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RecruitingNCT06958211

Study to Evaluate the Efficacy and Safety of Ruxolitinib Cream in Participants With Hidradenitis Suppurativa (TRuE-HS2)

A Phase 3, Double-Blind, Randomized, Vehicle-Controlled, Efficacy and Safety Study of Ruxolitinib Cream in Participants With Hidradenitis Suppurativa

Status
Recruiting
Phase
Phase 3
Study type
Interventional
Enrollment
550 (estimated)
Sponsor
Incyte Corporation · Industry
Sex
All
Age
12 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to evaluate the efficacy and safety of ruxolitinib cream in participants with hidradenitis suppurativa.

Conditions

Interventions

TypeNameDescription
DRUGRuxolitinib CreamRuxolitinib cream applied topically to the affected area as a thin film twice daily.
DRUGVehicle CreamMatching vehicle cream applied topically to the affected area as a thin film twice daily.

Timeline

Start date
2025-06-12
Primary completion
2026-10-09
Completion
2027-07-11
First posted
2025-05-06
Last updated
2026-04-08

Locations

107 sites across 9 countries: United States, Belgium, Bulgaria, Canada, France, Germany, Netherlands, Poland, Spain

Regulatory

Source: ClinicalTrials.gov record NCT06958211. Inclusion in this directory is not an endorsement.

Study to Evaluate the Efficacy and Safety of Ruxolitinib Cream in Participants With Hidradenitis Suppurativa (TRuE-HS2) (NCT06958211) · Clinical Trials Directory