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
2/3상
조기 종료
NCT06241573
| 대상 질환 | Hidradenitis Suppurativa |
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| 임상 단계 | 2/3상 |
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| 스폰서 | Boehringer Ingelheim |
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| 상태 | 조기 종료 |
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| 참여자 수 | 39 명 |
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| 중재(약물) | Spesolimab |
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| 시작일 | 2024년 5월 8일 |
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| 완료일 | 2025년 4월 11일 |
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| 결과 공개일 | 2026년 6월 17일 |
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요약
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.
Occurrence of Treatment Emergent Adverse Events (TEAE) up to the End of Maintenance Treatment Period
From first drug administration, up to 16 weeks after last administration, up to 39 weeks. · Participants
| Spesolimab Low Dose | 3 Participants |
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| Spesolimab High Dose | 6 Participants |
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| Spesolimab High Dose With Prior Placebo | 5 Participants |
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BENITIONS에서 보기
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