Multiple Myeloma Clinical Trial

Interferon Alfa and Interleukin-6 in Treating Patients With Recurrent Multiple Myeloma

Summary

RATIONALE: Interferon alfa may interfere with the growth of cancer cells. Interleukin-6 may stimulate the white blood cells to kill cancer cells. Giving interferon alfa together with interleukin-6 may kill more cancer cells.

PURPOSE: This clinical trial is studying the side effects and how well giving interferon alfa together with interleukin-6 works in treating patients with recurrent multiple myeloma.

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Full Description

OBJECTIVES:

Determine the response rate in patients with recurrent multiple myeloma treated with recombinant interferon alfa and recombinant interleukin-6.
Determine the safety and optimal dose of this regimen in these patients.
Determine the toxicity of this regimen in these patients.
Determine the impact of this regimen on clonogenic growth of myeloma cells in serial in vitro assays.

OUTLINE: This is a pilot study.

Patients receive recombinant interferon alfa subcutaneously (SC) once daily. Beginning 1 month later, patients also receive recombinant interleukin-6 SC once daily. Treatment continues for up to 6 months in the absence of disease progression or unacceptable toxicity.

PROJECTED ACCRUAL: A total of 27 patients will be accrued for this study.

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Eligibility Criteria

DISEASE CHARACTERISTICS:

Diagnosis of recurrent multiple myeloma
Must have received ≥ 2 prior therapies

PATIENT CHARACTERISTICS:

Performance status 0-3

PRIOR CONCURRENT THERAPY:

See Disease Characteristics

Study is for people with:

Multiple Myeloma

Phase:

Early Phase 1

Estimated Enrollment:

3

Study ID:

NCT00470093

Recruitment Status:

Terminated

Sponsor:

Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins

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There is 1 Location for this study

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Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
Baltimore Maryland, 21231, United States

How clear is this clinincal trial information?

Study is for people with:

Multiple Myeloma

Phase:

Early Phase 1

Estimated Enrollment:

3

Study ID:

NCT00470093

Recruitment Status:

Terminated

Sponsor:


Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins

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