Kokai-Kun John F, Bristol J Andrew, Setser John, Schlosser Michael
Synthetic Biologics, Inc, Rockville, MD, USA
Synthetic Biologics, Inc, Rockville, MD, USA.
Int J Toxicol. 2016 May;35(3):309-16. doi: 10.1177/1091581815623236. Epub 2015 Dec 23.
SYN-004 is a first in class, recombinant β-lactamase that degrades β-lactam antibiotics and has been formulated to be administered orally to patients receiving intravenous β-lactam antibiotics including cephalosporins. SYN-004 is intended to degrade unmetabolized antibiotics excreted into the intestines and thus has the potential to protect the gut microbiome from disruption by these antibiotics. Protection of the gut microbiome is expected to protect against opportunistic enteric infections such as Clostridium difficile infection as well as antibiotic-associated diarrhea. In order to demonstrate that oral SYN-004 is safe for human clinical trials, 2 Good Laboratory Practice-compliant toxicity studies were conducted in Beagle dogs. In both studies, SYN-004 was administered orally 3 times per day up to the maximum tolerated dose of the formulation. In the first study, doses of SYN-004 administered over 28 days were safe and well tolerated in dogs with the no-observed-adverse-effect level at the high dose of 57 mg/kg/day. Systemic absorption of SYN-004 was minimal and sporadic and showed no accumulation during the study. In the second study, doses up to 57 mg/kg/day were administered to dogs in combination with an intravenous dose of ceftriaxone (300 mg/kg) given once per day for 14 days. Coadministration of oral SYN-004 with intravenous ceftriaxone was safe and well tolerated, with SYN-004 having no noticeable effect on the plasma pharmacokinetics of ceftriaxone. These preclinical studies demonstrate that SYN-004 is well tolerated and, when coadministered with ceftriaxone, does not interfere with its systemic pharmacokinetics. These data supported advancing SYN-004 into human clinical trials.
SYN-004是首个此类重组β-内酰胺酶,可降解β-内酰胺类抗生素,其制剂设计用于口服给药,适用于接受包括头孢菌素在内的静脉β-内酰胺类抗生素治疗的患者。SYN-004旨在降解排泄到肠道中的未代谢抗生素,因此有可能保护肠道微生物群免受这些抗生素的破坏。保护肠道微生物群有望预防机会性肠道感染,如艰难梭菌感染以及抗生素相关性腹泻。为了证明口服SYN-004在人体临床试验中是安全的,在比格犬身上进行了2项符合良好实验室规范的毒性研究。在两项研究中,SYN-004均每天口服3次,直至制剂的最大耐受剂量。在第一项研究中,连续28天给予SYN-剂量在高剂量57毫克/千克/天时对犬安全且耐受性良好。SYN-004的全身吸收极少且偶发,在研究期间未显示出蓄积。在第二项研究中,每天给犬口服高达57毫克/千克/天的剂量,并联合静脉注射头孢曲松(300毫克/千克),每天1次,共14天。口服SYN-004与静脉注射头孢曲松联合给药安全且耐受性良好,SYN-004对头孢曲松的血浆药代动力学没有明显影响。这些临床前研究表明,SYN-004耐受性良好,与头孢曲松联合给药时不会干扰其全身药代动力学。这些数据支持将SYN-004推进人体临床试验。