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The introduction of Janus Kinase inhibitors (JAKi) seems to revolutionize the field of alopecia areata (AA) therapeutics. However, the ideal JAKi is not yet settled and the real-world data are still missing. To provide evidence about effectiveness and safety of different JAKi including tofacitinib, baricitinib, ritlecitinib,abrocitinib, upadacitinib and ifidancitinib in real-world settings and describe baseline disease characteristics and patients profiles that are considered good candidates for JAKi in the daily practice. Furthermore, we intended to investigate the efficacy and safety of JAK Inhibitors in patients With AA, as well as to provide clinical evidence for the clinicians and patients when they formulate individualized treatment plans.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Tofacitinib treated group | In the real-world settings, patients with AA treated with tofacitinib. |
| |
| Baritinib treated group | In the real-world settings, patients with AA treated with baritinib. |
| |
| Ruxolitinib treated group | In the real-world settings, patients with AA treated with ruxolitinib |
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| Upadacitinib treated group | In the real-world settings, patients with AA treated with upadacitinib. |
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| Abrocitinib treated group | In the real-world settings, patients with AA treated with abhicitinib. |
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| Ritlecitinib treated group | In the real-world settings, patients with AA treated with ritlecitinib. |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Tofacitinib | Drug | In the real-world settings, patients with AA treated with tofacitinib. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Mean SALT | Reduction of Severity of Alopecia Tool (SALT) score compared with baseline | at week 24 |
| SALT50 | Percentage of patient with more than 50% improvement in SALT score | at week 24 |
| SALT75 | Percentage of patient with more than 70% improvement in SALT score | at week 24 |
| Measure | Description | Time Frame |
|---|---|---|
| Mean SALT | Reduction of Severity of Alopecia Tool (SALT) score compared with baseline | at week 12, 36, 48, 56 |
| SALT50 | Percentage of patient with more than 75% improvement in SALT score |
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Inclusion Criteria:
Exclusion Criteria:
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Patients diagnosed with alopecia areata treated with JAKi including tofacitinib, baricitinib, ritlecitinib,abrocitinib, upadacitinib and ifidancitinib for more than 3 months in Department of Dermatology, Second Affiliated Hospital, Zhejiang University School of Medicine
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Ru Dai, MD | Contact | 15982215914 | dairu@zju.edu.cn | |
| Wu | Contact | wuxianjie@zju.edu.cn |
| Name | Affiliation | Role |
|---|---|---|
| Xianjie Wu, Ph.D | Second Affiliated Hospital, School of Medicine, Zhejiang University | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Second Affiliated Hospital, School of Medicine, Zhejiang University, China | Recruiting | Hangzhou | Zhejiang | 310009 | China |
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| ID | Term |
|---|---|
| D000506 | Alopecia Areata |
| ID | Term |
|---|---|
| D000505 | Alopecia |
| D007039 | Hypotrichosis |
| D006201 | Hair Diseases |
| D012871 | Skin Diseases |
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| ID | Term |
|---|---|
| C479163 | tofacitinib |
| C000596027 | baricitinib |
| C540383 | ruxolitinib |
| C000613732 | upadacitinib |
| C000634427 | abrocitinib |
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| Baricitinib | Drug | In the real-world settings, patients with AA treated with Baricitinib. |
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| Ruxolitinib | Drug | In the real-world settings, patients with AA treated with Ruxolitinib. |
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| Upadacitinib | Drug | In the real-world settings, patients with AA treated with Upadacitinib. |
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| Abrocitinib | Drug | In the real-world settings, patients with AA treated with Abrocitinib. |
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| Ritlecitinib | Drug | In the real-world settings, patients with AA treated with Ritlecitinib. |
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| at week 12, 36, 48, 56 |
| SALT75 | Percentage of patient with more than 50% improvement in SALT score | at week 12, 36, 48, 56 |
| Safety profile | Any adverse events including infection, hypohepatia, thrombus, gastrointestinal reaction and any other system events. | at week 4, 8, 12, 16, 20, 24, 28, 32, 36, 40, 44, 48, 52, 56 |
| D017437 |
| Skin and Connective Tissue Diseases |