A Study to Test Long-term Treatment With Spesolimab in People With a Skin Condition Disease Called Hidradenitis Suppurativa (HS) Who Took Part in a Previous Study With Spesolimab

Stopped early · Phase 2/Phase 3 · Has a placebo group

Conditions studied: Hidradenitis Suppurativa (HS)

In brief

This study is open to people with hidradenitis suppurativa (HS) who have completed another study with spesolimab (study 1368-0098 (NCT05819398) or study 1368-0100). The purpose of this study is to find out how well people tolerate spesolimab and whether it helps people with HS in the long-term. For about 1.5 years, participants get spesolimab injections under the skin every 2 weeks. Participants are in the study for about 2 years. During this time, participants have 41 visits. 24 visits are done at the study site. 17 visits can be done by video call at the participant's home. At study visits, doctors check the severity of the participant's HS and collect information on any health problems of the participants.

Key facts

Study ID

NCT06241573

Run by

Boehringer Ingelheim

People needed

39

Starts

2024-05-08

Expected to finish

2025-04-11

Last updated by the study team

2026-06-17

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Signed and dated written informed consent in accordance with ICH Harmonized Guideline for Good Clinical Practice (ICH-GCP) and local legislation prior to admission to the trial.
• Participants must be within the defined Residual Effect Period corresponding to 16 weeks since last spesolimab administration.
• Participants who have completed treatment in the parent hidradenitis suppurativa (HS) spesolimab trial (1368-0098 (NCT05819398) or 1368-0100) without premature discontinuation and are willing and able to continue treatment in this trial.
• Woman of childbearing potential (WOCBP) must be ready and able to use highly effective methods of birth control per ICH M3 (R2) that result in a low failure rate of less than 1% per year when used consistently and correctly.

You may not qualify if…

• Women who are pregnant, nursing, or who plan to become pregnant while in the trial.
• Use of any drug considered by the investigator likely to interfere with the safe conduct of the trial since the last visit of the parent trials.
• Use of immunomodulatory biologics or investigational agents since the last visit of the parent trials.
• Participants who require / intend to use certain restricted medications such as immunomodulatory biologics or other investigational drugs/devices during the course of the trial.
• Relevant chronic or acute infections including human immunodeficiency virus (HIV) and viral hepatitis. The corresponding laboratory tests will be performed at Visit 1. A participant can be re-screened if the participant was treated and is cured from the acute infection.
• Further exclusion criteria apply.

Where it is running

• First OC Dermatology — Fountain Valley, California, United States
• Dermatology Research Associates — Los Angeles, California, United States
• Integrative Skin Science and Research-Sacramento-69402 — Sacramento, California, United States
• Clinical Trials Research Institute — Thousand Oaks, California, United States
• STAT Research — CABA, Argentina
• Hospital Italiano de Buenos Aires — CABA, Argentina
• Hospital Alemán — Capital Federal, Argentina
• Holdsworth House Medical Practice — Sydney, New South Wales, Australia
• Alfred Hospital — Melbourne, Victoria, Australia
• Medical Center "Kordis" — Pleven, Bulgaria
• ASMC-IPSMC-skin and Veneral Diseases — Sofia, Bulgaria
• SimcoDerm Medical and Surgical Dermatology Centre — Barrie, Ontario, Canada
• Guelph Dermatology Research — Guelph, Ontario, Canada
• Dr. S. K. Siddha Medicine Professional Corporation — Newmarket, Ontario, Canada
• HOP Privé Antony — Antony, France
• Hôpital Edouard Herriot — Lyon, France
• Fachklinik Bad Bentheim — Bad Bentheim, Germany
• Hautmedizin Saar — Merzig, Germany
• Kurume University Hospital — Fukuoka, Kurume, Japan
• Ogaki Municipal Hospital — Gifu, Ogaki, Japan
• The University of Tokyo Hospital — Tokyo, Bunkyo-ku, Japan
• Nihon University Itabashi Hospital — Tokyo, Itabashi-ku, Japan
• Tokyo Medical University Hospital — Tokyo, Shinjuku-ku, Japan
• Hospital of Lithuanian University of Health Sciences Kauno Klinikos — Kaunas, Lithuania
• Vilnius University Hospital, Santariskiu — Vilnius, Lithuania

Full record on ClinicalTrials.gov

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