Multiple Myeloma Clinical Trial

Safety and Efficacy Study of Imexon for Treatment of Multiple Myeloma Patients

Summary

AMP-007 is a Phase 1/2 study for the treatment of advanced, previously treated multiple myeloma. The first phase of the study is designed to determine a safe dose of imexon that can be given to patients with advanced, previously-treated multiple myeloma. The Phase 2 part of the study is designed to provide additional safety data and to gain an understanding of whether imexon can improve the outcome for patients with multiple myeloma

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Advanced myeloma, with measurable disease as defined in the protocol.
Prior treatment, at least 2 prior regimens are required. This may include prior treatment with investigational products.
Able to perform the activities of daily living.
Off prior therapy for at least 2-4 weeks depending on the drug.
Blood counts and blood chemistries in or near normal range.
If female, neither pregnant nor nursing.
Willing to use contraceptives to prevent pregnancy.
No other serious illnesses.
No other active malignancy.
No serious infections.
No current other drug therapy for the myeloma except for steroid therapy under certain circumstances. Biphosphonate therapy is permitted.
Prior radiation is permitted.

Exclusion Criteria:

Use of corticosteroids for amyloid disorders, or high dose chronic steroids.

Study is for people with:

Multiple Myeloma

Phase:

Phase 1

Study ID:

NCT00327249

Recruitment Status:

Completed

Sponsor:

AmpliMed Corporation

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There are 2 Locations for this study

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Investigational Site 025
Little Rock Arkansas, 72206, United States
Investigational Site 008
Houston Texas, 77030, United States

How clear is this clinincal trial information?

Study is for people with:

Multiple Myeloma

Phase:

Phase 1

Study ID:

NCT00327249

Recruitment Status:

Completed

Sponsor:


AmpliMed Corporation

How clear is this clinincal trial information?

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