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Monoclonal Antibodies

Guselkumab for Scalp Psoriasis

Phase 4
Recruiting
Led By Raymond Cho, MD, PhD
Research Sponsored by University of California, San Francisco
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 baseline and 9 months
Awards & highlights

Study Summary

This trial looks at how an injection can reduce scalp psoriasis symptoms by blocking immune cells.

Who is the study for?
This trial is for individuals with moderate to severe scalp psoriasis, indicated by a PSSI score of 12 or higher. It's not suitable for those who've used systemic immunosuppressives recently, are pregnant or breastfeeding, have severe immune deficiencies, active serious infections like tuberculosis, any current cancers, or men trying to conceive.Check my eligibility
What is being tested?
The study focuses on Guselkumab and its effects on the immune cells in scalp psoriasis lesions. Specifically, it looks at how blocking IL-23 with this medication influences the condition.See study design
What are the potential side effects?
Guselkumab may cause side effects such as injection site reactions (like pain or swelling), headaches, joint pain, stomach issues and potential increased risk of infections due to its impact on the immune system.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline and 9 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and baseline and 9 months for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Change in psoriasis scalp severity index score (PSSI)

Side effects data

From 2020 Phase 4 trial • 1027 Patients • NCT03573323
9%
Injection site reaction
8%
Upper respiratory tract infection
7%
Nasopharyngitis
100%
80%
60%
40%
20%
0%
Study treatment Arm
Ixekizumab
Ixekizumab Post-Treatment Follow Up
Guselkumab
Guselkumab Post-Treatment Follow Up

Trial Design

1Treatment groups
Experimental Treatment
Group I: Guselkumab treatmentExperimental Treatment1 Intervention
Guselkumab treatment for ~ 9 months
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Guselkumab
2015
Completed Phase 4
~5990

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
Common treatments for scalp psoriasis include topical corticosteroids, vitamin D analogs, and biologics like IL-23 inhibitors. Guselkumab, an IL-23 blocker, works by targeting the IL-23 cytokine, which plays a crucial role in the inflammatory process of psoriasis. By inhibiting IL-23, Guselkumab reduces the activation and proliferation of T-cells that contribute to the psoriatic plaques. Understanding these mechanisms is important for patients as it helps them comprehend how these treatments can effectively reduce inflammation and improve symptoms, leading to better management of their condition.

Find a Location

Who is running the clinical trial?

University of California, San FranciscoLead Sponsor
2,517 Previous Clinical Trials
15,241,019 Total Patients Enrolled
Janssen Scientific Affairs, LLCIndustry Sponsor
159 Previous Clinical Trials
580,509 Total Patients Enrolled
Raymond Cho, MD, PhDPrincipal InvestigatorUniversity of California, San Francisco
4 Previous Clinical Trials
57 Total Patients Enrolled

Media Library

Guselkumab (Monoclonal Antibodies) Clinical Trial Eligibility Overview. Trial Name: NCT05858632 — Phase 4
Scalp Psoriasis Research Study Groups: Guselkumab treatment
Scalp Psoriasis Clinical Trial 2023: Guselkumab Highlights & Side Effects. Trial Name: NCT05858632 — Phase 4
Guselkumab (Monoclonal Antibodies) 2023 Treatment Timeline for Medical Study. Trial Name: NCT05858632 — Phase 4
Scalp Psoriasis Patient Testimony for trial: Trial Name: NCT05858632 — Phase 4
~7 spots leftby Jun 2026