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NCT00710736 · ClinicalTrials.gov registry record · Phase 1

A Study of ARRY-334543 and Capecitabine in Patients With Advanced Cancer

A Phase 1 study, sponsored by Array Biopharma, now a wholly owned subsidiary of Pfizer.

Completed
Registry status
Phase 1
Development phase
29
Enrollment target

NCT00710736: Completed Phase 1 study, sponsored by Array Biopharma, now a wholly owned subsidiary of Pfizer.

NCT00710736 is a Phase 1 study that has completed, run by Array Biopharma, now a wholly owned subsidiary of Pfizer. The registered enrollment target is 29 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (52% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00710736, a Phase 1 study, has completed, sponsored by Array Biopharma, now a wholly owned subsidiary of Pfizer.

COMPLETED
Registry status
Phase 1
Development phase
29 participants
Enrollment target

Study Summary

This is a Phase 1 study during which patients with advanced/metastatic solid tumors will receive investigational study drug ARRY-334543 and capecitabine. Patients will receive increasing doses of study drug in combination with capecitabine in order to achieve the highest dose of study drug possible that will not cause unacceptable side effects. Patients will be followed to see what side effects the combination causes and what effectiveness the combination has, if any, in treating the cancer. Approximately 30 patients from the US and Canada will be enrolled in this study.

Interventions

  • DRUG ARRY-334543, EGFR/ErbB2 inhibitor; oral
  • DRUG Capecitabine, 5-fluorouracil prodrug; oral

Trial Details

FieldValue
Enrollment Target 29 participants
Start Date 2008-06
Est. Completion 2011-04
Phase Phase 1

What the finished NCT00710736 record still lists

NCT00710736 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 29 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (52% lower).

The record links to 0 conditions, and to 2 interventions - of which ARRY-334543, EGFR/ErbB2 inhibitor; oral is the first listed.

NCT00710736 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00710736 about?

NCT00710736 is a clinical study titled "A Study of ARRY-334543 and Capecitabine in Patients With Advanced Cancer". This is a Phase 1 study during which patients with advanced/metastatic solid tumors will receive investigational study drug ARRY-334543 and capecitabine. Patients will receive increasing doses of study drug in combination with capecitabine in order to achieve the highest dose of study drug possible ...

What is the current status of trial NCT00710736?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 29 participants. The study started on 2008-06. Estimated completion is 2011-04.

What interventions are being tested in trial NCT00710736?

The interventions under investigation include: ARRY-334543, EGFR/ErbB2 inhibitor; oral (DRUG), Capecitabine, 5-fluorouracil prodrug; oral (DRUG).

Who is sponsoring clinical trial NCT00710736?

This trial is sponsored by Array Biopharma, now a wholly owned subsidiary of Pfizer, which has 21 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00710736's enrollment target sits among peer trials

29 1440th of 2000 higher than 554 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 NCT00710736, the US trial registry maintained by the National Library of Medicine. NCT00710736 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.