Unspecified Adult Solid Tumor, Protocol Specific Clinical Trial
Official title:
Phase I Study To Determine The Safety Of Halofuginone In Patients With A Solid Progressive Tumor
RATIONALE: Halofuginone hydrobromide may stop the growth of solid tumors by stopping blood
flow to the tumor.
PURPOSE: Phase I trial to study the effectiveness of halofuginone hydrobromide in treating
patients who have progressive advanced solid tumors.
OBJECTIVES:
- Determine the toxicity profile, maximum tolerated dose, and dose-limiting toxic effects
of halofuginone hydrobromide in patients with progressive advanced solid tumors.
- Establish a recommended dose of this drug for phase II study.
OUTLINE: This is a dose-escalation, multicenter study.
Patients receive oral halofuginone hydrobromide once daily on days 1 and 4-14 of course 1
and on days 1-14 of subsequent courses. Treatment repeats every 14 days in the absence of
disease progression or unacceptable toxicity.
Cohorts of 1-3 patients receive escalating doses of halofuginone hydrobromide until the
maximum tolerated dose (MTD) is determined. The MTD is defined as the dose at which 20% of
patients experience acute dose-limiting toxicity. After the MTD is reached, 6-12 additional
patients are treated at dose levels preceding the MTD until the recommended dose for phase
II study is determined. The recommended dose for phase II study is defined as the dose
preceding the MTD that allows a 90% dose intensity for 2 months with no greater than grade 2
toxicity in 80% of the patients.
Patients are followed every 8 weeks until disease progression or initiation of another
treatment.
PROJECTED ACCRUAL: Approximately 7-40 patients will be accrued for this study.
;
Primary Purpose: Treatment
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