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Efficacy, Safety, and Systemic Exposure of Once-Daily Indacaterol Acetate in Pediatric Asthma: A Randomized, Double-Blind, Controlled Dose-Finding Study.
Sekerel, Bulent Enis; Nell, Haylene; Laki, Istvan; Pak, Tatiana; Contreras, Edgar; Kolarz, Adam; D'Andrea, Peter; Manga, Volkan; Jain, Monish; Vaidya, Soniya; Valentin, Michele; Sen, Biswajit.
Afiliación
  • Sekerel BE; Pediatric Allergy and Asthma Division, Hacettepe University Faculty of Medicine, Ankara, Turkey. b_sekerel@yahoo.com.
  • Nell H; Tiervlei Trial Centre, Karl Bremer Hospital, Cape Town, South Africa.
  • Laki I; Department of Pediatric Pulmonology, Institute of Pulmonology, Törökbálint, Hungary.
  • Pak T; LLC PiterClinica, Saint-Petersburg, Russian Federation.
  • Contreras E; Médico Neumólogo e Internista, Director del Centro de Investigaciones de Latinoamerica, Guatemala City, Guatemala.
  • Kolarz A; Novartis Pharma AG, Basel, Switzerland.
  • D'Andrea P; Novartis Pharmaceuticals Corporation, East Hanover, NJ, USA.
  • Manga V; Novartis Pharmaceuticals Corporation, East Hanover, NJ, USA.
  • Jain M; Novartis Institutes for BioMedical Research, Cambridge, MA, USA.
  • Vaidya S; Novartis Institutes for BioMedical Research, Cambridge, MA, USA.
  • Valentin M; Novartis Pharmaceuticals Corporation, East Hanover, NJ, USA.
  • Sen B; Novartis Healthcare Pvt. Ltd, Hyderabad, India.
Clin Drug Investig ; 43(9): 719-728, 2023 Sep.
Article en En | MEDLINE | ID: mdl-37682405
ABSTRACT

BACKGROUND:

Indacaterol acetate (IND), a long-acting ß2-agonist in combination with mometasone furoate (MF), an inhaled corticosteroid (ICS), is being explored as a once-daily (od) treatment for asthma in children. This study examined the efficacy, safety, and systemic exposure of IND 75 µg and IND 150 µg in children with persistent asthma.

METHODS:

In this Phase IIb, multicenter, randomized, double-blind, parallel-group study, pediatric patients (aged ≥ 6 to < 12 years) with persistent asthma were randomized (11) to receive either IND 75 µg od or IND 150 µg od via Breezhaler® in combination with ICS background therapy. The primary endpoint was change from baseline in pre-dose trough forced expiratory volume in one second (FEV1) after two weeks of treatment.

RESULTS:

In total, 80 patients received IND 75 µg (n = 39) or IND 150 µg (n = 41). The study met its primary endpoint; both doses demonstrated improvements in pre-dose trough FEV1 from baseline to Day 14 (mean change [Δ] 212 mL, IND 75 µg; 171 mL, IND 150 µg). The secondary spirometry parameters (post-dose FEV1 after 1-h, post-dose forced vital capacity; morning and evening peak expiratory flow) also improved. Overall, 36.1% in IND 75 µg group and 25% patients in IND 150 µg group achieved a decrease from baseline in Pediatric Interviewer-administered Asthma Control Questionnaire score of ≥ 0.5 units. A dose-dependent increase in plasma IND concentration was noted between the two groups. Both IND doses demonstrated an acceptable safety profile.

CONCLUSIONS:

Once-daily IND 75 µg and IND 150 µg via Breezhaler® in combination with background ICS therapy provided substantial bronchodilation in children with asthma and were well tolerated. Taken together, these clinical and systemic exposure findings support IND 75 µg as the most appropriate dose for evaluation in Phase III trials in combination with MF in pediatric asthma. TRIAL REGISTRATION ClinicalTrials.gov (NCT02892019; 08-Sep-2016).
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Asma Tipo de estudio: Clinical_trials / Diagnostic_studies Límite: Child / Humans Idioma: En Revista: Clin Drug Investig Asunto de la revista: FARMACOLOGIA / TERAPIA POR MEDICAMENTOS Año: 2023 Tipo del documento: Article País de afiliación: Turquía

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Asma Tipo de estudio: Clinical_trials / Diagnostic_studies Límite: Child / Humans Idioma: En Revista: Clin Drug Investig Asunto de la revista: FARMACOLOGIA / TERAPIA POR MEDICAMENTOS Año: 2023 Tipo del documento: Article País de afiliación: Turquía