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 (NCT05889182)
M23-698
The M23-698 trial is a study designed to evaluate the safety and efficacy of a potential new medication compared to placebo in reducing symptoms and improving the quality of life for participants living with Hidradenitis Supparativa (HS). Participants receive either trial medication or a placebo (something that looks like the trial drug but has no effect on the body), both administered as oral treatments. The study will involve 19 study visits over the course of approximately two years.
Program & service
This trial is being run with the Specialty Medicine service, and as part of the Dermatology program.
Trial phase
Phase 3
Trial participation type
This trial has been designed for the Clinical Research of a Drug.
Principal investigator
Professor Johannes S Kern
Key inclusion data
Are 18 years or older
Have been diagnosed with HS for at least 6 months
Have not seen improvement from a previous HS treatment
More information
To find out more about this clinical trial, please review full details on the ANZCTR website.
View on ANZCTRIf you would like further details or have any questions about this clinical trial, we encourage you to get in touch with us and a member of our team will be happy to provide you with more information.