Purpose of this Study
We are doing this study to find out if an experimental drug called upadacitinib (the study drug) is a safe and effective option for people with moderate to severe hidradenitis suppurativa (HS) who did not get adequate relief from standard treatment.
Who Can Participate?
Eligibility
Adults and children ages 12+ who:
- Are diagnosed with HS
- Weigh at least 30 kg (66 pounds)
- Have measurable HS lesions in at least 2 distinct areas of the body
Age Range
12-110
Looking for Healthy Participants
No
What is Involved?
Description
This study is divided into 5 periods:Physical exam
Blood draws
Skin exam
Questionnaires
If you are eligible to join based on screening, you will proceed to study drug administration Period 1 and get a random assignment (like a coin flip) to either take a 30 mg dose of the study drug each day or to take a placebo (inactive substance that has no drug in it). This is a "blinded" study and you will not know if you are using the study drug or placebo. Study drug administration Period 1 will last for 16 weeks.
When Period 1 ends, you will begin Period 2. During Period 2, one of the following will occur:
- Screening period
- Study drug administration Period 1
- Study drug administration Period 2
- Study drug administration Period 3
- Follow-up period
- If you were taking the placebo during Period 1, you might be switched to a 30 mg dose of the study drug or you might continue to take the placebo.
- If you were taking the study drug during Period 1, you might be switched to a 15 mg dose of the study drug or you might continue to take the 30 mg dose.
Locations
Duke University Hospital
Visit Timing
Weekdays
Compensation
Yes
Spanish Materials Available
Yes
Study Details
Full Title
A Phase 3, Randomized, Placebo-Controlled, Double-Blind Study to Evaluate Efficacy and Safety of Upadacitinib in Adult and Adolescent Subjects with Moderate to Severe Hidradenitis Suppurativa Who Have Failed Anti-TNF Therapy
Principal Investigator
Tarannum
Jaleel
Protocol Number
PRO00114013
NCT ID
NCT05889182
Phase
III
Enrollment Status
Open to Enrollment