Ignite Creation Date:
2025-12-24 @ 4:18 PM
Ignite Modification Date:
2026-02-20 @ 6:40 PM
Study NCT ID:
NCT00868166
Status:
COMPLETED
Last Update Posted:
2020-02-25
First Post:
2009-03-23
Is NOT Gene Therapy:
True
Has Adverse Events:
True
Brief Title:
Safety and Efficacy of TRO19622 as add-on Therapy to Riluzole Versus Placebo in Treatment of Patients Suffering From ALS
Sponsor:
Hoffmann-La Roche
Organization:
Study Overview
Official Title:
Phase II/III, Multicenter, Randomized, Parallel Group, Double-blind, Placebo Controlled Study to Assess Safety and Efficacy of TRO19622 in Amyotrophic Lateral Sclerosis (ALS) Patients Treated With Riluzole
Status:
COMPLETED
Status Verified Date:
2020-02
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:
MITOTARGET
Brief Summary:
The purpose of the assay is to assess the safety and the efficacy of TRO19622 330 mg QD as add-on therapy to riluzole 50 mg bid in the treatment of patients suffering from ALS, as compared to placebo, assessed by the 18-month survival rate.
Detailed Description:
A stand alone treatment with TRO19622 is not acceptable for ethical reasons. Riluzole is an approved and widely used ALS treatment in the European community, in Japan and in the USA.
Therefore, in this study, TRO19622 will be assessed as add-on to riluzole in patients suffering from ALS.
At the start of the study, patients will be randomized to one of two groups : TRO19622 (330 mg QD or placebo (once a day).
Each treatment will be administered for 18 months under double-blind conditions. The product under evaluation will be administered to patients receiving the standard of care for ALS, including riluzole.
Riluzole dosage (50 mg bid) must be stable and well tolerated for at least one month prior to inclusion into the study.
After the double-blind period, open-label administration of TRO19622 will be allowed for safety and survival assessments and until efficacy results are available.
A separate open-label protocol will be written 6 months after the randomization of the last patient into the study.
Therefore, in this study, TRO19622 will be assessed as add-on to riluzole in patients suffering from ALS.
At the start of the study, patients will be randomized to one of two groups : TRO19622 (330 mg QD or placebo (once a day).
Each treatment will be administered for 18 months under double-blind conditions. The product under evaluation will be administered to patients receiving the standard of care for ALS, including riluzole.
Riluzole dosage (50 mg bid) must be stable and well tolerated for at least one month prior to inclusion into the study.
After the double-blind period, open-label administration of TRO19622 will be allowed for safety and survival assessments and until efficacy results are available.
A separate open-label protocol will be written 6 months after the randomization of the last patient into the study.
Study Oversight
Has Oversight DMC:
True
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?: