Key result
A single 1.0 mg oral dose of riociguat in patients with renal impairment resulted in reduced renal clearance and prolonged terminal half-life compared to healthy controls.
Why the study?
How do renal impairment and smoking status affect the pharmacokinetics and safety of a single oral dose of riociguat in comparison to healthy controls?
How do renal impairment and smoking status affect the pharmacokinetics and safety of a single oral dose of riociguat in comparison to healthy controls?
Renal impairment reduces riociguat clearance and prolongs its half-life, though exposure remains highly variable and overlaps with healthy controls, while nonsmokers appear to have greater exposure than smokers.
May warrant riociguat dose caution in renal impairment; nonrandomized data leave smoking effects on exposure open for confirmation.
Renal impairment is a common comborbidity in patients with pulmonary hypertension. The breakdown of riociguat, an oral soluble guanylate cyclase stimulator used to treat pulmonary hypertension, may be affected by smoking because polycyclic aromatic hydrocarbons in tobacco smoke induce expression of one of the metabolizing enzymes, CYP1A1. Two nonrandomized, nonblinded studies were therefore performed to investigate the pharmacokinetics and safety of a single oral dose of riociguat 1.0 mg in individuals with mild, moderate, or severe renal impairment compared with age-, weight-, and sex-matched healthy controls, including either smokers and nonsmokers (study I) or nonsmokers alone (study II). Pharmacokinetic analyses focused on the integrated per-protocol data set of both studies (N = 63). In patients with renal impairment, the renal clearance of riociguat was reduced and its terminal half-life prolonged compared with those in healthy controls. There was a monotonic relationship between creatinine clearance on treatment day and riociguat renal clearance (R (2) = 0.62). However, increased riociguat exposure with decreasing renal function was not strictly proportional. Riociguat exposure appeared to be greater in nonsmokers than in the combined population of smokers and nonsmokers, irrespective of renal function. Adverse events were mild to moderate and in line with the mode of action of riociguat. No serious adverse events occurred. In conclusion, renal impairment was associated with reduced riociguat clearance compared with that in controls; however, riociguat exposure in patients with renal impairment was highly variable, and ranges overlapped with those observed in healthy controls.
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Frey et al. (2016) studied Renal impairment (n=63). Riociguat vs. Age-, weight-, and sex-matched healthy controls was evaluated on Pharmacokinetics and safety. A single 1.0 mg oral dose of riociguat in patients with renal impairment resulted in reduced renal clearance and prolonged terminal half-life compared to healthy controls.
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