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A Study to Evaluate the Efficacy and Safety of Imsidolimab (ANB019) in the Treatment of Participants With Hidradenitis Suppurativa

NCT04856930 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 149

Last updated 2025-09-22

Study results available
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Summary

Efficacy and safety of imsidolimab (ANB019) in participants with Hidradenitis Suppurativa

Conditions

Interventions

BIOLOGICAL

Imsidolimab

Humanized Monoclonal Antibody

BIOLOGICAL

Placebo

Placebo

Sponsors & Collaborators

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-07-07
Primary Completion
2022-07-15
Completion
2022-12-14
FDA Drug
Yes

Countries

  • United States
  • Canada
  • Georgia
  • Poland

Study Locations

More Related Trials

Entities

Drugs
Diseases
Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04856930 on ClinicalTrials.gov