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NCT00001573 · ClinicalTrials.gov registry record · Phase 1

A Phase I Study of SU101 in Pediatric Patients With Refractory Malignancy

A Phase 1 study of Sarcoma and Glioma, sponsored by National Cancer Institute (NCI).

Completed
Registry status
Phase 1
Development phase
30
Enrollment target
1
Study location

NCT00001573 is a Phase 1 study of Sarcoma and Glioma that has completed, run by National Cancer Institute (NCI). The registered enrollment target is 30 participants, below the 921-participant average among 122 other Sarcoma trials with a reported enrollment target (97% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT00001573, a Phase 1 study of Sarcoma and Glioma, has completed, sponsored by National Cancer Institute (NCI).

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

Study Summary

A dose escalation scale consisting of 5 dosage levels is being used to determine the maximum tolerated dose (MTD) of SU101. A minimum of 3 and a maximum of 6 patients will be enrolled at each dose level. MTD is defined as the dose level immediately below that at which 2 or more patients exhibit dose limiting toxicity. Each treatment cycle is 21 days. Patients receive a 96 hour continuous IV infusion of SU101 on days 1-4.

Conditions Studied

Interventions

  • DRUG SU101

Study Locations (1)

Maryland

  • National Cancer Institute (NCI) - Bethesda

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 1997-03
Est. Completion 2000-05
Phase Phase 1

Sponsor

National Cancer Institute (NCI)

3,257 total trials

What the Registry Record Tells You About NCT00001573

The ClinicalTrials.gov registry entry for NCT00001573 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 30 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 921-participant average among 122 other Sarcoma trials with a reported enrollment target (97% lower). The listed sponsor is National Cancer Institute (NCI), which has 3,257 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Sarcoma appearing as the primary indexed condition, and to 1 intervention - of which SU101 is the first listed.

NCT00001573 reports 1 study location spanning 1 distinct geographic area - top geographies include Maryland.

Frequently Asked Questions

What is clinical trial NCT00001573 about?

NCT00001573 is a clinical study titled "A Phase I Study of SU101 in Pediatric Patients With Refractory Malignancy". A dose escalation scale consisting of 5 dosage levels is being used to determine the maximum tolerated dose (MTD) of SU101. A minimum of 3 and a maximum of 6 patients will be enrolled at each dose level. MTD is defined as the dose level immediately below that at which 2 or more patients exhibit dose...

What is the current status of trial NCT00001573?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 30 participants. The study started on 1997-03. Estimated completion is 2000-05.

What conditions does trial NCT00001573 study?

This clinical trial studies the following conditions: Sarcoma, Glioma.

What interventions are being tested in trial NCT00001573?

The interventions under investigation include: SU101 (DRUG).

Who is sponsoring clinical trial NCT00001573?

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

Where is trial NCT00001573 being conducted?

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

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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.