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Safety and Effectiveness of Topotecan HCl to Treat HIV-Infected Patients With AIDS-Related Progressive Multifocal Leukoencephalopathy (PML)

An Open, Comparative Phase II Study of Immediate Versus Delayed Treatment With Topotecan HCl Given as a Continuous 21-Day Infusion Every 28 Days to Patients With AIDS-Related Progressive Multifocal Leukoencephalopathy

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00002395
Enrollment
54
Registered
2001-08-31
Start date
Unknown
Completion date
Unknown
Last updated
2005-06-24

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

Conditions

HIV Infections, Leukoencephalopathy, Progressive Multifocal

Keywords

AIDS-Related Opportunistic Infections, Leukoencephalopathy, Progressive Multifocal, Infusions, Intravenous, Drug Administration Schedule, Topotecan

Brief summary

The purpose of this study is to see if it is safe and effective to give topotecan through a vein to treat HIV-infected patients with PML, an opportunistic (AIDS-related) infection caused by a virus that infects brain tissue and causes damage to the brain and the spinal cord. Topotecan fights HIV and the JC virus (the virus that causes PML) in laboratory experiments.

Detailed description

Topotecan, a cytotoxic DNA topoisomerase-I inhibitor that crosses the blood-brain barrier, inhibits the replication of JC virus (the virus that causes PML) in vitro, at concentrations that are not toxic to human cells. Topotecan also inhibits the replication of HIV-1 and the function of Tat (which upregulates the replication of JC virus). Patients are randomized to be treated immediately with topotecan or to have treatment delayed for 8 weeks. The dosing schedule for patients receiving immediate or delayed treatment is topotecan as a continuous 21-day intravenous infusion every 28 days. All patients must have received optimal, stable antiretroviral therapy for 3 weeks prior to entry and preferably will continue that therapy during the study.

Interventions

DRUGTopotecan

Sponsors

SmithKline Beecham
Lead SponsorINDUSTRY

Study design

Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

Patients may be eligible for this study if they: * Are HIV-positive. * Have PML, including symptoms of PML. * Are able to complete the study. * Agree to have a catheter inserted in a vein. * Have taken at least 3 weeks of a stable anti-HIV drug combination (unless they are unable to take anti-HIV drugs). * Are at least 18 years old. * Agree to use effective methods of birth control.

Exclusion criteria

Patients will not be eligible for this study if they: * Have a history of certain central nervous system (CNS) diseases. * Have a history of certain psychiatric disorders, such as bipolar disorder or schizophrenia. * Have syphilis that has not been treated. * Have certain severe medical problems, including AIDS-related opportunistic infections (such as PCP) that require treatment. * Have received chemotherapy in the past 30 days. * Have ever received chemotherapy for PML. * Are pregnant or breast-feeding. * Are taking certain medications, including any other investigational drugs.

Countries

United States

Outcome results

None listed

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