Clinafloxacin is an investigationalfluoroquinoloneantibiotic. Despite its promising antibiotic activity, the clinical development of clinafloxacin has been hampered by its risk for inducing serious side effects.
Medical uses
Clinafloxacin has not been approved for any indication. The investigational new drug application was withdrawn by the manufacturer in 1999, citing safety concerns.[4]
Available forms
Clinafloxacin is available in both oral and intravenous formulations.[1]
Specific populations
There is a warning against using clinafloxacin in pregnant patients, due to possible damage to the developing fetus.[5]
The phototoxicity with clinafloxacin has been more associated with oral dosing as compared to intravenous dosing, though the studies that described this were subject to confounding by study site (that is, patients that received intravenous clinafloxacin were less mobile, and thereby received less sunlight exposure).[1]
The mechanism for clinafloxacin's phototoxicity involves the chlorine atom at position 8. In the presence of ultraviolet light, the chemical structure of clinafloxacin is degraded, resulting in the formation of toxic, reactive oxygen species that can damage cellular structures—including DNA. For this reason clinafloxacin can also be classified as a photocarcinogen (a chemical that can cause light-induced cancer), though the risk of developing cancer in humans taking the medication is small.[1]
The mechanism for clinafloxacin's effect on blood glucose is thought to involve stimulation of the pancreatic beta cells, which produce insulin (a hormone that lowers blood glucose levels).[1]
The symptoms of clinafloxacin overdose are unknown.[7]
Interactions
Drug-drug interactions
Clinafloxacin inhibits multiple CYP450 drug metabolizing enzymes, especially CYP1A2.[1] Clinafloxacin has induced the accumulation of CYP1A2 substrates, including theophylline, at therapeutic doses.[1] This can also affect the metabolism of caffeine, another CYP1A2 substrate. Caffeine consumption must be limited while taking clinafloxacin to prevent caffeine accumulation and overdose.[2]
There is also a known interaction of clinafloxacin with phenytoin, resulting in a decrease in the clearance of phenytoin from the body.[1] The increase in INR seen in patients taking both clinafloxacin and the anticoagulantwarfarin has yet to be fully elucidated.[1]
Food-drug interactions
There are no known food-drug interactions with clinafloxacin.[2]
The time that it takes for serum concentrations of clinafloxacin to reach the maximum concentration (Cmax) in healthy volunteers after taking a dose by mouth is 0.7 hours.[3] The elimination half-life in humans is 6.1 hours.[3]Steady state levels of clinafloxacin are achieved in 3 days of twice daily dosing by mouth in healthy volunteers.[1]
About half of an administered clinafloxacin dose is found unchanged in the urine, meaning that the drug is cleared from the blood stream roughly equally by hepatic metabolism (liver-induced degradation) and renal elimination (kidney-mediated removal).[1]
Chemistry
Clinafloxacin is a fluoroquinolone, structurally related to other fluoroquinolones like ciprofloxacin.[5] It is soluble in methanol (about 2 mg/mL at 25 °C) and water.[9]
^ abcdefghijklmnoGrayson ML, Crowe SM, McCarthy JS, Mills J, Mouton JW, Norrby SR, Paterson DL, Pfaller MA (2012). Kucers' the use of antibiotics a clinical review of antibacterial, antifungal, antiparasitic and antiviral drugs (6th ed.). Boca Raton, FL: CRC Press. pp. 1542–1546. ISBN978-1444147520.
^ abcdPranger AD, Alffenaar JW, Aarnoutse RE (2011). "Fluoroquinolones, the cornerstone of treatment of drug-resistant tuberculosis: a pharmacokinetic and pharmacodynamic approach". Current Pharmaceutical Design. 17 (27): 2900–30. doi:10.2174/138161211797470200. PMID21834759.
