Evidence map›Paper›PMID 26342289›Full record

Trial reportInflammation research : official journal of the European Histamine Research Society ... [et al.]2015

Biological effects and clinical efficacy of a topical Toll-like receptor 7 agonist in seasonal allergic rhinitis: a parallel group controlled phase IIa study.

Lennart Greiff, Cecilia Ahlström-Emanuelsson, Mikaela Alenäs, Gun Almqvist, Morgan Andersson, Anders Cervin, Jan Dolata, Sam Lindgren, Anders Mårtensson, Barbara Young and 1 more

Registry-linked trialAbstract readClinical Trial, Phase IIRandomized Controlled Trial
PubMed Publisher
In one paragraph

Trial report in Inflammation research : official journal of the European Histamine Research Society ... [et al.], 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00770003 (A Double-blind, Placebo Controlled, Randomized, Parallel Group Study to Investigate the Tolerability, Safety, Pharmacodynamics and Pharmacokinetics of Repeated Weekly Doses of AZD8848 Administered Intranasally to Seasonal Allergic Rhinitis Patients), which is not on this map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.3field-weighted citation impact, top 12% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT00770003 phase1completednot on this map

A Double-blind, Placebo Controlled, Randomized, Parallel Group Study to Investigate the Tolerability, Safety, Pharmacodynamics and Pharmacokinetics of Repeated Weekly Doses of AZD8848 Administered Intranasally to Seasonal Allergic Rhinitis Patients

TypeinterventionalSponsorAstraZenecaRan2008 to 2010Enrolled103ConditionsAllergic RhinitisArmsAZD8848, Placebo
3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 27 citations in OpenAlex.

  1. Nasal administration of a probiotic assemblage in allergic rhinitis: A randomised placebo-controlled crossover trial.Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology · 2022
    Trial
  2. Trial
  3. Review
  4. Review
  5. Review
  6. Article
  7. EAACI Allergen Immunotherapy User's Guide.Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology · 2020
    Review
  8. Article
  9. Targeting Antiviral Pathways for Treatment of Allergic Diseases.Journal of the Pediatric Infectious Diseases Society · 2018
    Article
  10. Article
  11. Review
  12. Toll-Like Receptor 7-Targeted Therapy in Respiratory Disease.Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie · 2016
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 4 institutions in 2 countries.

Lennart GreiffDepartment of ORL, Head & Neck Surgery, Skåne University Hospital, Getingevägen 4, 221 85, Lund, Sweden. lennart.greiff@skane.se.
Cecilia Ahlström-EmanuelssonDepartment of ORL, Head & Neck Surgery, Skåne University Hospital, Getingevägen 4, 221 85, Lund, Sweden.
Mikaela AlenäsResearch & Development, AstraZeneca, Lund, Sweden.
Gun AlmqvistResearch & Development, AstraZeneca, Mölndal, Sweden.
Morgan AnderssonDepartment of ORL, Head & Neck Surgery, Skåne University Hospital, Getingevägen 4, 221 85, Lund, Sweden.
Anders CervinDepartment of ORL, Helsingborg Hospital, Helsingborg, Sweden.
Jan DolataDepartment of ORL, Helsingborg Hospital, Helsingborg, Sweden.
Sam LindgrenResearch & Development, AstraZeneca, Mölndal, Sweden.
Anders MårtenssonDepartment of ORL, Helsingborg Hospital, Helsingborg, Sweden.
Barbara YoungResearch & Development, AstraZeneca, Loughborough, UK.
Henrik WidegrenDepartment of ORL, Head & Neck Surgery, Skåne University Hospital, Getingevägen 4, 221 85, Lund, Sweden.
AstraZeneca (Sweden) · SEGetinge (Sweden) · SEHelsingborgs lasarett · SELoughborough University · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

OBJECTIVE AND

designThe purpose of the study was to examine effects of pre-treatment with a Toll-like receptor 7 (TLR7) agonist (AZD8848) in allergic rhinitis and to evaluate clinical effects of two dosing regimens. SUBJECTS: The study involved 83 patients with allergic rhinitis. Data on effects of AZD8848 on symptoms were analysed with data from a previous study (n = 68) of identical double blind, parallel group design (NCT00770003). TREATMENT: The treatment involved intranasal AZD8848 20 µg three times weekly, 60 µg once weekly, or placebo for 5 weeks.

methodsNasal lavage and plasma were analysed for proof-of-mechanism markers. Daily nasal allergen challenges were given for 7 days, starting 24 h after the final AZD8848 dose. Symptoms were monitored after each challenge and every morning and evening.

resultsMarkers of TLR-activation increased following AZD8848 administration (CXCL10, TNFα, IL-6, IFNγ). Symptoms recorded soon after allergen challenge were reduced up to eight days after the final dose of AZD8848. Morning and evening symptoms were also reduced, and these changes reached statistical significance for morning observations. Adverse effects were more frequent in the 20 µg three times weekly group.

conclusionsRepeated administration of AZD8848 activated TLR7 and produced IFN-induced effects. This was associated with a sustained reduction in allergen responsiveness.

Indexed as

AdenosineAdministration, TopicalAdolescentAdultAllergensAnti-Allergic AgentsBetulaCytokinesDouble-Blind MethodFemaleGene ExpressionHumansMaleMiddle AgedNasal Lavage FluidPhenylacetatesAdenosineAllergensAnti-Allergic AgentsAZD8848CytokinesPhenylacetatesTLR7 protein, humanToll-Like Receptor 7Allergen challengeBiomarkersCXCL-10IFNγIntranasal TLR7 stimulationNasal lavage

Identifiers

PMID26342289
OpenAlexW2108375278

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.