Ignite Creation Date:
2024-05-05 @ 4:35 PM
Last Modification Date:
2024-10-26 @ 9:22 AM
Study NCT ID:
NCT00279058
Status:
COMPLETED
Last Update Posted:
2015-04-21
First Post:
2006-01-17
Brief Title:
The Role of Peptide-loaded Dendritic Cells to Augment the Therapeutic Effect of Interleukin-2
Sponsor:
Hadassah Medical Organization
Organization:
Hadassah Medical Organization
Study Overview
Official Title:
The Role of Autologous Dendritic Cells Pulsed by Melanoma Associated Peptides to Augment the Therapeutic Effect of Interleukin-2
Status:
COMPLETED
Status Verified Date:
2007-04
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:
Melanoma is the main cause of death in patients with skin cancer Once it has metastasized this cancer has been shown to respond to chemotherapy only in rare cases Immunotherapy represents an approach to treatment based on the immune response to cancer antigens
The principal objective of the study is to identify whether a dendritic cell-based vaccine can increase the moderate therapeutic effect of bolus high dose IL-2 in patients with metastatic melanoma For this purposepatients with metastatic melanoma who have a certain blood type HLA-A201 will be treated systemically with high dose IL-2 In one group of patients the IL-2 will be preceded by three doses of autologous dendritic cell pulsed with melanoma antigens appropriate for their blood type Two cycles of three DC vaccines will be administered every 14 days by intra-lymph node injections followed by high dose IL-2 treatment Responding patients will receive additional DC vaccines at 1 month and 2 months intervals
In a second group patients will receive the standard high dose IL-2 protocol within a comparable period of time
Each group will include 12 patients
A complete evaluation of evaluable lesions will be performed prior to accrual after initial 3 DC vaccines six weeks after first IL-2 treatment after a total of 6 DC vaccines and 6 weeks after second cycle of IL-2 treatment
The principal objective of the study is to identify whether a dendritic cell-based vaccine can increase the moderate therapeutic effect of bolus high dose IL-2 in patients with metastatic melanoma For this purposepatients with metastatic melanoma who have a certain blood type HLA-A201 will be treated systemically with high dose IL-2 In one group of patients the IL-2 will be preceded by three doses of autologous dendritic cell pulsed with melanoma antigens appropriate for their blood type Two cycles of three DC vaccines will be administered every 14 days by intra-lymph node injections followed by high dose IL-2 treatment Responding patients will receive additional DC vaccines at 1 month and 2 months intervals
In a second group patients will receive the standard high dose IL-2 protocol within a comparable period of time
Each group will include 12 patients
A complete evaluation of evaluable lesions will be performed prior to accrual after initial 3 DC vaccines six weeks after first IL-2 treatment after a total of 6 DC vaccines and 6 weeks after second cycle of IL-2 treatment
Detailed Description:
None
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