Efficacy of fixed-dose combination artesunate-amodiaquine versus artemether-lumefantrine for uncomplicated childhood Plasmodium falciparum malaria in Democratic Republic of Congo: a randomized non-inferiority trial
© Espié et al.; licensee BioMed Central Ltd. 2012
Received: 8 February 2012
Accepted: 25 May 2012
Published: 25 May 2012
In 2005, the Democratic Republic of Congo (DRC) adopted artesunate and amodiaquine (ASAQ) as first-line anti-malarial treatment. In order to compare the efficacy of the fixed-dose formulation ASAQ versus artemether-lumefantrine (AL), a randomized, non-inferiority open-label trial was conducted in Katanga.
Children aged six and 59 months with uncomplicated Plasmodium falciparum malaria were enrolled and randomly allocated into one of the two regimens. The risk of recurrent parasitaemia by day 42, both unadjusted and adjusted by PCR genotyping to distinguish recrudescence from new infection, was analysed.
Between April 2008 and March 2009, 301 children were included: 156 with ASAQ and 145 with AL. No early treatment failures were reported. Among the 256 patients followed-up at day 42, 32 patients developed late clinical or parasitological failure (9.9% (13/131) in the ASAQ group and 15.2% (19/125) in the AL group). After PCR correction, cure rates were 98.3% (95%CI, 94.1-99.8) in the ASAQ group and 99.1% (95%CI, 94.9-99.9) in the AL group (difference −0.7%, one sided 95% CI −3.1). Kaplan-Meier PCR-adjusted cure rates were similar. Both treatment regimens were generally well tolerated.
Both ASAQ and AL are highly effective and currently adequate as the first-line treatment of uncomplicated falciparum malaria in this area of Katanga, DRC. However, in a very large country, such as DRC, and because of possible emergence of resistance from other endemic regions, surveillance of efficacy of artemisinin-based combination treatments, including other evaluations of the resistance of ASAQ, need to be done in other provinces.
The protocol was registered with the clinicaltrials.gov, open clinical trial registry under the identifier number NCT01567423.
Despite recent progress in access to effective preventive and therapeutic measures to control malaria, it remains one of the leading causes of morbidity and mortality worldwide, and especially in Democratic Republic of Congo (DRC) . In this country, malaria cases was reported to represent up to 68% of outpatient visits and 30% of hospital admissions and accounted for an estimated 42% mortality in children under five, all over the country . Malaria is seasonal, with transmission peaking during the rainy season from September to May and Plasmodium falciparum accounts for nearly 95% of all malaria cases in this region .
In 2005, following increased reports of sulphadoxine-pyrimethamine (SP) resistance , the National Malaria Control Programme the Ministry of Health of DRC decided to replace SP by artesunate (AS) combined with amodiaquine (AQ), as first-line treatment, following WHO guidelines recommendation to use artemisinin-based combination therapy (ACT) for uncomplicated malaria . The association was initially only available in loose combination of ASAQ in blister pack.
Until 2007, the combination of artemether-lumefantrine (AL) was the only fixed-dose ACT registered to international standards that was widely available in malaria-endemic countries. A new fixed-dose combination of artesunate and amodiaquine (ASAQ Winthrop®), developed by the Drugs for Neglected Diseases Initiative (DNDi) in collaboration with Sanofi-Aventis, was pre-qualified by the WHO in 2008.
Current international guidelines advocate that once a new anti-malarial treatment is introduced in a country, the efficacy of such novel regimens needs to be monitored regularly in order to detect early signs of declining efficacy, which can have implications for policy markers . The few studies conducted in eastern DRC showed that the efficacy of ASAQ by day 28 varied between 84.9% and 93.3% in children less than 5 years old [4, 6, 7]. As DRC is a very large country of approximately 2,345,000 km2, repeated evaluations of the ACT efficacy are needed in different regions.
Given that the transition in drug policy from a loose to a fixed dose combination would be easier option for uncomplicated malaria treatment, it was decided to assess the efficacy of the new fixed-dose combination of artesunate and amodiaquine (ASAQ) in comparison with the fixed-dose combination of artemeter and lumefantrine (AL), in the province of Katanga, south-eastern DRC.
The aims of the study were to compare (i) treatment efficacy of fixed-dose ASAQ and its alternative AL, expressed as product limit estimates of failure from survival analysis and as simple proportions from per protocol analysis, on day 42, and (ii) analysis of adjusted and unadjusted results by genotyping.
Study design and site
This protocol was registered with ClinicalTrials.gov, under the idenfier number NCT01567423.
Children aged between six and 59 months and with a body weight ≥ 5 kg were eligible for enrolment if they had P. falciparum infections (density threshold at inclusion between 2,000 and 200,000/μl), fever or history of fever in the previous 24 hours, no signs of severe malaria, no reported hypersensitivities of the studied drugs, and no serious concomitant febrile illness .
The children included were randomized in one of the two treatment arms, in a 1:1 ratio without stratification. The randomization list was generated by a computer in blocks of six. Treatment allocations were kept in sealed and numbered opaque envelopes. Participants were enrolled in the same order in which they were diagnosed.
ASAQ (ASAQ Winthrop®, Sanofi-Aventis) was administered once daily for three days, as follows: one tablet of artesunate 25 mg/amodiaquine 67.5 mg for children between 5 to 8.9 kg, artesunate 50 mg/amodiaquine 135 mg for children between 9 to 17.9 kg. One tablet of artemether 20 mg/lumefantrine 120 mg (Coartem®, Novartis Pharma, Basel, Switzerland) was administered twice daily for three days to children with a body weight of 5 to 14.9 kg and two tablets were administered twice daily for three days to children with a body weight of 15 to 24.9 kg. All doses were administered under direct observation for the three days. Full doses of drugs were re-administered if a patient vomited within 30 min after receipt. Patients who vomited more than twice were excluded from the study and were treated with oral quinine 10 mg/kg/8 h for 7 days.
Signs of severe malaria or any other serious health condition (e.g. severe malnutrition), intake of anti-malarial treatment in the last seven days, and mixed malaria infection were also excluded from the study.
Clinical assessment (including measurement of axillary temperature), tick and thin smears and haemoglobin measurement were performed on days 2, 3, 7, 14, 21, 28, 35 and 42 or any day in between in the event of illness.
Malaria outcome classification
Outcomes were classified according to 2009 WHO guidelines as adequate clinical and parasitological response (ACPR), early treatment failure (ETF), late clinical failure (LCF), late parasitological failure (LPF) or follow-up interrupted . Follow-up interrupted included treatment protocol violation, lost to follow-up, use of other anti-malarials outside the study protocol or withdrawal of consent prohibiting further follow-up. Drug tolerability was also assessed clinically. An adverse event was defined as any undesirable symptom in a patient during the study regardless of whether it was related to the treatment.
In areas of intense transmission, where multiple genotype infections are common , a second episode of malaria or a recurrent parasitaemia during the drug-free follow-up period may be due to the same infection or a different infection (a recrudescence, thus a treatment failure, or a new infection, respectively). To distinguish these two events, polymorphic P. falciparum genes, such as the merozoite surface protein 1 and 2 genes (msp1 and msp2) and the glutamate-rich protein gene (glurp) were genotyped by PCR, as previously described . PCR analyses, conducted at the Epicentre research base, Mbarara, Uganda, were performed using paired samples from all patients experiencing late clinical or parasitologic failure. Blood samples were collected on Whatman FTA® Cards (GE Healthcare UK Limited, Buckinghamshire, United Kingdom) on the day of enrollment and the day treatment failure occurred. The genotypic profiles for pre- and post-treatment parasites were compared; patients in which pre- and post-treatment genotypes were identical were considered as recrudescences and patients in which pre- and post-treatment genotypes were different were considered as new infections .
All ETFs were considered to be due to recrudescence. Patients meeting the criteria for LCF or LPF in whom genotyping was done; according to the results, patients were classified as either (i) resolved by PCR and further categorized as recrudescences or new infections or (ii) unsuccessfully genotyped with the reason recorded (missing sample, PCR not done or result inconclusive).
This study underwent ethical review and was approved by Ethical Committee of the School of Public Health, University of Kinshasa, DRC, the ethical review board of Médecins Sans Frontières and the Comité de Protection des Personnes “Ile de France XI”, St Germain en Laye, France. The study was authorized by the relevant health authority. Written informed consent was obtained from the parents or legal guardians of the enrolled children.
Based on previous data for AL efficacy [12–14], efficacy rate, defined as the PCR-adjusted parasitological cure rate at day 42, was estimated of 95% for both treatments. With a 7% non-inferiority margin, a power of 80%, and a test significant level (one side) of 5%, the sample size required to conclude to non inferiority was 150 per treatment group, taking into account an increase of 20% for loss to follow-up or premature withdrawals [nQuery Advisor v6].
The primary outcome was the PCR-adjusted parasitological cure rate up to day 42 of the follow-up period. Two analytical approaches were used to assess efficacy data. First, a per protocol (PP) analysis was performed including only the patients who were followed throughout the protocol, defined follow-up period and in whom a clear treatment outcome can be determined. The risk of failure for each treatment group was calculated as the proportion of patients classified as failure (the numerator) divided by the number of patients in the evaluable population (the denominator). In the second approach, survival analysis was performed and patients with incomplete follow-up who did not reach the primary outcome interest were included in the analysis as non-failures, but censored on the last day of follow-up. The risk of failure was calculated using the Kaplan-Meier product limit formula with data censored for patients who were not classified as failures and with interrupted follow-up. Patients wrongly included, who did not meet study inclusion criteria, were excluded from both analyses.
In the PP analysis (adjusting by genotyping), the evaluable population included only patients classified as ACPR, ETF or LCF/LPF due to recrudescence. In the survival analysis, the evaluable population for adjusted and unadjusted calculations included all patients enrolled in the study, with the exception that LCF/LPF outcomes with unsuccessful genotyping outcomes were excluded from the adjusted calculations. For the unadjusted calculations, patients with follow-up interrupted and non-falciparum new infections were censored on the last day of observation. For the adjusted calculations, censored patients also included those with new P. falciparum infections.
Other variables were compared using the chi2 test or Fisher’s exact test for variables and Student’s test for continuous variables.
Data were double entered and validated using Epidata version 3.1 (Odense, Danemark). All analyses were performed with Stata, version 10 (Stats-Corp, College Station, Texas). A p-value < 0.05 was considered statistically significant.
Baseline characteristics of trial participants, by treatment group
27.6 (6–59; 14.3)
27.4 (6–59; 15.0)
10.3 (5.1-17.0; 2.7)
10.2 (5.3-16.0; 2.6)
Axillary temperature (°C)
37.6 (34–40.5; 1.3)
37.6 (35.2-40.0; 1.1)
Patients with fever (T° ≥ 37.5°C)
9.0 (4.0-13.3; 1.9)
9.0 (5.3-15.5; 2.1)
Anaemia 5- < 8 g/dl
> 11 g/dl
Geometric mean parasite density (/μL) (IQR)
Proportion ≥ 100,000 para/μL
Patients with gametocytes
Adequate clinical and parasitological response and treatment cure rates
Treatment outcomes after 42 days for episodes of uncomplicated Plasmodium falciparum malaria
Treatment group, No. (%)
ASAQ (n = 156)
AL (n = 145)
No treatment outcome
Lost to follow-up
Other protocol deviations
Adequate clinical and parasitological response
Recurrent parasitaemia (including LCF and LPF)
Recurrent malaria due to non-falciparum species
Genotyping not performed
Among the 32 children with recurrent parasitaemia after day 7, PCR genotyping was successfully performed on 31 (96.8%) of 32 blood samples (Table 2). PCR-corrected cure rates by day 42 were 98.3% (95%CI, 94.1-99.8) following completion of the ASAQ regimen and 99.1% (95%CI, 94.9-99.9) following completion of the AL regimen (difference −0.7%, one sided 95% CI −3.1).
Efficacy outcome for ASAQ and AL on day 42, calculated by PP analysis and Kaplan-Meier analysis
PP cure rate analysis
Kaplan Meier cure rate analysis
% efficacy [CI95%]
% difference (LLCI*)
% efficacy [CI95%]
% difference (LLCI*)
Parasite and fever clearance, and gametocyte carriage
Clearance of fever (defined as a temperature <37.5°C) was more rapid in patients given ASAQ than in patients given AL, one day after treatment initiation. Among patient who had fever at inclusion, one (1.3%) of 79 ASAQ recipients and eight (11.3%) of 71 AL recipients remained febrile (p-value = 0.002). By day 2, nearly all fevers had resolved and the two regimens did not differ (p-value = 0.38). Rapid clinical improvement was recorded within the two treatment groups.
By day 2, parasite clearance did not differ between the two regimens, with positive slide results observed for nine (6.0%) of 150 ASAQ-treated patients and for seven (4.9%) or the 143 AL-treated patients (p-value = 0.68). By day 3 and day 7, only one patient (respectively in the AL group and in the ASAQ group) had not yet cleared all parasites.
At baseline, gametocyte carriage rates were low in both regimen groups (Table 1). Gametocytes were detected more often with ASAQ than with AL, respectively by day 2, 11.9% and 4.8%, by day 3, 10.6% and 4.2%, and by day 7, 6.3% and 1.5% (p-value < 0.05).
Both treatment regimens were generally well tolerated. Twelve patients (ten (6.4%) in the ASAQ group and two (1.4%) in the AL group) vomited within 30 min after the administration of the dose; nine of them (all in the ASAQ group) had received a second dose and none was excluded from the study.
No deaths occurred during the follow-up period, but six patients (one in the ASAQ group and five in the AL group) developed moderate or severe adverse events associated with clinically suspected severe malaria (anaemia, lethargy, convulsions). All patients were transfused and one received the rescue treatment consisting on intravenous quinine (loading dose 20 mg/kg given over 4 hours, then 10 mg/kg given 8 hours after the loading dose was started, followed by 10 mg/kg every 8 hours for 7 days). Four of these six patients (all in the AL group) were hospitalized for two to six days. Thus, these events could not be attributed to the intervention drugs.
Other mild side-effects were less common and were not related to a specific treatment: lower acute respiratory infections (54.6% in the ASAQ group and 51.3% in the AL group), conjunctivitis (16% in the ASAQ group and 10.8% in the AL group), abdominal pains and diarrhoea (8% in the ASAQ group and 14.9% in the AL group).
The results of this randomized trial of Congolese children in Katanga province with uncomplicated falciparum malaria and follow-up patients for 42 days show that the efficacy of fixed-dose combination of ASAQ is non-inferior to fixed-dose combination of AL, with regard to the margin prespecified at 7%.
High PCR adjusted cure rates of 98.3% to 98.4% (depending on the analysis population) were seen in patients assigned to ASAQ, compared with rates of 99.1% to 99.2% in patients assigned to AL. These results are comparable to those from previous studies where AS+AQ were routinely used as multiple tablets (loose combination) in other sub-Saharan countries [12–14], but higher than those reported by Bonnet et al. in Equatorial province of DRC . They are also consistant with those from recent studies which studied efficacy of fixed-dose combination of ASAQ after 28 days of follow-up [15, 16].
As with other malaria efficacy studies conducted in areas of high transmission , the unadjusted efficacy rates, which were significantly different between the two treatment arms, largely reflect a difference in rates of new infection than in rates of recrudescence. Thus, in this study, a significant proportion of new infections was reported, most prominently in the AL group, which reflect partially the prophylactic effect of the drugs.
In this study, the adjusted estimates of treatment efficacy derived from the two statistical approaches were not significantly different. New infection with P. falciparum usually constitutes an additional confounding factor for the adjusted analysis. Whereas patients with such infections are removed from the PP analyses, they are censored in the survival analysis after contributing a period of observation to the cumulative risk during which treatment failure was not observed . This discrepancy was particularly apparent in the high transmission sites in Africa where new infections were highest, but it was not observed in this study.
Survival analysis allows for more available data to contribute to the analysis, thus increasing the precision of the derived estimates. It avoids systematic biases introduced by dropping from the analysis patients who do not complete follow-up [8, 18, 19], even if in this study, the proportion of these patients was 10.3%, which could be considered as acceptable.
During the first days of treatment, a rapid decrease of fever, parasitaemia and gametocyte carriage was observed in the two regimen groups. These findings confirmed the results of efficacy studies on artemisinin-containing combination which led to lower gametocyte carriage, improving the cure rates, decreasing the transmission of falciparum malaria and reducing the spread of resistance to non-artemisinin drugs [20, 21]. Parasite clearance has became an important indicator in the evaluation of ACT, especially following the emergence of artemisinin resistance in Cambodia and the Thai-Burmese border [22–24]. Here the proportion of patients with low parasitaemia at day 2 and 3 is giving new important indication of the parasite early response following ACT .
This study showed that both combinations were well tolerated, with only 6% of children with drug-induced vomiting. Nevertheless, differents between treatment arms were observed in the first few days following treatment; vomiting was higher in the ASAQ group compared to AL. Only four patients developed severe malaria, and no deaths occurred during the course of the study. It is worth mentioning that the study was not designed nor power to compare tolerabilty between the two combinations. The ASAQ FDC presents the advantage of requiring one intake per day while AL is twice per day . However, the tolerability, in particular vomiting may impact the effectiveness of the treatment and should be assessed, particularly while used in home management of malaria  or as intermittent preventive therapy in children .
A limitation of this study was that pharmacology measures were not performed. It would improve the differentiation between true recrudescence to a problem of absorption . The limited reliability of the electric supply and the absence at that time of standardized PK measure on filter paper were among the reasons why these measures were not implemented.
According to WHO guidelines, which recommend a change in anti-malarial treatment policy when the cure rate for the current recommended therapy falls below 90% , this study showed that both ASAQ and AL are currently adequate as the first-line treatment of uncomplicated falciparum malaria in this area of the Katanga province. Surveillance of ACT efficacy in a very large country such as DRC remains a technical, financial and logistic challenge, illustrated by the limited number of published and unpublished efficacy studies in the past decade [4, 6, 7, 30].
While emergence of artemisinin resistance in South East Asia is of serious concern [22, 23], possible emergence of resistance from other endemic regions is triggering renewed attention in monitoring anti-malarial efficacy. More financial resources are now available in particular from Global Funds, World Bank or PMI to support this surveillance. However, the current recommended protocol for monitoring anti-malarial efficacy can be very challenging to implement, in particular, in remote study sites. In this particular study, the difficulties to supply equipment, drugs, consumables, establishing external quality assurance processes and accessing the site were among daily challenges. The follow-up of patients in particular in a border area was also a major issue for the study team. Research is needed to develop simpler methods to monitor efficacy, e.g., shorter follow-up of patients, and validate molecular marker of artemisinin resistance.
Initiatives, including development of paediatric formulations, home-based management of malaria and improving public sector procurement and supply chains should make ACT more accessible for sub-Saharan African children [31, 32].
We thank the patients and their families, the medical staff of the reference hospital of Pweto, the MSF-OCBA team of Pweto and Lubumbashi and the following trial team members: Daniel Iñiguez, Arnald García, Céline Langendorf, Mercè Claret Traïd, Gaspard Bossou and Akoi Koivogui.
We thank Mercè Claret Traïd and the parasitological laboratory of Drassanes Tropical Diseases and International Health Unit, Barcelona, Spain, for the External Quality Control.
We thank also Elisabeth Baudin, Loretxu Pinoges and Sarala Nicholas for the statistical support, Elisabeth Ashley and Patrice Piola for precious advice on malaria efficacy studies.
This study was funded by Médecins Sans Frontières-OCBA, Barcelona, Spain.
- Hay SI, Okiro EA, Gething PW, Patil AP, Tatem AJ, Guerra CA, Snow RW: Estimating the global clinical burden of Plasmodium falciparum malaria in 2007. PLoS Med. 2010, 7: e1000290-10.1371/journal.pmed.1000290.PubMed CentralView ArticlePubMedGoogle Scholar
- WHO: Malaria Control and Treatment in the Eastern Region of the Democratic Republic of the Congo (DRC). 2006, WHO, Geneva, [http://www.who.int/hac/crises/cod/appeal/DRC_Malaria_control_east_Feb06.pdf]Google Scholar
- WHO: World malaria report 2009. Country Profile : Democratic Republic of Congo. 2009b, WHO, Geneva, 96-98. [http://whqlibdoc.who.int/publications/2009/9789241563901_eng_Profiles.pdf]Google Scholar
- Alker AP, Kazadi WM, Kutelemeni AK, Bloland PB, Tshefu AK, Meshnick SR: dhfr and dhps genotype and sulfadoxine-pyrimethamine treatment failure in children with falciparum malaria in the Democratic Republic of Congo. Trop Med Int Health. 2008, 13: 1384-1391. 10.1111/j.1365-3156.2008.02150.x.PubMed CentralView ArticlePubMedGoogle Scholar
- WHO: Methods for surveillance of antimalarial drug efficacy. 2009, WHO, [http://whqlibdoc.who.int/publications/2009/9789241597531_eng.pdf]Google Scholar
- Swarthout TB, Broek IV, Kayembe G, Pota H, Roper C: Artesunate + amodiaquine and artesunate + sulphadoxine-pyrimethamine for treatment of uncomplicated malaria in Democratic Republic of Congo: a clinical trial with determination of sulphadoxine and pyrimethamine-resistant haplotypes. Trop Med Int Health. 2006, 11: 1503-1511. 10.1111/j.1365-3156.2006.01710.x.View ArticlePubMedGoogle Scholar
- Bonnet M, Broek I, van Herp M, Urrutia PP, van Overmeir C, Kyomuhendo J, Ndosimao CN, Ashley E, Guthmann JP: Varying efficacy of artesunate + amodiaquine and artesunate + sulphadoxine-pyrimethamine for the treatment of uncomplicated falciparum malaria in the Democratic Republic of Congo: a report of two in-vivo studies. Malar J. 2009, 8: 192-10.1186/1475-2875-8-192.PubMed CentralView ArticlePubMedGoogle Scholar
- Price RN, Dorsey G, Ashley EA, Barnes KI, Baird JK, d'Alessandro U, Guerin PJ, Laufer MK, Naidoo I, Nosten F, Olliaro P, Plowe CV, Ringwald P, Sibley CH, Stepniewska K, White NJ: World Antimalarial Resistance Network I: clinical efficacy of antimalarial drugs. Malar J. 2007, 6: 119-10.1186/1475-2875-6-119.PubMed CentralView ArticlePubMedGoogle Scholar
- Greenhouse B, Dokomajilar C, Hubbard A, Rosenthal PJ, Dorsey G: Impact of transmission intensity on the accuracy of genotyping to distinguish recrudescence from new infection in antimalarial clinical trials. Antimicrob Agents Chemother. 2007, 51 (9): 3096-3103. 10.1128/AAC.00159-07.PubMed CentralView ArticlePubMedGoogle Scholar
- Collins WJ, Greenhouse B, Rosenthal PJ, Dorsey G: The use of genotyping in antimalarial clinical trials: a systematic review of published studies from 1995–2005. Malar J. 2006, 5: 122-10.1186/1475-2875-5-122.PubMed CentralView ArticlePubMedGoogle Scholar
- Methods and techniques for clinical trials on antimalarial drug effi cacy: genotyping to identify parasite populations: informal consultation organized by the Medicines for Malaria Venture and cosponsored by the World Health Organization, 29–31. 2007, WHO, [http://whqlibdoc.who.int/publications/2008/9789241596305_eng.pdf], May , Amsterdam, The Netherlands
- Mårtensson A, Strömberg J, Sisowath C, Msellem MI, Gil JP, Montgomery SM, Olliaro P, Ali AS, Björkman A: Efficacy of artesunate plus amodiaquine versus that of artemether-lumefantrine for the treatment of uncomplicated childhood Plasmodium falciparum malaria in Zanzibar, Tanzania. Clin Infect Dis. 2005, 41: 1079-1086. 10.1086/444460.View ArticlePubMedGoogle Scholar
- Yeka A, Dorsey G, Kamya MR, Talisuna A, Lugemwa M, Rwakimari JB, Staedke SG, Rosenthal PJ, Wabwire-Mangen F, Bukirwa H: Artemether-lumefantrine versus dihydroartemisinin-piperaquine for treating uncomplicated malaria: a randomized trial to guide policy in Uganda. PLoS One. 2008, 3: e2390-10.1371/journal.pone.0002390.PubMed CentralView ArticlePubMedGoogle Scholar
- Zongo I, Dorsey G, Rouamba N, Tinto H, Dokomajilar C, Guiguemde RT, Rosenthal PJ, Ouedraogo JB: Artemether-lumefantrine versus amodiaquine plus sulfadoxine-pyrimethamine for uncomplicated falciparum malaria in Burkina Faso: a randomised non-inferiority trial. Lancet. 2007, 369: 491-498. 10.1016/S0140-6736(07)60236-0. Erratum in: Lancet. 2007, 369:826View ArticlePubMedGoogle Scholar
- Ndiaye JL, Faye B, Gueye A, Tine R, Ndiaye D, Tchania C, Ndiaye I, Barry A, Cissé B, Lameyre V, Gaye O: Repeated treatment of recurrent uncomplicated Plasmodium falciparum malaria in Senegal with fixed-dose artesunate plus amodiaquine versus fixed-dose artemether plus lumefantrine: a randomized, open-label trial. Malar J. 2011, 10: 237-10.1186/1475-2875-10-237.PubMed CentralView ArticlePubMedGoogle Scholar
- Sirima SB, Tiono AB, Gansané A, Diarra A, Ouédraogo A, Konaté AT, Kiechel JR, Morgan CC, Olliaro PL, Taylor WR: The efficacy and safety of a new fixed-dose combination of amodiaquine and artesunate in young African children with acute uncomplicated Plasmodium falciparum. Malar J. 2009, 8: 48-10.1186/1475-2875-8-48.PubMed CentralView ArticlePubMedGoogle Scholar
- Verret WJ, Dorsey G, Nosten F, Price RN: The effect of varying analytical methods on estimates of anti-malarial clinical efficacy. Malar J. 2009, 8: 77-10.1186/1475-2875-8-77.PubMed CentralView ArticlePubMedGoogle Scholar
- Guthmann JP, Pinoges L, Checchi F, Cousens S, Balkan S, van Herp M, Legros D, Olliaro P: Methodological issues in the assessment of antimalarial drug treatment: analysis of 13 studies in eight African countries from 2001 to 2004. Antimicrob Agents Chemother. 2006, 50: 3734-3739. 10.1128/AAC.01618-05.PubMed CentralView ArticlePubMedGoogle Scholar
- Ashley EA, Pinoges L, Turyakira E, Dorsey G, Checchi F, Bukirwa H, van den Broek I, Zongo I, Urruta PP, van Herp M, Balkan S, Taylor WR, Olliaro P, Guthmann JP: Different methodological approaches to the assessment of in vivo efficacy of three artemisinin-based combination antimalarial treatments for the treatment of uncomplicated falciparum malaria in African children. Malar J. 2008, 7: 154-10.1186/1475-2875-7-154.PubMed CentralView ArticlePubMedGoogle Scholar
- Nosten F, Brasseur P: Combination therapy for malaria: the way forward?. Drugs. 2002, 62: 1325-1329.View ArticleGoogle Scholar
- Stepniewska K, Price RN, Sutherland CJ, Drakeley CJ, von Seidlein L, Nosten F, White NJ: Plasmodium falciparum gametocyte dynamics in areas of different malaria endemicity. Malar J. 2008, 7: 249-10.1186/1475-2875-7-249.PubMed CentralView ArticlePubMedGoogle Scholar
- Dondorp AM, Nosten F, Yi P, Das D, Phyo AP, Tarning J, Lwin KM, Ariey F, Hanpithakpong W, Lee SJ, Ringwald P, Silamut K, Imwong M, Chotivanich K, Lim P, Herdman T, An SS, Yeung S, Singhasivanon P, Day NP, Lindegardh N, Socheat D, White NJ: Artemisinin resistance in Plasmodium falciparum malaria. N Engl J Med. 2009, 361: 455-467. 10.1056/NEJMoa0808859. Erratum in: N Engl J Med 2009, 361:1714PubMed CentralView ArticlePubMedGoogle Scholar
- Noedl H, Se Y, Schaecher K, Smith BL, Socheat D, Fukuda MM: Artemisinin Resistance in Cambodia 1 (ARC1) Study Consortium. Evidence of artemisinin-resistant malaria in western Cambodia. N Engl J Med. 2008, 359: 2619-2620. 10.1056/NEJMc0805011.View ArticlePubMedGoogle Scholar
- Phyo AP, Nkhoma S, Stepniewska K, Ashley EA, Nair S, McGready R, Ler Moo C, Al-Saai S, Dondorp AM, Lwin KM, Singhasivanon P, Day NP, White NJ, Anderson TJ, Nosten F: Emergence of artemisinin-resistant malaria on the western border of Thailand: a longitudinal study. Lancet. 2012Google Scholar
- Stepniewska K, Ashley E, Lee SJ, Anstey N, Barnes KI, Binh TQ, D'Alessandro U, Day NP, de Vries PJ, Dorsey G, Guthmann JP, Mayxay M, Newton PN, Olliaro P, Osorio L, Price RN, Rowland M, Smithuis F, Taylor WR, Nosten F, White NJ: In vivo parasitological measures of artemisinin susceptibility. J Infect Dis. 2010, 201: 570-579. 10.1086/650301.PubMed CentralView ArticlePubMedGoogle Scholar
- Taylor WR, Terlouw DJ, Olliaro PL, White NJ, Brasseur P, ter Kuile FO: Use of weight-for-age-data to optimize tablet strength and dosing regimens for a new fixed-dose artesunate-amodiaquine combination for treating falciparum malaria. Bull World Health Organ. 2006, 84: 956-964. 10.2471/BLT.06.031492.PubMed CentralView ArticlePubMedGoogle Scholar
- Ratsimbasoa A, Ravony H, Vonimpaisomihanta JA, Raherinjafy R, Jahevitra M, Rapelanoro R, Rakotomanga Jde D, Malvy D, Millet P, Ménard D: Compliance, safety, and effectiveness of fixed-dose artesunate-amodiaquine for presumptive treatment of non severe malaria in the context of home management of malaria in Madagascar. AmJTrop Med Hyg. 2012, 86: 203-210.View ArticleGoogle Scholar
- Ahorlu CK, Koram KA, Seake-Kwawu A, Weiss MG: Two-year evaluation of Intermittent Preventive Treatment for Children (IPTc) combined with timely home treatment for malaria control in Ghana. Malar J. 2011, 10: 127-10.1186/1475-2875-10-127.PubMed CentralView ArticlePubMedGoogle Scholar
- White NJ, Stepniewska K, Barnes K, Price RN, Simpson J: Simplified antimalarial therapeutic monitoring: using the day-7 drug level?. Trends Parasitol. 2008, 24: 159-163. 10.1016/j.pt.2008.01.006.View ArticlePubMedGoogle Scholar
- WHO: Global report on antimalarial drug efficacy and drug resistance: 2000–2010. 2010, WHO, Geneva, [http://whqlibdoc.who.int/publications/2010/9789241500470_eng.pdf]Google Scholar
- Yeka A, Harris JC: Treating uncomplicated malaria in children: comparing artemisinin-based combination therapies. Curr Opin Pediatr. 2010, 22: 798-803. 10.1097/MOP.0b013e32833fac44.PubMed CentralView ArticlePubMedGoogle Scholar
- Kurth F, Bélard S, Adegnika AA, Gaye O, Kremsner PG, Ramharter M: Do paediatric drug formulations of artemisinin combination therapies improve the treatment of children with malaria? A systematic review and meta-analysis. Lancet Infect Dis. 2010, 10: 125-132. 10.1016/S1473-3099(09)70327-5.View ArticlePubMedGoogle Scholar
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