Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Boehringer Ingelheim
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Male or female adult patients, 18 years of age or older
Signed and dated written informed consent in accordance with International Council on Harmonisation (ICH) Good Clinical Practice (GCP) and local legislation prior to the start of any screening procedures
Moderate to severe Hidradenitis suppurativa (HS), based on International Hidradenitis Suppurativa Severity Score System (IHS4) criteria, for at least 1 year prior to the baseline visit, as determined by the investigator through participant interview and/or review of the medical history. (If IHS4 scoring is not available, equivalent scoring based on scoring systems as HS-PGA or Hurley are acceptable based on documented investigator assessment)
HS lesions in at least 2 distinct anatomic area (right/left axillary, inguinal, inframammary, perineal)
Biologic naive or TNF inhibitor (TNFi)-failure for HS
Inadequate response to an adequate course of appropriate oral antibiotics for treatment of HS in the last 1 year, as per investigator discretion. This is not applicable for TNFi-failure patients
Total abscess and inflammatory nodule (AN) count of greater than or equal to 5
You may not be if
Presence of active skin lesions other than HS that interfere with the assessment of HS
Use of restricted medications as below:
* Topical corticosteroids over HS lesions within 1 week of Visit 2
* Systemic antibiotics within 4 weeks of visit 2
* Systemic non-biologic immunomodulatory and/or immunosuppressive agents use for HS within 4 weeks (or 5 half lives, whichever is longer) of visit 2
* Biologic agents use within 12 weeks or 5 half-lives, whichever is longer, prior to visit 2
* Opioid analgesics within 2 weeks of visit 2
* Live virus vaccine within 6 weeks of visit 2
Prior exposure to any immunosuppressive biologic other than TNFi for HS
Prior exposure to Interleukin 36 Receptor (IL-36R) inhibitors including spesolimab
Treatment with any investigational device or investigational drug of chemical or biologic nature within a minimum of 30 days or 5 half-lives of the drug, whichever is longer, prior to visit 2
Women who are pregnant, nursing, or who plan to become pregnant while in the trial. Women who stop nursing before the study drug administration do not need to be excluded from participating
History of allergy/hypersensitivity to the systemically administered trial medication agent or its excipients
Clareo Health | A Study to Test Whether Spesolimab Helps People With a Skin Disease Called Hidradenitis Suppurativa
