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Clinical Trials in the EU / 2025-522376-82-00
Authorised Phase III

Intralymphatic Allergen Immunotherapy (ILIT) in grass pollen allergy: a randomized controlled trial

2025-522376-82-00 · tracked via the Priya Life Science EU tracker
Sponsor
University Of Foggia
Sponsor type
Educational Institution
Therapeutic area
Immune System Phenomena
Decision date
28/10/2025
Enrollment target
70
Sites
Italy

Condition studied

allergic diseases (allergic rhinosinusitis, allergic asthma, allergy to Hymenoptera venoms)

Investigational medicinal product(s)

Sodium chloride 9mg/1000ml-

Eligibility

Age group
18-64 years, 65+ years
Sex
Female, Male

Primary endpoint

1. Symptom scores (SS) (primary endpoint), ranging from 0 to 18 points, with 3 nasal and 3 ocular symptoms (runny nose, blocked nose, sneezing, red eyes, itchy eyes and watery eyes), each of which scored from 0 (no symptoms) to 3 (severe symptoms);, 2. Medication scores (MS), taking into account the exact number of anti-histamine tablets, nasal corticosteroid puffs, eye drops, 3. Rhino-conjunctivitis Quality of Life Questionnaire (RQLQ)

Official registry record

This page summarises publicly available CTIS data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View 2025-522376-82-00 on CTIS ↗ ← All trials in the EU