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Monoclonal Antibodies

Dupilumab for Chronic Sinusitis

Phase 2
Recruiting
Led By Jody Tversky
Research Sponsored by Johns Hopkins University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Age 18-75 with history of chronic sinusitis without polyps
Be older than 18 years old
Must not have
Use of any biologic medication within the last 5 months or 5 half-lives whichever is longer
History of cancer not in remission at least 5 years prior to the date informed consent
Timeline
Screening 3 weeks
Treatment Varies
Follow Up continuous during entire length of study which is three years.
Awards & highlights
All Individual Drugs Already Approved

Summary

This trial aims to test the effectiveness of dupilumab, a medication that targets specific immune responses, in treating chronic sinus disease without nasal polyps. The study focuses on patients who have limited treatment options and suffer from long-term sinus issues. Dupilumab works by blocking proteins that cause inflammation, potentially offering a new solution for these patients. Dupilumab is a novel monoclonal antibody that recently received approval for the treatment of chronic rhinosinusitis with nasal polyps.

Who is the study for?
This trial is for adults aged 18-75 with chronic sinusitis without nasal polyps, a certain level of sinus infection severity, and specific blood or allergy test results. Participants must agree to use effective contraception if applicable and can't be on certain medications or have conditions like uncontrolled asthma, immune deficiencies, recent biologic medication use, or serious illnesses.
What is being tested?
The study tests the effectiveness of Dupilumab in treating chronic rhinosinusitis without nasal polyps compared to a placebo. It aims to understand how well Dupilumab works for different underlying causes of this condition by also looking at secondary outcomes.
What are the potential side effects?
Dupilumab may cause side effects such as allergic reactions at the injection site, eye inflammation or irritation, joint pain, and possibly an increased risk of infections. The exact side effects will be monitored throughout the trial.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
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I am between 18 and 75 years old and have chronic sinusitis without polyps.

Exclusion Criteria

You may be eligible for the trial if you check “No” for criteria below:
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I haven't taken any biologic medication in the past 5 months or longer.
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My previous cancer has been in remission for at least 5 years.
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I currently have a fungal infection in my sinuses.
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I have had hepatitis B or C in the past.
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I have not been on immunosuppression, except for oral steroids, in the last 3 months.
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I am scheduled for sinus surgery.
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I have major issues with the structure of my nose.
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I have been diagnosed with primary ciliary dyskinesia.
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I have not been treated for worm infections in the last 6 months.
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I have a known immunodeficiency disorder, including HIV.
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I am not taking any immunosuppressive medications like methotrexate or cyclosporine.
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I currently have a sinus infection.
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My asthma is not well-managed.
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I have cystic fibrosis.
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I currently have a fever of 100.4°F or higher.
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I do not have serious heart or lung conditions that are not being treated.
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I take more than 81mg of aspirin daily.
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I have had nasal polyps in the last 3 years or they were seen in a recent CT scan or endoscopy.
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I haven't taken any anti-interleukin therapy in the last 5 months or longer.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~continuous during entire length of study which is three years.
This trial's timeline: 3 weeks for screening, Varies for treatment, and continuous during entire length of study which is three years. for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
SNOT-22
Secondary study objectives
Adverse event rate
CT Score
Drop out rate rate
+4 more

Side effects data

From 2023 Phase 4 trial • 40 Patients • NCT04203797
5%
Asthma
5%
Rhinitis
5%
Injection site erythema
5%
Immunisation reaction
5%
Cough
5%
Sinus pain
100%
80%
60%
40%
20%
0%
Study treatment Arm
Dupilumab 300 mg Q2W
Placebo

Awards & Highlights

All Individual Drugs Already Approved
Therapies where all constituent drugs have already been approved are likely to have better-understood side effect profiles.

Trial Design

2Treatment groups
Experimental Treatment
Placebo Group
Group I: dupilumab treatment groupExperimental Treatment1 Intervention
dupilumab treatment group
Group II: placebo groupPlacebo Group1 Intervention
placebo group
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Dupilumab
FDA approved

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 Chronic Sinusitis, such as Dupilumab, work by targeting specific pathways in the immune system to reduce inflammation. Dupilumab inhibits the signaling of interleukins IL-4 and IL-13, which are crucial in the inflammatory process associated with Chronic Sinusitis. By blocking these cytokines, Dupilumab helps to decrease the inflammation and swelling in the nasal passages, leading to improved sinus drainage and reduced symptoms. This mechanism is particularly important for Chronic Sinusitis patients as it addresses the underlying inflammation rather than just alleviating symptoms, potentially leading to more effective and long-term relief.

Find a Location

Who is running the clinical trial?

Regeneron PharmaceuticalsIndustry Sponsor
665 Previous Clinical Trials
385,691 Total Patients Enrolled
8 Trials studying Sinusitis
1,445 Patients Enrolled for Sinusitis
Johns Hopkins UniversityLead Sponsor
2,323 Previous Clinical Trials
14,874,257 Total Patients Enrolled
3 Trials studying Sinusitis
62 Patients Enrolled for Sinusitis
Jody TverskyPrincipal InvestigatorJohns Hopkins University

Media Library

Dupilumab (Monoclonal Antibodies) Clinical Trial Eligibility Overview. Trial Name: NCT04362501 — Phase 2
Sinusitis Research Study Groups: dupilumab treatment group, placebo group
Sinusitis Clinical Trial 2023: Dupilumab Highlights & Side Effects. Trial Name: NCT04362501 — Phase 2
Dupilumab (Monoclonal Antibodies) 2023 Treatment Timeline for Medical Study. Trial Name: NCT04362501 — Phase 2
~4 spots leftby Mar 2025