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Monoclonal Antibodies

Imsidolimab for Generalized Pustular Psoriasis (GEMINI-2 Trial)

Phase 3
Waitlist Available
Research Sponsored by AnaptysBio, Inc.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up week 24
Awards & highlights
Pivotal Trial

Summary

This trial is testing a new medication called imsidolimab to see if it can help adults with a severe skin condition called generalized pustular psoriasis. The medication works by blocking certain proteins that cause inflammation and skin problems. Imsidolimab has shown promising results for treating pustular psoriasis.

Who is the study for?
This trial is for adults with generalized pustular psoriasis who completed at least the first week of a previous Phase 3 study without using any rescue or prohibited medications. Candidates must be deemed in need of long-term treatment by the investigator.
What is being tested?
The trial is testing the long-term safety and effectiveness of Imsidolimab, an investigational drug, against a placebo in managing symptoms and flare-ups associated with generalized pustular psoriasis.
What are the potential side effects?
While specific side effects are not listed here, common side effects for drugs treating psoriasis may include skin irritation, headaches, fatigue, nausea, and potential immune system changes.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~week 24
This trial's timeline: 3 weeks for screening, Varies for treatment, and week 24 for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Incidence of adverse events

Awards & Highlights

Pivotal Trial
The final step before approval, pivotal trials feature drugs that have already shown basic safety & efficacy.

Trial Design

4Treatment groups
Active Control
Placebo Group
Group I: SC ImsidolimabActive Control1 Intervention
Subcutaneous Imsidolimab
Group II: IV +SC ImsidolimabActive Control1 Intervention
IV loading dose followed by subcutaneous Imsidolimab
Group III: Standard of CareActive Control1 Intervention
Any available therapy
Group IV: SC PlaceboPlacebo Group1 Intervention
Subcutaneous Placebo

Research Highlights

Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.
Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
The most common treatments for Pustular Psoriasis often involve biologic agents that target specific interleukin pathways, such as IL-17, IL-23, and IL-36. These treatments work by inhibiting the activity of these cytokines, which are key drivers of the inflammatory process in psoriasis. For instance, IL-17 and IL-23 inhibitors reduce the proliferation of keratinocytes and the infiltration of inflammatory cells in the skin. Imsidolimab, an Anti-IL-36 Receptor Antibody, specifically targets the IL-36 pathway, which is implicated in the pathogenesis of pustular psoriasis by promoting inflammation and pustule formation. Understanding these mechanisms is crucial for patients as it helps in selecting targeted therapies that can effectively manage their symptoms and improve their quality of life.

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Who is running the clinical trial?

AnaptysBio, Inc.Lead Sponsor
16 Previous Clinical Trials
1,606 Total Patients Enrolled
Bruce Randazzo, MDStudy DirectorAnaptysBio, Inc.
10 Previous Clinical Trials
777 Total Patients Enrolled

Media Library

Imsidolimab (Monoclonal Antibodies) Clinical Trial Eligibility Overview. Trial Name: NCT05366855 — Phase 3
Pustular Psoriasis Research Study Groups: SC Imsidolimab, IV +SC Imsidolimab, SC Placebo, Standard of Care
Pustular Psoriasis Clinical Trial 2023: Imsidolimab Highlights & Side Effects. Trial Name: NCT05366855 — Phase 3
Imsidolimab (Monoclonal Antibodies) 2023 Treatment Timeline for Medical Study. Trial Name: NCT05366855 — Phase 3
Pustular Psoriasis Patient Testimony for trial: Trial Name: NCT05366855 — Phase 3
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