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Impact of AIT on Allergic Rhinitis and Asthma

Impact of AIT on Allergic Rhinitis and Asthma Using Real World Evidence

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04125888
Enrollment
92048
Registered
2019-10-14
Start date
2019-07-22
Completion date
2021-04-16
Last updated
2021-06-02

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

Conditions

Allergy, Respiratory Disease

Brief summary

The study will assess the effectiveness of AIT treatment in real clinical practice in Germany.

Detailed description

Allergic rhinitis (AR) affects 23-30% of the European population and is associated with a major burden on public health. AR and asthma frequently coexist, and may both be caused by allergen exposure. While the efficacy of AIT, i.e. reduce symptoms and medication use in patients with AR and asthma, has been demonstrated in several randomized clinical trials, little is known about the use and effectiveness of AIT in real world clinical practice. This study is a retrospective database study that uses real-world data from Germany. The study population consists of AR patients with and without asthma treated with AIT and matched controls not treated with AIT. Information about the patients and treatments will be obtained from the 'BKK German Sickness Fund Database' from 2007 until 2017.

Interventions

DRUGAllergy immunotherapy (AIT)

Immunotherapy for different types of allergies

Sponsors

ALK-Abelló A/S
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL

Inclusion criteria

for the AIT cohort: * At least two index-AIT prescriptions during the first FU-year * At least one confirmed AR diagnosis during the study period * Continuous enrollment (no gaps in insurance time-defined by days) for 12 months before the index event (in the pre-index period) * Continuous enrollment (no gaps in insurance time-defined by days) for at least 12 months after the index event (in the post-index period) Inclusion Criteria for the Control Cohort: \- For the control groups, the same inclusion criteria will apply, with the exception of inclusion criterion 1, i.e. controls have not received AIT before baseline.

Exclusion criteria

\- AIT prescription 12 months before the index event (in the pre-index period) for the AIT treatment group

Design outcomes

Primary

MeasureTime frameDescription
Allergic rhinitis medication useFrom pre-index year to follow-up year(s), assessed from 2007 and up to 2017Number of patients with an AR prescription and number of prescriptions by drug class

Secondary

MeasureTime frameDescription
Asthma medication useFrom pre-index to follow-up year(s), assessed from 2007 and up to 2017Number of patients with an asthma prescription and number of prescriptions by drug class
Change in asthma disease severityFrom pre-index to follow-up year(s), assessed from 2007 and up to 2017Change in asthma disease severity assessed by asthma diagnoses, asthma medication use and severe asthma exacerbation

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 20, 2026