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DOI 10.1089/cap.2012.0126

Медицинская библиотека · Journal of child and adolescent psychopharmacology · 2014

Safety and tolerability of desvenlafaxine in children and adolescents with major depressive disorder.

Findling Robert L, Groark James, Chiles Deborah, Ramaker Sara, Yang Lingfeng, Tourian Karen A

СтатьяМногоцентровое исследованиеРандомизированное исследованиеПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

OBJECTIVE

The purpose of this study was to assess long-term safety and tolerability of desvenlafaxine (administered as desvenlafaxine succinate) in children and adolescents with major depressive disorder (MDD).

METHODS

An 8 week, multicenter, open-label, fixed-dose study of children (ages 7-11 years) and adolescents (ages 12-17 years) with MDD was followed by a 6 month, flexible-dose extension study. Patients were administered desvenlafaxine 10-100 mg/day (children) or 25-200 mg/day (adolescents) for a total of 8 months. Treatment-emergent adverse events (AEs), withdrawals because of AEs, laboratory tests, vital signs, and the Columbia Suicide-Severity Rating Scale (C-SSRS) were collected. Eight month safety results from the lead-in plus extension studies are reported for extension study participants, using lead-in study day -1 as baseline.

RESULTS

Forty patients were enrolled in both studies (20 children; 20 adolescents). Of those, four children and three adolescents withdrew because of AEs. Treatment-emergent AEs reported by three or more patients were upper abdominal pain (15%) and headache (15%) in children, and somnolence (30%), nausea (20%), upper abdominal pain (15%), and headache (15%) in adolescents. Negativism (oppositional behavior) in a child was the single serious AE reported. No deaths occurred during the lead-in or extension studies. Mean pulse rates demonstrated statistically significant increases from lead-in study baseline to final evaluation (children, +5.2 bpm; adolescents, +5.9 bpm; p≤0.05). No statistically significant change in blood pressure was observed at final evaluation. Two adolescents (0 children) reported suicidal ideation on the C-SSRS at screening assessment and during the lead-in and/or extension trials; one adolescent reported suicidal ideation after screening only.

CONCLUSIONS

Long-term (8 month) treatment with desvenlafaxine was generally safe and well tolerated in depressed children and adolescents.

Для цитирования: Findling Robert L, Groark James, Chiles Deborah, Ramaker Sara, Yang Lingfeng, Tourian Karen A. Safety and tolerability of desvenlafaxine in children and adolescents with major depressive disorder.. Journal of child and adolescent psychopharmacology. 2014. DOI: 10.1089/cap.2012.0126.

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