The Safety and Efficacy of Intralymphatic Immunotherapy in Pollen Allergic Adolescents and Young Adults With Asthma

Karolinska Institute

Status and phase

Completed

Phase 3

Phase 2

Conditions

Asthma

Rhinitis

Allergy

Treatments

Drug: ALK diluent 0,3% human albumin

Drug: ALK Alutard birch or 5-grasses

Study type

Interventional

Funder types

Other

Identifiers

NCT03394508

DNR 2012/701 EPN Lund

Details and patient eligibility

About

The study evaluates the safety and efficacy of intralymphatic allergen-specific immunotherapy given to adolescents and young adults who are allergic to grass or birch pollen and have mild or moderate asthma. Patients will be treated with three intralymphatic injections; 1000 SQ-U x3 with 4-5 weeks interval, or placebo with 4-5 weeks interval. The patients receiving treatment will be given a fourth injection one year after the initial injections. The study is conducted in collaboration between Professor Lars Olof Cardell (ENT), prof Gunilla Hedlin (Pediatrics) and prof Marianne van Hage (Immunology)".

Full description

30 patients with seasonal allergic rhinitis due to birch or grass pollen are included. Study subjects are randomized to intralymphatic injections with placebo or ALK Alutard 5-grasses / birch or placebo. The patients receiving treatment will be given a fourth injection one year after the initial injections.

Enrollment

30 patients

Sex

All

Ages

16 to 50 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Allergic rhinitis due to grass or birch pollen
Mild to moderate asthma with a positive methacholine challenge
Accepted and signed informed consent.

Exclusion criteria

Previously subcutaneous immunotherapy (SCIT) with total symptom relief.
Previously SCIT but no symptom improvement at all.
Sensitizations to house dust mite or furry animals, with ongoing exposure and symptoms.
Severe atopic dermatitis.
Patients with significant diseases other than allergic rhinitis. A significant disease is defined as a disease which in the opinion of the investigator may either put the patient at risk because of participation in the study or a disease which may influence the results of the study or the patient's ability to participate in the study.
Patients with a respiratory tract infection in the past 4 weeks prior to Visit 2.
Pregnant or nursing women or women of childbearing potential not using a medically approved means of contraception (i.e., oral contraceptives, intrauterine devices, diaphragm, or subdermal implants).
Known autoimmune or collagen disease
Cardiovascular disease
Hepatic disease
Known renal insufficiency
Cancer
Hematologic disease
Chronic infectious disease
Any medication with a possible side-effect of interfering with the immune response
Previous immuno- or chemotherapy
Disease or conditions rendering the treatment of anaphylactic reactions difficult (symptomatic coronary heart diseases, severe arterial hypertension and treatment with β-blockers)
Major metabolic disease
Known or suspected allergy to the study product
Obesity with BMI > 30 since subcutaneous fat makes ultrasound imaging of lymph nodes harder which may risk the correct placement of injection.
Patients who, in the opinion of the investigator, abuse alcohol or drugs within 2 years prior to Visit 1.
Patients who have taken an investigational drug within 1 month or six half lives, whichever is greater, prior to Visit 1.
Mental incapability of coping with the study
Withdrawal of informed consent