Ignite Creation Date:
2024-05-05 @ 11:35 AM
Last Modification Date:
2024-10-26 @ 9:10 AM
Study NCT ID:
NCT00083460
Status:
COMPLETED
Last Update Posted:
2010-08-02
First Post:
2004-05-24
Brief Title:
Study of Combination PS-341 and Thalidomide in Multiple Myeloma
Sponsor:
University of Arkansas
Organization:
University of Arkansas
Study Overview
Official Title:
UARK 2001-37 A Phase I Exploratory Study of Combination PS-341 and Thalidomide in Refractory Multiple Myeloma
Status:
COMPLETED
Status Verified Date:
2010-07
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The purpose of this study is to assess the toxicity of PS-341 combined with one of four doses of thalidomide in patients with refractory multiple myeloma and to find the most appropriate doses of PS-341 and thalidomide in the combination
Detailed Description:
Patients will be enrolled in groups of 6-10 patients each receiving a low dose of PS-341 10 mgm2 and different dose levels of thalidomide 50 100 150 and 200 mg The first six patients in each group will receive PS-341 alone for the first cycle and thalidomide will be added on day 22 If the combination is found to be safe in these first 6 patients the remaining patients in each group will be enrolled Initially these patients will receive PS-341 alone and thalidomide will be added subsequently if deemed safe based on the first 6 patients in each thalidomide dose cohort
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None