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Use of Topotecan in Patients With Refractory Acute Leukemia

Study of Topoisomerase Inhibition in the Treatment of Acute Leukemia

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00100477
Enrollment
10
Registered
2004-12-31
Start date
1998-08-31
Completion date
2001-06-30
Last updated
2013-09-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Leukemia, Non-Hodgkin's Lymphoma

Keywords

Multiple Myeloma, Lymphoma, Leukemia, Etoposide, Drug Therapy, Clinical Trials

Brief summary

The purpose of this study is to identify the highest tolerated doses in drugs used to treat aggressive leukemia, lymphoma or multiple myeloma not responding to standard chemotherapy treatment. The drugs being used in this study include drugs frequently used in treating such diseases (mitoxantrone and etoposide) as well as a newer drug that has also been shown to be effective (topotecan).

Detailed description

The purpose of this study is to identify the highest tolerated doses in drugs used to treat aggressive leukemia, lymphoma or multiple myeloma not responding to standard chemotherapy treatment. The drugs being used in this study include drugs frequently used in treating such diseases (mitoxantrone and etoposide) as well as a newer drug that has also been shown to be effective (topotecan).

Interventions

DRUGEtoposide
DRUGTopotecan
DRUGMitozantrone

Sponsors

Immunex Corporation
CollaboratorINDUSTRY
SmithKline Beecham
CollaboratorINDUSTRY
Amgen
CollaboratorINDUSTRY
US Department of Veterans Affairs
Lead SponsorFED

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

Patients in the following disease categories will be considered eligible for this study: * Any acute leukemia beyond an initial attempt to induce a remission or after relapse * Chronic Myelogenous Leukemia in Blast Phase * Refractory Multiple Myeloma * Refractory non-Hodgkin's and Hodgkin's Lymphoma * Patients must be more than 14 days beyond prior myelotoxic chemotherapy * Several other eligibility criteria apply.

Exclusion criteria

* None

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026