Ignite Creation Date:
2024-05-05 @ 8:02 PM
Last Modification Date:
2024-10-26 @ 9:57 AM
Study NCT ID:
NCT00793156
Status:
UNKNOWN
Last Update Posted:
2010-02-04
First Post:
2008-11-17
Brief Title:
A Randomized-Withdrawal Phase 3 Study Evaluating the Safety and Efficacy of Oral Nalfurafine HCl AC-820in Subjects on Hemodialysis With Uremic Pruritus Renal Itch
Sponsor:
Acologix Inc
Organization:
Acologix Inc
Study Overview
Official Title:
A Randomized-Withdrawal Phase 3 Study Evaluation the Safety and Efficacy of Oral Nalfurafine HCl AC-820in Subjects on Hemodialysis With Uremic Pruritus Renal Itch
Status:
UNKNOWN
Status Verified Date:
2010-02
Last Known Status:
NOT_YET_RECRUITING
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:
AC120-8231
Brief Summary:
Primary objective of this multicenter double-blind placebo controlled randomized withdrawal study are to determine the effectiveness and safety of orally administered AC-820 in doses of 25 µg and 50 µg daily in patients with moderate to severe itching associated with end-stage renal disease and hemodialysis and perform a population PK analysis
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