status
Phase 1
Development phase
17 participants
Enrollment target

Study Summary

This is a standard Phase 1b and 2a, multi-center, study design that will examine the safety, tolerability, and maximum tolerated dose of tivozanib (AV-951) with this dosing schedule, as well as overall response rate of tivozanib (AV-951) administration in NSCLC.

Interventions

  • DRUG Tivozanib (AV-951)

Trial Details

FieldValue
Enrollment Target 17 participants
Start Date 2009-01
Est. Completion 2011-05
Phase Phase 1
AVEO Pharmaceuticals

27 total trials

What the finished NCT00826878 record still lists

NCT00826878 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 17 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (72% lower).

The record links to 0 conditions, and to 1 intervention - of which Tivozanib (AV-951) is the first listed.

NCT00826878 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00826878 about?

NCT00826878 is a clinical study titled "An Open-Label Study of QD Oral Administration of Tivozanib (AV-951) in Subjects With Non-Small Cell Lung Cancer (NSCLC)". This is a standard Phase 1b and 2a, multi-center, study design that will examine the safety, tolerability, and maximum tolerated dose of tivozanib (AV-951) with this dosing schedule, as well as overall response rate of tivozanib (AV-951) administration in NSCLC.

What is the current status of trial NCT00826878?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 17 participants. The study started on 2009-01. Estimated completion is 2011-05.

What interventions are being tested in trial NCT00826878?

The interventions under investigation include: Tivozanib (AV-951) (DRUG).

Who is sponsoring clinical trial NCT00826878?

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 NCT00826878's enrollment target sits among peer trials

17 1785th of 2000 higher than 215 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 NCT00826878, the US trial registry maintained by the National Library of Medicine. NCT00826878 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.