نتایج جستجو برای: mefloquine

تعداد نتایج: 976  

Journal: :Antimicrobial agents and chemotherapy 1998
M van Vugt A Brockman B Gemperli C Luxemburger I Gathmann C Royce T Slight S Looareesuwan N J White F Nosten

An open, randomized comparison of artemether-benflumetol (CGP 56 697; Novartis) with artesunate-mefloquine was conducted in 617 patients with acute uncomplicated multidrug-resistant falciparum malaria on the western border of Thailand. Both treatments rapidly and reliably cleared fever and parasitemia, and there was no significant difference in the initial therapeutic response parameters. Paras...

Journal: :The Journal of infectious diseases 2005
Anne-Catrin Uhlemann Michael Ramharter Bertrand Lell Peter G Kremsner Sanjeev Krishna

The study of molecular markers of drug resistance is particularly important in surveillance studies of drugs, such as mefloquine, that still retain efficacy in sub-Saharan Africa yet have encountered resistance elsewhere. In a recent study in Thailand, we identified amplification of the Plasmodium falciparum multidrug resistance gene 1 (pfmdr1) as being the most important predictor of in vitro ...

2006
Udomsak Silachamroon U Silachamroon

The combination of artesunate and mefloquine is currently one of the most effective treatments for multidrug-resistant Plasmodium falciparum malaria. Simultaneous, rather than sequential treatment with the two drugs, would allow better patient compliance. We therefore evaluated threeday treatment with artesunate combined with either 2 or 3 days of mefloquine co-administered once a day with arte...

Journal: :Antimicrobial agents and chemotherapy 1997
R G Ridley H Matile C Jaquet A Dorn W Hofheinz W Leupin R Masciadri F P Theil W F Richter M A Girometta A Guenzi H Urwyler E Gocke J M Potthast M Csato A Thomas W Peters

The S,S enantiomer of the bisquinoline trans-N1,N2-bis(7-chloroquinolin-4-yl)cyclohexane-1,2-diamine, Ro 47-7737, is significantly more potent against chloroquine-resistant Plasmodium falciparum than the R,R enantiomer and the previously described racemate. Both the enantiomers and the racemate are more potent inhibitors of heme polymerization than chloroquine, and their activities are probably...

2013
Katrin Ingram Urs Duthaler Mireille Vargas William Ellis Jennifer Keiser

21 Chronic Schistosoma mansoni infections lead to severe tissue destructions of the gut wall 22 and liver and can influence drug disposition. This study aimed to investigate the impact of a 23 chronic S. mansoni infection on pharmacokinetic (PK) parameters of two promising 24 antischistosomal lead candidates (mefloquine and enpiroline) in mice. Studies were 25 conducted in two different mouse c...

Journal: :Antimicrobial agents and chemotherapy 2015
Caroline Petit Vincent Jullien Adeline Samson Jérémie Guedj Jean-René Kiechel Sarah Zohar Emmanuelle Comets

The objectives of this study were to design a pharmacokinetic (PK) study by using information about adults and evaluate the robustness of the recommended design through a case study of mefloquine. PK data about adults and children were available from two different randomized studies of the treatment of malaria with the same artesunate-mefloquine combination regimen. A recommended design for ped...

Journal: :Bulletin of the World Health Organization 1994
A L Fontanet B D Johnston A M Walker Y Bergqvist U Hellgren W Rooney

Reported are the results of a randomized trial of a single dose of mefloquine (15 mg/kg or 25 mg/kg body weight) for the treatment of uncomplicated multidrug-resistant falciparum malaria. Of the 110 adult patients enrolled in the study 57 were randomly assigned to the 15 mg/kg group and 53 to the 25 mg/kg group. The baseline characteristics of the patients did not differ significantly in the tw...

Journal: :Antimicrobial agents and chemotherapy 2010
Pharath Lim Chansuda Wongsrichanalai Pheaktra Chim Nimol Khim Saorin Kim Sophy Chy Rithy Sem Sina Nhem Poravuth Yi Socheat Duong Denis Mey Bouth Blaise Genton Hans-Peter Beck Jean Gerard Gobert William O Rogers Jean-Yves Coppee Thierry Fandeur Odile Mercereau-Puijalon Pascal Ringwald Jacques Le Bras Frederic Ariey

This study describes the results of in vitro antimalarial susceptibility assays and molecular polymorphisms of Plasmodium falciparum isolates from Cambodia. The samples were collected from patients enrolled in therapeutic efficacy studies (TES) conducted by the Cambodian National Malaria Control Program for the routine efficacy monitoring of artemisinin-based combination therapy (ACT) (artesuna...

Journal: :Journal of the American Chemical Society 2012
Manuel Schmidt Han Sun Per Rogne Gerhard K E Scriba Christian Griesinger Lars T Kuhn Uwe M Reinscheid

Even though the important antimalaria drug rac-erythro-mefloquine HCl has been on the market as Lariam for decades, the absolute configurations of its enantiomers have not been determined conclusively. This is needed, since the (-) enantiomer is believed to cause adverse side effects in malaria treatment resulting from binding to the adenosine receptor in the human brain. Since there are confli...

Journal: :Clinical infectious diseases : an official publication of the Infectious Diseases Society of America 2004
Mayfong Mayxay Maniphone Khanthavong Niklas Lindegårdh Siamphay Keola Marion Barends Tiengkham Pongvongsa Ratsuda Yapom Anna Annerberg Samlane Phompida Rattanaxay Phetsouvanh Nicholas J White Paul N Newton

BACKGROUND Recent clinical trials in the Lao People's Democratic Republic have demonstrated that chloroquine and sulfadoxine-pyrimethamine, which are national malaria treatment policy, are no longer effective in the treatment of uncomplicated Plasmodium falciparum malaria. METHODS A randomized comparison of 3 oral antimalarial combinations--chloroquine plus sulfadoxine-pyrimethamine versus ar...

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