ClinConnect ClinConnect Logo
Search / Trial NCT04881461

A Study in Adults With Grass Pollen-induced Rhinoconjunctivitis

Launched by ALK-ABELLÓ A/S · May 10, 2021

Trial Information

Current as of May 28, 2025

Completed

Keywords

Allergic Rhinoconjunctivitis Adults Grass

ClinConnect Summary

This trial is a 2 year, parallel-group, double-blind, placebo-controlled phase III trial to evaluate efficacy and safety of the 5-grass mix SLIT-drops in adults with grass pollen-induced rhinoconjunctivitis with or without asthma. Approximately 440 adults will be enrolled in the trial and will receive the 5-grass mix SLIT-drops or placebo. The trial is conducted in several European countries.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • 1. Male or female aged ≥18 years on the day informed consent is obtained
  • 2. A clinical history of grass pollen-induced allergic rhinoconjunctivitis for two years or more with or without asthma
  • 3. A clinical history of severe allergic rhinoconjunctivitis symptoms (interfering with usual daily activities or sleep) induced by grass pollen, which remain troublesome despite symptomatic treatment with antihistamines, nasal steroids or eye drops during the previous grass pollen season
  • 4. Positive specific immunoglobulin E (IgE) (defined as ≥class 2, ≥0.70 kU/l) against grass: Phleum pratense
  • 5. Positive skin prick test to Phleum pratense at screening
  • Exclusion Criteria:
  • 1. Has a clinically relevant history of symptomatic seasonal and/or perennial allergic rhinoconjunctivitis and/or asthma caused by an allergen other than grass pollen, to which the subject is exposed, which could potentially overlap with the efficacy assessment periods
  • 2. Within the last 3 months before the randomisation visit, has had an occurrence of any clinical deterioration of asthma that resulted in emergency treatment, hospitalisation, or treatment with systemic corticosteroids
  • 3. SLIT treatment with any grass pollen AIT for more than 1 month within the last 5 years. In addition, any SLIT treatment with grass pollen AIT within the previous 12 months
  • 4. SCIT treatment with any grass AIT reaching the maintenance dose within the last 5 years. In addition, any SCIT treatment with grass AIT within the previous 12 months
  • 5. Ongoing treatment with any allergy immunotherapy product
  • 6. Uncontrolled or severe asthma requiring daily use of more than 800 mcg budesonide or equivalent at screening

About Alk Abelló A/S

ALK-Abelló A/S is a global biopharmaceutical company specializing in the development of innovative allergy immunotherapy treatments. With a strong commitment to improving patient outcomes, ALK focuses on research and development of products that address various allergic conditions, including asthma, rhinitis, and food allergies. Leveraging advanced scientific expertise and a robust pipeline of therapies, ALK aims to enhance the quality of life for individuals affected by allergies while adhering to the highest standards of safety and efficacy in clinical trial practices. The company is dedicated to advancing the field of allergy treatment through collaboration and innovation.

Locations

Tallinn, , Estonia

Strasbourg, , France

Kaunas, , Lithuania

Poznań, , Poland

Jablonec Nad Nisou, , Czechia

Jihlava, , Czechia

Tábor, , Czechia

Brno, , Czechia

Liberec, , Czechia

Litomyšl, , Czechia

Pardubice, , Czechia

Trutnov, , Czechia

české Budějovice, , Czechia

Loiré, Saint étienne, France

Fenouillet, , France

Hyeres, , France

Joué Lés Tours, , France

Paris, , France

Rezé, , France

Saint Quentin, , France

Toulouse, , France

Balvi, , Latvia

Daugavpils, , Latvia

Riga, , Latvia

Riga, , Latvia

Rēzekne, , Latvia

ādaži, , Latvia

Kaunas, , Lithuania

Klaipėda, , Lithuania

Vilnius, , Lithuania

Vilnius, , Lithuania

Vilnius, , Lithuania

Vilnius, , Lithuania

Vilnius, , Lithuania

Kraków, Malopolskie, Poland

Tarnów, Maopolskie, Poland

Poznań, Wielkopolskie, Poland

Kielce, , Poland

Kraków, , Poland

Kraków, , Poland

Kraków, , Poland

Lublin, , Poland

Poznań, , Poland

Rzeszów, , Poland

Tomaszów Mazowiecki, , Poland

Wrocław, , Poland

Wrocław, , Poland

Wrocław, , Poland

Kaunas, Kauno Apskritis, Lithuania

Patients applied

0 patients applied

Trial Officials

Laurent Guilleminault, MD

Principal Investigator

CHU Hôpital Larrey

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

Similar Trials