Five new drugs aim to tame painful skin condition
NCT ID NCT03827798
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests five different investigational drugs (iscalimab, LYS006, MAS825, remibrutinib, and ianalumab) in 248 adults with moderate to severe hidradenitis suppurativa, a chronic skin condition causing painful lumps. The main goal is to see if these drugs reduce abscesses and inflammatory nodules by at least 50% without increasing draining tunnels. Participants are randomly assigned to receive a drug or a placebo, and neither they nor their doctors know which they get.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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248 people
The number who actually took part.
- Started
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Feb 2019
- Expected to finish
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Dec 2026
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 65 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patients with moderate to severe HS based on the number of lesions, fistulae and anatomical areas involved * Minimal body weight of 50 kg * Able to communicate well with the investigator and understand and comply with the requirements of the study, and the ability and willingness to conduct study visits as per the study schedule Exclusion Criteria: * Use of other investigational drugs at the time of screening or before * Women physiologically capable of becoming pregnant, unless they are using highly effective methods of contraception * Pregnant or lactating women Other protocol-defined inclusion/exclusion criteria may apply
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Advanced Medical Research
Sandy Springs, Georgia, 30328, United States
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Dawes Fretzin Clinical Rea Group
Indianapolis, Indiana, 46256, United States
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Medical University of South Carolina MUSC
Charleston, South Carolina, 29425, United States
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NorthShore University Health System
Evanston, Illinois, 60201, United States
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Novartis Investigative Site
Graz, 8036, Austria
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Novartis Investigative Site
Brussels, 1070, Belgium
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Novartis Investigative Site
Prague, Prague 1, 11000, Czechia
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Novartis Investigative Site
Copenhagen, 2400, Denmark
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Novartis Investigative Site
Roskilde, 4000, Denmark
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Novartis Investigative Site
Antony, 92160, France
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Novartis Investigative Site
Lyon, 69003, France
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Novartis Investigative Site
Marseille, 13885, France
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Novartis Investigative Site
Nice, 06202, France
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Novartis Investigative Site
Reims, 51100, France
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Novartis Investigative Site
Rouen, 76031, France
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Novartis Investigative Site
Bochum, 44791, Germany
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Novartis Investigative Site
Frankfurt, 60590, Germany
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Novartis Investigative Site
Hamburg, 20246, Germany
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Novartis Investigative Site
Schwerin, 19055, Germany
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Novartis Investigative Site
Pécs, Baranya, 7623, Hungary
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Novartis Investigative Site
Debrecen, Hajdu Bihar Megye, 4032, Hungary
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Novartis Investigative Site
Budapest, H-1083, Hungary
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Novartis Investigative Site
Szeged, H 6725, Hungary
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Novartis Investigative Site
Kopavogur, 201, Iceland
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Novartis Investigative Site
Rotterdam, South Holland, 3015 GD, Netherlands
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Novartis Investigative Site
Groningen, 9713 GZ, Netherlands
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Novartis Investigative Site
Granada, Andalusia, 18014, Spain
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Novartis Investigative Site
Sabadell, Barcelona, 08208, Spain
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Novartis Investigative Site
Manises, Valencia, 46940, Spain
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Novartis Investigative Site
Barcelona, 08041, Spain
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Novartis Investigative Site
Las Palmas GC, 35010, Spain
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Novartis Investigative Site
Valencia, 46026, Spain
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Olympian Clinical Research
Clearwater, Florida, 33609, United States
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Park Avenue Dermatology PA
Orange Park, Florida, 32073, United States
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Penn State Milton S Hershey Medical Center
Hershey, Pennsylvania, 17033-0850, United States
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University Of South Florida
Tampa, Florida, 33612, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Phase 2, randomized, parallel-group, double-blind, placebo-controlled study of sonelokimab in patients with active moderate to severe hidradenitis suppurativa
- Can a mediterranean diet tame hidradenitis suppurativa?
- Can we predict the path of chronic skin disease?
- Can a pill that degrades IRAK4 tame autoimmune inflammation?
- Could childhood trauma fuel skin inflammation?
- Head-to-Head: which pill tames hidradenitis suppurativa best?