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SB-715992 in Treating Patients With Metastatic or Recurrent Malignant Melanoma

Phase 2
Completed
Conditions
Melanoma (Skin)
Registration Number
NCT00095953
Lead Sponsor
NCIC Clinical Trials Group
Brief Summary

RATIONALE: Drugs used in chemotherapy, such as SB-715992, work in different ways to stop tumor cells from dividing so they stop growing or die.

PURPOSE: This phase II trial is studying how well SB-715992 works in treating patients with metastatic or recurrent malignant melanoma.

Detailed Description

OBJECTIVES:

* Determine the efficacy of SB-715992, in terms of response rate, in patients with previously untreated metastatic or recurrent malignant melanoma.

* Determine the toxic effects of this drug in these patients.

* Determine the early progression rate and response duration in patients treated with this drug.

* Determine the pharmacokinetics of this drug in these patients.

* Correlate pharmacokinetics with safety and efficacy endpoints of this drug in these patients.

* Correlate β-tubulin and kinesin spindle protein expression in tumor tissue with clinical outcomes in patients treated with this drug.

OUTLINE: This is a nonrandomized, multicenter study.

Patients receive SB-715992 IV over 1 hour on day 1. Courses repeat every 21 days in the absence of disease progression or unacceptable toxicity.

All patients are followed at 4 weeks after completion of protocol therapy. Patients with ongoing complete response, partial response, or stable disease are followed every 3 months thereafter until relapse.

PROJECTED ACCRUAL: A total of 15-25 patients will be accrued for this study within 12-14 months.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
17
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Primary Outcome Measures
NameTimeMethod
Response2 years
Secondary Outcome Measures
NameTimeMethod
Pharmacokinetics at day 1 of course 1 (day 1 of course 2 if dose is changed)2 years
Molecular correlates on archival tissue, fresh tumor tissue, and peripheral blood mononuclear cells (PVMCs)2 years
Toxicity2 years

Trial Locations

Locations (7)

Fraser Valley Cancer Centre at British Columbia Cancer Agency

🇨🇦

Surrey, British Columbia, Canada

British Columbia Cancer Agency - Vancouver Cancer Centre

🇨🇦

Vancouver, British Columbia, Canada

Toronto Sunnybrook Regional Cancer Centre at Sunnybrook and Women's College Health Sciences Centre

🇨🇦

Toronto, Ontario, Canada

Nova Scotia Cancer Centre at Queen Elizabeth II Health Sciences Centre

🇨🇦

Halifax, Nova Scotia, Canada

British Columbia Cancer Agency - Centre for the Southern Interior

🇨🇦

Kelowna, British Columbia, Canada

Margaret and Charles Juravinski Cancer Centre

🇨🇦

Hamilton, Ontario, Canada

Centre Hospitalier de l'Universite de Montreal

🇨🇦

Montreal, Quebec, Canada

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