Ignite Creation Date:
2024-05-05 @ 11:49 AM
Last Modification Date:
2024-10-26 @ 9:14 AM
Study NCT ID:
NCT00144703
Status:
COMPLETED
Last Update Posted:
2012-01-26
First Post:
2005-09-01
Brief Title:
Sirolimus With Tacrolimus for Graft-vs-Host Disease Prophylaxis After Related Stem Cell Transplantation
Sponsor:
Dana-Farber Cancer Institute
Organization:
Dana-Farber Cancer Institute
Study Overview
Official Title:
Open Label Phase II Trial of Sirolimus in Combination With Tacrolimus for Graft-vs-Host Disease Prophylaxis After Matched Related Allogeneic Hematopoietic Stem Cell Transplantation
Status:
COMPLETED
Status Verified Date:
2009-01
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 evaluate the ability of sirolimus to prevent graft versus host disease GVHD in patients following stem cell transplant from a related donor
Detailed Description:
Therapy to prevent GVHD will consist of an infusion of tacrolimus intravenously and sirolimus orally once per day starting 3 days before stem cell infusion This will take place in the hospital where the patient will remain for the duration of the transplant
Sirolimus will continue for 9 weeks at at stable dose then will be tapered by 13 on week 9 and 13 on week 17 It will be stopped on week 26 if there is no significant evidence of GVHD These dose modifications will occur at home and patients will be seen weekly for the first 2 months after discharge
If GVHD is present the tapering schedule wil be slower and based upon the patients clinical condition
Tacrolimus will be given orally once the patient is discharged from the hospital and will be tapered at the same schedule as sirolimus Blood levels of both tacrolimus and sirolimus will be monitored and the dose adjusted accordingly
During the year following stem cell transplant blood work will be performed to evaluate the immune system and GVHD
Sirolimus will continue for 9 weeks at at stable dose then will be tapered by 13 on week 9 and 13 on week 17 It will be stopped on week 26 if there is no significant evidence of GVHD These dose modifications will occur at home and patients will be seen weekly for the first 2 months after discharge
If GVHD is present the tapering schedule wil be slower and based upon the patients clinical condition
Tacrolimus will be given orally once the patient is discharged from the hospital and will be tapered at the same schedule as sirolimus Blood levels of both tacrolimus and sirolimus will be monitored and the dose adjusted accordingly
During the year following stem cell transplant blood work will be performed to evaluate the immune system and GVHD
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