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Clinical Trials in Germany / NCT07412990
Recruiting Observational

GRASS (Grass MATA MPL Real-world Assessment Study)

NCT07412990 · tracked via the Priya Life Science Germany tracker
Phase
Observational
Started
2026-03-11
Last updated
2026-03-20

Condition(s) studied

Grass Pollen Allergy

Investigational drug(s) / intervention(s)

Grassmuno®

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)

Trial sites (1)

FacilityCityRegionStatus
Dr. Kasche Hamburg Germany Recruiting

More Allergy Therapeutics trials in Germany

Official registry record

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.

View NCT07412990 on ClinicalTrials.gov ↗ ← All trials in Germany