Weiner Iddo, Kahan-Hanum Maya, Buchstab Nufar, Zelcbuch Lior, Navok Sharon, Sherman Irit, Nicenboim Julian, Axelrod Tim, Berko-Ashur Dikla, Olshina Maya, Mordoch Ron, Jablonska Jagoda, Gera-Inbar Tamar, Vainberg-Slutskin Ilya, Blumenfeld Britny, Sberro-Livnat Hila, Moses Ayelet, Nevenzel Hadas, Levy-Saar Inbal, Gold Jenia, Goldberg Meital, Tchernorudsky Nina, Ben-Yishay Noa, Cohen Tal, Kario Edith, Levovich Inesa, Safonov Roman, Tzur Yaron, Zarchin Yulia, Lev Vered, Elharar Yifat, Safyon-Gartman Einav, Gahali-Sass Inbar, Puttagunta Sailaja, Ussery Xilla, Vilchez Regis, Rappo Urania, Zak Naomi, Golembo Myriam, Cohen Ariel, Koff Jon, Kerem Eitan, Sorek Rotem, Bassan Merav
BiomX Ltd, Ness Ziona, Israel.
BiomX Inc, Cambridge, MA, USA.
Nat Commun. 2025 Jul 1;16(1):5579. doi: 10.1038/s41467-025-60598-4.
Cystic fibrosis is a monogenetic disease complicated by recurrent bacterial lung infections that require chronic antibiotics. Pseudomonas aeruginosa is an increasingly antibiotic-resistant pathogen associated with cystic fibrosis morbidity and mortality. Here, we describe the development of a three-phage cocktail (BX004-A) designed to target a wide range of P. aeruginosa strains. We evaluated BX004-A in Part 1 of a first-in-human double-blind placebo-controlled phase 1b/2a clinical trial, which included nine adult cystic fibrosis patients chronically infected with P. aeruginosa (NCT05010577). BX004-A met the primary endpoints of safety and tolerability. Exploratory endpoints included pharmacokinetics and Pseudomonas aeruginosa sputum density reduction. Efficient phage delivery to the lower respiratory tract was observed, and a potential reduction in P. aeruginosa sputum burden was noted in the phage arm. However, due to the study's small sample size, definitive conclusions regarding efficacy are limited. These data pave the way toward further development of novel phage-based therapeutics in antibiotic-resistant pulmonary bacterial infections.
囊性纤维化是一种单基因疾病,常并发反复的细菌性肺部感染,需要长期使用抗生素。铜绿假单胞菌是一种抗生素耐药性日益增强的病原体,与囊性纤维化的发病率和死亡率相关。在此,我们描述了一种三噬菌体组合制剂(BX004-A)的研发情况,该制剂旨在靶向多种铜绿假单胞菌菌株。我们在一项首次人体双盲安慰剂对照1b/2a期临床试验的第一部分中对BX004-A进行了评估,该试验纳入了9名长期感染铜绿假单胞菌的成年囊性纤维化患者(NCT05010577)。BX004-A达到了安全性和耐受性的主要终点。探索性终点包括药代动力学和铜绿假单胞菌痰液密度降低情况。观察到噬菌体有效地递送至下呼吸道,并且在噬菌体治疗组中注意到铜绿假单胞菌痰液负担可能有所减轻。然而,由于该研究的样本量较小,关于疗效的确定性结论有限。这些数据为进一步开发用于抗生素耐药性肺部细菌感染的新型噬菌体疗法铺平了道路。