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NCT00030615 · ClinicalTrials.gov registry record · Phase 1

Decitabine in Treating Patients With Advanced Solid Tumors

A Phase 1 study of Unspecified Adult Solid Tumor, Protocol Specific and Stage IV Breast Cancer, sponsored by National Cancer Institute (NCI).

Completed
Registry status
Phase 1
Development phase
24
Enrollment target
1
Study location

NCT00030615 is a Phase 1 study of Unspecified Adult Solid Tumor, Protocol Specific and Stage IV Breast Cancer that has completed, run by National Cancer Institute (NCI). The registered enrollment target is 24 participants, below the 501-participant average among 83 other Unspecified Adult Solid Tumor, Protocol Specific trials with a reported enrollment target (95% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT00030615, a Phase 1 study of Unspecified Adult Solid Tumor, Protocol Specific and Stage IV Breast Cancer, has completed, sponsored by National Cancer Institute (NCI).

COMPLETED
Registry status
Phase 1
Development phase
24 participants
Enrollment target
1
Study location

Study Summary

This phase I trial is studying the side effects and best dose of decitabine in treating patients with advanced solid tumors that have not responded to previous treatment. Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die

Interventions

  • OTHER laboratory biomarker analysis
  • OTHER pharmacological study
  • DRUG decitabine

Study Locations (1)

California

  • University of Southern California - Los Angeles

Trial Details

FieldValue
Enrollment Target 24 participants
Start Date 2001-12
Phase Phase 1

Sponsor

National Cancer Institute (NCI)

3,257 total trials

What the Registry Record Tells You About NCT00030615

The ClinicalTrials.gov registry entry for NCT00030615 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 24 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 501-participant average among 83 other Unspecified Adult Solid Tumor, Protocol Specific trials with a reported enrollment target (95% lower). The listed sponsor is National Cancer Institute (NCI), which has 3,257 total studies on file at ClinicalTrials.gov.

The record links to 9 conditions, with Unspecified Adult Solid Tumor, Protocol Specific appearing as the primary indexed condition, and to 3 interventions - of which laboratory biomarker analysis is the first listed.

NCT00030615 reports 1 study location spanning 1 distinct geographic area - top geographies include California.

Frequently Asked Questions

What is clinical trial NCT00030615 about?

NCT00030615 is a clinical study titled "Decitabine in Treating Patients With Advanced Solid Tumors". This phase I trial is studying the side effects and best dose of decitabine in treating patients with advanced solid tumors that have not responded to previous treatment. Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die

What is the current status of trial NCT00030615?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 24 participants. The study started on 2001-12.

What conditions does trial NCT00030615 study?

This clinical trial studies the following conditions: Unspecified Adult Solid Tumor, Protocol Specific, Stage IV Breast Cancer, Recurrent Melanoma, Recurrent Breast Cancer, Male Breast Cancer.

What interventions are being tested in trial NCT00030615?

The interventions under investigation include: laboratory biomarker analysis (OTHER), pharmacological study (OTHER), decitabine (DRUG).

Who is sponsoring clinical trial NCT00030615?

This trial is sponsored by National Cancer Institute (NCI), which has 3,257 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00030615 being conducted?

This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Unspecified Adult Solid Tumor, Protocol Specific

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

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.