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The study drug consists of an oral investigational treatment, or a placebo (with no active treatment), that will be administered once daily for 12 weeks. You will have 2 to 1 odds of receiving the 400 mg study treatment vs placebo.

Following in the treatment period of the study, participants will be asked to return to complete a follow-up appointment after 4 weeks l to assess safety and efficacy.  

Several blood samples will be collected and a physical evaluation of your Hidradenitis Suppurativa and overall health will be done with the study team During the study visits.

This study will last a period of up to 20 weeks and includes 7 visits; the screening visit may take up to 3 hours and the remaining visits will take approximately 1 to 4 hours each to complete.

 Compensation for your time and travel may be available. There will be no cost to you for taking part in this study. You will be provided with all study medication, examinations and medical care related to the study at no cost to you.


Visites
Médicament administré à quels jours
Total
Durée
Procédures
Durée de l'étude
Jours
Week 0, 2, 4, 8 and 12
Total
7
Durée
1 to 4 hours
Procédures
Blood samples
Durée de l'étude
Up to 20 weeks
Résumé
We are currently recruiting patients aged 18+ old with hidradenitis suppurativa for a study that evaluates the safety and efficacy of an oral investigational treatment.
Problème de santé
Hidradénite suppurée
Traitement
RIST4721

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(feet)
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Cette étude est disponible à 3 endroits

SKiN Health

SKiN Health

Cobourg, Ontario, K9A0Z4, Canada
Progressive Clinical Research

Progressive Clinical Research

San Antonio, Texas, 78213, United States
The Indiana Clinical Trials Center

The Indiana Clinical Trials Center

Plainfield, Indiana, 46168, United States
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