New antibody shows promise for painful skin condition
NCT ID NCT04856930
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This phase 2 trial tested a drug called imsidolimab (ANB019) in 149 people with hidradenitis suppurativa, a chronic skin condition causing painful abscesses and nodules. Participants received either the drug or a placebo to see if it could reduce the number of inflamed lesions. The study is complete, and results will show whether this antibody approach is safe and effective.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- imsidolimab (ANB019), a lab-made antibody
- What this could lead to
- If it works, this could point toward a new treatment option for hidradenitis suppurativa, reducing painful abscesses and nodules.
- What could go wrong
- This is a mid-stage trial with only 149 participants, so results may not apply to everyone. The drug may not work better than placebo, and side effects are possible.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
-
149 people
The number who actually took part.
- Started
-
Jul 2021
- Finished
-
Dec 2022
- Lead sponsor
-
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
-
18 to 75 years
- Sex
-
Anyone
- Healthy volunteers
-
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: 1. Clinically confirmed diagnosis of active HS with a disease duration of greater than or equal to (≥) 6 months before Day 1. 2. HS lesions present in at least 2 distinct anatomical areas. 3. Total Abscess and inflammatory nodule (AN) count ≥ 5. 4. Draining fistulas less than or equal to (≤) 20. 5. Stable HS for at least 6 weeks prior to Day 1 visit. Exclusion Criteria: 1\. Concomitant dermatological or medical conditions that may interfere with the Investigators' ability to evaluate the participant's response to therapy.
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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
-
Site 10-101
Fort Gratiot, Michigan, 48059, United States
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Site 10-102
Sacramento, California, 95817, United States
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Site 10-103
Portsmouth, New Hampshire, 03801, United States
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Site 10-104
Fountain Valley, California, 92708, United States
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Site 10-105
Norfolk, Virginia, 23502, United States
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Site 10-106
Spokane, Washington, 99202, United States
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Site 10-107
Largo, Florida, 33770, United States
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Site 10-108
Birmingham, Alabama, 35224, United States
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Site 10-109
Coral Gables, Florida, 33134, United States
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Site 10-110
Sandy Springs, Georgia, 30328, United States
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Site 10-111
Tampa, Florida, 33607, United States
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Site 10-112
Pflugerville, Texas, 78660, United States
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Site 10-113
Greenville, South Carolina, 29615, United States
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Site 10-115
Warwick, Rhode Island, 02886, United States
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Site 10-117
San Antonio, Texas, 78213, United States
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Site 10-118
Houston, Texas, 77056, United States
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Site 10-119
Northridge, California, 91324, United States
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Site 11-101
Saint-Jérôme, Quebec, J7Z 7E2, Canada
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Site 11-102
Markham, Ontario, L3P 1X3, Canada
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Site 11-103
Cobourg, Ontario, K9A 0Z4, Canada
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Site 11-105
Québec, Quebec, G1N 4V3, Canada
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Site 11-106
Calgary, Alberta, T2J7E1, Canada
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Site 30-103
Ossy, Silesian Voivodeship, 42-624, Poland
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Site 30-104
Rzeszów, Podkarpackie Voivodeship, 35-055, Poland
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Site 30-106
Olsztyn, 10-229, Poland
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Site 30-107
Krakow, Malopolska, 30-074, Poland
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Site 30-108
Katowice, Silesian Voivodeship, 40-611, Poland
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Site 30-109
Lodz, 90-265, Poland
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Site 59-102
Tbilisi, 112, Georgia
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Site 59-103
Tbilisi, 160, Georgia
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Site 59-104
Tbilisi, 159, Georgia
-
Site 59-105
Tbilisi, 160, Georgia
-
Site 59-106
Batumi, 6000, Georgia
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Site 59-107
Tbilisi, 162, Georgia
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can a Weight-Loss drug also calm a painful skin disease?
- Viruses that kill bacteria: a new weapon against superbugs?
- Can an injected drug calm the painful flares of hidradenitis suppurativa?
- Nanobody drug tested against painful skin condition
- Can a mediterranean diet tame hidradenitis suppurativa?
- Can we predict the path of chronic skin disease?