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Sökning: onr:"swepub:oai:DiVA.org:uu-366950" > Relative bioavailab...

Relative bioavailability of bedaquiline tablets suspended in water : Implications for dosing in children

Svensson, Elin, 1985- (författare)
Uppsala universitet,Institutionen för farmaceutisk biovetenskap,Radboud Univ Nijmegen Med Ctr, Radboud Inst Hlth Sci, Dept Pharm, Nijmegen, Netherlands
du Bois, Jeannine (författare)
TASK Appl Sci, Cape Town, South Africa
Kitshoff, Rene (författare)
TASK Appl Sci, Cape Town, South Africa
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de Jager, Veronique R. (författare)
TASK Appl Sci, Cape Town, South Africa
Wiesner, Lubbe (författare)
Univ Cape Town, Div Clin Pharmacol, Dept Med, Cape Town, South Africa
Norman, Jennifer (författare)
Univ Cape Town, Div Clin Pharmacol, Dept Med, Cape Town, South Africa
Nachman, Sharon (författare)
SUNY Stony Brook, Dept Pediat, Stony Brook, NY 11794 USA
Smith, Betsy (författare)
NIAID, Div Aids, NIH, Bethesada, MA USA
Diacon, Andreas H. (författare)
TASK Appl Sci, Cape Town, South Africa;Stellenbosch Univ, Div Med Physiol, Fac Med & Hlth Sci, Stellenbosch, South Africa
Hesseling, Anneke C. (författare)
Stellenbosch Univ, Dept Paediat & Child Hlth, Desmond Tutu TB Ctr, Fac Med & Hlth Sci, Cape Town, South Africa
Garcia-Prats, Anthony J. (författare)
Stellenbosch Univ, Dept Paediat & Child Hlth, Desmond Tutu TB Ctr, Fac Med & Hlth Sci, Cape Town, South Africa
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 (creator_code:org_t)
2018-08-10
2018
Engelska.
Ingår i: British Journal of Clinical Pharmacology. - : Wiley. - 0306-5251 .- 1365-2125. ; 84:10, s. 2384-2392
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Aims: Bedaquiline is an important novel drug for treatment of multidrug-resistant tuberculosis, but no paediatric formulation is yet available. This work aimed to explore the possibility of using the existing tablet formulation in children by evaluating the relative bioavailability, short-term safety, acceptability and palatability of suspended bedaquiline tablets compared to whole tablets.Methods: A randomized, open-label, two-period cross-over study was conducted in 24 healthy adult volunteers. Rich pharmacokinetic sampling over 48h was conducted at two occasions 14days apart in each participant after administration of 400mg bedaquiline (whole or suspended in water). The pharmacokinetic data were analysed with nonlinear mixed-effects modelling. A questionnaire was used to assess palatability and acceptability.Results: There was no statistically significant difference in the bioavailability of the suspended bedaquiline tables compared to whole. The nonparametric 95% confidence interval of the relative bioavailability of suspended bedaquiline tablets was 94-108% of that of whole bedaquiline tablets; hence, the predefined bioequivalence criteria were fulfilled. There were no Grade 3 or 4 or serious treatment emergent adverse events recorded in the study and no apparent differences between whole tablets and suspension regarding taste, texture or smell.Conclusions: The bioavailability of bedaquiline tablets suspended in water was the same as for tablets swallowed whole and the suspension was well tolerated. This suggests that the currently available bedaquiline formulation could be used to treat multidrug-resistant tuberculosis in children, to bridge the gap between when paediatric dosing regimens have been established and when a paediatric dispersible formulation is routinely available.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Farmaceutiska vetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Pharmaceutical Sciences (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Mikrobiologi inom det medicinska området (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Microbiology in the medical area (hsv//eng)

Nyckelord

bedaquiline
bioavailability
paediatric dosing
population PK
suspended tablets

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