Salomon-Zimri Shiran, Kerem Nitai, Linares Gabriel R, Russek-Blum Niva, Ichida Justin K, Tracik Ferenc
NeuroSense Therapeutics, Ltd., Ha-Menofim 11, Herzliya 4672562, Israel.
Department of Stem Cell Biology and Regenerative Medicine, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033, USA.
Pharmaceuticals (Basel). 2025 Apr 3;18(4):524. doi: 10.3390/ph18040524.
Amyotrophic lateral sclerosis (ALS) is a multifactorial neurodegenerative disease characterized by the involvement of multiple pathways and mechanisms. The complexity of its pathophysiology is reflected in the diverse hypotheses relating to its underlying causes. Given this intricate interplay of processes, a combination therapy approach offers a promising strategy. Combination therapies have demonstrated significant success in treating complex diseases, where they aim to achieve synergistic therapeutic effects and reduce drug dosage. PrimeC is an oral combination treatment composed of a patented novel formulation consisting of specific and unique doses of two well-characterized drugs (ciprofloxacin and celecoxib). It aims to synergistically inhibit the progression of ALS by addressing key elements of its pathophysiology. Demonstrating the synergistic effect of the PrimeC combination compared to each of its individual components, celecoxib and ciprofloxacin, and assessing its ability to improve the drug concentration profile and efficacy. The efficacy of the PrimeC combination was assessed in a survival assay using human induced pluripotent stem cell (iPSC)-derived motor neurons. Additionally, a drug profiling study was conducted, measuring drug levels in the brain and serum of C57BL mice treated with a single compound versus the combination. Motor neurons modeling ALS treated with the PrimeC combination exhibited better survival rates compared to treatment with either individual compound alone. The enhanced efficacy of the combination was further supported by a drug concentration profiling study in rodents, demonstrating that the PrimeC combination resulted in increased ciprofloxacin concentrations in both brain tissue and serum-highlighting the optimized interaction and synergistic potential of its two comprising agents. Our findings support the potential of combination therapy as an effective strategy for ALS treatment. Specifically, the PrimeC combination demonstrated promising therapeutic effects, providing a strong rationale for its ongoing development as a targeted treatment for ALS.
肌萎缩侧索硬化症(ALS)是一种多因素神经退行性疾病,其特征是涉及多种途径和机制。其病理生理学的复杂性体现在与其潜在病因相关的多种假设中。鉴于这些过程之间复杂的相互作用,联合治疗方法提供了一种有前景的策略。联合疗法在治疗复杂疾病方面已取得显著成功,其目标是实现协同治疗效果并降低药物剂量。PrimeC是一种口服联合治疗药物,由一种专利新型制剂组成,该制剂包含两种特性明确的药物(环丙沙星和塞来昔布)的特定且独特剂量。它旨在通过解决其病理生理学的关键要素来协同抑制ALS的进展。证明PrimeC联合用药与其各个单独成分(塞来昔布和环丙沙星)相比的协同作用,并评估其改善药物浓度分布和疗效的能力。在使用人诱导多能干细胞(iPSC)衍生的运动神经元进行的生存试验中评估了PrimeC联合用药的疗效。此外,还进行了一项药物分析研究,测量用单一化合物与联合用药治疗的C57BL小鼠大脑和血清中的药物水平。与单独使用任何一种化合物治疗相比,用PrimeC联合用药治疗的模拟ALS的运动神经元表现出更好的存活率。啮齿动物的药物浓度分析研究进一步支持了联合用药增强的疗效,表明PrimeC联合用药导致脑组织和血清中环丙沙星浓度增加,突出了其两种组成药物的优化相互作用和协同潜力。我们的研究结果支持联合治疗作为ALS治疗有效策略的潜力。具体而言,PrimeC联合用药显示出有前景的治疗效果,为其作为ALS的靶向治疗药物的持续开发提供了有力的理论依据。