Andosan in Allergic and Asthma Patients
Primary Purpose
Allergic Asthma, Allergic Rhinoconjunctivitis, Immune Tolerance
Status
Completed
Phase
Not Applicable
Locations
Norway
Study Type
Interventional
Intervention
Andosan
Placebo
Sponsored by

About this trial
This is an interventional other trial for Allergic Asthma focused on measuring ASIT, SLIT, Andosan
Eligibility Criteria
Inclusion Criteria:
- FOR PART 1
- Asthma or allergy patients that are eligible for ASIT (Allergen specific immunotherapy).
- Age above 18.
- Able to understand written and oral Norwegian
- FOR PART 2
- Positive metacholine provocation test (Newly diagnosed with asthma)
- Age above 18.
- Able to perform spirometry at home independently.
Exclusion Criteria:
- none other than not meeting the inclusion criteria
Sites / Locations
- Akershus university hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Andosan
Placebo
Arm Description
The Agaricus blazei Murill-based mushroom extract, Andosan™, is given as one dosage 100 ml/day orally for 1 month. The intervention solution is given in a neutral plastic container
The placebo is drinking water with brownish food coloring, given as one dosage 100 ml/day orally for 1 month. The placebo solution is given in a neutral plastic container (same as for intervention/experimental solution).
Outcomes
Primary Outcome Measures
FEV1
Change in FEV1 within-day variation (%) from run-in-period of last five days of intervention.
Secondary Outcome Measures
Oscillometry
change in small airway obstruction as measured by the R5Hz and R5-20Hz level in oscillometry.
Questionnaire ACT
Change in asthma symptoms, as measured by the asthma control test
Questionnaire RQLQ
Change in burden of asthma symptoms measured by RQLQ (Respiratory questionnaire of life quality)
Mast cell activation in serum
Difference in activation of mast cells measured in serum before and after intervention
Immunoglobulin E in serum
difference in concentration before and after intervention
Eosinophiles
difference in eosinophile count before and after intervention.
Full Information
NCT ID
NCT05192720
First Posted
September 2, 2021
Last Updated
February 2, 2023
Sponsor
University Hospital, Akershus
Collaborators
Oslo University Hospital, ImmunoPharma AS
1. Study Identification
Unique Protocol Identification Number
NCT05192720
Brief Title
Andosan in Allergic and Asthma Patients
Official Title
Effect of Supplementary Treatment With Agaricus Blazei Based Mushroom Extract, Andosan, on Patients With Asthma and Allergy
Study Type
Interventional
2. Study Status
Record Verification Date
February 2023
Overall Recruitment Status
Completed
Study Start Date
August 31, 2021 (Actual)
Primary Completion Date
December 31, 2022 (Actual)
Study Completion Date
December 31, 2022 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Hospital, Akershus
Collaborators
Oslo University Hospital, ImmunoPharma AS
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Examine whether daily oral ingestion of a immunomodulatory mushroom extract (AndoSanTM) in patients with asthma and allergy, undergoing allergen specific immunotherapy or who have asthma proven by metacholine provocation test, experience clinical and biochemical improvement in their disease.
A prospective randomised study comparing the mushroom extract with placebo.
Detailed Description
Asthma and allergy are increasing in Norway and Western countries. Treatment is still mostly symptomatic. Extracts of the immunomodulatory and edible mushroom Agaricus blazei, such as Andosan™, have been shown to protect against asthma and allergy in murine models by changing the T helper cell 1(upregulation)-T helper cell 2 (downregulation) balance in the immune system. Positive effects on allergy were also shown in a RCT on blood donors with selfreported allergy. Andosan™ is produced in Japan and approved as food (mushroom juice) in Norway.
The aim of this study is to examine whether Andosan™ i) has similar clinical effects against allergy and asthma in patients as it has in mice, and as earlier shown in a study on blood donors with allergy ii) wether patients taking Andosan has any clinical impact on asthma while taken as supplementary treatment in addition to other medication compared to a placebo group while going through allergen specific immunotherapy (ASIT).
iii) Investigate if Andosan taken for two weeks has any effect on bronchial reactivity measured through spirometry done five days (as home spirometry twice daily) before and after treatment with Andosan in patients proven to have asthma with bronchial provocation test.
If the extract shows effect on these patients it support the hypotheses that Andosan helps against atopic diseases and facilitate the shift from Th-2 to Th-1 responses at a cellular level.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Allergic Asthma, Allergic Rhinoconjunctivitis, Immune Tolerance
Keywords
ASIT, SLIT, Andosan
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
25-30 patients in each arm receiving Andosan or placebo.
Masking
Participant
Masking Description
the patients do not know if they get Andosan or placebo.
Allocation
Randomized
Enrollment
34 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Andosan
Arm Type
Experimental
Arm Description
The Agaricus blazei Murill-based mushroom extract, Andosan™, is given as one dosage 100 ml/day orally for 1 month. The intervention solution is given in a neutral plastic container
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
The placebo is drinking water with brownish food coloring, given as one dosage 100 ml/day orally for 1 month. The placebo solution is given in a neutral plastic container (same as for intervention/experimental solution).
Intervention Type
Dietary Supplement
Intervention Name(s)
Andosan
Intervention Description
See also detailed study design, Mushroom juice based on Agaricus Blazei and two other types of mushroom.
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo
Intervention Description
drinking water with food colour
Primary Outcome Measure Information:
Title
FEV1
Description
Change in FEV1 within-day variation (%) from run-in-period of last five days of intervention.
Time Frame
20 days
Secondary Outcome Measure Information:
Title
Oscillometry
Description
change in small airway obstruction as measured by the R5Hz and R5-20Hz level in oscillometry.
Time Frame
20 days to four weeks
Title
Questionnaire ACT
Description
Change in asthma symptoms, as measured by the asthma control test
Time Frame
four weeks
Title
Questionnaire RQLQ
Description
Change in burden of asthma symptoms measured by RQLQ (Respiratory questionnaire of life quality)
Time Frame
four weeks
Title
Mast cell activation in serum
Description
Difference in activation of mast cells measured in serum before and after intervention
Time Frame
four weeks
Title
Immunoglobulin E in serum
Description
difference in concentration before and after intervention
Time Frame
four weeks
Title
Eosinophiles
Description
difference in eosinophile count before and after intervention.
Time Frame
20 days
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
FOR PART 1
Asthma or allergy patients that are eligible for ASIT (Allergen specific immunotherapy).
Age above 18.
Able to understand written and oral Norwegian
FOR PART 2
Positive metacholine provocation test (Newly diagnosed with asthma)
Age above 18.
Able to perform spirometry at home independently.
Exclusion Criteria:
- none other than not meeting the inclusion criteria
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Faiza Mahmood
Organizational Affiliation
University Hospital, Akershus
Official's Role
Principal Investigator
Facility Information:
Facility Name
Akershus university hospital
City
Lørenskog
State/Province
Viken
ZIP/Postal Code
1478
Country
Norway
12. IPD Sharing Statement
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Andosan in Allergic and Asthma Patients
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