Ignite Creation Date:
2024-05-06 @ 7:10 PM
Last Modification Date:
2024-10-26 @ 3:01 PM
Study NCT ID:
NCT05917561
Status:
RECRUITING
Last Update Posted:
2023-12-22
First Post:
2023-05-31
Brief Title:
Efficacy and Tolerance of the Association of ANIFROLUMAB 300mg IV Every Four Weeks and Phototherapy Versus Phototherapy in Adults With Progressive Vitiligo
Sponsor:
University Hospital Bordeaux
Organization:
University Hospital Bordeaux
Study Overview
Official Title:
Efficacy and Tolerance of the Association of ANIFROLUMAB 300mg IV Every Four Weeks and Phototherapy Versus Phototherapy in Adults With Progressive Vitiligo a Randomized Double Blind Prospective Non Comparative Proof of Concept Phase II Study
Status:
RECRUITING
Status Verified Date:
2023-12
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:
VITANI
Brief Summary:
The purpose of this phase 2 study is to evaluate the effect and the safety of the combination of ANIFROLUMAB in combination with phototherapy in adult participants with non-segmental progressive vitiligo
Detailed Description:
Treatment Strategy Multicentric parallel double blind randomized phase 2 prospective study comparing ANIFROLUMAB 300mgmonth narrowband UVB TL01 versus placebo narrowband UVB TL01 Follow-up of the study patients included in this study will start ANIFROLUMAB 3 months before starting narrowband UVB TL01 Phototherapy will be performed twice a week during 6 months Follow-up visit will be done at week 12 24 36 and 48
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None