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Enrolling By InvitationNCT07007637

A Study to Evaluate the Long-term Safety, Tolerability, and Efficacy of Subcutaneous Sonelokimab in Participants With Moderate to Severe Hidradenitis Suppurativa

A Phase 3, Multicenter, Open-label Extension Study to Evaluate the Long-term Safety, Tolerability, and Efficacy of Subcutaneous Sonelokimab in Participants With Moderate to Severe Hidradenitis Suppurativa

Status
Enrolling By Invitation
Phase
Phase 3
Study type
Interventional
Enrollment
835 (estimated)
Sponsor
MoonLake Immunotherapeutics AG · Industry
Sex
All
Age
12 Years
Healthy volunteers
Not accepted

Summary

This is a study to evaluate the long-term safety, tolerability, and efficacy of sonelokimab in participants with moderate to severe hidradenitis suppurativa who were previously enrolled in a parental study.

Conditions

Interventions

TypeNameDescription
DRUGSonelokimabSonelokimab

Timeline

Start date
2025-06-27
Primary completion
2028-06-13
Completion
2028-06-13
First posted
2025-06-06
Last updated
2026-03-09

Locations

88 sites across 11 countries: United States, Belgium, Bulgaria, Canada, France, Germany, Hungary, Italy, Norway, Poland, Spain

Regulatory

Source: ClinicalTrials.gov record NCT07007637. Inclusion in this directory is not an endorsement.