Two Phase II randomized trials on the CRTh2 antagonist AZD1981 in adults with asthma

Piotr Kuna,1 Leif Bjermer,2 Göran Tornling3,4 1Department of Internal Medicine, Asthma and Allergy, Barlicki University Hospital, Medical University of Łódz, Łódz, Poland; 2Department of Respiratory Medicine and Allergology, Skane University Hospital, Lund University,...

Full description

Bibliographic Details
Main Authors: Kuna P, Bjermer L, Tornling G
Format: Article
Language:English
Published: Dove Medical Press 2016-08-01
Series:Drug Design, Development and Therapy
Subjects:
Online Access:https://www.dovepress.com/two-phase-ii-randomized-trials-on-the-crth2-antagonist-azd1981-in-adul-peer-reviewed-article-DDDT
_version_ 1819176717453885440
author Kuna P
Bjermer L
Tornling G
author_facet Kuna P
Bjermer L
Tornling G
author_sort Kuna P
collection DOAJ
description Piotr Kuna,1 Leif Bjermer,2 Göran Tornling3,4 1Department of Internal Medicine, Asthma and Allergy, Barlicki University Hospital, Medical University of Łódz, Łódz, Poland; 2Department of Respiratory Medicine and Allergology, Skane University Hospital, Lund University, 3AstraZeneca Research and Development, Molndal, 4Respiratory Medicine Unit, Department of Medicine Solna and CMM, Karolinska Institute and Karolinska University Hospital, Solna, Sweden Background: Chemoattractant receptor-homologous molecule expressed on T helper type 2 (Th2) cell (CRTh2) receptor antagonists is being investigated for asthma.Objectives: The aim of this study was to assess the effects of the CRTh2 receptor antagonist, AZD1981 (with/without inhaled corticosteroids [ICSs]), on lung function and asthma control.Patients and methods: Adults aged 18–60 years were enrolled in two randomized, placebo-controlled, parallel-group trials (protocol number: D9830C00003 [study 1, n=209] and protocol number: D9830C00004 [study 2, n=510]). In study 1, patients with stable asthma (forced expiratory volume in 1 second [FEV1]: 65%-110%) were withdrawn from ICS (<400 µg/d) and randomized to AZD1981 1,000 mg twice daily (bid) or placebo. In study 2, patients with uncontrolled asthma (FEV1: 40%-85%) despite ICS therapy (≥500 µg/d) were randomized to 50 mg, 400 mg, or 1,000 mg bid AZD1981 or placebo. The primary efficacy variable for both trials was the change in morning peak expiratory flow after 4 weeks of treatment. Secondary variables included Asthma Control Questionnaire (ACQ-5) scores, FEV1 assessments, safety, and tolerability. In study 2, efficacy was also assessed according to atopic status.Results: Following 4 weeks of treatment, there was a nonsignificant increase in morning peak expiratory flow on AZD1981 1,000 mg bid (9.5 L/min vs placebo, P=0.086 [study 1] and 12 L/min vs placebo, P=0.16 [study 2]). In study 2, all doses of AZD1981 provided significant improvements in ACQ-5 scores (0.26–0.3 units vs placebo, P=0.010–0.022); however, there was no dose–response relationship. Improved ACQ-5 scores and FEV1 were observed in the majority of atopic patients treated with AZD1981. AZD1981 was well tolerated across treatment groups.Conclusion: Further research may be warranted in atopic patients to fully evaluate the clinical efficacy of AZD1981. Keywords: CRTh2 receptor, efficacy, Phase II, respiratory, Th2 cells, prostaglandin D2
first_indexed 2024-12-22T21:15:12Z
format Article
id doaj.art-4ff84bcda2df4fcebf28e440aa45dc24
institution Directory Open Access Journal
issn 1177-8881
language English
last_indexed 2024-12-22T21:15:12Z
publishDate 2016-08-01
publisher Dove Medical Press
record_format Article
series Drug Design, Development and Therapy
spelling doaj.art-4ff84bcda2df4fcebf28e440aa45dc242022-12-21T18:12:22ZengDove Medical PressDrug Design, Development and Therapy1177-88812016-08-01Volume 102759277028686Two Phase II randomized trials on the CRTh2 antagonist AZD1981 in adults with asthmaKuna PBjermer LTornling GPiotr Kuna,1 Leif Bjermer,2 Göran Tornling3,4 1Department of Internal Medicine, Asthma and Allergy, Barlicki University Hospital, Medical University of Łódz, Łódz, Poland; 2Department of Respiratory Medicine and Allergology, Skane University Hospital, Lund University, 3AstraZeneca Research and Development, Molndal, 4Respiratory Medicine Unit, Department of Medicine Solna and CMM, Karolinska Institute and Karolinska University Hospital, Solna, Sweden Background: Chemoattractant receptor-homologous molecule expressed on T helper type 2 (Th2) cell (CRTh2) receptor antagonists is being investigated for asthma.Objectives: The aim of this study was to assess the effects of the CRTh2 receptor antagonist, AZD1981 (with/without inhaled corticosteroids [ICSs]), on lung function and asthma control.Patients and methods: Adults aged 18–60 years were enrolled in two randomized, placebo-controlled, parallel-group trials (protocol number: D9830C00003 [study 1, n=209] and protocol number: D9830C00004 [study 2, n=510]). In study 1, patients with stable asthma (forced expiratory volume in 1 second [FEV1]: 65%-110%) were withdrawn from ICS (<400 µg/d) and randomized to AZD1981 1,000 mg twice daily (bid) or placebo. In study 2, patients with uncontrolled asthma (FEV1: 40%-85%) despite ICS therapy (≥500 µg/d) were randomized to 50 mg, 400 mg, or 1,000 mg bid AZD1981 or placebo. The primary efficacy variable for both trials was the change in morning peak expiratory flow after 4 weeks of treatment. Secondary variables included Asthma Control Questionnaire (ACQ-5) scores, FEV1 assessments, safety, and tolerability. In study 2, efficacy was also assessed according to atopic status.Results: Following 4 weeks of treatment, there was a nonsignificant increase in morning peak expiratory flow on AZD1981 1,000 mg bid (9.5 L/min vs placebo, P=0.086 [study 1] and 12 L/min vs placebo, P=0.16 [study 2]). In study 2, all doses of AZD1981 provided significant improvements in ACQ-5 scores (0.26–0.3 units vs placebo, P=0.010–0.022); however, there was no dose–response relationship. Improved ACQ-5 scores and FEV1 were observed in the majority of atopic patients treated with AZD1981. AZD1981 was well tolerated across treatment groups.Conclusion: Further research may be warranted in atopic patients to fully evaluate the clinical efficacy of AZD1981. Keywords: CRTh2 receptor, efficacy, Phase II, respiratory, Th2 cells, prostaglandin D2https://www.dovepress.com/two-phase-ii-randomized-trials-on-the-crth2-antagonist-azd1981-in-adul-peer-reviewed-article-DDDTCRTh2 receptorefficacyphase IIrespiratoryTh2 cellsprostaglandin D2
spellingShingle Kuna P
Bjermer L
Tornling G
Two Phase II randomized trials on the CRTh2 antagonist AZD1981 in adults with asthma
Drug Design, Development and Therapy
CRTh2 receptor
efficacy
phase II
respiratory
Th2 cells
prostaglandin D2
title Two Phase II randomized trials on the CRTh2 antagonist AZD1981 in adults with asthma
title_full Two Phase II randomized trials on the CRTh2 antagonist AZD1981 in adults with asthma
title_fullStr Two Phase II randomized trials on the CRTh2 antagonist AZD1981 in adults with asthma
title_full_unstemmed Two Phase II randomized trials on the CRTh2 antagonist AZD1981 in adults with asthma
title_short Two Phase II randomized trials on the CRTh2 antagonist AZD1981 in adults with asthma
title_sort two phase ii randomized trials on the crth2 antagonist azd1981 in adults with asthma
topic CRTh2 receptor
efficacy
phase II
respiratory
Th2 cells
prostaglandin D2
url https://www.dovepress.com/two-phase-ii-randomized-trials-on-the-crth2-antagonist-azd1981-in-adul-peer-reviewed-article-DDDT
work_keys_str_mv AT kunap twophaseiirandomizedtrialsonthecrth2antagonistazd1981inadultswithasthma
AT bjermerl twophaseiirandomizedtrialsonthecrth2antagonistazd1981inadultswithasthma
AT tornlingg twophaseiirandomizedtrialsonthecrth2antagonistazd1981inadultswithasthma