Clinical Pharmacology and Pharmacometrics, Biogen, 225 Binney Street, Cambridge, MA, USA.
Kowalski PMetrics Consulting, LLC, 44569 Larchwood Drive, Northville, MI, USA.
J Pharmacokinet Pharmacodyn. 2023 Feb;50(1):45-62. doi: 10.1007/s10928-022-09839-3. Epub 2023 Jan 4.
Clinical Dementia Rating-Sum of Boxes (CDR-SB) assessments from two Phase 3 studies (ENGAGE and EMERGE) of aducanumab in subjects with early Alzheimer's disease (AD) were pooled to develop an exposure-response (ER) model. A linear model in the logit-transformed scaled CDR-SB best characterized the time profile for placebo- and aducanumab-treated subjects, with concentration as the exposure metric. The model allowed delineation of slow (4%), typical (86%), and fast (10%) progressing subpopulations in the data. The estimated drug effect on the disease progression rate was significant, 2.05 L/(g·year), with a 95% confidence interval (1.60, 2.50) that did not include zero. Following an evaluation of a series of ER model forms including differential drug and null effects either between the studies or among the three progression classes, the final ER model with a common (pooled) estimate of the drug effect between the studies and among the three progression classes was considered parsimonious. The final model provides supportive evidence that the two studies demonstrate a common intrinsic pharmacology. None of the identified covariates (Mini-Mental State Examination-BL score and Asian race) were clinically meaningful. Finally, simulations demonstrated that the intrinsic pharmacology remained consistent between the two Phase 3 studies.
对来自两项 aducanumab 治疗早期阿尔茨海默病(AD)的 3 期研究(ENGAGE 和 EMERGE)的临床痴呆评定量表总和评分(CDR-SB)进行了汇总,以建立暴露-反应(ER)模型。对数转换后的 CDR-SB 中线性模型最能描述安慰剂和 aducanumab 治疗组的时间曲线,以浓度作为暴露指标。该模型允许对数据中的缓慢(4%)、典型(86%)和快速(10%)进展亚群进行区分。药物对疾病进展速度的估计影响显著,为 2.05 L/(g·年),95%置信区间(1.60,2.50)不包括零。在评估了一系列 ER 模型形式后,包括研究之间或三种进展类别之间的药物和无效效应的差异,最终 ER 模型考虑了研究之间和三种进展类别之间药物效应的共同(汇总)估计,被认为是简约的。最终模型提供了支持性证据,表明这两项研究显示出共同的内在药理学。未发现有临床意义的识别变量(简易精神状态检查-基础评分和亚洲种族)。最后,模拟结果表明,两种 3 期研究中的内在药理学保持一致。