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NCT00473577 · ClinicalTrials.gov registry record · Phase 1

Study of the Tolerability, Safety, and Pharmacokinetics of CRA-024781 in Cancer Patients

A Phase 1 study, sponsored by Pharmacyclics.

Completed
Registry status
Phase 1
Development phase
40
Enrollment target

NCT00473577: Completed Phase 1 study, sponsored by Pharmacyclics.

NCT00473577 is a Phase 1 study that has completed, run by Pharmacyclics. The registered enrollment target is 40 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (33% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00473577, a Phase 1 study, has completed, sponsored by Pharmacyclics.

COMPLETED
Registry status
Phase 1
Development phase
40 participants
Enrollment target

Study Summary

To determine the maximum tolerated dose (MTD) of CRA-024781 IV given by 2-hour intravenous infusions in patients with refractory solid or hematologic malignancies. To evaluate safety and tolerability, pharmacokinetics and pharmacodynamics, and to evaluate bioavailability of CRA-024781 IV when administered in a single oral dose.

Interventions

  • DRUG CRA-24781

Trial Details

FieldValue
Enrollment Target 40 participants
Start Date 2005-08
Est. Completion 2007-12
Phase Phase 1
Pharmacyclics

54 total trials

What the finished NCT00473577 record still lists

NCT00473577 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 40 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (33% lower).

The record links to 0 conditions, and to 1 intervention - of which CRA-24781 is the first listed.

NCT00473577 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00473577 about?

NCT00473577 is a clinical study titled "Study of the Tolerability, Safety, and Pharmacokinetics of CRA-024781 in Cancer Patients". To determine the maximum tolerated dose (MTD) of CRA-024781 IV given by 2-hour intravenous infusions in patients with refractory solid or hematologic malignancies. To evaluate safety and tolerability, pharmacokinetics and pharmacodynamics, and to evaluate bioavailability of CRA-024781 IV when admini...

What is the current status of trial NCT00473577?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 40 participants. The study started on 2005-08. Estimated completion is 2007-12.

What interventions are being tested in trial NCT00473577?

The interventions under investigation include: CRA-24781 (DRUG).

Who is sponsoring clinical trial NCT00473577?

This trial is sponsored by Pharmacyclics, which has 54 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00473577's enrollment target sits among peer trials

40 1130th of 2000 higher than 810 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 NCT00473577, the US trial registry maintained by the National Library of Medicine. NCT00473577 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.