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
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.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
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
Trial Officials
Laurent Guilleminault, MD
Principal Investigator
CHU Hôpital Larrey
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
Similar Trials