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NCT00519233 · ClinicalTrials.gov registry record · Phase 1

AGS-1C4D4 in Patients With Advanced Hormone Refractory Prostate Cancer

A Phase 1 study, sponsored by Astellas Pharma.

Completed
Registry status
Phase 1
Development phase
13
Enrollment target

NCT00519233: Completed Phase 1 study, sponsored by Astellas Pharma.

NCT00519233 is a Phase 1 study that has completed, run by Astellas Pharma. The registered enrollment target is 13 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (78% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00519233, a Phase 1 study, has completed, sponsored by Astellas Pharma.

COMPLETED
Registry status
Phase 1
Development phase
13 participants
Enrollment target

Study Summary

The present study will investigate the safety, tolerability and spectrum of side effects of AGS-1C4D4. As such, this study will characterize the dose limiting toxicities (DLT) and potentially the maximum tolerated dose (MTD) of AGS-1C4D4 in patients with advanced HRPC.

Interventions

  • DRUG AGS-1C4D4

Trial Details

FieldValue
Enrollment Target 13 participants
Start Date 2007-09
Est. Completion 2009-09
Phase Phase 1
Astellas Pharma

165 total trials

What the finished NCT00519233 record still lists

NCT00519233 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 13 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (78% lower).

The record links to 0 conditions, and to 1 intervention - of which AGS-1C4D4 is the first listed.

NCT00519233 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00519233 about?

NCT00519233 is a clinical study titled "AGS-1C4D4 in Patients With Advanced Hormone Refractory Prostate Cancer". The present study will investigate the safety, tolerability and spectrum of side effects of AGS-1C4D4. As such, this study will characterize the dose limiting toxicities (DLT) and potentially the maximum tolerated dose (MTD) of AGS-1C4D4 in patients with advanced HRPC.

What is the current status of trial NCT00519233?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 13 participants. The study started on 2007-09. Estimated completion is 2009-09.

What interventions are being tested in trial NCT00519233?

The interventions under investigation include: AGS-1C4D4 (DRUG).

Who is sponsoring clinical trial NCT00519233?

This trial is sponsored by Astellas Pharma, which has 165 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00519233's enrollment target sits among peer trials

13 1847th of 2000 higher than 149 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 NCT00519233, the US trial registry maintained by the National Library of Medicine. NCT00519233 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.