Propanc Biopharma, Inc. 计划在澳大利亚提交临床试验申请，旨在启动一项涉及30至40名晚期癌症患者的1B期研究。这一举措标志着该公司在推进其新型癌症治疗方案的临床开发道路上迈出了关键一步。研究将聚焦于评估候选疗法的安全性、耐受性及初步疗效，目标人群是那些已接受过标准治疗但疾病仍出现进展的患者。
该1B期研究的设计旨在收集至关重要的临床数据，为后续更广泛的临床试验奠定基础。在澳大利亚提交CTA的决定，反映了公司利用该国高效监管框架和强大临床研究生态系统的战略考量。成功完成此阶段研究，有望为Propanc Biopharma, Inc.的核心产品管线带来重要的价值提升，并为其针对难治性癌症的开发策略提供关键支持。
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