Multiple Myeloma Clinical Trial

Combination Bisphosphonate and Anti-Angiogenesis Therapy With Pamidronate and Thalidomide

Summary

The purpose of this research is to study how helpful the combination of thalidomide and Pamidronate or thalidomide and Zometa is in controlling the myeloma disease and to study any side effects.

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Full Description

Recently laboratory research found that thalidomide can inhibit the formation of new blood vessels that are necessary for the growth and spread of cancer. In order to grow and increase in size tumors require new blood vessels to supply them with the necessary blood to grow. If we can prevent these new blood vessels feeding the tumor from being formed by using thalidomide we might slow or stop the growth of the tumor. This concept is called "anti-angiogenesis" It is hoped that thalidomide will slow or stop the growth myeloma. However, it cannot be guaranteed that you will benefit if you take part in this study. The treatment you receive may even be harmful.

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Eligibility Criteria

Inclusion Criteria:

Patients must have a diagnosis of Smoldering or Indolent myeloma
All patients must be informed of the investigational nature of this study and must sign a written informed consent in accordance with UAMS Human Research Advisory Committee and federal guidelines.

Exclusion Criteria:

Prior bisphosphonate therapy within 30 days prior to study entry.
Serum creatinine > 5 mg/dl, ascites, or serum direct bilirubin > 2.5 mg/dl.
Prior plicamycin or calcitonin within 2 weeks of study entry.
Severe cardiac disease, unstable thyroid disease, or epilepsy.
Prior radiation therapy to > 20% of the skeleton.

Study is for people with:

Multiple Myeloma

Phase:

Phase 2

Estimated Enrollment:

83

Study ID:

NCT00083382

Recruitment Status:

Completed

Sponsor:

University of Arkansas

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There is 1 Location for this study

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University of Arkansas for Medical Sciences/MIRT
Little Rock Arkansas, 72205, United States

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Study is for people with:

Multiple Myeloma

Phase:

Phase 2

Estimated Enrollment:

83

Study ID:

NCT00083382

Recruitment Status:

Completed

Sponsor:


University of Arkansas

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