An Observational, Prospective Study to Assess the Efficacy and Safety of Adalloce in Patients With Rheumatoid Arthritis and Ankylosing Spondylitis

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

This Study is to Assess the Efficacy and Safety of Adalloce in Patients With Rheumatoid Arthritis and Ankylosing Spondylitis, An Observational, Prospective Study

Eligibility
Participation Requirements
Sex: All
Minimum Age: 19
Maximum Age: 74
Healthy Volunteers: f
View:

• Men and women between the ages of over 19 and under 75 at the time of consent

• Patients diagnosed with RA or AS at least 3 months prior to the study registration

• Patients who are scheduled to be prescribed Adalloce according to the doctor's opinions

• Patients who have never received Adalloce

• Patients who voluntarily gave their written consent after being sufficiently explained about the purpose and contents of this study

Locations
Other Locations
Republic of Korea
Daegu Catholic University Medical Center
RECRUITING
Daegu
Contact Information
Primary
Hee Suh
hee1110@yuhan.co.kr
+82-2-828-0231
Time Frame
Start Date: 2023-01-26
Estimated Completion Date: 2026-08
Participants
Target number of participants: 1000
Sponsors
Leads: Yuhan Corporation

This content was sourced from clinicaltrials.gov