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Clinical Trials/KCT0009141
KCT0009141
Recruiting
未知

An observational, prospective study to assess the efficacy and safety of Adalloce in patients with Rheumatoid Arthritis (RA) and Ankylosing Spondylitis (AS)

Yuhan0 sites1,000 target enrollmentTBD
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ConditionsDiseases of the musculoskeletal system and connective tissue

Overview

Phase
未知
Intervention
Not specified
Conditions
Diseases of the musculoskeletal system and connective tissue
Sponsor
Yuhan
Enrollment
1000
Status
Recruiting
Last Updated
2 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Observational Study
Sex
All

Investigators

Sponsor
Yuhan

Eligibility Criteria

Inclusion Criteria

  • •1\. Men and women between the ages of over 19 and under 75 at the time of consent
  • •2\. Patients diagnosed with RA or AS at least 3 months prior to the study registration
  • •3\. Patients who are scheduled to be prescribed Adalloce according to the doctor's opinions
  • •4\. Patients who have never received Adalloce
  • •5\. Patients who voluntarily gave their written consent after being sufficiently explained about the purpose and contents of this study

Exclusion Criteria

  • •1\. Patients with hypersensitivity to this drug or its components
  • •2\. Patients with active tuberculosis or other severe infection such as sepsis or opportunistic infection
  • •3\. Patients with moderate to severe heart failure (NYHA class III/IV)
  • •4\. Patients who are judged to be inappropriate for Adalloce administration according to the approved conditions
  • •5\. Patients who are not suitable for participation in this study according to the judgment of the investigator
  • •6\. Patients participating in other drug clinical trials (Adalloce PMS participants cannot participate in this study)

Outcomes

Primary Outcomes

Not specified

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