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Safety Study of Single-Dose Intravenously Administered DOTA-Siglec-9 Peptide in Sprague Dawley Rats

机译:单剂量静脉给药DOTA-Siglec-9肽对Sprague Dawley大鼠的安全性研究

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摘要

The peptide-based radioactive compound [68Ga]Ga-DOTA-Siglec-9 is a novel agent for imaging of inflammation with positron emission tomography. The drug target of [68Ga]Ga-DOTA-Siglec-9 is vascular adhesion protein 1. Previous studies have obtained promising results with [68Ga]Ga-DOTA-Siglec-9 in experimental animals. However, before taking this novel imaging agent into clinical trials, safety and toxicological studies need to be performed with the nonradioactive precursor compound DOTA-Siglec-9. This extended single-dose toxicity study was designed to provide information on the major toxic effects of DOTA-Siglec-9 and to indicate possible target organs after a single intravenous (iv) injection in rats. The study was performed using 60 adult Hsd: Sprague Dawley rats and included a control group and a treatment group to investigate the toxicity of DOTA-Siglec-9 solution at a final concentration of 0.2 mg/mL after a single iv injection of 582 µg/kg. The maximum dose tested was 1,000-fold the clinical dose on a mg/kg basis as indicated in European Medicines Agency International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use guideline M3(R2). The planned human clinical dose is approximately 0.582 µg of DOTA-Siglec-9 per kg of body mass. This study demonstrates that iv administration of DOTA-Siglec-9 at a dose of 582 µg/kg was well tolerated in rats and did not produce toxicologically significant adverse effects.
机译:基于肽的放射性化合物[ 68 Ga] Ga-DOTA-Siglec-9是用正电子发射断层显像技术对炎症成像的新型药物。 [ 68 Ga] Ga-DOTA-Siglec-9的药物靶标是血管粘附蛋白1。先前的研究[[sup> 68 Ga] Ga-DOTA-实验动物中的Siglec-9。但是,在将该新型显像剂用于临床试验之前,需要对非放射性前体化合物DOTA-Siglec-9进行安全性和毒理学研究。这项扩展的单剂量毒性研究旨在提供有关DOTA-Siglec-9的主要毒性作用的信息,并指示在大鼠中单次静脉内(iv)注射后可能的靶器官。这项研究是使用60只成年Hsd:Sprague Dawley大鼠进行的,包括对照组和治疗组,以单次静脉注射582 µg / ml的终浓度为0.2 mg / mL的DOTA-Siglec-9溶液的毒性进行研究。公斤。如欧洲药品管理局国际人用药品技术要求协调委员会M3(R2)指南所述,所测试的最大剂量是mg / kg基础剂量的1000倍。计划的人类临床剂量约为每千克体重0.582 µg DOTA-Siglec-9。这项研究表明,以582 µg / kg的剂量静脉内给药DOTA-Siglec-9在大鼠中具有良好的耐受性,并且在毒理学上不会产生明显的不良影响。

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