A Study to Evaluate the Efficacy and Safety of AVTX-009 in Patients with Moderate to Severe Hidradenitis Suppurativa
Hidradenitis SuppurativaThe main purpose of this study is to evaluate the efficacy and safety of AVTX-009 compared with placebo in patients with moderate to severe Hidradenitis Suppurativa (HS).
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Conditions de participation
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Sexe:
ALL -
Âges admissibles:
18 and up
Critères de participation
Inclusion Criteria:
1. Signs and symptoms of hidradenitis suppurativa (HS) for at least 6 months prior to Screening.
2. At least 5 inflammatory lesions in at least 2 distinct anatomical areas, at least 1 of which is Hurley Stage 2 or 3.
Exclusion Criteria:
1. Has a draining fistula count of ≥ 20.
2. Has another active skin inflammatory condition, infection (viral, bacterial, or fungal), or another active ongoing inflammatory disease (other than HS) that requires treatment with a prohibited medication, which could interfere with the assessment of HS.
3. History of chronic or recurrent infectious disease, including but not limited to chronic renal infection, chronic lung infection, recurrent urinary tract infection, or open, draining or infected skin wounds or ulcers (not related to HS).
4. Has severe, progressive and/or uncontrolled renal, hepatic, hematologic, endocrine, pulmonary, cardiac, neurologic or immunosuppressive disease.
Lieu de l'étude
Clinical Site 1103
Clinical Site 1103Barrie, Ontario
Canada
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Clinical Site 1107
Clinical Site 1107London, Ontario
Canada
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Clinical Site 1104
Clinical Site 1104Hamilton, Ontario
Canada
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Clinical Site 1106
Clinical Site 1106Toronto, Ontario
Canada
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Clinical Site 1101
Clinical Site 1101Saskatoon, Saskatchewan
Canada
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- Étude parrainée par
- Avalo Therapeutics, Inc.
- Participants recherchés
- Plus d'informations
- ID de l'étude:
NCT06603077