Evidence Gaps in Clinical Trials of Pharmacologic Treatment for H1-Antihistamine-Refractory Chronic Spontaneous Urticaria: A Systematic Review and Future Perspectives

No data addressing issues concerning disparities in participant and trial characteristics and trial outcome reporting have been established in clinical trials for H1-antihistamine-refractory chronic spontaneous urticaria (CSU). To better harmonize and compare the different treatment interventions, w...

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Main Authors: Surapon Nochaiwong (Author), Mati Chuamanochan (Author), Chidchanok Ruengorn (Author), Kednapa Thavorn (Author)
Format: Book
Published: MDPI AG, 2022-10-01T00:00:00Z.
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100 1 0 |a Surapon Nochaiwong  |e author 
700 1 0 |a Mati Chuamanochan  |e author 
700 1 0 |a Chidchanok Ruengorn  |e author 
700 1 0 |a Kednapa Thavorn  |e author 
245 0 0 |a Evidence Gaps in Clinical Trials of Pharmacologic Treatment for H1-Antihistamine-Refractory Chronic Spontaneous Urticaria: A Systematic Review and Future Perspectives 
260 |b MDPI AG,   |c 2022-10-01T00:00:00Z. 
500 |a 10.3390/ph15101246 
500 |a 1424-8247 
520 |a No data addressing issues concerning disparities in participant and trial characteristics and trial outcome reporting have been established in clinical trials for H1-antihistamine-refractory chronic spontaneous urticaria (CSU). To better harmonize and compare the different treatment interventions, we systematically evaluated the overall landscape of pharmacological treatments for H1-antihistamine-refractory CSU clinical trials published between 2000 and 2021. This systematic review included 23 randomized clinical trials involving 2480 participants from 22 countries. We found significant increases in the number of globally published and newly tested drugs, especially biologic drugs. Regarding relatively small trials, we found that people living with H1-antihistamine-refractory CSU who were identified as members of minority groups (non-white population), populations of regions other than North America/Europe, and populations of low- to lower/upper-middle-income countries are underrepresented. Most trials were designed to evaluate treatment efficacy and safety profiles; however, less than half of the included trials reported the patient's perspective in terms of patient-reported outcomes. Disparities in outcome reporting, including clinimetric tools for assessing treatment response and outcome sets, were observed. To close the evidence gap in H1-antihistamine-refractory CSU trials, strategies for improving trial and participant enrollment and standardizing core outcome sets for trial reporting are needed. 
546 |a EN 
690 |a biologic agents 
690 |a chronic spontaneous urticaria 
690 |a clinical trials 
690 |a core outcomes sets 
690 |a evidence gaps 
690 |a H1-antihistamine-refractory 
690 |a Medicine 
690 |a R 
690 |a Pharmacy and materia medica 
690 |a RS1-441 
655 7 |a article  |2 local 
786 0 |n Pharmaceuticals, Vol 15, Iss 10, p 1246 (2022) 
787 0 |n https://www.mdpi.com/1424-8247/15/10/1246 
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