Dupilumab in Allergic Fungal Rhinosinusitis (AFRS) (LIBERTY-AFRS-AI)
|
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details. |
| ClinicalTrials.gov Identifier: NCT04684524 |
|
Recruitment Status :
Recruiting
First Posted : December 24, 2020
Last Update Posted : May 15, 2023
|
Sponsor:
Sanofi
Collaborator:
Regeneron Pharmaceuticals
Information provided by (Responsible Party):
Sanofi
- Study Details
- Tabular View
- No Results Posted
- Disclaimer
- How to Read a Study Record
Brief Summary:
Primary Objective:
- To evaluate the efficacy of treatment with dupilumab to reduce sinus opacification in a population with allergic fungal rhinosinusitis (AFRS)
Secondary Objectives:
- To evaluate the efficacy of treatment with dupilumab to reduce sinus opacification in a population with allergic fungal rhinosinusitis (AFRS) at Week 24
- To assess the efficacy of dupilumab to reduce the need for rescue treatments
- To evaluate the efficacy of treatment with dupilumab in improving symptoms in AFRS
- To evaluate the efficacy of dupilumab to reduce nasal polyp formation in participants with AFRS
- To evaluate the efficacy of dupilumab in improving overall symptom severity and quality of life in AFRS
- To evaluate the efficacy of dupilumab in improving sense of smell in participants with AFRS
- To explore the effect of dupilumab as assessed by three-Dimensional CT volumetric measurement of the paranasal sinuses
- To evaluate the safety and tolerability of dupilumab when administered to participants with AFRS
- To evaluate the pharmacokinetics (PK) of dupilumab in participants with AFRS
- To characterize the effect of dupilumab on total IgE and specific IgE
- To assess immunogenicity to dupilumab in participants with AFRS
| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Allergic Fungal Rhinosinusitis | Drug: Dupilumab SAR231893 Drug: Placebo | Phase 3 |
| Study Type : | Interventional (Clinical Trial) |
| Estimated Enrollment : | 62 participants |
| Allocation: | Randomized |
| Intervention Model: | Parallel Assignment |
| Masking: | Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor) |
| Primary Purpose: | Treatment |
| Official Title: | A Randomized Double-blind Placebo-controlled Parallel Group Study Assessing the Efficacy and Safety of Dupilumab in Patients With Allergic Fungal Rhinosinusitis (AFRS) |
| Actual Study Start Date : | December 1, 2020 |
| Estimated Primary Completion Date : | December 27, 2024 |
| Estimated Study Completion Date : | March 21, 2025 |
Resource links provided by the National Library of Medicine
MedlinePlus related topics:
Molds
Drug Information
available for:
Dupilumab
| Arm | Intervention/treatment |
|---|---|
|
Experimental: Dupilumab
Dupilumab administered every 2 or 4 weeks based on weights
|
Drug: Dupilumab SAR231893
Pharmaceutical form:Injection solution Route of administration: Subcutaneous |
|
Placebo Comparator: Matching placebo
Placebo administered every 2 or 4 weeks based on weights
|
Drug: Placebo
Pharmaceutical form:Injection solution Route of administration: Subcutaneous |
Primary Outcome Measures :
- Change from baseline in sinus opacifications assessed by computerized tomography (CT) scans using the Lund Mackay (LMK) score at Week 52 [ Time Frame: Baseline to Week 52 ]LMK total score is based on assessment of the CT scan findings for each sinus area. The extent of opacification is rated between 0 (normal) to 24 (total opacification).
Secondary Outcome Measures :
- Change from baseline in sinus opacifications assessed by CT scans using the LMK score at Week 24 [ Time Frame: Baseline to Week 24 ]LMK total score is based on assessment of the CT scan findings for each sinus area. The extent of opacification is rated between 0 (normal) to 24 (total opacification).
- Proportion of patients who receive systemic corticosteroids (SCS) and/or undergo/plan to undergo surgery for AFRS during the planned study treatment period [ Time Frame: Baseline to Week 52 ]
- Change from baseline in monthly average nasal congestion/obstruction score from the Nasal symptom Diary at Week 24 and Week 52 [ Time Frame: Baseline to Week 24 and Week 52 ]The nasal congestion/obstruction scores are scored from 0 ('No symptoms') to 3 ('Severe symptoms').
- Change from Baseline in the monthly average anterior/posterior rhinorrhea score from the Nasal Symptom Diary at Week 24 and Week 52 [ Time Frame: Baseline to Week 24 and Week 52 ]The rhinorrhea scores are scored from 0 ('No symptoms') to 3 ('Severe symptoms').
- Change from baseline in endoscopic NPS compared to placebo at Week 24 and Week 52 [ Time Frame: Baseline to Week 24 and Week 52 ]The total nasal polyps score (NPS) is the sum of the right and left nostrils, ranging from 0 (no polyps) to 8 (large polyps causing complete obstruction).
- Change from baseline in 22-item sino-nasal outcome test (SNOT-22) total score at Week 24 and Week 52 [ Time Frame: Baseline to Week 24 and Week 52 ]SNOT-22 is a patient-reported outcome (PRO) questionnaire. Score ranges from 0 to 110 with higher score indicating greater rhinosinusitis related health burden.
- Change from baseline in monthly average total symptom score (TSS) derived from the Nasal Symptom Diary at Week 24 and Week 52 [ Time Frame: Baseline to Week 24 and Week 52 ]TSS ranges from 0 to 9. Higher scores on the TSS indicate greater symptom severity.
- Change from baseline in visual analog scale (VAS) rhinosinusitis at Week 24 and Week 52 [ Time Frame: Baseline to Week 24 and Week 52 ]VAS score ranges from 0 ('not troublesome') to 10 ('worst thinkable troublesome').
- Change from baseline in University of Pennsylvania smell identification test (UPSIT) at Week 24 and Week 52 [ Time Frame: Baseline to Week 24 and Week 52 ]The UPSIT score ranges from 0 to 40, with 40 being the best possible score.
- Change from baseline in the score of decreased/loss of smell using the Nasal Symptom Diary at Week 24 and Week 52 [ Time Frame: Baseline to Week 24 and Week 52 ]The decreased/loss of smell scores are scored from 0 ('No symptoms') to 3 ('Severe symptoms').
- Change from baseline to Week 52 in three Dimensional CT volumetric measurement of the paranasal sinuses [ Time Frame: Baseline to Week 52 ]
- Incidence of treatment-emergent adverse events (TEAEs) or serious adverse events (SAEs) [ Time Frame: Baseline to Week 64 ]
- Dupilumab concentration in serum over time [ Time Frame: Baseline to Week 52 ]
- Percent change from baseline in total IgE in serum compared to placebo over the 52 weeks treatment period [ Time Frame: Baseline to Week 52 ]
- Percent change from baseline in fungal-specific IgE in serum compared to placebo over the 52 weeks treatment period [ Time Frame: Baseline to Week 52 ]
- Incidence of treatment-emergent anti-drug antibodies (ADA) to dupilumab over time [ Time Frame: Baseline to Week 64 ]Enter Endpoint Secondary
Information from the National Library of Medicine
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
| Ages Eligible for Study: | 6 Years and older (Child, Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
Participant must be at least 6 years of age (or the minimum legal age for adolescents in the country of the investigational site) at the time of signing the informed consent.
Participants with the diagnosis of AFRS adapted from criteria by Bent and Kuhn (meeting all):
- IgE mediated inflammatory response to fungal hyphae (specific IgE serology or skin test) Evidence of sensitization to fungus by skin testing (at screening or documented historical positive skin test in the previous 12 months), or positive fungal-specific IgE in serum at screening.
- Nasal polyposis confirmed by nasal endoscopy at screening.
-
Characteristic CT signs to be performed during screening period and can include any of the below signs as assessed by central reader:
- hyperdensities
- bony demineralization
- bone erosion of sinus
- Eosinophilic mucin/mucus identified within 5 years prior to screening or at screening with or without positive fungal stain
AFRS patients with the following:
- An endoscopic NPS of at least 2 out of 4 for unilateral polyps or 3 out of 8 for bilateral polyps at Visit 1 (central reading) and Visit 2 (local reading) and,
- Sinus opacification in CT scan with an LMK score of 9 for patients with unilateral polyps or 12 for patients with bilateral polyps during screening period and,
Body weight ≥15 kg
Exclusion Criteria:
- Patients with nasal conditions/concomitant nasal diseases making them non-evaluable at Visit 1 or for the primary efficacy
- Nasal cavity malignant tumor and benign tumors.
- Known of fungal invasion into sinus tissue.
- Severe concomitant illness(es) that, in the investigator's judgment, would adversely affect the patient's participation in the study
- Active tuberculosis or non-tuberculous mycobacterial infection, or a history of incompletely treated tuberculosis unless documented adequately treated.
- Diagnosed active endoparasitic infections; suspected or high risk of endoparasitic infection
- Known or suspected immunodeficiency
- Active chronic or acute infection requiring treatment with systemic antibiotics, antivirals, or antifungals within 2 weeks before the Screening Visit 1 or during the screening period.
- History of systemic hypersensitivity or anaphylaxis to dupilumab or any of its excipients.
- Treatment with commercially available dupilumab within 12 months, participation in prior dupilumab clinical trial, or discontinued dupilumab use due to adverse event.
- Patients who are treated with intranasal corticosteroid drops; intranasal steroid emitting devices/stents; nasal spray using exhalation delivery system, such as Xhance™, during screening period.
- Patients who are on intranasal corticosteroids (INCS) spray unless they have received stable dose for at least 4 weeks prior to Visit 1.
- Patients who have undergone sinus intranasal surgery (including polypectomy) within 6 months prior to Visit 1.
-
Patients who have taken:
- Biologic therapy/systemic immunosuppressant to treat inflammatory disease or autoimmune disease within 5 half-lives prior to Visit 1
- Any investigational mAb within 5 half-lives prior to Visit 1
- Anti-IgE therapy (omalizumab) within 4 months prior to Visit 1. - Treatment with a live (attenuated) vaccine within 4 weeks prior to Visit 1
- Leukotriene antagonists/modifiers unless patient is on a continuous treatment for at least 30 days prior to Visit 1.
- Initiation of allergen immunotherapy within 3 months prior to Visit 1 or a plan to begin therapy or change its dose during the screening or treatment period. - Patients received SCS during screening period. - Either intravenous immunoglobulin therapy and/or plasmapheresis within 30 days prior to Screening Visit (Visit 1).
The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.
Information from the National Library of Medicine
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04684524
Contacts
| Contact: Trial Transparency email recommended (Toll free number for US & Canada) | 800-633-1610 ext option 6 | Contact-US@sanofi.com |
Locations
Show 45 study locations
Sponsors and Collaborators
Sanofi
Regeneron Pharmaceuticals
Investigators
| Study Director: | Clinical Sciences & Operations | Sanofi |
| Responsible Party: | Sanofi |
| ClinicalTrials.gov Identifier: | NCT04684524 |
| Other Study ID Numbers: |
EFC16724 2020-002999-12 ( EudraCT Number ) U1111-1246-7549 ( Registry Identifier: ICTRP ) |
| First Posted: | December 24, 2020 Key Record Dates |
| Last Update Posted: | May 15, 2023 |
| Last Verified: | May 9, 2023 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | Yes |
| Plan Description: | Qualified researchers may request access to patient level data and related study documents including the clinical study report, study protocol with any amendments, blank case report form, statistical analysis plan, and dataset specifications. Patient level data will be anonymized and study documents will be redacted to protect the privacy of trial participants. Further details on Sanofi's data sharing criteria, eligible studies, and process for requesting access can be found at: https://vivli.org |
| Studies a U.S. FDA-regulated Drug Product: | Yes |
| Studies a U.S. FDA-regulated Device Product: | No |
| Product Manufactured in and Exported from the U.S.: | Yes |
Additional relevant MeSH terms:
|
Sinusitis Allergic Fungal Sinusitis Respiratory Tract Infections Infections Paranasal Sinus Diseases Nose Diseases Respiratory Tract Diseases |
Otorhinolaryngologic Diseases Mycoses Bacterial Infections and Mycoses Respiratory Hypersensitivity Hypersensitivity, Immediate Hypersensitivity Immune System Diseases |