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TransCon CNP,一种持续释放的 C 型利钠肽前药,一种用于治疗成纤维细胞生长因子受体 3 相关骨骼发育不良相关合并症的潜在安全有效的新型治疗方法。

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.

机构信息

Ascendis Pharma A/S, Hellerup, Denmark (V.M.B., C.E.R., P.H.M., M.K.-H.); and Ascendis Pharma GmbH, Heidelberg, Germany (F.F., A.B., J.Z., U.H.)

Ascendis Pharma A/S, Hellerup, Denmark (V.M.B., C.E.R., P.H.M., M.K.-H.); and Ascendis Pharma GmbH, Heidelberg, Germany (F.F., A.B., J.Z., U.H.).

出版信息

J Pharmacol Exp Ther. 2019 Sep;370(3):459-471. doi: 10.1124/jpet.119.258251. Epub 2019 Jun 24.

Abstract

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. for the CNP-39 molecule (20 g/kg) was approximately 100-fold higher, compared with the peak CNP level associated with administration of 100 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. SIGNIFICANCE STATEMENT: The hormone C-type natriuretic peptide (CNP) is in clinical development for the treatment of comorbidities associated with achondroplasia, the most common form of human dwarfism. The TransCon Technology was used to design TransCon CNP, a prodrug that slowly releases active CNP in the body over several days. Preclinical data show great promise for TransCon CNP to be an effective and well-tolerated drug that provides sustained levels of CNP in a convenient once-weekly dose, while avoiding high systemic CNP bolus concentrations that can induce cardiovascular side effects.

摘要

经交联的 CNP(TransCon CNP)是一种 C 型利钠肽(CNP-38),通过可切割的连接子与聚乙二醇载体分子连接,旨在通过每周皮下给药提供持续的全身 CNP 水平。TransCon CNP 正在开发中,用于治疗软骨发育不全相关的合并症。在小鼠和食蟹猴中,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 耐受性良好,在暴露水平超过预期临床治疗暴露水平时,未观察到不良心血管影响。在等效剂量水平下,单次皮下注射未缀合的 CNP-38 分子或每日 CNP-39 分子(与 Vosoritide 相同的氨基酸序列,USAN:INN)后,可观察到血压降低和/或心率增加。在食蟹猴中,每日 CNP-39 分子的半衰期估计为 20 分钟,而从 TransCon CNP 释放的 CNP-38 为 90 小时。与每日 CNP-39 分子(20 g/kg)相比,每日 CNP-39 分子的峰值 CNP 水平大约高 100 倍,与给予 100 g/kg CNP 作为 TransCon CNP 的峰值 CNP 水平相关。此外,每日 CNP-39 分子的 CNP 暴露仅在给药后 2 小时内可见(定量下限 37 pmol/l),而 TransCon CNP 至少在给药后 7 天内引起 CNP-38 的全身暴露。与半衰期短的 CNP 分子相比,由于更好的治疗药物覆盖和降低低血压风险,与 TransCon CNP 给药相关的 CNP 暴露延长和相关的血流动力学安全的峰值血清浓度被认为可提高疗效。意义陈述:激素 C 型利钠肽(CNP)正在开发中,用于治疗软骨发育不全相关的合并症,软骨发育不全是最常见的人类侏儒症形式。TransCon 技术用于设计 TransCon CNP,这是一种前药,可在数天内在体内缓慢释放活性 CNP。临床前数据表明,TransCon CNP 有望成为一种有效且耐受性良好的药物,可提供方便的每周一次给药,持续 CNP 水平,同时避免可引起心血管副作用的高全身 CNP 爆发浓度。

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