Ignite Creation Date:
2024-05-06 @ 1:48 AM
Last Modification Date:
2024-10-26 @ 11:10 AM
Study NCT ID:
NCT01906658
Status:
COMPLETED
Last Update Posted:
2017-01-06
First Post:
2013-07-15
Brief Title:
A Study to Explore the Safety and Tolerability of Acthar in Patients With Amyotrophic Lateral Sclerosis
Sponsor:
Mallinckrodt
Organization:
Mallinckrodt
Study Overview
Official Title:
A Study to Explore the Safety and Tolerability of Acthar in Patients With Amyotrophic Lateral Sclerosis
Status:
COMPLETED
Status Verified Date:
2016-11
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:
This 8-week randomized open-label evaluation will examine the acute safety and tolerability of 4 different dosing regimens of Acthar to inform dose selection for future studies of Acthar in patients with Amyotrophic Lateral Sclerosis ALS The study will also investigate the mean rate of change in the ALSFRS-R total score as an exploratory endpoint to help design future studies
This study will enroll up to 40 patients and include an optional 28-week open-label extension period plus a 3-week treatment taper and 1-week follow up period After completion of Week 8 patients enrolled in a treatment group that is considered safe and tolerable at that time have the option to continue into the open-label extension period A 3-week treatment taper and a follow-up visit are planned for all patients enrolled in the study beginning either at Week 8 or at Week 36 if a patient continues into the optional open-label extension period
This study will enroll up to 40 patients and include an optional 28-week open-label extension period plus a 3-week treatment taper and 1-week follow up period After completion of Week 8 patients enrolled in a treatment group that is considered safe and tolerable at that time have the option to continue into the open-label extension period A 3-week treatment taper and a follow-up visit are planned for all patients enrolled in the study beginning either at Week 8 or at Week 36 if a patient continues into the optional open-label extension period
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