Key result
A fixed-dose combination of amlodipine, losartan, and hydrochlorothiazide more than doubled hydrochlorothiazide plasma levels and slightly increased losartan levels compared to individual components.
Why the study?
Does a fixed-dose combination of amlodipine, losartan, and hydrochlorothiazide alter their pharmacokinetics compared to individual administration in healthy volunteers?
RCT (n=26)
Crossover
Does a fixed-dose combination of amlodipine, losartan, and hydrochlorothiazide alter their pharmacokinetics compared to individual administration in healthy volunteers?
A fixed-dose combination of amlodipine, losartan, and hydrochlorothiazide results in significant pharmacokinetic interactions, notably doubling hydrochlorothiazide exposure, which requires further clinical evaluation.
Doubled hydrochlorothiazide exposure with the fixed-dose combination warrants caution in use; leaves open clinical relevance pending patient outcome trials.
The fixed-dose combinations of drugs are alternatives for a major control of chronical diseases such hypertension. Amlodipine, losartan and hydrochlorothiazide are widely used as pharmacological treatment of this cardiovascular disorder. Since these drugs have different mechanism of action, it could be assumed that a fixed-dose combination containing them will provide therapeutic advantages and greater adherence to the treatment. However, firstly is necessary to verify a possible pharmacokinetic interaction between the components. In this study, the oral pharmacokinetics of amlodipine, losartan and hydrochlorothiazide in a fixed-dose combination formulation were evaluated and compared against the individual components in 26 healthy volunteers. After an overnight fast subjects received an oral dose of losartan (50 mg), hydrochlorothiazide (12.5 mg), amlodipine (5 mg) or the same doses in fixed-dose combination formulation in four periods according to a randomized crossover design. Blood samples were obtained at selected times for a period of 72 h. Plasma was obtained and stored frozen at -80EC until analyzed by ultra performance liquid chromatography coupled with tandem mass spectrometry. The treatments were well tolerated. No changes were observed in the pharmacokinetic parameters of amlodipine. For losartan and losartan acid the plasma levels were slightly higher whereas for hydrochlorothiazide greatly increase more than twice their plasma levels with fixed-dose combination formulation. These results suggest pharmacokinetic interactions between these compounds. Further studies are necessary in order to establish the mechanisms of these interactions, however, clinical relevance should be evaluated in clinical studies in patients in which this fixed-dose combination formulation could be a therapeutic alternative.
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Santos-Cab et al. (2016) conducted an RCT in Healthy volunteers (n=26). Fixed-dose combination of amlodipine, losartan, and hydrochlorothiazide vs. Individual components was evaluated on Pharmacokinetic parameters (plasma levels). A fixed-dose combination of amlodipine, losartan, and hydrochlorothiazide more than doubled hydrochlorothiazide plasma levels and slightly increased losartan levels compared to individual components.
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