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NCT00585000 · ClinicalTrials.gov registry record · Phase 1

A Study To Assess The Safety Of Administering CP-675,206 As A One Hour Infusion In Patients With Surgically Incurable Advanced Melanoma

A Phase 1 study, sponsored by AstraZeneca.

Terminated
Registry status
Phase 1
Development phase
49
Enrollment target

NCT00585000: Clinical Trial Phase 1 study, sponsored by AstraZeneca.

NCT00585000 is a Phase 1 study that was terminated before completion, run by AstraZeneca. The registered enrollment target is 49 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (18% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00585000, a Phase 1 study, was terminated before completion, sponsored by AstraZeneca.

TERMINATED
Registry status
Phase 1
Development phase
49 participants
Enrollment target

Study Summary

This will show if CP-675,206 can be administered safely as an intravenous infusion lasting one hour. CP 675,206 already has been administered to 835 subjects over 1.0 - 7.5 hours.

Interventions

  • DRUG CP-675,206

Trial Details

FieldValue
Enrollment Target 49 participants
Start Date 2007-12
Est. Completion 2010-01
Phase Phase 1
AstraZeneca

1,285 total trials

Why NCT00585000 stopped before completion

NCT00585000 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 49 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (18% lower).

The record links to 0 conditions, and to 1 intervention - of which CP-675,206 is the first listed.

NCT00585000 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00585000 about?

NCT00585000 is a clinical study titled "A Study To Assess The Safety Of Administering CP-675,206 As A One Hour Infusion In Patients With Surgically Incurable Advanced Melanoma". This will show if CP-675,206 can be administered safely as an intravenous infusion lasting one hour. CP 675,206 already has been administered to 835 subjects over 1.0 - 7.5 hours.

What is the current status of trial NCT00585000?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 49 participants. The study started on 2007-12. Estimated completion is 2010-01.

What interventions are being tested in trial NCT00585000?

The interventions under investigation include: CP-675,206 (DRUG).

Who is sponsoring clinical trial NCT00585000?

This trial is sponsored by AstraZeneca, which has 1,285 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00585000's enrollment target sits among peer trials

49 1017th of 2000 higher than 976 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 NCT00585000, the US trial registry maintained by the National Library of Medicine. NCT00585000 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.