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NCT06707246 · ClinicalTrials.gov record · last posted 2024-11-27

A Randomized Trial Comparing the Efficacy and Safety of Secukinumab with Tofacitinib in the Treatment of Moderate to Severe Hidradenitis Suppurativa in Chinese Patients

StatusRecruiting
PhaseNot applicable
Started2024-12-15
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from the ClinicalTrials.gov record
The goal of this clinical trial is to compare the efficacy secukimumab versus tofacitinib in patients with moderate to severe hidradenitis suppurativa (HS)in adults. It will also learn about the safety of secukimumab and tofacitinib. The main questions it aims to answer are: * Which treatment is more effective in patients with moderate to severe HS? * What medical problems do participants have when taking secukimumab versus tofacitinib? Researchers will compare secukimumab versus tofacitinib to see which treatment works better to treat moderate to severe HS. Participants will: * Half of participants will take secukimumab every week in the first month and every four weeks thereafter till 1 year * Another half of participants will take tofacitinib a tablet daily for 1 year * Visit the clinic once every 2 weeks for checkups and tests in the first month, and every 4 weeks thereafter * Keep a diary of their symptoms and the number of times they use a rescue inhaler

Protocol amendment history 1 change detected by DataLookout

2026-08-09
notable
Sponsor changed: Second Affiliated Hospital, School of Medicine, Zhejiang University → Second Affiliated Hospital, Zhejiang University, School of Medicine
WasSecond Affiliated Hospital, School of Medicine, Zhejiang University
NowSecond Affiliated Hospital, Zhejiang University, School of Medicine
Trial Details
NCT Number NCT06707246
Lead Sponsor Second Affiliated Hospital, School of Medicine, Zhejiang University
Collaborators: First Affiliated Hospital of Wenzhou Medical University, Jinhua Central Hospital, Affiliated Hospital of Jiaxing University, Ningbo No. 1 Hospital, The First People's Hospital of Huzhou
Conditions Hidradenitis Suppurativa
Enrollment 60 participants
Start Date 2024-12-15
Primary Completion 2026-10 (estimated)
Study Completion 2027-10 (estimated)
Updated on ClinicalTrials.gov 2024-11-27