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Intralymphatic Immunotherapy Enhanced by Vitamin-D, a Randomized Placebo-controlled Trial and Comparison With SLIT

Intralymphatic Immunotherapy Enhanced by Vitamin-D, a Randomized Placebo-controlled Trial and Comparison With SLIT

Recruiting
18-60 years
All
Phase 2/3

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Overview

A national, multicenter, randmised double blind study with parallell arms. 360 patients with grass induced allergic rhinitis will be open randomised 1:2 to 3 years Grazax sublingual immunotherapy or 3 intralymphatic injections with ALK Alutard Timothy. In a second step, the ILIT group will be double blind randomised 1:1 to an intramuscular injection of Vitamin D Vicotrat or placebo, 4 week before the start of the intralymphatic treatment. The primary outcome measure is daily combined symptoms and medication scores during grass pollen season.

Eligibility

Inclusion Criteria:

  • moderate to severe allergic rhinitis due to grass pollen, with Rhinitis Total Symptom Score >/= 8.
  • informed consent

Exclusion Criteria:

  • chronic rhinosinusitis
  • Previous immunotherapy
  • BMI > 35
  • house dust mite allergy with symptoms or allergy towards furry animals with exposition
  • 25(OH)Vitamin D levels < 25 or > 75 nmol/L
  • uncontrolled asthma
  • severe atopic dermatitis
  • pregnancy or nursing
  • autoimmune disease
  • hyper IgE-syndrome
  • cardiovascular disease
  • lung disease
  • liver or kidney disease
  • hematologic disorder
  • metabolic disease
  • chronic infectious disese
  • medications interacting with the immune system
  • cancer
  • previous cytostatic therapy
  • medication with beta-blockers or ACE-inhibiters, if medication cannot be paused at the day for treatment
  • medication with antiepileptic drugs, glykosides, orlistat, statines, thiazide diuretics
  • Mb Paget, osteoporosis or sarcidosis
  • Hyperparathyroidism or other disease conferring risk of hypercalcemia
  • malabsorption or bowel disease with diarrea
  • tendency for formation of kidney stones
  • hereditary pseudohypoparathyroidism with decreased phosphorous secretion
  • use of Vitamin D supplementation or excessive use of sun tanning booths
  • drug abuse
  • intake of other study product within 1 month or 6 half times, which ever is longest, before visit 1
  • Mental incapacity to follow study protocol
  • withdrawn consent
  • other significant disease
  • allergy towards study medication

Study details
    Allergic Rhinitis Due to Grass Pollen

NCT06061848

Lars Olaf Cardell

26 January 2024

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