Page last updated: 2024-10-22

amodiaquine and Recrudescence

amodiaquine has been researched along with Recrudescence in 34 studies

Amodiaquine: A 4-aminoquinoline compound with anti-inflammatory properties.
amodiaquine : A quinoline having a chloro group at the 7-position and an aryl amino group at the 4-position.

Research Excerpts

ExcerptRelevanceReference
"Artemether-lumefantrine plus amodiaquine provides an alternative to artemether-lumefantrine alone as first-line treatment for multidrug-resistant P falciparum malaria in the Greater Mekong subregion, and could prolong the therapeutic lifetime of artemether-lumefantrine in malaria-endemic populations."9.51Triple therapy with artemether-lumefantrine plus amodiaquine versus artemether-lumefantrine alone for artemisinin-resistant, uncomplicated falciparum malaria: an open-label, randomised, multicentre trial. ( Amaratunga, C; Callery, JJ; Chau, NH; Chotivanich, K; Chotsiri, P; Day, NPJ; Dhorda, M; Dondorp, AM; Duanguppama, J; Dung, NTP; Hien, TT; Hoglund, RM; Imwong, M; Lek, D; Long, LT; Maude, RJ; Miotto, O; Mukaka, M; Nghia, HDT; Nguon, C; Peto, TJ; Rekol, H; Ruecker, A; Sokha, M; Sovann, Y; Tarning, J; Thuong, NTH; Tripura, R; van der Pluijm, RW; Van Luong, V; von Seidlein, L; Waithira, N; White, NJ, 2022)
" The objective was to assess the efficacy and safety of repeated administrations of two fixed-dose presentations of ACT--artesunate plus amodiaquine (ASAQ) and artemether-lumefantrine (AL)--in subsequent episodes of Plasmodium falciparum malaria."9.15Repeated 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. ( Barry, A; Cissé, B; Faye, B; Gaye, O; Gueye, A; Lameyre, V; Ndiaye, D; Ndiaye, I; Ndiaye, JL; Tchania, C; Tine, R, 2011)
" In the present study, the efficacies of chloroquine (CQ) or amodiaquine (AQ) in the oral treatment of acute, symptomatic, uncomplicated, Plasmodium falciparum malaria were compared with those of oral treatments with the combination of CQ or AQ with pyrimethamine-sulfadoxine (PS)."9.10A randomized comparison of chloroquine, amodiaquine and their combination with pyrimethamine-sulfadoxine in the treatment of acute, uncomplicated, Plasmodium falciparum malaria in children. ( Sowunmi, A, 2002)
"Twenty-eight day in-vivo efficacy trial of amodiaquine-artesunate in 103 children aged 6-59 months in western Kenya with smear-confirmed uncomplicated Plasmodium falciparum malaria."7.75In-vivo efficacy of amodiaquine-artesunate in children with uncomplicated Plasmodium falciparum malaria in western Kenya. ( Desai, M; Hamel, MJ; Kariuki, S; McMorrow, M; Newman, RD; Odero, CO; Odhiambo, FO; Ord, R; Otieno, KO; Roper, C; Slutsker, L; Thwing, JI; Vulule, J, 2009)
" The findings indicate that - at least at the dosing regimen used in the present study and among children with acute, uncomplicated, P."6.71A randomized comparison of chloroquine and chloroquine plus ketotifen in the treatment of acute, uncomplicated, Plasmodium falciparum malaria in children. ( Sowunmi, A, 2003)
"AS-MQ and AL are more effective than DP and AS-AQ FDC in preventing gametocytaemia shortly after treatment, suggesting that the non-artemisinin partner drug or the timing of artemisinin dosing are important determinants of post-treatment gametocyte dynamics."6.53Gametocyte carriage in uncomplicated Plasmodium falciparum malaria following treatment with artemisinin combination therapy: a systematic review and meta-analysis of individual patient data. ( , 2016)
"Artemether-lumefantrine plus amodiaquine provides an alternative to artemether-lumefantrine alone as first-line treatment for multidrug-resistant P falciparum malaria in the Greater Mekong subregion, and could prolong the therapeutic lifetime of artemether-lumefantrine in malaria-endemic populations."5.51Triple therapy with artemether-lumefantrine plus amodiaquine versus artemether-lumefantrine alone for artemisinin-resistant, uncomplicated falciparum malaria: an open-label, randomised, multicentre trial. ( Amaratunga, C; Callery, JJ; Chau, NH; Chotivanich, K; Chotsiri, P; Day, NPJ; Dhorda, M; Dondorp, AM; Duanguppama, J; Dung, NTP; Hien, TT; Hoglund, RM; Imwong, M; Lek, D; Long, LT; Maude, RJ; Miotto, O; Mukaka, M; Nghia, HDT; Nguon, C; Peto, TJ; Rekol, H; Ruecker, A; Sokha, M; Sovann, Y; Tarning, J; Thuong, NTH; Tripura, R; van der Pluijm, RW; Van Luong, V; von Seidlein, L; Waithira, N; White, NJ, 2022)
" The objective was to assess the efficacy and safety of repeated administrations of two fixed-dose presentations of ACT--artesunate plus amodiaquine (ASAQ) and artemether-lumefantrine (AL)--in subsequent episodes of Plasmodium falciparum malaria."5.15Repeated 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. ( Barry, A; Cissé, B; Faye, B; Gaye, O; Gueye, A; Lameyre, V; Ndiaye, D; Ndiaye, I; Ndiaye, JL; Tchania, C; Tine, R, 2011)
" In the present study, the efficacies of chloroquine (CQ) or amodiaquine (AQ) in the oral treatment of acute, symptomatic, uncomplicated, Plasmodium falciparum malaria were compared with those of oral treatments with the combination of CQ or AQ with pyrimethamine-sulfadoxine (PS)."5.10A randomized comparison of chloroquine, amodiaquine and their combination with pyrimethamine-sulfadoxine in the treatment of acute, uncomplicated, Plasmodium falciparum malaria in children. ( Sowunmi, A, 2002)
"Artesunate-amodiaquine (AS-AQ) is one of the most widely used artemisinin-based combination therapies (ACTs) to treat uncomplicated Plasmodium falciparum malaria in Africa."4.91The effect of dosing strategies on the therapeutic efficacy of artesunate-amodiaquine for uncomplicated malaria: a meta-analysis of individual patient data. ( Adjuik, MA; Allan, R; Anvikar, AR; Ashley, EA; Ba, MS; Barennes, H; Barnes, KI; Bassat, Q; Baudin, E; Björkman, A; Bompart, F; Bonnet, M; Borrmann, S; Brasseur, P; Bukirwa, H; Checchi, F; Cot, M; D'Alessandro, U; Dahal, P; Deloron, P; Desai, M; Diap, G; Djimde, AA; Dorsey, G; Doumbo, OK; Espié, E; Etard, JF; Fanello, CI; Faucher, JF; Faye, B; Flegg, JA; Gaye, O; Gething, PW; González, R; Grandesso, F; Guerin, PJ; Guthmann, JP; Hamour, S; Hasugian, AR; Hay, SI; Humphreys, GS; Ibrahim, LM; Jullien, V; Juma, E; Kamya, MR; Karema, C; Kiechel, JR; Kremsner, PG; Krishna, S; Lameyre, V; Lee, SJ; Lell, B; Mårtensson, A; Massougbodji, A; Menan, H; Ménard, D; Menéndez, C; Meremikwu, M; Moreira, C; Nabasumba, C; Nambozi, M; Ndiaye, JL; Nikiema, F; Nsanzabana, C; Ntoumi, F; Ogutu, BR; Olliaro, P; Osorio, L; Ouédraogo, JB; Penali, LK; Pene, M; Pinoges, L; Piola, P; Price, RN; Roper, C; Rosenthal, PJ; Rwagacondo, CE; Same-Ekobo, A; Schramm, B; Seck, A; Sharma, B; Sibley, CH; Sinou, V; Sirima, SB; Smith, JJ; Smithuis, F; Somé, FA; Sow, D; Staedke, SG; Stepniewska, K; Swarthout, TD; Sylla, K; Talisuna, AO; Tarning, J; Taylor, WR; Temu, EA; Thwing, JI; Tine, RC; Tinto, H; Tjitra, E; Vaillant, MT; Valecha, N; Van den Broek, I; White, NJ; Yeka, A; Zongo, I, 2015)
"Twenty-eight day in-vivo efficacy trial of amodiaquine-artesunate in 103 children aged 6-59 months in western Kenya with smear-confirmed uncomplicated Plasmodium falciparum malaria."3.75In-vivo efficacy of amodiaquine-artesunate in children with uncomplicated Plasmodium falciparum malaria in western Kenya. ( Desai, M; Hamel, MJ; Kariuki, S; McMorrow, M; Newman, RD; Odero, CO; Odhiambo, FO; Ord, R; Otieno, KO; Roper, C; Slutsker, L; Thwing, JI; Vulule, J, 2009)
" Follow-up visits were performed on days 3, 7, 14, 21, and 28 to evaluate clinical and parasitological resolution of their malaria episode as well as adverse events."2.80Effectiveness and safety of artemether-lumefantrine versus artesunate-amodiaquine for unsupervised treatment of uncomplicated falciparum malaria in patients of all age groups in Nanoro, Burkina Faso: a randomized open label trial. ( Derra, K; Diallo-Nakanabo, S; Guiguemde, TR; Kazienga, A; Ouedraogo, JB; Owusu-Dabo, E; Sondo, P; Sorgho, H; Tarnagda, Z; Tinto, H; Valea, I; Zampa, O, 2015)
"Nearly all recurrences were due to new infections."2.73Artemether-lumefantrine versus amodiaquine plus sulfadoxine-pyrimethamine for uncomplicated falciparum malaria in Burkina Faso: a randomised non-inferiority trial. ( Dokomajilar, C; Dorsey, G; Guiguemde, RT; Ouedraogo, JB; Rosenthal, PJ; Rouamba, N; Tinto, H; Zongo, I, 2007)
" The findings indicate that - at least at the dosing regimen used in the present study and among children with acute, uncomplicated, P."2.71A randomized comparison of chloroquine and chloroquine plus ketotifen in the treatment of acute, uncomplicated, Plasmodium falciparum malaria in children. ( Sowunmi, A, 2003)
"AS-MQ and AL are more effective than DP and AS-AQ FDC in preventing gametocytaemia shortly after treatment, suggesting that the non-artemisinin partner drug or the timing of artemisinin dosing are important determinants of post-treatment gametocyte dynamics."2.53Gametocyte carriage in uncomplicated Plasmodium falciparum malaria following treatment with artemisinin combination therapy: a systematic review and meta-analysis of individual patient data. ( , 2016)
"Recrudescence was detected by a thick blood smear and confirmed by polymerase chain reaction."1.35Some features of primary and recrudescent amodiaquine-resistant Plasmodium falciparum infections in Nigerian children. ( Balogun, ST; Gbotosho, GO; Happi, CT; Sowunmi, A, 2008)

Research

Studies (34)

TimeframeStudies, this research(%)All Research%
pre-19906 (17.65)18.7374
1990's3 (8.82)18.2507
2000's11 (32.35)29.6817
2010's12 (35.29)24.3611
2020's2 (5.88)2.80

Authors

AuthorsStudies
Dentinger, CM1
Rakotomanga, TA1
Rakotondrandriana, A1
Rakotoarisoa, A1
Rason, MA1
Moriarty, LF1
Steinhardt, LC1
Kapesa, L1
Razafindrakoto, J1
Svigel, SS1
Lucchi, NW1
Udhayakumar, V2
Halsey, ES2
Ratsimbasoa, CA1
Peto, TJ1
Tripura, R1
Callery, JJ1
Lek, D1
Nghia, HDT1
Nguon, C1
Thuong, NTH1
van der Pluijm, RW1
Dung, NTP1
Sokha, M1
Van Luong, V1
Long, LT1
Sovann, Y1
Duanguppama, J1
Waithira, N1
Hoglund, RM1
Chotsiri, P1
Chau, NH1
Ruecker, A1
Amaratunga, C1
Dhorda, M1
Miotto, O1
Maude, RJ1
Rekol, H1
Chotivanich, K1
Tarning, J2
von Seidlein, L1
Imwong, M1
Mukaka, M1
Day, NPJ1
Hien, TT1
White, NJ2
Dondorp, AM1
Andrianaranjaka, V1
Lin, JT1
Golden, C1
Juliano, JJ1
Randrianarivelojosia, M1
Muhindo Mavoko, H1
Nabasumba, C2
Tinto, H4
D'Alessandro, U2
Grobusch, MP1
Lutumba, P1
Van Geertruyden, JP1
Adjuik, MA1
Allan, R1
Anvikar, AR1
Ashley, EA1
Ba, MS1
Barennes, H1
Barnes, KI1
Bassat, Q1
Baudin, E1
Björkman, A2
Bompart, F1
Bonnet, M1
Borrmann, S1
Brasseur, P1
Bukirwa, H1
Checchi, F1
Cot, M1
Dahal, P1
Deloron, P2
Desai, M2
Diap, G1
Djimde, AA1
Dorsey, G4
Doumbo, OK1
Espié, E1
Etard, JF1
Fanello, CI1
Faucher, JF1
Faye, B2
Flegg, JA1
Gaye, O2
Gething, PW1
González, R1
Grandesso, F1
Guerin, PJ1
Guthmann, JP1
Hamour, S1
Hasugian, AR2
Hay, SI1
Humphreys, GS1
Jullien, V1
Juma, E1
Kamya, MR1
Karema, C1
Kiechel, JR1
Kremsner, PG1
Krishna, S1
Lameyre, V3
Ibrahim, LM1
Lee, SJ1
Lell, B1
Mårtensson, A1
Massougbodji, A1
Menan, H1
Ménard, D1
Menéndez, C1
Meremikwu, M1
Moreira, C1
Nambozi, M1
Ndiaye, JL2
Nikiema, F1
Nsanzabana, C1
Ntoumi, F2
Ogutu, BR1
Olliaro, P1
Osorio, L1
Ouédraogo, JB5
Penali, LK1
Pene, M1
Pinoges, L1
Piola, P1
Price, RN2
Roper, C2
Rosenthal, PJ5
Rwagacondo, CE1
Same-Ekobo, A1
Schramm, B1
Seck, A1
Sharma, B1
Sibley, CH1
Sinou, V1
Sirima, SB1
Smith, JJ1
Smithuis, F1
Somé, FA1
Sow, D1
Staedke, SG1
Stepniewska, K1
Swarthout, TD1
Sylla, K1
Talisuna, AO1
Taylor, WR1
Temu, EA1
Thwing, JI2
Tjitra, E2
Tine, RC1
Vaillant, MT1
Valecha, N1
Van den Broek, I1
Yeka, A1
Zongo, I4
Sondo, P1
Derra, K1
Diallo-Nakanabo, S1
Tarnagda, Z1
Zampa, O1
Kazienga, A1
Valea, I1
Sorgho, H1
Owusu-Dabo, E1
Guiguemde, TR1
Ndounga, M1
Casimiro, PN1
Koukouikila-Koussounda, F1
Bitemo, M1
Diassivy Matondo, B1
Ndounga Diakou, LA1
Basco, LK1
Paczkowski, M1
Mwandama, D1
Marthey, D1
Luka, M1
Makuta, G1
Sande, J1
Ali, D1
Troell, P1
Mathanga, DP1
Gutman, J1
Siqueira, AM1
Alencar, AC1
Melo, GC1
Magalhaes, BL1
Machado, K1
Alencar Filho, AC1
Kuehn, A1
Marques, MM1
Manso, MC1
Felger, I1
Vieira, JL1
Daniel-Ribeiro, CT1
Lacerda, MV1
Plucinski, MM1
Dimbu, PR1
Macaia, AP1
Ferreira, CM1
Samutondo, C1
Quivinja, J1
Afonso, M1
Kiniffo, R1
Mbounga, E1
Kelley, JS1
Patel, DS1
He, Y1
Talundzic, E1
Garrett, DO1
Ringwald, P1
Fortes, F1
Ratcliff, A1
Siswantoro, H1
Kenangalem, E1
Wuwung, RM1
Purba, HL1
Piera, KA1
Chalfien, F1
Marfurt, J1
Penttinen, PM1
Russell, B1
Anstey, NM1
Sowunmi, A3
Balogun, ST1
Gbotosho, GO1
Happi, CT1
Odero, CO1
Odhiambo, FO1
Otieno, KO1
Kariuki, S1
Ord, R1
McMorrow, M1
Vulule, J1
Slutsker, L1
Newman, RD1
Hamel, MJ1
Somé, AF1
Séré, YY1
Dokomajilar, C3
Rouamba, N2
Greenhouse, B1
Gueye, A1
Tine, R1
Ndiaye, D1
Tchania, C1
Ndiaye, I1
Barry, A1
Cissé, B1
Sutanto, I1
Suprianto, S1
Widiaty, A1
Ruckert, P1
von Bethmann, A1
de Monbrison, F1
Picot, S1
Laihad, F1
Baird, JK1
Cattamanchi, A1
Kyabayinze, D1
Hubbard, A1
LOVE, J1
FOULK, R1
WILLIAMS, RG1
MITCHELL, RB1
Lankoande, ZM1
Lemnge, M1
Alifrangis, M1
Kafuye, MY1
Segeja, MD1
Gesase, S1
Minja, D1
Massaga, JJ1
Rønn, AM1
Bygbjerg, IC1
Holmgren, G1
Gil, JP1
Morrow, RH1
Guiguemde, RT1
Watkins, WM1
Sixsmith, DG1
Spencer, HC1
Boriga, DA1
Kariuki, DM1
Kipingor, T1
Koech, DK1
al-Yaman, F1
Genton, B1
Mokela, D1
Narara, A2
Raiko, A1
Alpers, MP1
Domarle, O1
Migot-Nabias, F1
Mvoukani, JL1
Lu, CY1
Nabias, R1
Mayombo, J1
Tiga, H1
Sapak, P1
Garner, P1
Baea, M1
Heywood, P1
Alpers, M1
Glew, RH1
Miller, LH1
Collins, WE1
Howard, WA1
Wyler, DJ1
Chaves-Carballo, E1
Neva, FA1
Weise, HJ1
Troidl, H1
Lorenz, W1
Barth, H1
Seidel, W1
Rohde, H1
Goecke, K1
Schmal, A1
Hamelmann, H1
Bruce-Chwatt, LJ1

Clinical Trials (5)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
A Multi-centre, Open-label Randomised Trial to Assess the Efficacy, Safety and Tolerability of the Triple ACT Artemether-lumefantrine+Amodiaquine (AL+AQ) Compared to the ACT Artemether-lumefantrine (AL) in Uncomplicated Falciparum Malaria in Cambodia and [NCT03355664]Phase 3310 participants (Actual)Interventional2018-03-19Completed
A Randomized Clinical Trial to Measure the Impact of Retreatment With an Artemisinin-based Combination on Malaria Incidence and Its Potential Selection of Resistant Strains[NCT01374581]Phase 32,117 participants (Actual)Interventional2012-05-31Completed
Pharmacovigilance for Artemisinin-based Combination Treatments in Africa[NCT01232530]3,176 participants (Actual)Observational2010-06-30Completed
A Randomised Comparative Study to Assess the Efficacy and Tolerability of Blood Schizonticidal Treatments With Artesunate Amodiaquine Winthrop® / Coarsucam (ASAQ) Versus Chloroquine (CQ) for Uncomplicated Plasmodium Vivax Monoinfection Malaria[NCT01378286]Phase 3380 participants (Actual)Interventional2012-01-31Completed
A Randomized Study to Compare Artesunate + Amiodaquine Versus Artemether + Lumefantrine in the Treatment of Repeated Uncomplicated Plasmodium Falciparum Malaria Attacks Occurring During 2 Years in a Cohort in Senegal[NCT00540410]Phase 4366 participants (Actual)Interventional2007-09-30Completed
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trial Outcomes

Fever Clearance Time

The time taken for the tympanic temperature to fall below 37.5˚C and remain there for at least 24 hours (NCT03355664)
Timeframe: 42 day

InterventionHours to fever clearance (Mean)
Artemether-lumefantrine for 3 Days Plus Primaquine at Hour 2418.3
Artemether-lumefantrine for 3 Days Plus Amodiaquine for 3 Days Plus Primaquine at Hour 2414.9

Incidence of Adverse Events Concerning Markers of Hepatic or Renal Toxicity

Total bilirubin, Alanine transaminase, Aspartate transaminase, Alkaline phosphatase and creatinine will be measured (NCT03355664)
Timeframe: 42 day

InterventionEvents (Number)
Artemether-lumefantrine for 3 Days Plus Primaquine at Hour 2453
Artemether-lumefantrine for 3 Days Plus Amodiaquine for 3 Days Plus Primaquine at Hour 2463

Incidence of Prolongation of the Corrected QT Interval

We record the number of events where the QT interval exceeds 500ms or increases by 60ms or greater. (NCT03355664)
Timeframe: 28 day

InterventionEvents (Number)
Artemether-lumefantrine for 3 Days Plus Primaquine at Hour 240
Artemether-lumefantrine for 3 Days Plus Amodiaquine for 3 Days Plus Primaquine at Hour 240

Number of Severe Adverse Events by Study Arm

"All numerators in AE tables mean that the AE was reported as present according to the definitions defined in the US government DAIDS 2017 grading tables for reporting of adverse events. The AEs are reported without grading in this table, but are graded in the paper reporting this clinical trial.~All Primary analyses are reported (also in the accepted manuscript) along with the secondary outcomes needed to support the primary analysis. Secondary outcomes not involving the randomised comparison will be updated when the analyses are available. Please note that analyses of these Secondary outcomes will take time." (NCT03355664)
Timeframe: 42 days

InterventionParticipants (Number)
Artemether-lumefantrine for 3 Days Plus Primaquine at Hour 242
Artemether-lumefantrine for 3 Days Plus Amodiaquine for 3 Days Plus Primaquine at Hour 245

Parasite Clearance Half-life

Parasite clearance half-life assessed by microscopy as primary parameter to determine parasite clearance (NCT03355664)
Timeframe: 42 day

InterventionHours (Mean)
Artemether-lumefantrine for 3 Days Plus Primaquine at Hour 245
Artemether-lumefantrine for 3 Days Plus Amodiaquine for 3 Days Plus Primaquine at Hour 245.5

Polymerase Chain Reaction Corrected Efficacy Defined as Adequate Clinical and Parasitological Response (ACPR) by Study Arm

Efficacy is defined as participants, following initial parasite and fever clearance, not having a recrudescence of the original plasmodium infection and fever, up to 42 days of follow up. (NCT03355664)
Timeframe: 42 days

InterventionParticipants (Count of Participants)
Artemether-lumefantrine for 3 Days Plus Primaquine at Hour 24146
Artemether-lumefantrine for 3 Days Plus Amodiaquine for 3 Days Plus Primaquine at Hour 24151

Prolongation of the Corrected QT Interval

We record the number of events where the QT interval exceeds 500ms or increases by 60ms or greater. There were zero events of this at any time point in either study arm. So no further analyses are possible. (NCT03355664)
Timeframe: Hour 4, Hour 24, Hour 28, Hour 48, Hour 52, Hour 60, Hour 64, Day 7 and Day 28 and between these time points

InterventionEvents (Number)
Artemether-lumefantrine for 3 Days Plus Primaquine at Hour 240
Artemether-lumefantrine for 3 Days Plus Amodiaquine for 3 Days Plus Primaquine at Hour 240

42-day Polymerase Chain Reaction Corrected Efficacy According to Site/Geographic Region

42-day polymerase chain reaction corrected efficacy defined as adequate clinical and parasitological response (ACPR) according to site/geographic region. (NCT03355664)
Timeframe: 42 day

,
InterventionParticipants (Count of Participants)
West CambodiaEast CambodiaVietnam
Artemether-lumefantrine for 3 Days Plus Amodiaquine for 3 Days Plus Primaquine at Hour 24359026
Artemether-lumefantrine for 3 Days Plus Primaquine at Hour 24329123

Reviews

3 reviews available for amodiaquine and Recrudescence

ArticleYear
The effect of dosing strategies on the therapeutic efficacy of artesunate-amodiaquine for uncomplicated malaria: a meta-analysis of individual patient data.
    BMC medicine, 2015, Mar-31, Volume: 13

    Topics: Africa; Amodiaquine; Antimalarials; Artemisinins; Dose-Response Relationship, Drug; Drug Combination

2015
Gametocyte carriage in uncomplicated Plasmodium falciparum malaria following treatment with artemisinin combination therapy: a systematic review and meta-analysis of individual patient data.
    BMC medicine, 2016, May-24, Volume: 14

    Topics: Amodiaquine; Antimalarials; Artemisinins; Child, Preschool; Drug Combinations; Drug Therapy, Combina

2016
[Importation of malaria into the Federal Republic of Germany including Berlin (West) in the last ten years (1963-1972)].
    Deutsche medizinische Wochenschrift (1946), 1974, Volume: 99, Issue:18

    Topics: Africa; Age Factors; Aircraft; Amodiaquine; Antimalarials; Asia; Berlin; Chloroquine; Disease Outbre

1974

Trials

14 trials available for amodiaquine and Recrudescence

ArticleYear
Efficacy of artesunate-amodiaquine and artemether-lumefantrine for uncomplicated Plasmodium falciparum malaria in Madagascar, 2018.
    Malaria journal, 2021, Nov-03, Volume: 20, Issue:1

    Topics: Adolescent; Amodiaquine; Antimalarials; Artemether, Lumefantrine Drug Combination; Artemisinins; Chi

2021
Triple therapy with artemether-lumefantrine plus amodiaquine versus artemether-lumefantrine alone for artemisinin-resistant, uncomplicated falciparum malaria: an open-label, randomised, multicentre trial.
    The Lancet. Infectious diseases, 2022, Volume: 22, Issue:6

    Topics: Amodiaquine; Antimalarials; Artemether; Artemether, Lumefantrine Drug Combination; Artemisinins; Dru

2022
Impact of retreatment with an artemisinin-based combination on malaria incidence and its potential selection of resistant strains: study protocol for a randomized controlled clinical trial.
    Trials, 2013, Sep-23, Volume: 14

    Topics: Amodiaquine; Antimalarials; Artemether, Lumefantrine Drug Combination; Artemisinins; Child, Preschoo

2013
Effectiveness and safety of artemether-lumefantrine versus artesunate-amodiaquine for unsupervised treatment of uncomplicated falciparum malaria in patients of all age groups in Nanoro, Burkina Faso: a randomized open label trial.
    Malaria journal, 2015, Aug-20, Volume: 14

    Topics: Amodiaquine; Antimalarials; Artemether, Lumefantrine Drug Combination; Artemisinins; Burkina Faso; C

2015
Artesunate-amodiaquine versus artemether-lumefantrine for the treatment of acute uncomplicated malaria in Congolese children under 10 years old living in a suburban area: a randomized study.
    Malaria journal, 2015, Oct-29, Volume: 14

    Topics: Amodiaquine; Anemia, Sickle Cell; Antimalarials; Artemether, Lumefantrine Drug Combination; Artemisi

2015
In vivo efficacy of artemether-lumefantrine and artesunate-amodiaquine for uncomplicated Plasmodium falciparum malaria in Malawi, 2014.
    Malaria journal, 2016, Apr-26, Volume: 15

    Topics: Amodiaquine; Antimalarials; Artemether, Lumefantrine Drug Combination; Artemisinins; Child, Preschoo

2016
Fixed-Dose Artesunate-Amodiaquine Combination vs Chloroquine for Treatment of Uncomplicated Blood Stage P. vivax Infection in the Brazilian Amazon: An Open-Label Randomized, Controlled Trial.
    Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2017, Jan-15, Volume: 64, Issue:2

    Topics: Adolescent; Adult; Aged; Amodiaquine; Antimalarials; Artemisinins; Brazil; Child; Child, Preschool;

2017
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.
    Malaria journal, 2011, Aug-12, Volume: 10

    Topics: Adolescent; Adult; Aged; Amodiaquine; Antimalarials; Artemether, Lumefantrine Drug Combination; Arte

2011
Good efficacy of artemether-lumefantrine for uncomplicated falciparum malaria in eastern Sumba, East Nusatenggara, Indonesia.
    Acta medica Indonesiana, 2012, Volume: 44, Issue:3

    Topics: Amodiaquine; Antimalarials; Artemether, Lumefantrine Drug Combination; Artemisinins; Drug Combinatio

2012
A randomized comparison of chloroquine and chloroquine plus ketotifen in the treatment of acute, uncomplicated, Plasmodium falciparum malaria in children.
    Annals of tropical medicine and parasitology, 2003, Volume: 97, Issue:2

    Topics: Acute Disease; Administration, Oral; Amodiaquine; Analysis of Variance; Antimalarials; Child; Child,

2003
Amodiaquine resistance is not related to rare findings of pfmdr1 gene amplifications in Kenya.
    Tropical medicine & international health : TM & IH, 2006, Volume: 11, Issue:12

    Topics: Amodiaquine; Animals; Antimalarials; Child; Drug Resistance, Multiple; Follow-Up Studies; Gene Ampli

2006
Artemether-lumefantrine versus amodiaquine plus sulfadoxine-pyrimethamine for uncomplicated falciparum malaria in Burkina Faso: a randomised non-inferiority trial.
    Lancet (London, England), 2007, Feb-10, Volume: 369, Issue:9560

    Topics: Amodiaquine; Antimalarials; Artemether, Lumefantrine Drug Combination; Artemisinins; Burkina Faso; C

2007
Effectiveness of amodiaquine as treatment for chloroquine-resistant Plasmodium falciparum infections in Kenya.
    Lancet (London, England), 1984, Feb-18, Volume: 1, Issue:8373

    Topics: Adolescent; Amodiaquine; Blood; Child; Chloroquine; Drug Combinations; Drug Resistance, Microbial; F

1984
A randomized comparison of chloroquine, amodiaquine and their combination with pyrimethamine-sulfadoxine in the treatment of acute, uncomplicated, Plasmodium falciparum malaria in children.
    Annals of tropical medicine and parasitology, 2002, Volume: 96, Issue:3

    Topics: Acute Disease; Amodiaquine; Antimalarials; Child; Child, Preschool; Chloroquine; Drug Therapy, Combi

2002

Other Studies

17 other studies available for amodiaquine and Recrudescence

ArticleYear
Activation of minority-variant Plasmodium vivax hypnozoites following artesunate + amodiaquine treatment in a 23-year old man with relapsing malaria in Antananarivo, Madagascar.
    Malaria journal, 2013, May-31, Volume: 12

    Topics: Adult; Amodiaquine; Antimalarials; Artemisinins; Drug Combinations; Humans; Madagascar; Malaria, Viv

2013
Efficacy of artemether-lumefantrine, artesunate-amodiaquine, and dihydroartemisinin-piperaquine for treatment of uncomplicated Plasmodium falciparum malaria in Angola, 2015.
    Malaria journal, 2017, 02-02, Volume: 16, Issue:1

    Topics: Amodiaquine; Angola; Antimalarials; Artemether, Lumefantrine Drug Combination; Artemisinins; Child;

2017
In vivo and in vitro efficacy of amodiaquine monotherapy for treatment of infection by chloroquine-resistant Plasmodium vivax.
    Antimicrobial agents and chemotherapy, 2009, Volume: 53, Issue:3

    Topics: Adolescent; Age Distribution; Amodiaquine; Animals; Antimalarials; Chloroquine; Confidence Intervals

2009
Some features of primary and recrudescent amodiaquine-resistant Plasmodium falciparum infections in Nigerian children.
    Memorias do Instituto Oswaldo Cruz, 2008, Volume: 103, Issue:8

    Topics: Acute Disease; Amodiaquine; Animals; Antimalarials; Case-Control Studies; Child; Child, Preschool; D

2008
In-vivo efficacy of amodiaquine-artesunate in children with uncomplicated Plasmodium falciparum malaria in western Kenya.
    Tropical medicine & international health : TM & IH, 2009, Volume: 14, Issue:3

    Topics: Amodiaquine; Animals; Antimalarials; Artemisinins; Child, Preschool; Drug Combinations; Drug Resista

2009
Selection of known Plasmodium falciparum resistance-mediating polymorphisms by artemether-lumefantrine and amodiaquine-sulfadoxine-pyrimethamine but not dihydroartemisinin-piperaquine in Burkina Faso.
    Antimicrobial agents and chemotherapy, 2010, Volume: 54, Issue:5

    Topics: Amodiaquine; Antimalarials; Artemether; Artemisinins; Burkina Faso; Drug Combinations; Drug Resistan

2010
Distinguishing recrudescence from reinfection in a longitudinal antimalarial drug efficacy study: comparison of results based on genotyping of msp-1, msp-2, and glurp.
    The American journal of tropical medicine and hygiene, 2003, Volume: 68, Issue:2

    Topics: Amodiaquine; Animals; Antigens, Protozoan; Antimalarials; Artemisinins; Artesunate; Child, Preschool

2003
Evaluation of amodiaquin (camoquin) in the treatment of relapsing vivax malaria.
    The American journal of the medical sciences, 1953, Volume: 225, Issue:1

    Topics: Amodiaquine; Malaria; Malaria, Vivax; Recurrence

1953
Roles of specific Plasmodium falciparum mutations in resistance to amodiaquine and sulfadoxine-pyrimethamine in Burkina Faso.
    The American journal of tropical medicine and hygiene, 2006, Volume: 75, Issue:1

    Topics: Amodiaquine; Animals; Antimalarials; Burkina Faso; Dihydropteroate Synthase; Drug Combinations; Drug

2006
High reinfection rate and treatment failures in children treated with amodiaquine for falciparum malaria in Muheza villages, Northeastern Tanzania.
    The American journal of tropical medicine and hygiene, 2006, Volume: 75, Issue:2

    Topics: Amodiaquine; Animals; Antimalarials; Child, Preschool; Cohort Studies; Haplotypes; Hematocrit; Human

2006
Antimalarial drug combinations in vastly different settings.
    Lancet (London, England), 2007, Feb-10, Volume: 369, Issue:9560

    Topics: Amodiaquine; Animals; Antimalarials; Artemether, Lumefantrine Drug Combination; Artemisinins; Burkin

2007
Resistance of Plasmodium falciparum malaria to amodiaquine, chloroquine and quinine in the Madang Province of Papua New Guinea, 1990-1993.
    Papua and New Guinea medical journal, 1996, Volume: 39, Issue:1

    Topics: Acute Disease; Amodiaquine; Animals; Antimalarials; Case-Control Studies; Child; Child, Preschool; C

1996
Factors influencing resistance to reinfection with Plasmodium falciparum.
    The American journal of tropical medicine and hygiene, 1999, Volume: 61, Issue:6

    Topics: Adolescent; Adult; Amodiaquine; Animals; Antibodies, Protozoan; Antimalarials; Child; Child, Prescho

1999
Ineffectiveness of amodiaquine against Plasmodium falciparum malaria in symptomatic young children living in an endemic malarious area of Papua New Guinea.
    Journal of tropical pediatrics, 1991, Volume: 37, Issue:4

    Topics: Age Factors; Amodiaquine; Child; Child, Preschool; Drug Resistance; Female; Humans; Infant; Malaria,

1991
Response to treatment in man of multi-drug resistant Plasmodium falciparum from Panama.
    The American journal of tropical medicine and hygiene, 1974, Volume: 23, Issue:1

    Topics: Adult; Amodiaquine; Animals; Anopheles; Antimalarials; Chloroquine; Drug Resistance, Microbial; Drug

1974
Studies on a mechanism of enhancement of maximum gastric secretory response: its possible importance in recurrent ulcers after surgical treatment.
    Research in experimental medicine. Zeitschrift fur die gesamte experimentelle Medizin einschliesslich experimenteller Chirurgie, 1972, Volume: 157, Issue:3

    Topics: Amodiaquine; Animals; Dogs; Female; Gastric Juice; Gastric Mucosa; Histamine; Histamine Antagonists;

1972
The role of drugs in a malaria program.
    The American journal of tropical medicine and hygiene, 1972, Volume: 21, Issue:5

    Topics: Amodiaquine; Antimalarials; Chloroquine; Dose-Response Relationship, Drug; Humans; Malaria; Primaqui

1972