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PYC Therapeutics公司在获得安全性批准后,将治疗视神经萎缩的药物推进至多剂量研究阶段;股价上涨7%。

-- 据周三提交给澳大利亚证券交易所的文件显示,PYC Therapeutics(ASX:PYC)已获得安全审查委员会的批准,可将候选药物PYC-001推进至针对常染色体显性遗传性视神经萎缩(ADOA)患者的多剂量递增研究。此前,该药物在60微克单次递增剂量试验中取得了积极的四周安全性和耐受性结果。 文件称,该公司目前正在评估ADOA患者的重复给药方案,以评估其安全性和初步疗效,旨在启动全球注册试验以支持新药申请之前,建立临床概念验证。 文件还补充道,正在进行的I期和II期多剂量递增研究的结果将于2026年和2027年陆续公布。 该公司股价在周三的交易中上涨了7%。

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