Chen Ruoyu, Fang Xian-Long, Raza Hafiz Khuram
Department of Clinical Transformation, Shanghai Yuansong Biotechnology Company Limited, Shanghai, 201499, China.
Pharm Res. 2025 Jun;42(6):917-933. doi: 10.1007/s11095-025-03863-x. Epub 2025 May 8.
Recombinant L-IFN Adenovirus (YSCH-01) is a modified oncolytic adenovirus, which showed good curative effects in a variety of solid tumors. The safety of YSCH-01 needs to be evaluated for non-clinical research.
This toxicity and distribution study of YSCH-01 injection via ITU/IV/IP injection in Syrian Hamster was conducted to prepare an investigational new drug (IND) application. The endpoints included mortality/moribundity, clinical observation, body weight, palpable mass examination, food consumption, ophthalmology, and clinical pathology. Toxicokinetics, ADA test, viral shedding, and tissue bio-distribution were analyzed.
The severely toxic dose in 10% of animals was 1 × 10 VP/animal, > 2 × 10 VP/kg, and 6.7 × 10 VP/kg for ITU groups, IV groups and IP groups, respectively. The antibody titers of recombinant L-IFN adenovirus were significantly increased following YSCH-01 administration, and slightly lower during recovery period. YSCH-01 gDNA can be shed through the administration site, saliva and feces, and almost no urine. In the ITU, IV, and IP injection groups, YSCH-01 was distributed in the whole blood and all collected organs with T in most whole blood/tissues of 2.00-4.00 days and L-IFN was detected in all tumor and serum samples, with a T of 2.00-4.00 days, full or partial clearance of YSCH-01 and L-IFN was noted in most tissues/organs or tumor and serum on D28.
Our study demonstrated the toxicity and potential toxicity of YSCH-01 in Syrian hamsters and evaluated its tissue distribution in hamsters after a single administration. STD10 results in hamsters support the safety of the estimated dosage for future clinical studies.
重组L-IFN腺病毒(YSCH-01)是一种经过改造的溶瘤腺病毒,在多种实体瘤中显示出良好的疗效。需要通过非临床研究评估YSCH-01的安全性。
通过在叙利亚仓鼠中进行ITU/IV/IP注射YSCH-01注射液的毒性和分布研究,以准备新药临床试验申请(IND)。观察终点包括死亡率/濒死率、临床观察、体重、可触及肿块检查、食物消耗、眼科检查和临床病理学。分析了毒代动力学、ADA检测、病毒排泄和组织生物分布。
ITU组、IV组和IP组中,10%动物的严重毒性剂量分别为1×10病毒粒子/动物、>2×10病毒粒子/千克和6.7×10病毒粒子/千克。给予YSCH-01后,重组L-IFN腺病毒的抗体滴度显著升高,恢复期略有降低。YSCH-01的gDNA可通过给药部位、唾液和粪便排出,几乎不会通过尿液排出。在ITU、IV和IP注射组中,YSCH-01分布于全血和所有采集的器官,大多数全血/组织中的半衰期为2.00-4.00天,所有肿瘤和血清样本中均检测到L-IFN,半衰期为2.00-4.00天,在第28天时,大多数组织/器官或肿瘤和血清中YSCH-01和L-IFN出现完全或部分清除。
我们的研究证明了YSCH-01在叙利亚仓鼠中的毒性和潜在毒性,并评估了单次给药后其在仓鼠体内的组织分布。仓鼠的STD10结果支持了未来临床研究中估计剂量的安全性。