首页> 外文期刊>The Journal of Pharmacology and Experimental Therapeutics: Official Publication of the American Society for Pharmacology and Experimental Therapeutics >TransCon CNP, a Sustained-Release C-Type Natriuretic Peptide Prodrug, a Potentially Safe and Efficacious New Therapeutic Modality for the Treatment of Comorbidities Associated with Fibroblast Growth Factor Receptor 3-Related Skeletal Dysplasias
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TransCon CNP, a Sustained-Release C-Type Natriuretic Peptide Prodrug, a Potentially Safe and Efficacious New Therapeutic Modality for the Treatment of Comorbidities Associated with Fibroblast Growth Factor Receptor 3-Related Skeletal Dysplasias

机译:Transcon CNP,一种持续释放的C型利钠肽前药,一种用于治疗与成纤维细胞生长因子受体3相关的骨骼发育不良相关的合并症的潜在安全和有效的新治疗模态

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摘要

TransCon CNP is a C-type natriuretic peptide (CNP-38) conjugated via a cleavable linker to a polyethylene glycol carrier molecule, designed to provide sustained systemic CNP levels upon weekly subcutaneous administration. TransCon CNP is in clinical development for the treatment of comorbidities associated with achondroplasia. In both mice and cynomolgus monkeys, sustained exposure to CNP via TransCon CNP was more efficacious in stimulating bone growth than intermittent CNP exposure. TransCon CNP was well tolerated with no adverse cardiovascular effects observed at exposure levels exceeding the expected clinical therapeutic exposure. At equivalent dose levels, reductions in blood pressure and/or an increase in heart rate were seen following single subcutaneous injections of the unconjugated CNP-38 molecule or a daily CNP-39 molecule (same amino acid sequence as Vosoritide, USAN:INN). The half-life of the daily CNP-39 molecule in cynomolgus monkey was estimated to be 20 minutes, compared with 90 hours for CNP-38, released from TransCon CNP. C(max )for the CNP-39 molecule (20 mu g/kg) was approximately 100-fold higher, compared with the peak CNP level associated with administration of 100 mu g/kg CNP as TransCon CNP. Furthermore, CNP exposure for the daily CNP-39 molecule was only evident for up to 2 hours postdose (lower limit of quantification 37 pmol/l), whereas TransCon CNP gave rise to systemic exposure to CNP-38 for at least 7 days postdose. The prolonged CNP exposure and associated hemodynamically safe peak serum concentrations associated with TransCon CNP administration are suggested to improve efficacy, compared with short-lived CNP molecules, due to better therapeutic drug coverage and decreased risk of hypotension.
机译:Transcon CNP是通过可切割的接头与聚乙二醇载体分子缀合的C型Natrieturetic肽(CNP-38),其旨在在每周皮下给药时提供持续的全身CNP水平。 Transcon CNP在临床开发中用于治疗与疼痛组织相关的合并症。在小鼠和鱼鹰猴中,通过Transcon CNP持续暴露于CNP,在刺激骨生长方面比间歇性CNP暴露更有效。 Transcon CNP耐受良好的耐受性,在暴露水平超过预期临床治疗性暴露时没有观察到不良心血管效应。在同等的剂量水平下,在未缀合的CNP-38分子或每日CNP-39分子(与vosoritide的相同氨基酸序列相同的氨基酸序列,Usan:Inn)后,观察到血压和/或心率增加的降低。每日CNP-39分子中的半衰期在Cynomolgus猴中估计为20分钟,与CNP-38的90小时相比,从Transcon CNP释放。 CNP-39分子(20μmmma)的C(max)较高约100倍,与施用100μg/ kg CNP作为Transcon CNP相关的峰CNP水平相比。此外,每日CNP-39分子的CNP暴露仅为持续2小时(定量37 pmol / L)的下限仅明显,而Transcon CNP将产生至少7天的系统暴露于CNP-38。延长的CNP暴露和相关的血流动力学安全峰与与转段CNP局部相关的血清浓度有关,与短寿命的CNP分子相比,有效,因为具有更好的治疗药物覆盖并降低了低血压的风险。

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