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NCT00451880 · ClinicalTrials.gov registry record · Phase 1

Study of XL281 in Adults With Solid Tumors

A Phase 1 study, sponsored by Exelixis.

Completed
Registry status
Phase 1
Development phase
180
Enrollment target

NCT00451880: Completed Phase 1 study, sponsored by Exelixis.

NCT00451880 is a Phase 1 study that has completed, run by Exelixis. The registered enrollment target is 180 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (200% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00451880, a Phase 1 study, has completed, sponsored by Exelixis.

COMPLETED
Registry status
Phase 1
Development phase
180 participants
Enrollment target

Study Summary

The purpose of this study is to determine the safest dose of the multiple Raf kinase inhibitor (including c-Raf, B-Raf, and the activated mutant B-RafV600E) XL281, how often it should be taken, and how well subjects with cancer tolerate XL281. This study will also determine how the body reacts to XL281 when it is taken with and without food, and with and without Pepcid (famotidine), a drug that inhibits stomach acid production.

Interventions

  • DRUG famotidine
  • DRUG XL281

Trial Details

FieldValue
Enrollment Target 180 participants
Start Date 2007-02
Est. Completion 2011-10
Phase Phase 1
Exelixis

48 total trials

What the finished NCT00451880 record still lists

NCT00451880 is an interventional study that assigns participants to a tested intervention. The registered 180 participants enrollment target is mid-sized for trials with a published cap, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (200% higher).

The record links to 0 conditions, and to 2 interventions - of which famotidine is the first listed.

NCT00451880 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00451880 about?

NCT00451880 is a clinical study titled "Study of XL281 in Adults With Solid Tumors". The purpose of this study is to determine the safest dose of the multiple Raf kinase inhibitor (including c-Raf, B-Raf, and the activated mutant B-RafV600E) XL281, how often it should be taken, and how well subjects with cancer tolerate XL281. This study will also determine how the body reacts to XL...

What is the current status of trial NCT00451880?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 180 participants. The study started on 2007-02. Estimated completion is 2011-10.

What interventions are being tested in trial NCT00451880?

The interventions under investigation include: famotidine (DRUG), XL281 (DRUG).

Who is sponsoring clinical trial NCT00451880?

This trial is sponsored by Exelixis, which has 48 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00451880's enrollment target sits among peer trials

180 299th of 2000 higher than 1,690 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 NCT00451880, the US trial registry maintained by the National Library of Medicine. NCT00451880 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.