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Avalo Study

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A Phase 2, Randomized, Double-blind, Placebocontrolled, Parallel-group Study to Evaluate the Efficacy and Safety of AVTX-009 in Patients with Moderate to Severe Hidradenitis Suppurativa (LOTUS)

  • Sex at Birth: Any
  • Age: Adult (18 - 64), Older Adult (65+)
  • Accepting Healthy People: No
  • Type: Interventional / Therapeutic
  • Trial Phase: Phase II
  • Conditions Being Studied:

Study Purpose

The 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).

Who Can Participate

Participants 18 - 80 years old with symptoms of hidradenitis suppurativa (HS) for at least 6 months prior to screening may be eligible for this study.

Principal Investigator
Neil Korman MD PhD
Department/Division
Dermatology (Dermatitis)

Locations

UH Cleveland Medical Center
11100 Euclid Avenue
Cleveland OH, 44106

  • UH IRB: STUDY20241432
  • StudyID: 2024-01582
  • ClinicalTrials.gov: NCT06603077
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