Key result
Co-administration of ximelagatran and digoxin in healthy volunteers showed no pharmacokinetic or pharmacodynamic interactions, with both drugs being well tolerated.
Why the study?
Does ximelagatran interact with digoxin pharmacokinetically or pharmacodynamically in healthy volunteers?
RCT (n=16)
Double-blind
2-way crossover
Does ximelagatran interact with digoxin pharmacokinetically or pharmacodynamically in healthy volunteers?
Co-administration of digoxin and ximelagatran does not result in clinically significant pharmacokinetic or pharmacodynamic interactions in healthy volunteers.
Answers are grounded in this paper and cite their sources.
Supports co-administration without dose adjustment; confirms no PK/PD interaction for this thrombin inhibitor.
The interaction potential of digoxin and ximelagatran, an oral direct thrombin inhibitor being developed for the prevention and treatment of thromboembolic disease, was investigated in this randomized, double-blind, 2-way crossover study. On 2 separate occasions, healthy female and male volunteers (n = 16) received ximelagatran 36 mg or placebo twice daily for 8 days separated by a 4- to 14-day washout period. All volunteers received a single oral dose of digoxin 0.5 mg on day 4 of both study periods. No interaction between ximelagatran and digoxin was detected in the pharmaco-kinetic parameters (using a 90% confidence interval [CI] of least squares mean estimate ratios), including melagatran (the active form of ximelagatran) AUC(tau) and C(max) and digoxin AUC(t) and C(max). Digoxin did not alter the melagatran-induced prolongation of the activated partial thromboplastin time, and both drugs were well tolerated when administered in combination. In conclusion, no pharmacokinetic or pharmacodynamic interaction between digoxin and ximelagatran was observed in this study.
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Sarich et al. (2004) conducted an RCT in Healthy volunteers (n=16). Ximelagatran + Digoxin vs. Placebo + Digoxin was evaluated on Pharmacokinetic parameters (melagatran and digoxin AUC and Cmax) and pharmacodynamic interaction (aPTT prolongation). Co-administration of ximelagatran and digoxin in healthy volunteers showed no pharmacokinetic or pharmacodynamic interactions, with both drugs being well tolerated.
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