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NCT00022607 · ClinicalTrials.gov registry record · Phase 2

Bevacizumab With or Without Thalidomide in Treating Patients With Relapsed or Refractory Multiple Myeloma

A Phase 2 study of Multiple Myeloma and Plasma Cell Neoplasm, sponsored by California Cancer Consortium.

Completed
Registry status
Phase 2
Development phase
4
Study locations

NCT00022607: Completed Phase 2 study of Multiple Myeloma and Plasma Cell Neoplasm, sponsored by California Cancer Consortium.

NCT00022607 is a Phase 2 study of Multiple Myeloma and Plasma Cell Neoplasm that has completed, run by California Cancer Consortium. The trial reports 4 study locations across 2 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00022607, a Phase 2 study of Multiple Myeloma and Plasma Cell Neoplasm, has completed, sponsored by California Cancer Consortium.

COMPLETED
Registry status
Phase 2
Development phase
4
Study locations

Study Summary

RATIONALE: Monoclonal antibodies, such as bevacizumab, can block cancer growth in different ways. Some block the ability of cancer cells to grow and spread. Others find cancer cells and help kill them or deliver cancer-killing substances to them. Thalidomide may stop the growth of cancer cells by stopping blood flow to the tumor. It is not yet known whether bevacizumab works better with or without thalidomide for multiple myeloma. PURPOSE: This randomized phase II trial is to see if bevacizumab works better with or without thalidomide in treating patients who have relapsed or refractory multiple myeloma.

Interventions

  • BIOLOGICAL bevacizumab
  • DRUG thalidomide

Study Locations (4)

California

  • City of Hope Comprehensive Cancer Center - Duarte
  • USC/Norris Comprehensive Cancer Center and Hospital - Los Angeles
  • University of California Davis Cancer Center - Sacramento

Illinois

  • University of Chicago Cancer Research Center - Chicago

Trial Details

FieldValue
Start Date 2002-01
Est. Completion 2006-05
Phase Phase 2
California Cancer Consortium

8 total trials

What the finished NCT00022607 record still lists

NCT00022607 is an interventional study that assigns participants to a tested intervention. An enrollment target was not published in the registry record, which is common for early-stage or observational entries.

The record links to 1 condition, with Multiple Myeloma and Plasma Cell Neoplasm appearing as the primary indexed condition, and to 2 interventions - of which bevacizumab is the first listed.

NCT00022607 reports a single indexed study location in California, Illinois.

Frequently Asked Questions

What is clinical trial NCT00022607 about?

NCT00022607 is a clinical study titled "Bevacizumab With or Without Thalidomide in Treating Patients With Relapsed or Refractory Multiple Myeloma". RATIONALE: Monoclonal antibodies, such as bevacizumab, can block cancer growth in different ways. Some block the ability of cancer cells to grow and spread. Others find cancer cells and help kill them or deliver cancer-killing substances to them. Thalidomide may stop the growth of cancer cells by st...

What is the current status of trial NCT00022607?

This trial is currently completed. It is a Phase 2 study. The study started on 2002-01. Estimated completion is 2006-05.

What conditions does trial NCT00022607 study?

This clinical trial studies the following conditions: Multiple Myeloma and Plasma Cell Neoplasm.

What interventions are being tested in trial NCT00022607?

The interventions under investigation include: bevacizumab (BIOLOGICAL), thalidomide (DRUG).

Who is sponsoring clinical trial NCT00022607?

This trial is sponsored by California Cancer Consortium, which has 8 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00022607 being conducted?

This trial has 4 study locations across California, Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Source: ClinicalTrials.gov NCT00022607, the US trial registry maintained by the National Library of Medicine. NCT00022607 (unsized enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.