Genentech, Inc. , South San Francisco , California , USA.
Hepatology. 2023 Sep 1;78(3):847-862. doi: 10.1002/hep.32742. Epub 2022 Sep 12.
BFKB8488A is a bispecific antibody targeting fibroblast growth factor receptor 1c and Klothoβ. This phase 1b study assessed safety, tolerability, pharmacokinetics, immunogenicity, and pharmacodynamics of BFKB8488A in patients with type 2 diabetes mellitus (T2DM) or NAFLD.
Patients were randomized to receive multiple doses of BFKB8488A at various dose levels and dosing intervals (weekly, every 2 weeks, or every 4 weeks) or placebo for 12 weeks. The primary outcome was the safety of BFKB8488A. Overall, 153 patients (T2DM: 91; NAFLD: 62) were enrolled and received at least one dose of treatment. Of these, 102 patients (62.7%) reported at least one adverse event (BFKB8488A: 83 [68.6%]; placebo: 19 [59.4%]). BFKB8488A exhibited nonlinear pharmacokinetics, with greater than dose-proportional increases in exposure. The treatment-emergent antidrug antibody incidence was 22.7%. Overall, trends in exposure-dependent increases in high-density lipoprotein (HDL) and decreases in triglyceride levels were observed. Decreases in alanine aminotransferase and aspartate aminotransferase were 0.7% and 9.2% for medium exposure and 7.3% and 11.2% for high-exposure tertiles, compared with increases of 7.5% and 17% in the placebo group, respectively, at Day 85. In patients with NAFLD, the mean decrease from baseline liver fat was 13.0%, 34.5%, and 49.0% in the low-, medium-, and high-exposure tertiles, respectively, compared with 0.1% with placebo at Day 85.
BFKB8488A was adequately tolerated in patients with T2DM or NAFLD, leading to triglyceride reduction, HDL improvements, and trends in improvement in markers of liver health for both populations and marked liver fat reduction in patients with NAFLD. ( ClinicalTrials.gov : NCT03060538).
BFKB8488A 是一种针对成纤维细胞生长因子受体 1c 和 Klothoβ 的双特异性抗体。这项 1b 期研究评估了 BFKB8488A 在 2 型糖尿病(T2DM)或非酒精性脂肪性肝病(NAFLD)患者中的安全性、耐受性、药代动力学、免疫原性和药效学。
患者被随机分配接受不同剂量水平和给药间隔(每周、每 2 周或每 4 周)的 BFKB8488A 多次给药或安慰剂治疗 12 周。主要结局是 BFKB8488A 的安全性。共有 153 名患者(T2DM:91 名;NAFLD:62 名)入组并接受了至少一剂治疗。其中,102 名患者(62.7%)报告了至少一次不良反应(BFKB8488A:83[68.6%];安慰剂:19[59.4%])。BFKB8488A 表现出非线性药代动力学特征,暴露量呈大于剂量比例的增加。治疗后出现抗药物抗体的发生率为 22.7%。总体而言,观察到与暴露相关的高密度脂蛋白(HDL)升高和甘油三酯水平降低的趋势。中暴露和高暴露 tertile 组丙氨酸氨基转移酶和天冬氨酸氨基转移酶分别降低 0.7%和 9.2%,安慰剂组分别升高 7.5%和 17%,在第 85 天。在 NAFLD 患者中,低、中、高暴露 tertile 组从基线肝脂肪的平均降低分别为 13.0%、34.5%和 49.0%,而安慰剂组在第 85 天则为 0.1%。
BFKB8488A 在 T2DM 或 NAFLD 患者中耐受良好,导致甘油三酯降低,高密度脂蛋白改善,两个人群的肝脏健康标志物均有改善趋势,NAFLD 患者的肝脂肪明显减少。(ClinicalTrials.gov:NCT03060538)