The LATITUDE HS Study will be evaluating options for adults with Hidradenitis Supportiva. Sign up for the WeConnect registry to be one of the first to be notified when the LATITUDE HS Study goes live.
Visit Takeda's Clinical Trials Transparency page to get in-depth information on all of Takeda's clinical research trials.
By joining WeConnect, you will be kept informed of trials that match your health needs so that you can have further conversations with your healthcare provider.
Hidradenitis Suppurativa (HS) is a long-term skin condition that can be painful and confusing. It causes bumps, boils, or sores to appear in places where skin rubs together, like under the arms, around the groin, on the buttocks, and under the breasts. These spots can hurt, swell, and sometimes leak fluid. Many people don’t know about HS, and it’s often mistaken for acne or simple skin infections. But HS is different, it lasts longer, often comes back, and can affect everyday life.
Doctors don’t know exactly what causes HS, but they do know some things that make it more likely:
It’s important to remember: HS is not contagious. You cannot catch it from someone else, and it is not because of being “dirty.”
Because HS can look like acne, ingrown hairs, or infections, it can be hard to diagnose. Doctors usually look at:
A dermatologist (a skin doctor) is usually the best person to figure out if it’s HS. Sometimes, other tests may be done to rule out different conditions, but there isn’t one single test that proves HS.
HS can be tough to live with. The sores may be painful, and people sometimes feel embarrassed or worried about their skin. It can also make daily life harder, choosing clothes, exercising, or even sitting can be uncomfortable.
Support from doctors, family, and friends is very important. Some people also find help by joining support groups where they can share their experiences with others who understand.
Taking care of mental health is just as important as treating the skin, because HS can affect confidence and mood.
Common symptoms
The main signs of HS include:
These symptoms often come and go. Some people may only get mild bumps, while others may have more serious flare-ups.
Management
There is no cure for HS yet, but there are ways to manage it and make life easier:
Everyone’s HS is different, so treatment is often a mix of several approaches.
Scientists are learning more about HS every year. Research is focused on:
Hidradenitis Suppurativa is a challenging skin condition, but it doesn’t define who someone is. With the right care, support, and new research on the horizon, people living with HS can find ways to manage their symptoms and live fulfilling lives.
Your experience with HS is valuable. Take the next step in supporting HS research.
Sign up for our patient registry today. Together, we can make a difference.
Now, you can relax while we keep you updated with notifications about Takeda’s clinical trials that might be just the right fit for you.
We know you're interested in signing up for Takeda's WeConnect to get direct communication about Takeda clinical trials, but just in case you are looking for other ways to get involved – please review the information below.
BioLife Plasma Services is Takeda’s global plasma collection network and an industry leader in the collection of high-quality plasma that is processed into life-saving plasma-based therapies that benefit thousands of people every day.
Learn more about plasma donation and how to help people who require life-saving plasma-based therapies by donating your plasma.
Our goal is to be readily available to support clinicians and researchers in whatever way we can. We believe the best way to improve disease outcomes is through robust and open communication about the science and clinical evidence.
That’s why we love to hear from medical professionals—to hear your questions, to understand what you’re seeing in the clinic, and to discuss research.