deltatrials
Enrolling By Invitation PHASE3 INTERVENTIONAL 1-arm NCT07007637

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

Sponsor: MoonLake Immunotherapeutics AG

Interventions Sonelokimab
Updated 4 times since 2025 Last updated: Mar 5, 2026 Started: Jun 27, 2025 Primary completion: Jun 13, 2028 Completion: Jun 13, 2028
This information is for research purposes only and is not medical advice. Consult a healthcare provider before making any medical decision.

This PHASE3 trial investigates Hidradenitis Suppurativa and is currently ongoing. MoonLake Immunotherapeutics AG leads this study, which shows 4 recorded versions since 2025 — indicating limited longitudinal coverage. The change history captured here reflects the iterative nature of clinical trial conduct.

Status Flow

~Jul 2025 – ~Aug 2025 · 31 days · monthly snapshotNot Yet Recruiting~Aug 2025 – ~Oct 2025 · 2 months · monthly snapshotEnrolling By Invitation~Oct 2025 – ~Mar 2026 · 5 months · monthly snapshotEnrolling By Invitation~Mar 2026 – present · 4 months · monthly snapshotEnrolling By Invitation

Change History

4 versions recorded
  1. Mar 2026 — Present [monthly]

    Enrolling By Invitation PHASE3

  2. Oct 2025 — Mar 2026 [monthly]

    Enrolling By Invitation PHASE3

  3. Aug 2025 — Oct 2025 [monthly]

    Enrolling By Invitation PHASE3

    Status: Not Yet RecruitingEnrolling By Invitation

  4. Jul 2025 — Aug 2025 [monthly]

    Not Yet Recruiting PHASE3

    First recorded

Jun 2025

Trial started

Per CT.gov start date — pre-dates our first snapshot

Eligibility Summary

No eligibility information available.

Contact Information

Sponsor contact:
  • MoonLake Immunotherapeutics AG
Data source: MoonLake Immunotherapeutics AG

For direct contact, visit the study record on ClinicalTrials.gov .