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NCT00668382 · ClinicalTrials.gov registry record · Phase 1

Evaluate The Toxicity And Feasibility Of Intra-Tumoral Injection

A Phase 1 study, sponsored by University of Massachusetts, Worcester.

Completed
Registry status
Phase 1
Development phase
11
Enrollment target

NCT00668382: Completed Phase 1 study, sponsored by University of Massachusetts, Worcester.

NCT00668382 is a Phase 1 study that has completed, run by University of Massachusetts, Worcester. The registered enrollment target is 11 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (82% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00668382, a Phase 1 study, has completed, sponsored by University of Massachusetts, Worcester.

COMPLETED
Registry status
Phase 1
Development phase
11 participants
Enrollment target

Study Summary

This is a Phase I pilot study to evaluate the toxicity and feasibility of intratumoral injection (Glycosphingolipids) GSL alpha-GAL (beta-galactosidase) in patients with advanced, refractory solid tumors who have failed standard therapies or are not eligible for standard treatment.

Primary Outcome

Grade 3/4 Toxicity occurring in a participant within a month of intratumoral injection

Interventions

  • BIOLOGICAL Alpha-Gal Glycosphingolipid

Trial Details

FieldValue
Enrollment Target 11 participants
Start Date 2007-07
Est. Completion 2011-07
Phase Phase 1

What the finished NCT00668382 record still lists

NCT00668382 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 11 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (82% lower).

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

NCT00668382 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00668382 about?

NCT00668382 is a clinical study titled "Evaluate The Toxicity And Feasibility Of Intra-Tumoral Injection". This is a Phase I pilot study to evaluate the toxicity and feasibility of intratumoral injection (Glycosphingolipids) GSL alpha-GAL (beta-galactosidase) in patients with advanced, refractory solid tumors who have failed standard therapies or are not eligible for standard treatment.

What is the current status of trial NCT00668382?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 11 participants. The study started on 2007-07. Estimated completion is 2011-07.

What interventions are being tested in trial NCT00668382?

The interventions under investigation include: Alpha-Gal Glycosphingolipid (BIOLOGICAL).

Who is sponsoring clinical trial NCT00668382?

This trial is sponsored by University of Massachusetts, Worcester, which has 240 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00668382's enrollment target sits among peer trials

11 1911th of 2000 higher than 88 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 NCT00668382, the US trial registry maintained by the National Library of Medicine. NCT00668382 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.