1. Safety and efficacy of azilsartan in paediatric patients with hypertension: a phase 3, single-arm, open-label, prospective study
- Author
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Kazuaki Enya, Kenkichi Sugiura, Yuya Nishiyama, and Shuichi Ito
- Subjects
Nephrology ,medicine.medical_specialty ,Adolescent ,Physiology ,Blood Pressure ,Physiology (medical) ,Internal medicine ,Azilsartan ,medicine ,Humans ,Prospective Studies ,Prospective cohort study ,Adverse effect ,Child ,Antihypertensive Agents ,Oxadiazoles ,business.industry ,Acute kidney injury ,medicine.disease ,Discontinuation ,Blood pressure ,Tolerability ,Hypertension ,Benzimidazoles ,business ,medicine.drug - Abstract
Background Azilsartan is an angiotensin II receptor blocker indicated for the treatment of adult hypertension. A previous single-dose study suggested that azilsartan may also be a promising agent for paediatric hypertension. However, the long-term safety and efficacy of azilsartan in children have not been established. Methods We conducted a phase 3, single-arm, open-label, prospective study to evaluate the safety and efficacy of azilsartan in pediatric patients with hypertension. Twenty-seven patients aged 6–15 years were treated with once-daily azilsartan for 52 weeks. The starting dose was 2.5 mg for patients weighing N = 22) and 5 mg for patients weighing ≥ 50 kg (N = 5), with doses titrated up to a maximum of 20 and 40 mg, respectively. Results Azilsartan showed acceptable tolerability at doses up to 20 mg in patients weighing Conclusions Our study suggests that azilsartan has an acceptable safety profile in hypertensive patients aged 6–15 years. Azilsartan may be a promising agent for treating paediatric hypertension.
- Published
- 2021