Roche Innovation Center, Shanghai, China.
Roche Innovation Center, Basel, Switzerland.
Clin Transl Sci. 2024 Aug;17(8):e13896. doi: 10.1111/cts.13896.
Ruzotolimod (Toll-like receptor 7 (TLR7) agonist, RG7854) is an oral, small molecule immuno-modulator activating the TLR 7 and is being evaluated in patients with CHB. As with other TLR7 agonists, the study drug-related adverse events of flu-like symptoms have been reported in some participants during phase I studies with ruzotolimod. An exploratory analysis of the relationship between pharmacokinetic (PK)/pharmacodynamic (PD) and flu-like symptoms was performed in participants from two phase I studies including both healthy volunteers and NUC-suppressed CHB patients who received either single or multiple ascending doses of orally administered ruzotolimod. Linear and logistic regression were used to explore potential relationships between dose, flu-like symptoms, PK, and PD. Generalized linear regression was performed to predict the probability of flu-like symptoms of all intensities at different RO7011785 (the active metabolite of the double prodrug ruzotolimod) PK exposure. This analysis showed that single or multiple doses of ruzotolimod at ⩾100 mg, the immune PD (IFN-α, neopterin, IP-10, and the transcriptional expression of ISG15, OAS-1, MX1, and TLR7) responses increase with the RO7011785 PK exposure, which increases linearly with the doses from 3 mg to 170 mg of ruzotolimod. The analysis also showed that the probability of flu-like symptoms occurrence increases with PD responses (IFN-α and IP-10). Dose reduction of ruzotolimod can be an effective way to reduce the magnitude of PD response, thus reducing the probability of study drug-related flu-like symptoms occurrence at all intensity in the participants who are highly sensitive to PD activation and intolerant to flu-like symptoms.
鲁唑替尼(Toll 样受体 7(TLR7)激动剂,RG7854)是一种口服小分子免疫调节剂,可激活 TLR7,目前正在慢性乙型肝炎(CHB)患者中进行评估。与其他 TLR7 激动剂一样,在鲁唑替尼的 I 期研究中,一些参与者报告了与研究药物相关的流感样症状不良事件。在包括健康志愿者和 NUC 抑制的 CHB 患者在内的两项 I 期研究中,对接受口服鲁唑替尼单剂量或多次递增剂量的参与者进行了探索性分析,以评估药代动力学(PK)/药效学(PD)与流感样症状之间的关系。线性和逻辑回归用于探索剂量、流感样症状、PK 和 PD 之间的潜在关系。广义线性回归用于预测不同 RO7011785(鲁唑替尼的双前药的活性代谢物)PK 暴露时所有强度流感样症状的概率。该分析表明,100mg 及以上的鲁唑替尼单剂量或多剂量,免疫 PD(IFN-α、新蝶呤、IP-10 以及 ISG15、OAS-1、MX1 和 TLR7 的转录表达)反应随 RO7011785 PK 暴露而增加,其随 3mg 至 170mg 鲁唑替尼剂量呈线性增加。分析还表明,流感样症状发生的概率随 PD 反应(IFN-α和 IP-10)增加而增加。鲁唑替尼剂量减少可能是降低 PD 反应幅度的有效方法,从而降低对 PD 激活敏感且不能耐受流感样症状的参与者中所有强度研究药物相关流感样症状发生的概率。