Ignite Creation Date:
2024-05-05 @ 11:23 AM
Last Modification Date:
2024-10-26 @ 9:06 AM
Study NCT ID:
NCT00010413
Status:
COMPLETED
Last Update Posted:
2008-10-02
First Post:
2001-02-02
Brief Title:
Phase II Study of High-Dose Cyclophosphamide in Patients With Refractory Pemphigus
Sponsor:
Johns Hopkins University
Organization:
Office of Rare Diseases ORD
Study Overview
Official Title:
None
Status:
COMPLETED
Status Verified Date:
2008-10
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:
OBJECTIVES
I Determine the response rate and 1-year event-free survival of patients with refractory pemphigus treated with high-dose cyclophosphamide
I Determine the response rate and 1-year event-free survival of patients with refractory pemphigus treated with high-dose cyclophosphamide
Detailed Description:
PROTOCOL OUTLINE Patients receive cyclophosphamide IV on days 1-4 and filgrastim G-CSF beginning on day 10 and continuing until blood counts recover
Patients are followed monthly for 6 months every 2 months for 6 months every 4 months for a year and then annually thereafter
Patients are followed monthly for 6 months every 2 months for 6 months every 4 months for a year and then annually thereafter
Study Oversight
Has Oversight DMC:
Is a FDA Regulated Drug?:
Is a FDA Regulated Device?:
Is an Unapproved Device?:
Is a PPSD?:
Is a US Export?:
Is an FDA AA801 Violation?:
Secondary IDs
| Secondary ID | Type | Domain | Link |
|---|---|---|---|
| JHOC-99022610 | None | None | None |
| JHOC-J9912 | None | None | None |