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Enrolling by invitationPhase 3

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

Key facts

Where
Alicante, Badalona, Barcelona, Cadiz, Córdoba, Granada, Granollers, Madrid, Málaga, Manises, Santiago de Compostela, Seville, and Valencia, SpainSee the 13 sites
Phase
Phase 3

Where in Spain

  • AlicanteHospital not named in the registryNo longer taking part
  • BadalonaHospital not named in the registryNo longer taking part
  • BarcelonaHospital not named in the registryNo longer taking part
  • CadizHospital not named in the registryNo longer taking part
  • CórdobaHospital not named in the registryNo longer taking part
  • GranadaHospital not named in the registryNo longer taking part
  • GranollersHospital not named in the registryNo longer taking part
  • MadridHospital not named in the registryNo longer taking part
  • MálagaHospital not named in the registryNo longer taking part
  • ManisesHospital not named in the registryNo longer taking part
  • Santiago de CompostelaHospital not named in the registryNo longer taking part
  • SevilleHospital not named in the registryNo longer taking part
  • ValenciaHospital not named in the registryNo longer taking part

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Trial details

Who runs it
MoonLake Immunotherapeutics AG
Trial code
NCT07007637
Record updated
8 June 2026
Original description
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.Read full original descriptionShow less

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

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.

Inclusion: Participants who have completed a parental study (M1095-HS-301 or M1095-HS-302 [adult studies] or M1095-HS-304 [adolescent study]) and are eligible to continue to receive sonelokimab at the time of completing the parental study; Female participants are eligible to participate if they are not pregnant or breastfeeding; Male participants must be willing to use a condom when sexually active with a partner of childbearing potential . Male participants must also agree to refrain from donating sperm during the study and for at least 8 weeks after the last dose of study treatment.

Exclusion: Participants who plan to participate in another interventional study for a drug or device during this study; Participants who meet any of the discontinuation criteria of the parental study at the time of enrollment in this OLE study; Participants who have ongoing or planned to use one or more of the prohibited HS or non-HS treatments specified in the protocol.

ClinicalTrials.gov NCT07007637