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A Registry Study Assessing PRO, Dosing Patterns, and Safety of Vunakizumab in Patients With General Rheumatic Diseases. (V-MIRACLE)

Zhejiang University logo

Zhejiang University

Status

Not yet enrolling

Conditions

Ankylosing Spondylitis (AS)
Polymyalgia Rheumatica (PMR)
Enthesitis-related Arthritis
Giant Cell Arteritis (GCA)
Behcet's Disease
Takayasu Arteritis (TAK)
Psoriatic Arthritis (PsA)
Nr-axSpA

Study type

Observational

Funder types

Other

Identifiers

NCT06766552
z220241396

Details and patient eligibility

About

Ankylosing spondylitis, radiographically negative axial spondyloarthritis, psoriatic arthritis, polymyalgia rheumatica, Takayasu arteritis, giant cell arteritis, non-ocular Behcet's disease, and enthesitis-related arthritis are common diseases in rheumatology. Traditional anti-rheumatic drugs are less effective and have greater side effects than biological agents. At present, there has been no large-scale registration study on rheumatic autoimmune diseases such as spondyloarthritis in China. However, data such as patient characteristics, medication patterns, and patient outcome reports of different rheumatology diseases can often serve as a reference for rheumatology clinicians to reasonably select treatment methods for different patients. Therefore, a large-scale registration study is needed to fill the gap in multi-disease registration studies in rheumatology departments in China.

Enrollment

10,000 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Diagnosed with rheumatic autoimmune diseases such as ankylosing spondylitis/radiologically negative axial spondyloarthritis/psoriatic arthritis/polymyalgia rheumatica/Takayasu arteritis/giant cell arteritis/ non-ocular Behcet's disease/ enthesitis-related arthritis;
  2. Currently receiving or planning to receive fulvezinib treatment;
  3. Can follow up according to the doctor's advice;
  4. Able to understand and sign the informed consent form, understand the purpose of this study, and voluntarily participate in this study.

Exclusion criteria

1.Investigator believes will prevent the subject from following and completing the study protocol

Trial contacts and locations

1

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Central trial contact

Huaxiang wu

Data sourced from clinicaltrials.gov

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