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NCT00510224 · ClinicalTrials.gov registry record · Phase 2

Sandostatin for Patients With Androgen Independent Prostate Cancer

A Phase 2 study, sponsored by University of California, San Francisco.

Terminated
Registry status
Phase 2
Development phase
13
Enrollment target

NCT00510224 is a Phase 2 study that was terminated before completion, run by University of California, San Francisco. The registered enrollment target is 13 participants.

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The verdict

NCT00510224, a Phase 2 study, was terminated before completion, sponsored by University of California, San Francisco.

TERMINATED
Registry status
Phase 2
Development phase
13 participants
Enrollment target

Study Summary

This is an open label, single center Phase II trial of Sandostatin LAR in patients with hormone refractory prostate cancer. Patients will receive Sandostatin LAR 30 mg intramuscularly every 28 days. Patients will be treated until the time of disease progression, unacceptable toxicity or withdrawal of consent. The study will require 27 evaluable patients.

Interventions

  • DRUG Sandostatin

Trial Details

FieldValue
Enrollment Target 13 participants
Start Date 2007-07
Est. Completion 2009-08
Phase Phase 2

What the Registry Record Tells You About NCT00510224

The ClinicalTrials.gov registry entry for NCT00510224 describes a study currently listed as terminated, categorized as Phase 2. The registered enrollment target is 13 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of California, San Francisco, which has 1,713 total studies on file at ClinicalTrials.gov.

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

NCT00510224 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00510224 about?

NCT00510224 is a clinical study titled "Sandostatin for Patients With Androgen Independent Prostate Cancer". This is an open label, single center Phase II trial of Sandostatin LAR in patients with hormone refractory prostate cancer. Patients will receive Sandostatin LAR 30 mg intramuscularly every 28 days. Patients will be treated until the time of disease progression, unacceptable toxicity or withdrawal o...

What is the current status of trial NCT00510224?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 13 participants. The study started on 2007-07. Estimated completion is 2009-08.

What interventions are being tested in trial NCT00510224?

The interventions under investigation include: Sandostatin (DRUG).

Who is sponsoring clinical trial NCT00510224?

This trial is sponsored by University of California, San Francisco, which has 1,713 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.