Grassmuno®: SCIT for grass pollen allergy, observational study
Study summary
Objective of this non-interventional study (NIS) is to collect data on the use of Grassmuno® in routine clinical practice.
Eligibility
Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
At the physician's discretion and based on the current Summary of Product Characteristics (SmPC), study participation may be offered to patients who
* are male and female patients
* are 18 years of age or older
* treated in accordance with the SmPC of Grassmuno® for IgE-mediated moderate to severe allergic rhinitis and/or rhinoconjunctivitis (without asthma or with well-controlled asthma) triggered by grass pollen.
* Patients will only be enrolled in the study after the treatment decision has been made
Exclusion Criteria:
At the physician's discretion, the study should not be offered to the following patients:
* Patients who are not sufficiently proficient in or do not adequately understand the German language, as this would prevent adequate comprehension of study-relevant documents.
* In addition, patients should not be included if any of the contraindications listed in the current Summary of Product Characteristics (SmPC) are present.
Primary outcome measure(s)
Treatment adherence — once a year for one year Absolute number and percentage of treatment adherent patients after the first treatment year
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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