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NCT00253344 · ClinicalTrials.gov registry record · Phase 1

Lenalidomide and Docetaxel in Treating Patients With Advanced Solid Tumors

A Phase 1 study of Unspecified Adult Solid Tumor, Protocol Specific, sponsored by Case Comprehensive Cancer Center.

Completed
Registry status
Phase 1
Development phase
33
Enrollment target
1
Study location

NCT00253344 is a Phase 1 study of Unspecified Adult Solid Tumor, Protocol Specific that has completed, run by Case Comprehensive Cancer Center. The registered enrollment target is 33 participants, below the 501-participant average among 83 other Unspecified Adult Solid Tumor, Protocol Specific trials with a reported enrollment target (93% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT00253344, a Phase 1 study of Unspecified Adult Solid Tumor, Protocol Specific, has completed, sponsored by Case Comprehensive Cancer Center.

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

Study Summary

RATIONALE: Lenalidomide may stop the growth of tumor cells by blocking blood flow to the tumor. Drugs used in chemotherapy, such as docetaxel, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving lenalidomide together with docetaxel may kill more tumor cells. PURPOSE: This phase I trial is studying the side effects and best dose of lenalidomide when given together with docetaxel in treating patients with advanced solid tumors.

Interventions

  • DRUG docetaxel
  • DRUG lenalidomide

Study Locations (1)

Ohio

  • Ireland Cancer Center at University Hosptials Case Medical Center, Case Comprehensive Cancer Center - Cleveland

Trial Details

FieldValue
Enrollment Target 33 participants
Start Date 2005-06
Est. Completion 2008-06
Phase Phase 1

Sponsor

Case Comprehensive Cancer Center

407 total trials

What the Registry Record Tells You About NCT00253344

The ClinicalTrials.gov registry entry for NCT00253344 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 33 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 (93% lower). The listed sponsor is Case Comprehensive Cancer Center, which has 407 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Unspecified Adult Solid Tumor, Protocol Specific appearing as the primary indexed condition, and to 2 interventions - of which docetaxel is the first listed.

NCT00253344 reports 1 study location spanning 1 distinct geographic area - top geographies include Ohio.

Frequently Asked Questions

What is clinical trial NCT00253344 about?

NCT00253344 is a clinical study titled "Lenalidomide and Docetaxel in Treating Patients With Advanced Solid Tumors". RATIONALE: Lenalidomide may stop the growth of tumor cells by blocking blood flow to the tumor. Drugs used in chemotherapy, such as docetaxel, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving lenalidomide together with do...

What is the current status of trial NCT00253344?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 33 participants. The study started on 2005-06. Estimated completion is 2008-06.

What conditions does trial NCT00253344 study?

This clinical trial studies the following conditions: Unspecified Adult Solid Tumor, Protocol Specific.

What interventions are being tested in trial NCT00253344?

The interventions under investigation include: docetaxel (DRUG), lenalidomide (DRUG).

Who is sponsoring clinical trial NCT00253344?

This trial is sponsored by Case Comprehensive Cancer Center, which has 407 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00253344 being conducted?

This trial has 1 study location across Ohio. 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 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.