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Phase 3 Trial of Crinecerfont in Pediatric Congenital Adrenal Hyperplasia

雄烯二酮 医学 先天性肾上腺增生 安慰剂 内科学 抗糖皮质激素 内分泌学 糖皮质激素 随机化 氢化可的松 随机对照试验 激素 糖皮质激素受体 雄激素 病理 替代医学
作者
Kyriakie Sarafoglou,Mimi S. Kim,Maya Lodish,Eric I. Felner,Lætitia Martinerie,Natalie Nokoff,María Clemente,Patricia Y. Fechner,Maria Vogiatzi,Phyllis Speiser,Henrik Falhammar,G Rosales,Ε. H. Roberts,George Jeha,Robert Farber,Jean L. Chan
出处
期刊:The New England Journal of Medicine [New England Journal of Medicine]
卷期号:391 (6): 493-503 被引量:4
标识
DOI:10.1056/nejmoa2404655
摘要

BackgroundChildren with classic congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency require treatment with glucocorticoids, usually at supraphysiologic doses, to address cortisol insufficiency and reduce excess adrenal androgens. However, such treatment confers a predisposition to glucocorticoid-related complications. In 2-week phase 2 trials, patients with CAH who received crinecerfont, a new oral corticotropin-releasing factor type 1 receptor antagonist, had decreases in androstenedione levels.MethodsIn this phase 3, multinational, randomized trial, we assigned pediatric participants with CAH, in a 2:1 ratio, to receive crinecerfont or placebo for 28 weeks. A stable glucocorticoid dose was maintained for 4 weeks, and the dose was then adjusted to a target of 8.0 to 10.0 mg per square meter of body-surface area per day (hydrocortisone dose equivalents), provided that the androstenedione level was controlled (≤120% of the baseline level or within the reference range). The primary efficacy end point was the change in the androstenedione level from baseline to week 4. A key secondary end point was the percent change in the glucocorticoid dose from baseline to week 28 while androstenedione control was maintained.ResultsA total of 103 participants underwent randomization, of whom 69 were assigned to the crinecerfont group and 34 to the placebo group; 100 (97%) remained in the trial at 28 weeks. At baseline, the mean glucocorticoid dose was 16.4 mg per square meter per day, and the mean androstenedione level was 431 ng per deciliter (15.0 nmol per liter). At week 4, the androstenedione level was substantially reduced in the crinecerfont group (−197 ng per deciliter [−6.9 nmol per liter]) but increased in the placebo group (71 ng per deciliter [2.5 nmol per liter]) (least-squares mean difference, −268 ng per deciliter [−9.3 nmol per liter]; P<0.001); the observed mean androstenedione value, obtained before the morning glucocorticoid dose, was 208 ng per deciliter (7.3 nmol per liter) in the crinecerfont group, as compared with 545 ng per deciliter (19.0 nmol per liter) in the placebo group. At week 28, the mean glucocorticoid dose had decreased (while androstenedione control was maintained) by 18.0% with crinecerfont but increased by 5.6% with placebo (least-squares mean difference, −23.5 percentage points; P<0.001). Headache, pyrexia, and vomiting were the most common adverse events.ConclusionsIn this phase 3 trial, crinecerfont was superior to placebo in reducing elevated androstenedione levels in pediatric participants with CAH and was also associated with a decrease in the glucocorticoid dose from supraphysiologic to physiologic levels while androstenedione control was maintained. (Funded by Neurocrine Biosciences; CAHtalyst Pediatric ClinicalTrials.gov number, NCT04806451.)
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