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Real Life Use of Omalizumab in Chronic Urticaria

Drug Survival of Omalizumab in Chronic Urticaria : a Retrospective Multicentric Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04584190
Acronym
XO-DS
Enrollment
700
Registered
2020-10-12
Start date
2020-07-01
Completion date
2020-12-30
Last updated
2020-10-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Urticaria

Keywords

Chronic urticaria treated with OMALIZUMAB

Brief summary

Chronic urticaria affects up to 1% of the population. Chronic urticaria refractory to updosing antihistamines can benefit from OMALIZUMAB, which is an anti-IgE IgG1 monoclonal antibody administrated every 4 weeks subcutaneously which represents a cost of nearly 800€/month excluding nurse fees. Efficacy and good tolerance have already been demonstrated in real-life large cohorts of patients. A 6 months treatment duration is proposed before evaluating the efficacy and discontinuating the treatment in the absence of adequate response. Mean duration of chronic urticaria is 3 to 5 years with high standard deviations. Therefore, optimal duration of treatment with OMALIZUMAB is unknown and discontinuation modalities differ between physicians. The aim of this study is to evaluate the mean duration between initiation and first discontinuation of OMALIZUMAB in patients treated for chronic urticaria and explore the different factors influencing this duration and its outcome.

Detailed description

Chronic urticaria affects up to 1% of the population. Rarely, chronic urticaria may be refractory to updosing four-fold antihistamine drugs and then can be improved with subcutaneous OMALIZUMAB. OMALIZUMAB is available for chronic urticaria since 2015. It is an IgG1 monoclonal antibody targeting IgE and administrated every 4 weeks which represent a cost of nearly 800€/month excluding nurse fees. Efficacy and good tolerance have already been demonstrated in real-life large cohorts of patients. A 6 months treatment duration is proposed before evaluating the efficacy and discontinuating the treatment in the absence of adequate response. Mean duration of chronic urticaria is 3 to 5 yearss with high standard deviations. Therefore, optimal duration of treatment with OMALIZUMAB is unknown and discontinuation modalities differ between physicians. The aim of this study is to evaluate the mean duration between initiation and first discontinuation of OMALIZUMAB in patients treated for chronic urticaria and explore the different factors influencing this duration and its outcome. To accomplish this, the investigators will conduct a restrospective analyse of all patients treated with OMALIZUMAB for chronic urticaria from 2010 to 2020 in the major French hospital reference centers for chronic urticaria management : Paris, Lyon, Grenoble, Lille, Bordeaux, Nantes, Rouen, Saint-Etienne, Montpellier.

Interventions

None listed

Sponsors

Lyon Civil Hospitals - Lyon Sud Hospital Center
CollaboratorUNKNOWN
Tenon Hospital, Paris
CollaboratorOTHER
Nantes University Hospital
CollaboratorOTHER
University Hospital, Grenoble
CollaboratorOTHER
University Hospital, Rouen
CollaboratorOTHER
Lille University Hospital
CollaboratorUNKNOWN
University Hospital, Bordeaux
CollaboratorOTHER
Centre Hospitalier Universitaire de Saint Etienne
CollaboratorOTHER
University Hospital, Montpellier
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* chronic spontaneous or inducible urticaria * treated with omalizumab * at least once between January the 1st 2010 and july 2020.

Exclusion criteria

* unknown intiation and discontinuation date of omalizumab * omalizumab initiated for asthma * other diagnosis (vascularitis, aquagenic pruritus)

Design outcomes

Primary

MeasureTime frameDescription
duration between initiation and first discontinuation of OMALIZUMAB1 dayassessed at the time of inclusion Description: duration between initiation and first discontinuation of OMALIZUMAB

Secondary

MeasureTime frameDescription
efficacy of omalizumab and relapse at discontinuation1 dayefficacy of omalizumab and relapse at discontinuation
discontinuation cause1 daydiscontinuation cause
predictive factors of duration between initiation and first discontinuation of omalizumab1 daypredictive factors of duration between initiation and first discontinuation of omalizumab
persistance of antihistamine intake at 1year, 2 years and 3 yearsat 1year, 2years and 3yearspersistance of antihistamine intake at 1year, 2 years and 3 years
mid and long-term tolerance of omalizumab.1 daymid and long-term tolerance of omalizumab.
rechallenge with omalizumab and efficacy1 dayrechallenge with omalizumab and efficacy

Countries

France

Contacts

Primary ContactJulie Litovsky, resident
julie.litovsky@gmail.com606934527
Backup ContactAurélie Du Thanh, MD, PhD
a-du_thanh@chu-montpellier.fr61148890

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026