Rheumatoid Arthritis (RA) Clinical Trials

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Comparison of Morning Versus Evening Oral Administration of a JAK Inhibitor in Rheumatoid Arthritis

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

The aim of this study is to offer patients two treatment options: morning or evening administration of a JAK inhibitor prescribed within the framework of its marketing authorization, according to the EULAR response. The objective is to determine whether evening administration in our patients with rheumatoid arthritis provides greater efficacy than morning administration in our patients taking JAK inhibitors once daily.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Patient aged over 18 years

• Patient with Rheumatoid Arthritis according to the 2010 ACR/EULAR criteria

• Patient meeting the criteria for initiation of a JAK inhibitor according to the marketing authorization and international recommendations

• Patient capable of providing informed, written, dated, and signed consent before the start of any trial-related procedure.

Locations
Other Locations
Monaco
Centre Hospitalier Princesse Grace
RECRUITING
Monaco
Contact Information
Primary
Olivier BROCQ, MD
recherche.clinique@chpg.mc
97 98 99 00
Backup
Nicolas RIJO
recherche.clinique@chpg.mc
97 98 99 00
Time Frame
Start Date: 2024-04-23
Estimated Completion Date: 2026-11
Participants
Target number of participants: 90
Treatments
JAK inhibitor morning then evening
JAK inhibitor intake every morning during 3 months then every evening during 3 months
JAK inhibitor evening then morning
JAK inhibitor intake every evening during 3 months then every morning during 3 months
Related Therapeutic Areas
Sponsors
Leads: Centre Hospitalier Princesse Grace

This content was sourced from clinicaltrials.gov