Gong Jue, Zhou Jie, Yuan Dongfen, Ma Xuewen, Vishwamitra Deeksha, Hilder Brandi, Masterson Tara J, Tolbert Jaszianne, Renaud Thomas, Heuck Christoph, Kane Colleen, Samtani Mahesh N, Girgis Suzette, Haddish-Berhane Nahor, Berdeja Jesus, Krishnan Amrita, Ouellet Daniele
Johnson & Johnson, Spring House, Pennsylvania, USA.
Johnson & Johnson, Raritan, New Jersey, USA.
Clin Pharmacol Ther. 2025 Oct;118(4):954-966. doi: 10.1002/cpt.70004. Epub 2025 Jul 24.
Talquetamab is the first and only GPRC5D × CD3 bispecific antibody approved for relapsed/refractory multiple myeloma (RRMM). In the phase I/II MonumenTAL-1 study, overall response rates (ORRs) were > 66% in patients with RRMM treated with subcutaneous talquetamab at the recommended phase II doses (RP2Ds): 0.4 mg/kg weekly and 0.8 mg/kg every other week. We characterized the pharmacokinetics (PK), pharmacodynamics, immunogenicity, and exposure-response relationships for efficacy and safety following talquetamab administration in phase I and II. In phase I, talquetamab exposure increased in an approximately dose-proportional manner across intravenous and subcutaneous doses and was maintained around or above the 90% maximum effective concentration identified in an ex vivo cytotoxic assay at the RP2Ds. Higher levels of T-cell activation and cytokine induction were observed at the RP2Ds compared with lower doses. Talquetamab demonstrated time-dependent clearance with a half-life of 7.56 days at initial treatment and 12.2 days at steady state. Patients with immunoglobulin G multiple myeloma and International Staging System (ISS) stage II/III exhibited higher clearance of talquetamab, which resulted in lower exposure. Dose adjustment based on myeloma subtype and ISS stage was not required. In exposure-response analyses, a near-flat relationship was demonstrated for ORR, duration of response, and progression-free survival at the exposure range of the RP2Ds. In safety exposure-response analyses, rates of grade 1/2 dysgeusia increased with higher exposures. The incidence of anti-talquetamab antibodies had no apparent impact on the PK, efficacy, or safety of talquetamab. These clinical pharmacology results support the selection of the talquetamab RP2Ds.
塔勒夸单抗是首个也是唯一获批用于复发/难治性多发性骨髓瘤(RRMM)的GPRC5D×CD3双特异性抗体。在I/II期MonumenTAL-1研究中,复发/难治性多发性骨髓瘤患者接受皮下注射塔勒夸单抗,按照推荐的II期剂量(RP2Ds):每周0.4mg/kg和每两周0.8mg/kg治疗,总体缓解率(ORR)>66%。我们对I期和II期给予塔勒夸单抗后的药代动力学(PK)、药效学、免疫原性以及疗效和安全性的暴露-反应关系进行了表征。在I期,塔勒夸单抗的暴露量在静脉注射和皮下注射剂量范围内以近似剂量比例的方式增加,并在RP2Ds下维持在体外细胞毒性试验确定的90%最大有效浓度左右或以上。与较低剂量相比,在RP2Ds下观察到更高水平的T细胞活化和细胞因子诱导。塔勒夸单抗表现出时间依赖性清除,初始治疗时半衰期为7.56天,稳态时为12.2天。免疫球蛋白G多发性骨髓瘤和国际分期系统(ISS)II/III期的患者对塔勒夸单抗的清除率较高,这导致暴露量较低。无需根据骨髓瘤亚型和ISS分期进行剂量调整。在暴露-反应分析中,在RP2Ds的暴露范围内,ORR、反应持续时间和无进展生存期呈现近似平坦的关系。在安全性暴露-反应分析中,1/2级味觉障碍的发生率随暴露量增加而升高。抗塔勒夸单抗抗体的发生率对塔勒夸单抗的PK、疗效或安全性没有明显影响。这些临床药理学结果支持了塔勒夸单抗RP2Ds的选择。