Phase I/II Study of hLL1 in Multiple Myeloma

Status Completed

Clinical Trial Summary

This is a Phase I/II, open-label, multi-center study conducted in patients with recurrent or refractory multiple myeloma who have failed at least two prior standard systemic treatments.

Clinical Trial Description

All patients receive hLL1 administered intravenously twice weekly for 4 consecutive weeks. Cohorts of 3-6 patients will receive escalating doses of hLL1 in order to determine the maximum tolerated dose (MTD) for this administration schedule. Up to approximately 30 additional patients will be entered at one or more dose levels at or below the MTD in order to determine the optimal dose for subsequent studies. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT00421525
Study type	Interventional
Source	Gilead Sciences
Contact
Status	Completed
Phase	Phase 1/Phase 2
Start date	January 2007
Completion date	June 2009

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See also
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