[Translation] An open-label, dose-escalation Phase I clinical study to evaluate the safety, tolerability, pharmacokinetic characteristics and preliminary efficacy of FP-208 monotherapy in patients with advanced solid tumors
主要目的是评估FP-208治疗晚期实体肿瘤患者的安全性和药代动力学特征,次要目的是初步评估抗肿瘤活性,并探索生物标志物pS6药物和疗效的关系。
[Translation] The primary objective is to evaluate the safety and pharmacokinetic characteristics of FP-208 in the treatment of patients with advanced solid tumors. The secondary objective is to preliminarily evaluate the anti-tumor activity and explore the relationship between the biomarker pS6 drug and efficacy.