Encore Medical
Research

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Hidradenitis Suppurativa (HS) Clinical Study Details

Struggling with moderate to severe HS? Join our clinical trial exploring a potential new treatment: expert care, no-cost participation, and a chance to improve your quality of life.

Recruiting- Male/Female - 18 to 70 years of age - Compensation Available

Apply To This Study Here

Please enter your name, a valid phone number, and a valid email address where you can be contacted.

Have you used opioid pain medications (except tramadol) in the last 4 weeks?

Are your HS pain medications (if any) stable and unchanged for at least 4 weeks?

Do you currently have periodontal (gum) disease that is being treated or needs dental work during the study?

Do you have any immune deficiency, frequent infections, or a history of serious infections (e.g., TB, fungal infections)?

Do you have HIV, active hepatitis B or C, or a history of liver disease with abnormal labs?

Are you between 18 and 80 years old?

Have you been diagnosed with Hidradenitis Suppurativa (HS) by a dermatologist or medical provider?

Do you currently have 6 or more inflammatory lesions (lumps, nodules, or abscesses) that have been present for at least 8 weeks?

Do you have any other skin conditions that might interfere with your HS evaluation?

Do you have HS lesions in at least 2 different body areas?

Do you have any serious health conditions like uncontrolled diabetes, heart failure, kidney disease, or autoimmune diseases like lupus or Crohn’s?

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Am I the right age to participate?

Yes, if you’re between 18 and 80 years old.

Do I need an official diagnosis of HS?

Yes, you must have been diagnosed with Hidradenitis Suppurativa (HS) by a dermatologist and had symptoms for at least 6 months.

How severe should my HS be?

To qualify, you need to have at least 6 active inflammatory HS lesions for 8 weeks or more and affected areas in at least two different parts of your body. At least one area must be moderate to severe (Hurley Stage II or III).

Are there any birth control or family planning requirements?

Yes. All participants must follow strict birth control guidelines during the study and for 90 days after their last dose, whether male or female. This includes using approved contraceptive methods.

Can I join if I’m planning to become pregnant or donate sperm?

No. You must agree not to become pregnant, donate sperm, or plan for pregnancy during the study and for 90 days after it ends.

What else is expected of me?

You must give written informed consent, attend all study visits, and follow all study-related procedures and instructions.

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Benefits of participating in this study

There are multiple ways you can benefit from joining us in this study. Here are some of them.

Innovative medical treatments

Gain access to investigational treatments not yet available to the public. Receive study-related medical care and close health monitoring at no cost. Help researchers better understand medical conditions and improve future treatment options . Contribute to science in a way that may benefit others — including friends, family, and future generations.

Transportation & meals

Complimentary meals and transportation included for your appointment day.

Compensation

Compensation provided for your time and inconvenience.

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