Department of Pharmaceutical Biosciences, Uppsala University, Uppsala, Sweden.
J Clin Pharmacol. 2013 Jun;53(6):589-600. doi: 10.1002/jcph.86. Epub 2013 Apr 22.
Predicting late phase outcomes from early-phase findings can help inform decisions in drug development. If the measurements in early-phase differ from those in late phase, forecasting is more challenging. In this paper, we present a model-based approach for predicting glycosylated hemoglobin (HbA1c) in late phase using glucose and insulin concentrations from an early-phase study, investigating an anti-diabetic treatment. Two previously published models were used; an integrated glucose and insulin (IGI) model for meal tolerance tests and an integrated glucose-red blood cell-HbA1c (IGRH) model predicting the formation of HbA1c from the average glucose concentration (Cg,av ). Output from the IGI model was used as input to the IGRH model. Parameters of the IGI model and drug effects were estimated using data from a phase1 study in 59 diabetic patients receiving various doses of a glucokinase activator. Cg,av values were simulated according to a Phase 2 study design and used in the IGRH model for predictions of HbA1c. The performance of the model-based approach was assessed by comparing the predicted to the actual outcome of the Phase 2 study. We have shown that this approach well predicts the longitudinal HbA1c response in a 12-week study using only information from a 1-week study where glucose and insulin concentrations were measured.
从早期发现预测后期结果有助于为药物开发决策提供信息。如果早期阶段的测量值与晚期阶段的测量值不同,则预测就更具挑战性。在本文中,我们提出了一种基于模型的方法,用于使用早期研究中的葡萄糖和胰岛素浓度来预测晚期糖化血红蛋白(HbA1c),研究一种抗糖尿病治疗方法。我们使用了两种以前发表的模型;用于餐耐量试验的整合葡萄糖和胰岛素(IGI)模型,以及从平均葡萄糖浓度(Cg,av)预测 HbA1c 形成的整合葡萄糖-红细胞-HbA1c(IGRH)模型。IGI 模型的输出被用作 IGRH 模型的输入。使用 59 名接受各种剂量葡萄糖激酶激活剂的糖尿病患者的 1 期研究中的数据来估计 IGI 模型的参数和药物作用。根据 2 期研究设计模拟 Cg,av 值,并在 IGRH 模型中用于预测 HbA1c。通过将预测值与 2 期研究的实际结果进行比较,评估了基于模型的方法的性能。我们已经表明,这种方法仅使用测量葡萄糖和胰岛素浓度的 1 周研究中的信息,就可以很好地预测 12 周研究中的纵向 HbA1c 反应。