Guselkumab vs Risankizumab for Crohn's Disease
(CHARGE Trial)
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial aims to compare the effectiveness of two treatments, guselkumab and risankizumab, for individuals with Crohn's Disease, a condition causing severe inflammation in the digestive tract. Participants will receive one of these treatments to determine which better manages symptoms. The trial targets those who have had Crohn's Disease for at least 12 weeks and are experiencing moderate to severe symptoms that significantly impact daily life. As a Phase 3 trial, it represents the final step before FDA approval, providing participants an opportunity to access potentially effective treatments early.
Do I need to stop my current medications for the trial?
The trial protocol does not specify if you need to stop your current medications, but it mentions that you must follow the requirements for other medications used to treat Crohn's Disease as outlined in the study. It's best to discuss this with the trial team or your doctor.
Is there any evidence suggesting that this trial's treatments are likely to be safe?
A previous study found guselkumab to be safe for people with Crohn's disease over one year of treatment. Its safety profile matched that of a placebo, with no unexpected side effects reported. Another study over five years confirmed that guselkumab was well-tolerated, with most participants continuing treatment without major issues.
Research indicates that risankizumab is also well-tolerated. One study found no new safety risks, and its safety remained consistent over time. Another study reported that only 6.9% of patients experienced unwanted effects, with only a few discontinuing treatment due to these effects.
Both guselkumab and risankizumab have generally been shown to be safe in these studies. However, consulting a healthcare provider is essential to understand what this means personally.12345Why are researchers excited about this trial's treatments?
Researchers are excited about these treatments for Crohn's Disease because they offer a novel approach compared to traditional options like corticosteroids and immunosuppressants. Guselkumab works by targeting a specific protein called interleukin-23 (IL-23), which plays a key role in inflammation, and is administered as an induction dose subcutaneously followed by a maintenance dose every four weeks. Risankizumab also targets IL-23 but is initially given intravenously, switching to a subcutaneous injection every eight weeks, potentially offering greater convenience and different dosing flexibility. Both treatments focus on reducing inflammation more precisely, which could lead to fewer side effects and better management of Crohn's Disease symptoms.
What evidence suggests that this trial's treatments could be effective for Crohn's Disease?
This trial will compare Guselkumab and Risankizumab for treating Crohn's Disease. Studies have shown that Guselkumab delivers strong results, with up to 97.7% of patients experiencing symptom relief when continuing treatment over five years. Another study found that 56.1% of patients felt better at week 12, outperforming those who took a placebo.
Risankizumab also shows promise. In one study, 78% of patients felt better after 12 weeks of treatment. Additionally, 46.7% of patients experienced symptom relief after the initial treatment phase, with some groups achieving even higher success rates. Both treatments have effectively reduced symptoms and improved the quality of life for people with moderate to severe Crohn's Disease. Participants in this trial will receive either Guselkumab or Risankizumab to further evaluate their effectiveness.36789Who Is on the Research Team?
Janssen Research & Development, LLC Clinical Trial
Principal Investigator
Janssen Research & Development, LLC
Are You a Good Fit for This Trial?
This trial is for people with moderately to severely active Crohn's disease, including those with fistulas, who have had the condition for at least 12 weeks. Participants must have confirmed Crohn's and meet certain activity scores based on symptoms and ulcers.Inclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants receive guselkumab or risankizumab with induction doses at Weeks 0, 4, and 8, followed by maintenance doses from Week 12 through Week 52
Follow-up
Participants are monitored for safety and effectiveness after treatment
Long-term safety follow-up
Participants are monitored for adverse events and laboratory abnormalities
What Are the Treatments Tested in This Trial?
Interventions
- Guselkumab
- Risankizumab
Trial Overview
The study compares two injectable medications—guselkumab and risankizumab—to see which works better in treating moderate to severe Crohn's disease. Participants are randomly assigned to one of the two treatments.
How Is the Trial Designed?
2
Treatment groups
Experimental Treatment
Participants will receive risankizumab induction dose intravenously (IV) at Weeks 0, 4, and 8 followed by risankizumab maintenance dose SC once every 8 weeks (q8w) from Week 12 through Week 52.
Participants will receive guselkumab induction dose subcutaneously (SC) at Weeks 0, 4, and 8 followed by guselkumab maintenance dose SC once every 4 weeks (q4w) from Week 12 through Week 52.
Find a Clinic Near You
Who Is Running the Clinical Trial?
Janssen Research & Development, LLC
Lead Sponsor
Joaquin Duato
Janssen Research & Development, LLC
Chief Executive Officer since 2022
MBA from ESADE, Master of International Management from Thunderbird School of Global Management
Dr. Jijo James, MD
Janssen Research & Development, LLC
Chief Medical Officer since 2014
MD from St. Johns Medical College, MPH from Columbia University
Citations
One-Year Efficacy of Guselkumab Versus Advanced ... - PMC
Guselkumab at doses of 100 mg and 200 mg was more effective than several treatments. Guselkumab 200 mg was significantly better than infliximab ...
Subcutaneous Guselkumab Is Effective for Both Induction ...
Results: At week 12, guselkumab was superior to placebo for clinical remission (56.1% vs 21.4%, P < 0.01) and endoscopic response (41.3% vs 21.4 ...
Results In Crohn's Disease (CD)
*Results are from a 48-week clinical trial of patients with moderately to severely active Crohn's disease: 225 patients started with TREMFYA® 400 mg SC doses ...
Five-year efficacy and safety of guselkumab for moderately to ...
Among those continuing treatment, with available data (as observed), 97.7% (n = 85 of 87) achieved clinical remission, 71.3% (n = 62 of 87) ...
Guselkumab Demonstrates Rapid and Lasting Results in ...
Subcutaneous guselkumab showed significant clinical remission and endoscopic response in moderate to severe Crohn's disease, with no added ...
48-week results from two phase 3, randomised, placebo ...
Coprimary composite endpoints (comparing each guselkumab regimen with placebo) were (1) clinical response at week 12 and clinical remission at week 48 and (2) ...
Results From the Phase 3 GRAVITI Study
Efficacy and safety of 48 weeks of guselkumab for patients with Crohn's disease: maintenance results from the phase 2, randomised, double-blind GALAXI-1 trial.
8.
jnjmedicalconnect.com
jnjmedicalconnect.com/media/attestation/congresses/immunology/2024/rhapp/efficacy-and-safety-of-guselkumab-induction-and-maintenance-therapy-in-patients-with-moderately-to-s.pdfResults of the GALAXI 2 & 3 Phase 3 Studies
Efficacy and Safety of Guselkumab Therapy in Patients With Moderately to. Severely Active Crohn's Disease: Results of the GALAXI 2 & 3 Phase 3 Studies. Remo ...
NCT03466411 | A Study of the Efficacy and Safety ...
Efficacy and safety of 48 weeks of guselkumab for patients with Crohn's disease: maintenance results from the phase 2, randomised, double-blind GALAXI-1 ...
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