miltefosine has been researched along with Leishmaniasis, American in 170 studies
miltefosine: hexadecyl phosphocholine derivative of cisplatin; did not substantially activate HIV long terminal repeat; less toxic than cisplatin
miltefosine : A phospholipid that is the hexadecyl monoester of phosphocholine.
Excerpt | Relevance | Reference |
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"To describe the characteristic clinical features and management of keratitis in the patients receiving miltefosine for post-kala-azar dermal leishmaniasis (PKDL)." | 8.02 | Keratitis occurring in patients treated with miltefosine for post-kala-azar dermal leishmaniasis. ( Ambasta, A; Arya, LK; Kusumesh, R; Mohan, N; Ravidas, V; Sinha, BP, 2021) |
"Miltefosine has not been readily available in the United States due to marketing delays and is expected to become available later this year." | 6.52 | Pharmacotherapy for leishmaniasis in the United States: focus on miltefosine. ( Fujinami, N; Shah, PJ; Vakil, NH, 2015) |
"Oral miltefosine was started at a dose of 150 mg/day but had to be stopped after 20 days as the patient developed diarrhea, bipedal edema, and renal impairment." | 5.56 | Case Report: Erysipeloid Cutaneous Leishmaniasis Treated with Oral Miltefosine. ( Adhikary, S; Karki, A; Parajuli, N; Tiwari, S, 2020) |
" We reported a case of acute anterior uveitis,a rare adverse effect, experienced by a patient treated with miltefosine for post-kala-azar dermal leishmaniasis." | 5.56 | Acute uveitis: A rare adverse effect of miltefosine in the treatment of post-kala-azar dermal leishmaniasis. ( Das, P; Das, VNR; Lal, CS; Pal, B; Pandey, K; Topno, RK, 2020) |
"Visceral leishmaniasis is an opportunistic infection that affects human immunodeficiency virus-infected persons in leishmaniasis-endemic areas." | 5.36 | Visceral Leishmaniasis treated with antimonials/paromomycin followed by itraconazole/miltefosine after standard therapy failures in a human immunodeficiency virus-infected patient. ( Barragán, P; López-Velez, R; Olmo, M; Podzamczer, D, 2010) |
"Although three new drugs or drug formulations, liposomal amphotericin B (AmBisome), miltefosine and paromomycin should be available for the treatment of visceral leishmaniasis (VL) within the next year, they all suffer from limitations of either cost, specific toxicities or parenteral administration." | 4.83 | Current scenario of drug development for leishmaniasis. ( Croft, SL; Seifert, K; Yardley, V, 2006) |
"To describe the characteristic clinical features and management of keratitis in the patients receiving miltefosine for post-kala-azar dermal leishmaniasis (PKDL)." | 4.02 | Keratitis occurring in patients treated with miltefosine for post-kala-azar dermal leishmaniasis. ( Ambasta, A; Arya, LK; Kusumesh, R; Mohan, N; Ravidas, V; Sinha, BP, 2021) |
" The presence of vesicles at the site of heat application was the most common adverse event reported associated with the use of TT; while vomiting (31." | 3.11 | A phase II multicenter randomized study to evaluate the safety and efficacy of combining thermotherapy and a short course of miltefosine for the treatment of uncomplicated cutaneous leishmaniasis in the New World. ( Alvarez, F; Arana, B; Boni, M; Echevarria, J; Jiménez, A; Llanos-Cuentas, A; López, L; Méndez, C; Quintero, J; Ramos, AP; Rode, J; Tabares, Y; Valencia, B; Vélez, I, 2022) |
"Miltefosine has proven efficacy for CL caused by L." | 3.01 | A Double-blind, Randomized Trial to Evaluate Miltefosine and Topical Granulocyte Macrophage Colony-stimulating Factor in the Treatment of Cutaneous Leishmaniasis Caused by Leishmania braziliensis in Brazil. ( Barral, A; Barral-Netto, M; Boaventura, V; Carvalho, EM; Corte, TWF; Guimarães, LH; Lago, T; Machado, PRL; Penna, G; Prates, FVO; Schriefer, A, 2021) |
" We aimed to characterize the intracellular PBMC miltefosine kinetics by developing a population pharmacokinetic (PK) model simultaneously describing plasma and intracellular PBMC pharmacokinetics." | 2.87 | Simultaneous population pharmacokinetic modelling of plasma and intracellular PBMC miltefosine concentrations in New World cutaneous leishmaniasis and exploration of exposure-response relationships. ( Beijnen, JH; Castro, MDM; Cossio, A; Dorlo, TPC; Gomez, MA; Kip, AE; Saravia, NG; Schellens, JHM, 2018) |
"Miltefosine was found to be effective and safe in the treatment of PKDL." | 2.80 | Efficacy and safety of miltefosine in treatment of post-kala-azar dermal leishmaniasis. ( Chakravarty, J; Rai, M; Singh, A; Sundar, S, 2015) |
" The adverse effects were primarily gastrointestinal for miltefosine and pain at the lesion site after treatment for thermotherapy." | 2.78 | Thermotherapy effective and safer than miltefosine in the treatment of cutaneous leishmaniasis in Colombia. ( Cruz, C; Godoy, G; López, L; Robledo, SM; Vélez, ID, 2013) |
"Oral miltefosine has not been evaluated for pediatric cutaneous leishmaniasis." | 2.77 | Noninferiority of miltefosine versus meglumine antimoniate for cutaneous leishmaniasis in children. ( Garcerant, D; Gore Saravia, N; Miranda, MC; Montero, LM; Muvdi Arenas, S; Nicholls, RS; Osorio, L; Pérez, M; Prager, M; Rodríguez-Barraquer, I; Rojas, MX; Rubiano, LC, 2012) |
"Miltefosine is an oral agent used for cutaneous leishmaniasis treatment." | 2.75 | Efficacy of miltefosine for the treatment of American cutaneous leishmaniasis. ( López, L; Mestra, L; Rodríguez, E; Rojas, C; Sánchez, X; Vélez, I, 2010) |
"Miltefosine was more effective than Sb(v) in the age group of 13-65 years-old compared to 2-12 years-old group (78." | 2.75 | Miltefosine in the treatment of cutaneous leishmaniasis caused by Leishmania braziliensis in Brazil: a randomized and controlled trial. ( Ampuero, J; Carvalho, EM; Guimarães, LH; Machado, PR; Penna, G; Rocha, AT; Schriefer, A; Sousa, RS; Talhari, A; Villasboas, L, 2010) |
" The safety of miltefosine-allopurinol combination therapy was confirmed by lack of effect on renal and hepatic parameters and adverse reactions." | 2.74 | Multicentric, controlled clinical study to evaluate effectiveness and safety of miltefosine and allopurinol for canine leishmaniosis. ( Bianciardi, P; Cañavate, C; Cruz, I; Miró, G; Mortarino, M; Oliva, G; Vischer, C, 2009) |
" Population pharmacokinetic modeling was performed with nonlinear mixed-effect modeling, using NONMEM." | 2.73 | Pharmacokinetics of miltefosine in Old World cutaneous leishmaniasis patients. ( Beijnen, JH; de Vries, HJ; de Vries, PJ; Dorlo, TP; Huitema, AD; Keizer, RJ; van Thiel, PP, 2008) |
"Miltefosine appears to be a safe and effective alternative to currently used therapies." | 2.73 | Miltefosine in cutaneous leishmaniasis. ( Mumtaz, N; Rahman, SB; ul Bari, A, 2007) |
"The miltefosine rate was lower than historic antimony cure rates of >90%." | 2.71 | Miltefosine for new world cutaneous leishmaniasis. ( Arana, BA; Arboleda, M; Berman, JD; Diaz, A; Engel, J; Gutierrez, P; Junge, K; Luz, M; Rizzo, N; Sindermann, H; Soto, J; Toledo, J; Vega, JC, 2004) |
" In this uncontrolled study of oral miltefosine for treatment of patients with American cutaneous leishmaniasis, a dosage of approximately 2." | 2.70 | Treatment of American cutaneous leishmaniasis with miltefosine, an oral agent. ( Berman, J; Engel, J; Fischer, C; Gutierrez, P; Nicholls, RS; Padilla, J; Soto, J; Toledo, J; Voss, A, 2001) |
" Moreover, VL and PKDL pharmacovigilance studies indicate a risk for serious adverse events, questioning the safety of MF." | 2.61 | The safety and efficacy of miltefosine in the long-term treatment of post-kala-azar dermal leishmaniasis in South Asia - A review and meta-analysis. ( den Boer, ML; Essink, DR; Pijpers, J; Ritmeijer, K, 2019) |
"Conventional treatment of cutaneous leishmaniasis involves intravenous or intralesional pentavalent antimonials." | 2.52 | Can a simple outpatient-based treatment be used to treat cutaneous leishmaniasis in young children? A Critically Appraised Topic. ( Burden-Teh, E; Williams, HC; Wootton, CI, 2015) |
"Miltefosine has not been readily available in the United States due to marketing delays and is expected to become available later this year." | 2.52 | Pharmacotherapy for leishmaniasis in the United States: focus on miltefosine. ( Fujinami, N; Shah, PJ; Vakil, NH, 2015) |
" These drugs were incorporated in conventional dosage forms or loaded in lipid nanocarries, which have been used mainly for improved skin delivery and antileishmanial activity." | 2.48 | Drug delivery systems for the topical treatment of cutaneous leishmaniasis. ( Aguiar, MG; Carneiro, G; Fernandes, AP; Ferreira, LA, 2012) |
"We report a 46-year-old patient with acquired immune deficiency syndrome who, 7 months after diagnosis of VL, developed PKDL and uveal leishmaniasis following HAART-induced immune recovery." | 2.44 | Post-kala-azar dermal leishmaniasis as an immune reconstitution inflammatory syndrome in a patient with acquired immune deficiency syndrome. ( Acquaviva, V; Antinori, S; Bestetti, G; Corbellino, M; Foschi, A; Longhi, E; Meroni, L; Parravicini, C; Piolini, R; Trovati, S, 2007) |
"Miltefosine is a lecithin analogue and its mechanism may be to inhibit phosphatidylcholine biosynthesis in the causative parasites." | 2.43 | Miltefosine to treat leishmaniasis. ( Berman, J, 2005) |
"Miltefosine was well tolerated, and as effective as historic values of antimony for treatment of L." | 2.43 | Treatment of New World cutaneous leishmaniasis with miltefosine. ( Berman, J; Soto, J, 2006) |
"Miltefosine is an alkylphosphocholine, originally developed for the treatment of cancer." | 2.43 | [Miltefosine: a new remedy for leishmaniasis]. ( Beijnen, JH; de Vries, PJ; Dorlo, TP; Eggelte, TA, 2006) |
"Recent developments in the treatment of simple cutaneous leishmaniasis are discussed followed by speculation about future therapies." | 2.42 | Cutaneous leishmaniasis: current and future management. ( Hepburn, NC, 2003) |
" Following the confirmation of significant in vitro activity, the performance of the maximum tolerated dose of OLPC was evaluated in an experimental murine model of CL followed by a dose-response titration and the efficacy evaluation of four OLPC formulations (two with a fast-release and two with a slow-release profile) using bioluminescent Leishmania major parasites." | 1.91 | Efficacy of oleylphosphocholine in experimental cutaneous leishmaniasis. ( Alavijeh, M; Croft, SL; Dixon, J; Harris, A; Mcarthur, KN; Platteeuw, JJ; Van Bocxlaer, K; Van Den Heuvel, D; Yardley, V, 2023) |
"Cutaneous leishmaniasis was not considered as an initial diagnosis because of the atypical appearance of the lesion as well as his residence in the hilly region of Nepal." | 1.62 | Case Report: An Atypical Erysipeloid Presentation of Cutaneous Leishmaniasis from the Hilly Region of Nepal. ( Nepal, S, 2021) |
"Miltefosine was orally administered for 27 patients with MA resistant ACL with approved L." | 1.62 | The effect of oral miltefosine in treatment of antimoniate resistant anthroponotic cutaneous leishmaniasis: An uncontrolled clinical trial. ( Darchini-Maragheh, E; Goyonlo, VM; Kiafar, B; Layegh, P; Tayyebi, M, 2021) |
"Treatment with miltefosine resulted in cure in 77 % (20/26) of cases, with cures among all species." | 1.62 | Efficacy and Tolerability of Miltefosine in the Treatment of Cutaneous Leishmaniasis. ( Brown, T; Nash, TE; Nutman, TB; O'Connell, EM; Talaat, KR; Ware, JM; Wetzler, L, 2021) |
" We reported a case of acute anterior uveitis,a rare adverse effect, experienced by a patient treated with miltefosine for post-kala-azar dermal leishmaniasis." | 1.56 | Acute uveitis: A rare adverse effect of miltefosine in the treatment of post-kala-azar dermal leishmaniasis. ( Das, P; Das, VNR; Lal, CS; Pal, B; Pandey, K; Topno, RK, 2020) |
"Oral miltefosine was started at a dose of 150 mg/day but had to be stopped after 20 days as the patient developed diarrhea, bipedal edema, and renal impairment." | 1.56 | Case Report: Erysipeloid Cutaneous Leishmaniasis Treated with Oral Miltefosine. ( Adhikary, S; Karki, A; Parajuli, N; Tiwari, S, 2020) |
"Prompt identification and treatment of cutaneous leishmaniasis caused by species with potential for mucocutaneous spread are key to limiting morbidity and mortality." | 1.56 | Cutaneous leishmaniasis successfully treated with miltefosine. ( Call, JE; Chan, CX; Chapman, MS; Glass, JS; Simmons, BJ; Yan, S, 2020) |
"In Brazil, cutaneous leishmaniasis is caused predominantly by L." | 1.51 | Investigation of the pathways related to intrinsic miltefosine tolerance in Leishmania (Viannia) braziliensis clinical isolates reveals differences in drug uptake. ( Alves, JM; Carvalho, EM; Coelho, AC; Cruz, AK; Cruz, MC; Espada, CR; Hornillos, V; Machado, PR; Magalhães, RM; Schriefer, A; Uliana, SRB, 2019) |
"Topical treatment for cutaneous leishmaniasis (CL) would be useful for treatment of some forms of the disease." | 1.51 | Anti-leishmanial activity of a topical miltefosine gel in experimental models of New World cutaneous leishmaniasis. ( Escobar, P; Mantilla, JC; Neira, LF, 2019) |
"Miltefosine was efficacious, safe and well tolerated, suggesting that it can play an important role in the treatment of severe PKDL also in East-African patients." | 1.51 | Severe post-kala-azar dermal leishmaniasis successfully treated with miltefosine in an Ethiopian HIV patient. ( Abongomera, C; Adera, C; Battaglioli, T; Ritmeijer, K, 2019) |
" This study aimed to investigate the feasibility of using focused pharmacovigilance for VL (VLPV) in Bangladesh's National Kala-azar Elimination Programme for the early detection and prevention of expected and unexpected adverse drug reactions (ADRs)." | 1.48 | Using focused pharmacovigilance for ensuring patient safety against antileishmanial drugs in Bangladesh's National Kala-azar Elimination Programme. ( Ahuja, V; Ghosh, P; Haque, R; Hossain, AFMA; Hossain, MA; Hossain, MS; Kumar, A; Mahshin, M; Maruf, S; Mondal, D; Shamsuzzaman, AKM; Sharma, A; Sharma, V, 2018) |
"Treatments by miltefosine, amphotericin B, N-methyl-glucamine antimoniate were subsequently initiated." | 1.46 | Recurrence of visceral and muco-cutaneous leishmaniasis in a patient under immunosuppressive therapy. ( Arrese Estrada, J; Cnops, L; Darcis, G; de Leval, L; Giot, JB; Hayette, MP; Leonard, P; Moutschen, M; Tassin, F; Van der Auwera, G, 2017) |
"Oral miltefosine has been shown to be non-inferior to first-line, injectable meglumine antimoniate (MA) for the treatment of cutaneous leishmaniasis (CL) in children." | 1.46 | Cost-effectiveness of meglumine antimoniate versus miltefosine caregiver DOT for the treatment of pediatric cutaneous leishmaniasis. ( Bartlett, AH; Berger, BA; Castro, MDM; Cossio, A; Pho, MT; Prada, S; Saravia, NG, 2017) |
"In the Netherlands, cutaneous leishmaniasis is most commonly seen in military personnel deployed on a mission or training abroad." | 1.46 | Two cases of cutaneous leishmaniasis in Dutch military personnel treated with oral miltefosine. ( Couwenberg, SM; Kortbeek, LM; Schadd, EM; Stijnis, C; van der Snoek, EM, 2017) |
"Tamoxifen was able to hinder the emergence of miltefosine resistance." | 1.43 | Efficacy of tamoxifen and miltefosine combined therapy for cutaneous leishmaniasis in the murine model of infection with Leishmania amazonensis. ( Coelho, AC; Reimão, JQ; Trinconi, CT; Uliana, SR, 2016) |
"In this study 86 confirmed cases of PKDL were treated with two different dosage regimens of miltefosine (Regimen I- 50mg twice daily for 90 days and Regimen II- 50 mg thrice for 60 days) and the clinical outcome assessed monthly." | 1.42 | Decline in Clinical Efficacy of Oral Miltefosine in Treatment of Post Kala-azar Dermal Leishmaniasis (PKDL) in India. ( Avishek, K; Deep, DK; Ramesh, V; Salotra, P; Singh, R; Verma, A; Verma, S, 2015) |
" Initial dose-response experiments showed that an oral daily dose of 40 mg/kg of OlPC was needed to impact time to cure and lesion sizes." | 1.40 | Direct comparison of the efficacy and safety of oral treatments with oleylphosphocholine (OlPC) and miltefosine in a mouse model of L. major cutaneous leishmaniasis. ( Bosschaerts, T; Caridha, DP; Fortin, A; Grogl, M; Hickman, MR; Hudson, TH; Leed, S; Ngundam, F; Parriott, S; Sena, J, 2014) |
"Treatment with meglumine antimoniate had to be interrupted in six patients, with QTc prolongation the reason for the interruption in three patients." | 1.39 | Cutaneous leishmaniasis in Switzerland: first experience with species-specific treatment. ( Blum, JA; Hatz, C; Mosimann, V; Neumayr, A, 2013) |
"Miltefosine is an alkylphospholipid analogue that exhibits potent activity against the different clinical manifestations of leishmaniasis." | 1.38 | Efficacy of miltefosine treatment in Leishmania amazonensis-infected BALB/c mice. ( de Souza, W; Godinho, JL; Rodrigues, JC; Silva, R; Simas-Rodrigues, C; Ürmenyi, TP, 2012) |
"Miltefosine treatment cured two patients with L." | 1.37 | A species-specific approach to the use of non-antimony treatments for cutaneous leishmaniasis. ( Fedorko, DP; Mahanty, S; Nash, TE; Ramanathan, R; Talaat, KR, 2011) |
" These observations illustrate the usability of quantifying parasite loads in skin lesions as a pharmacodynamic measure and quantitative descriptor of drug effect for CL supporting clinical assessment." | 1.37 | Dynamics of parasite clearance in cutaneous leishmaniasis patients treated with miltefosine. ( Beijnen, JH; de Vries, PJ; Dorlo, TP; Schoone, GJ; Stienstra, Y; van Thiel, PP; van Vugt, M, 2011) |
"Miltefosine treatment did not influence DC maturation (upregulation of major histocompatibility complex II [MHC II] or costimulatory molecules, e." | 1.36 | Miltefosine efficiently eliminates Leishmania major amastigotes from infected murine dendritic cells without altering their immune functions. ( Eichhorn, A; Gazeau, C; Griewank, K; von Stebut, E, 2010) |
"Visceral leishmaniasis is an opportunistic infection that affects human immunodeficiency virus-infected persons in leishmaniasis-endemic areas." | 1.36 | Visceral Leishmaniasis treated with antimonials/paromomycin followed by itraconazole/miltefosine after standard therapy failures in a human immunodeficiency virus-infected patient. ( Barragán, P; López-Velez, R; Olmo, M; Podzamczer, D, 2010) |
"Miltefosine has been established as the first oral administration drug against cutaneous and visceral leishmaniasis." | 1.35 | In vivo activity of perifosine against Leishmania amazonensis. ( Cabrera-Serra, MG; Piñero, JE; Valladares, B, 2008) |
"Mucocutaneous leishmaniasis is a serious preventable complication of cutaneous leishmaniasis." | 1.35 | [Mucosal complication of cutaneous leishmaniasis]. ( Figueroa, RA; Miranda, MC; Prager, M; Zea, DF, 2009) |
"Miltefosine was administered orally at 25 mg/kg/day for 10 days, while 10% paromomycin gel was applied topically twice a day for 10 days." | 1.35 | Combined topical paromomycin and oral miltefosine treatment of mice experimentally infected with Leishmania (Leishmania) major leads to reduction in both lesion size and systemic parasite burdens. ( Aguiar, MG; Fernandes, AP; Ferreira, LA; Nunan, EA; Nunan, FA; Silva, DL, 2009) |
"Miltefosine is a less toxic option to replace the antimony compounds." | 1.34 | [Cutaneous leishmaniasis]. ( Sunderkötter, C; von Stebut, E, 2007) |
"Miltefosine was given 100mg daily in divided doses for an initial 8 weeks." | 1.33 | Cure of antimony-unresponsive Indian post-kala-azar dermal leishmaniasis with oral miltefosine. ( Agrawal, D; Agrawal, S; Chakravarty, J; Chhabra, A; Kumar, K; Singh, V; Sundar, S, 2006) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 47 (27.65) | 29.6817 |
2010's | 87 (51.18) | 24.3611 |
2020's | 36 (21.18) | 2.80 |
Authors | Studies |
---|---|
Dorlo, TP | 3 |
van Thiel, PP | 4 |
Huitema, AD | 1 |
Keizer, RJ | 1 |
de Vries, HJ | 5 |
Beijnen, JH | 4 |
de Vries, PJ | 6 |
Griewank, K | 1 |
Gazeau, C | 1 |
Eichhorn, A | 1 |
von Stebut, E | 2 |
Stroppa, PHF | 2 |
Antinarelli, LMR | 1 |
Carmo, AML | 1 |
Gameiro, J | 1 |
Coimbra, ES | 2 |
da Silva, AD | 2 |
Temraz, MG | 1 |
Elzahhar, PA | 1 |
El-Din A Bekhit, A | 1 |
Bekhit, AA | 1 |
Labib, HF | 1 |
Belal, ASF | 1 |
Emiliano, YSS | 1 |
Almeida-Amaral, EE | 1 |
Monge-Maillo, B | 2 |
Norman, FF | 1 |
Chamorro-Tojeiro, S | 1 |
Gioia, F | 1 |
Pérez-Molina, JA | 1 |
Chicharro, C | 1 |
Moreno, J | 1 |
López-Vélez, R | 4 |
López, L | 3 |
Valencia, B | 1 |
Alvarez, F | 1 |
Ramos, AP | 1 |
Llanos-Cuentas, A | 2 |
Echevarria, J | 1 |
Vélez, I | 2 |
Boni, M | 1 |
Rode, J | 1 |
Quintero, J | 1 |
Jiménez, A | 1 |
Tabares, Y | 1 |
Méndez, C | 1 |
Arana, B | 3 |
Barba, PJ | 1 |
Morgado-Carrasco, D | 1 |
Quera, A | 1 |
Bano, S | 3 |
Bibi, M | 4 |
Farooq, S | 3 |
Zafar, H | 3 |
Shaikh, M | 3 |
Khoso, BK | 3 |
Yousuf, S | 3 |
Choudhary, MI | 3 |
Ferreira, BA | 1 |
Coser, EM | 1 |
Saborito, C | 1 |
Yamashiro-Kanashiro, EH | 1 |
Lindoso, JAL | 1 |
Coelho, AC | 5 |
Van Bocxlaer, K | 3 |
Dixon, J | 1 |
Platteeuw, JJ | 1 |
Van Den Heuvel, D | 1 |
Mcarthur, KN | 1 |
Harris, A | 1 |
Alavijeh, M | 1 |
Croft, SL | 6 |
Yardley, V | 5 |
Carregal, VM | 1 |
Lanza, JS | 1 |
Souza, DM | 1 |
Islam, A | 1 |
Demicheli, C | 1 |
Fujiwara, RT | 1 |
Rivas, L | 1 |
Frézard, F | 2 |
Meinel, RS | 1 |
Almeida, ADC | 1 |
Glanzmann, N | 1 |
Dar, MJ | 2 |
Khalid, S | 1 |
McElroy, CA | 1 |
Satoskar, AR | 1 |
Khan, GM | 3 |
Ramesh, V | 8 |
Dixit, KK | 1 |
Sharma, N | 1 |
Singh, R | 2 |
Salotra, P | 8 |
Topno, RK | 4 |
Rabi Das, VN | 1 |
Kumar, M | 1 |
Madhukar, M | 1 |
Pandey, K | 5 |
Verma, N | 4 |
Agrawal, K | 1 |
Lal, CS | 4 |
Siddiqui, NA | 2 |
Bimal, S | 3 |
Das, P | 5 |
Özbilgin, A | 2 |
Çavuş, İ | 2 |
Kaya, T | 1 |
Yıldırım, A | 1 |
Harman, M | 2 |
Mann, S | 1 |
Phupitakphol, T | 1 |
Davis, B | 1 |
Newman, S | 1 |
Suarez, JA | 1 |
Henao-Martínez, A | 1 |
Franco-Paredes, C | 1 |
Kabra, R | 1 |
Ingale, P | 1 |
Singh, S | 1 |
Peixoto, F | 1 |
Nascimento, MT | 1 |
Costa, R | 1 |
Silva, J | 1 |
Renard, G | 1 |
Guimarães, LH | 3 |
Penna, G | 4 |
Barral-Netto, M | 3 |
Carvalho, LP | 1 |
Machado, PRL | 3 |
Carvalho, EM | 5 |
Pinart, M | 1 |
Rueda, JR | 1 |
Romero, GA | 1 |
Pinzón-Flórez, CE | 1 |
Osorio-Arango, K | 1 |
Silveira Maia-Elkhoury, AN | 1 |
Reveiz, L | 1 |
Elias, VM | 1 |
Tweed, JA | 1 |
Prates, FVO | 1 |
Boaventura, V | 1 |
Lago, T | 1 |
Schriefer, A | 3 |
Corte, TWF | 1 |
Barral, A | 1 |
Kusumesh, R | 1 |
Ambasta, A | 1 |
Arya, LK | 1 |
Mohan, N | 1 |
Sinha, BP | 1 |
Ravidas, V | 1 |
Tunalı, V | 1 |
Gündüz, C | 1 |
Turgay, N | 1 |
Ollech, A | 2 |
Solomon, M | 2 |
Horev, A | 2 |
Reiss-Huss, S | 2 |
Ben-Amitai, D | 2 |
Zvulunov, A | 2 |
Friedland, R | 2 |
Atar-Snir, V | 2 |
Molho-Pessach, V | 1 |
Barzilai, A | 2 |
Greenberger, S | 2 |
Ware, JM | 1 |
O'Connell, EM | 1 |
Brown, T | 1 |
Wetzler, L | 1 |
Talaat, KR | 2 |
Nutman, TB | 1 |
Nash, TE | 2 |
Soto, JA | 1 |
Berman, JD | 3 |
Chan, CX | 1 |
Simmons, BJ | 1 |
Call, JE | 1 |
Yan, S | 1 |
Glass, JS | 1 |
Chapman, MS | 1 |
Pessach-Molcho, V | 1 |
Parajuli, N | 1 |
Adhikary, S | 1 |
Karki, A | 1 |
Tiwari, S | 1 |
Khan, AS | 1 |
Ud Din, F | 1 |
Ali, Z | 1 |
Zahid, F | 2 |
Zeb, A | 2 |
Mendes, L | 1 |
Guerra, JO | 1 |
Costa, B | 1 |
Silva, ASD | 1 |
Guerra, MDGB | 1 |
Ortiz, J | 1 |
Doria, SS | 1 |
Silva, GVD | 1 |
de Jesus, DV | 1 |
Pal, B | 2 |
Das, VNR | 2 |
Peralta, MF | 1 |
Usseglio, NA | 1 |
Bracamonte, ME | 1 |
Guzmán, ML | 1 |
Olivera, ME | 1 |
Marco, JD | 1 |
Barroso, PA | 1 |
Carrer, DC | 1 |
Kämink, S | 1 |
Masih, B | 1 |
Ali, N | 1 |
Ullah, A | 1 |
Khan, SJ | 1 |
Ashraf, S | 1 |
Pylypenko, T | 1 |
Grobusch, MP | 1 |
Fernhout, J | 1 |
den Boer, M | 1 |
Ritmeijer, K | 3 |
Batool, S | 1 |
Ud-Din, F | 1 |
Naz, SS | 1 |
Khan, MW | 1 |
Tayyebi, M | 1 |
Darchini-Maragheh, E | 1 |
Layegh, P | 1 |
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Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
---|---|---|---|---|---|---|---|
Pharmacokinetics of Miltefosine in Children and Adults: Implications for the Treatment of Cutaneous Leishmaniasis in Colombia.[NCT01462500] | Phase 4 | 60 participants (Actual) | Interventional | 2011-10-31 | Completed | ||
A Randomized, Open Label, Multicenter Study to Determine the Efficacy and Safety of Combining Thermotherapy and a Short Course of Miltefosine for the Treatment of Uncomplicated Cutaneous Leishmaniasis in the New World¨[NCT02687971] | Phase 2 | 130 participants (Actual) | Interventional | 2016-12-31 | Completed | ||
Miltefosine and GM-CSF in Cutaneous Leishmaniasis: a Randomized and Controlled Trial[NCT03023111] | Phase 3 | 300 participants (Actual) | Interventional | 2017-06-30 | Completed | ||
Documenting Clinical Outcomes of Patients Receiving Miltefosine for the Treatment of Complicated Cutaneous Leishmaniasis in Ethiopia[NCT04004754] | 94 participants (Actual) | Observational | 2019-05-07 | Completed | |||
Randomized Clinical Trial of the Efficacy and Tolerability of Oral Miltefosine Versus Parenteral Antimony for the Treatment of Pediatric Cutaneous Leishmaniasis in Colombia[NCT00487253] | Phase 3 | 150 participants (Anticipated) | Interventional | 2007-07-31 | Active, not recruiting | ||
Therapeutic Gain of Adding the Immunomodulator Pentoxifylline to the Treatment of Cutaneous Leishmaniasis[NCT01464242] | Phase 2/Phase 3 | 75 participants (Actual) | Interventional | 2011-11-30 | Completed | ||
Phase 3 Open-label Study of Efficacy and Safety of Miltefosine or Thermotherapy vs Glucantime for Cutaneous Leishmaniasis in Colombia.[NCT00471705] | Phase 3 | 437 participants (Actual) | Interventional | 2006-06-30 | Completed | ||
A Study for Safety and Efficacy of Miltefosine for Treatment of Children and Adolescents With Post-Kala-azar Dermal Leishmaniasis (PKDL) in Bangladesh and Association of Serum Vitamin E and Exposure to Arsenic With PKDL[NCT02193022] | Phase 3 | 80 participants (Actual) | Interventional | 2014-07-31 | Completed | ||
Evaluation of the Safety and Clinical Activity of Curaleish Lotion and Cream in the Topical Treatment of Cutaneous Leishmaniasis in Colombia[NCT04072874] | Phase 1/Phase 2 | 0 participants (Actual) | Interventional | 2021-01-31 | Withdrawn (stopped due to Tthe study is in the approval phase by local regulatory authorities) | ||
Randomized Clinical Trial to Evaluate the Safety and Therapeutic Response of Two ARNICA TINCTURE Treatment Regimes in the Topical Treatment of Uncomplicated Cutaneous Leishmaniasis in Colombia[NCT05094908] | Phase 1 | 16 participants (Anticipated) | Interventional | 2023-05-03 | Recruiting | ||
Clinical Trial to Assess Efficacy and Safety of Orally Administered Miltefosine in Brazilian Patients With Cutaneous Leishmaniasis Compared to the Standard Care as Active Control[NCT00600548] | Phase 2 | 180 participants (Actual) | Interventional | 2007-07-31 | Completed | ||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |
"Complete Clinical response: Initial cure plus the absence of recurrences or mucosal lesions for 6 months after the end of treatment.~Note: nitial cure: Complete re-epithelialization of all ulcers and complete disappearance of the induration up to 3 months after the end of treatment." (NCT00471705)
Timeframe: Until 6 months posttreatment
Intervention | participants (Number) |
---|---|
Miltefosine | 85 |
Glucantime® | 103 |
Thermotherapy | 86 |
At least 50% increase in lesion size at the end of treatment, absence of clinical response at 6 weeks, or any sign of lesion activity 3 months after the end of treatment (NCT00471705)
Timeframe: Until 3 months posttreatment
Intervention | participants (Number) |
---|---|
Miltefosine | 34 |
Glucantime® | 14 |
Thermotherapy | 42 |
Reactivation of the lesion at the original site after cure or mucosal compromise during follow-up. (NCT00471705)
Timeframe: Until 6 months post-treatment
Intervention | Participants (Number) |
---|---|
Miltefosine | 3 |
Glucantime® | 4 |
Thermotherapy | 6 |
23 reviews available for miltefosine and Leishmaniasis, American
Article | Year |
---|---|
Interventions for American cutaneous and mucocutaneous leishmaniasis.
Topics: Administration, Oral; Adult; Antiprotozoal Agents; Azithromycin; BCG Vaccine; Female; Humans; Hypert | 2020 |
Keratitis After Post-Kala-Azar Dermal Leishmaniasis.
Topics: Administration, Oral; Adult; Antiprotozoal Agents; Corneal Stroma; Eye Infections, Parasitic; Glucoc | 2018 |
Drug resistance and treatment failure in leishmaniasis: A 21st century challenge.
Topics: Amphotericin B; Antiprotozoal Agents; Drug Resistance; Drug Therapy, Combination; Humans; Leishmania | 2017 |
Interventions to treat cutaneous leishmaniasis in children: A systematic review.
Topics: Antiprotozoal Agents; Clinical Trials as Topic; Humans; Leishmania; Leishmaniasis, Cutaneous; Meglum | 2018 |
American tegumentary leishmaniasis in Brazil: a critical review of the current therapeutic approach with systemic meglumine antimoniate and short-term possibilities for an alternative treatment.
Topics: Antiprotozoal Agents; Brazil; Humans; Leishmania braziliensis; Leishmania guyanensis; Leishmaniasis, | 2019 |
The safety and efficacy of miltefosine in the long-term treatment of post-kala-azar dermal leishmaniasis in South Asia - A review and meta-analysis.
Topics: Antiprotozoal Agents; Asia; Humans; Leishmaniasis, Cutaneous; Leishmaniasis, Visceral; Phosphorylcho | 2019 |
Efficacy of miltefosine compared with glucantime for the treatment of cutaneous leishmaniasis: a systematic review and meta-analysis.
Topics: Humans; Leishmaniasis, Cutaneous; Meglumine Antimoniate; Non-Randomized Controlled Trials as Topic; | 2019 |
Can a simple outpatient-based treatment be used to treat cutaneous leishmaniasis in young children? A Critically Appraised Topic.
Topics: Administration, Cutaneous; Ambulatory Care; Aminoglycosides; Antiprotozoal Agents; Child, Preschool; | 2015 |
Miltefosine for visceral and cutaneous leishmaniasis: drug characteristics and evidence-based treatment recommendations.
Topics: Administration, Oral; Africa, Eastern; Antiprotozoal Agents; Bangladesh; Coinfection; Drug Therapy, | 2015 |
Pharmacotherapy for leishmaniasis in the United States: focus on miltefosine.
Topics: Antiprotozoal Agents; Drug Resistance; Humans; Leishmaniasis; Leishmaniasis, Cutaneous; Leishmaniasi | 2015 |
Treatment of leishmaniasis with miltefosine: 2008 status.
Topics: Administration, Oral; Adult; Antiprotozoal Agents; Child; Clinical Trials as Topic; Female; Humans; | 2008 |
Drug delivery systems for the topical treatment of cutaneous leishmaniasis.
Topics: Administration, Cutaneous; Aminoquinolines; Amphotericin B; Animals; Antiprotozoal Agents; Drug Deli | 2012 |
Orally effective drugs for kala-azar (visceral leishmaniasis): focus on miltefosine and sitamaquine.
Topics: Administration, Oral; Aminoquinolines; Animals; Antiprotozoal Agents; Clinical Trials as Topic; Dose | 2003 |
Cutaneous leishmaniasis: current and future management.
Topics: Amphotericin B; Animals; Antimony Sodium Gluconate; Humans; Immunotherapy; Leishmania; Leishmaniasis | 2003 |
Miltefosine to treat leishmaniasis.
Topics: Administration, Oral; Animals; Antiprotozoal Agents; Humans; Leishmaniasis, Cutaneous; Leishmaniasis | 2005 |
Current scenario of drug development for leishmaniasis.
Topics: Amphotericin B; Animals; Antiprotozoal Agents; Drug Design; Humans; Leishmania; Leishmaniasis; Leish | 2006 |
Current scenario of drug development for leishmaniasis.
Topics: Amphotericin B; Animals; Antiprotozoal Agents; Drug Design; Humans; Leishmania; Leishmaniasis; Leish | 2006 |
Current scenario of drug development for leishmaniasis.
Topics: Amphotericin B; Animals; Antiprotozoal Agents; Drug Design; Humans; Leishmania; Leishmaniasis; Leish | 2006 |
Current scenario of drug development for leishmaniasis.
Topics: Amphotericin B; Animals; Antiprotozoal Agents; Drug Design; Humans; Leishmania; Leishmaniasis; Leish | 2006 |
Miltefosine--discovery of the antileishmanial activity of phospholipid derivatives.
Topics: Animals; Antineoplastic Agents; Antiprotozoal Agents; Drug Design; Glycerylphosphorylcholine; Leishm | 2006 |
Treatment of New World cutaneous leishmaniasis with miltefosine.
Topics: Administration, Oral; Adult; Antiprotozoal Agents; Clinical Trials as Topic; Double-Blind Method; Dr | 2006 |
[Miltefosine: a new remedy for leishmaniasis].
Topics: Animals; Antiprotozoal Agents; Humans; Leishmaniasis, Cutaneous; Leishmaniasis, Visceral; Phosphoryl | 2006 |
Cutaneous leishmaniasis treatment.
Topics: Administration, Cutaneous; Administration, Oral; Aminoquinolines; Amphotericin B; Animals; Antimony; | 2007 |
Post-kala-azar dermal leishmaniasis as an immune reconstitution inflammatory syndrome in a patient with acquired immune deficiency syndrome.
Topics: Acquired Immunodeficiency Syndrome; Americas; Antiprotozoal Agents; Antiretroviral Therapy, Highly A | 2007 |
Development status of miltefosine as first oral drug in visceral and cutaneous leishmaniasis.
Topics: Administration, Oral; Adult; Antiprotozoal Agents; Child; Child, Preschool; Clinical Trials as Topic | 2001 |
Chemotherapy of cutaneous leishmaniasis: a review.
Topics: Antifungal Agents; Antimony; Leishmaniasis, Cutaneous; Meglumine; Meglumine Antimoniate; Ointments; | 2001 |
23 trials available for miltefosine and Leishmaniasis, American
Article | Year |
---|---|
Pharmacokinetics of miltefosine in Old World cutaneous leishmaniasis patients.
Topics: Adult; Afghanistan; Animals; Antiprotozoal Agents; Chromatography, Liquid; Female; Humans; Leishmani | 2008 |
A phase II multicenter randomized study to evaluate the safety and efficacy of combining thermotherapy and a short course of miltefosine for the treatment of uncomplicated cutaneous leishmaniasis in the New World.
Topics: Adult; Antiprotozoal Agents; Humans; Hyperthermia, Induced; Leishmaniasis, Cutaneous; Meglumine; Meg | 2022 |
A Double-blind, Randomized Trial to Evaluate Miltefosine and Topical Granulocyte Macrophage Colony-stimulating Factor in the Treatment of Cutaneous Leishmaniasis Caused by Leishmania braziliensis in Brazil.
Topics: Antimony; Antiprotozoal Agents; Brazil; Granulocyte-Macrophage Colony-Stimulating Factor; Granulocyt | 2021 |
Association of miltefosine with granulocyte and macrophage colony-stimulating factor (GM-CSF) in the treatment of cutaneous leishmaniasis in the Amazon region: A randomized and controlled trial.
Topics: Administration, Oral; Administration, Topical; Adolescent; Adult; Antiprotozoal Agents; Female; Gran | 2021 |
A Pilot Randomized Clinical Trial: Oral Miltefosine and Pentavalent Antimonials Associated With Pentoxifylline for the Treatment of American Tegumentary Leishmaniasis.
Topics: Antiprotozoal Agents; Humans; Leishmaniasis, Cutaneous; Pentoxifylline; Phosphorylcholine; Pilot Pro | 2021 |
Simultaneous population pharmacokinetic modelling of plasma and intracellular PBMC miltefosine concentrations in New World cutaneous leishmaniasis and exploration of exposure-response relationships.
Topics: Adult; Child; Child, Preschool; Colombia; Dose-Response Relationship, Drug; Female; Humans; Leishman | 2018 |
Thermotherapy effective and safer than miltefosine in the treatment of cutaneous leishmaniasis in Colombia.
Topics: Adult; Antiprotozoal Agents; Colombia; Follow-Up Studies; Humans; Hyperthermia, Induced; Leishmanias | 2013 |
[Cutaneous leishmaniasis. Diagnosis and therapy in northern Afghanistan].
Topics: Administration, Topical; Adult; Afghanistan; Antimony Sodium Gluconate; Antiprotozoal Agents; Combin | 2014 |
Efficacy and safety of miltefosine in treatment of post-kala-azar dermal leishmaniasis.
Topics: Antiprotozoal Agents; Female; Humans; Leishmaniasis, Cutaneous; Leishmaniasis, Visceral; Male; Phosp | 2015 |
Inadequacy of 12-Week Miltefosine Treatment for Indian Post-Kala-Azar Dermal Leishmaniasis.
Topics: Adolescent; Adult; Antiprotozoal Agents; Child; Drug Administration Schedule; Female; Humans; Leishm | 2015 |
Safety and efficacy of a combination of paromomycin and miltefosine for two vs. three courses in patients with post-kala-azar dermal leishmaniasis: an observational pilot study.
Topics: Administration, Oral; Adult; Antiprotozoal Agents; Drug Administration Schedule; Drug Therapy, Combi | 2017 |
Multicentric, controlled clinical study to evaluate effectiveness and safety of miltefosine and allopurinol for canine leishmaniosis.
Topics: Allopurinol; Animals; Dog Diseases; Dogs; Drug Therapy, Combination; Female; Leishmaniasis, Cutaneou | 2009 |
Efficacy of miltefosine for the treatment of American cutaneous leishmaniasis.
Topics: Adult; Antiprotozoal Agents; Capsules; Humans; Injections, Intramuscular; Leishmania; Leishmaniasis, | 2010 |
Efficacy of miltefosine for the treatment of American cutaneous leishmaniasis.
Topics: Adult; Antiprotozoal Agents; Capsules; Humans; Injections, Intramuscular; Leishmania; Leishmaniasis, | 2010 |
Efficacy of miltefosine for the treatment of American cutaneous leishmaniasis.
Topics: Adult; Antiprotozoal Agents; Capsules; Humans; Injections, Intramuscular; Leishmania; Leishmaniasis, | 2010 |
Efficacy of miltefosine for the treatment of American cutaneous leishmaniasis.
Topics: Adult; Antiprotozoal Agents; Capsules; Humans; Injections, Intramuscular; Leishmania; Leishmaniasis, | 2010 |
Cutaneous leishmaniasis (Leishmania major infection) in Dutch troops deployed in northern Afghanistan: epidemiology, clinical aspects, and treatment.
Topics: Adult; Afghanistan; Antiprotozoal Agents; Cryotherapy; Humans; Leishmania major; Leishmaniasis, Cuta | 2010 |
Miltefosine in the treatment of cutaneous leishmaniasis caused by Leishmania braziliensis in Brazil: a randomized and controlled trial.
Topics: Abdominal Pain; Administration, Oral; Adolescent; Adult; Aged; Antimony; Antiprotozoal Agents; Brazi | 2010 |
Noninferiority of miltefosine versus meglumine antimoniate for cutaneous leishmaniasis in children.
Topics: Administration, Oral; Antiprotozoal Agents; Child; Child, Preschool; Colombia; Female; Humans; Leish | 2012 |
Oral miltefosine for Indian post-kala-azar dermal leishmaniasis: a randomised trial.
Topics: Administration, Oral; Adolescent; Adult; Female; Follow-Up Studies; Humans; Leishmaniasis, Cutaneous | 2013 |
Miltefosine for new world cutaneous leishmaniasis.
Topics: Administration, Oral; Adult; Animals; Antiprotozoal Agents; Colombia; Double-Blind Method; Drug Tole | 2004 |
Oral miltefosine to treat new world cutaneous leishmaniasis.
Topics: Administration, Oral; Animals; Antiprotozoal Agents; Humans; Leishmania braziliensis; Leishmaniasis, | 2007 |
Miltefosine in cutaneous leishmaniasis.
Topics: Adult; Antimony; Antiprotozoal Agents; Female; Humans; Leishmaniasis, Cutaneous; Male; Meglumine; Me | 2007 |
Comparison of miltefosine and meglumine antimoniate for the treatment of zoonotic cutaneous leishmaniasis (ZCL) by a randomized clinical trial in Iran.
Topics: Adolescent; Adult; Animals; Antiprotozoal Agents; Female; Humans; Iran; Leishmaniasis, Cutaneous; Ma | 2007 |
Efficacy of miltefosine for Bolivian cutaneous leishmaniasis.
Topics: Adolescent; Adult; Animals; Antiprotozoal Agents; Bolivia; Child; Female; Humans; Leishmania brazili | 2008 |
Efficacy of miltefosine for Bolivian cutaneous leishmaniasis.
Topics: Adolescent; Adult; Animals; Antiprotozoal Agents; Bolivia; Child; Female; Humans; Leishmania brazili | 2008 |
Efficacy of miltefosine for Bolivian cutaneous leishmaniasis.
Topics: Adolescent; Adult; Animals; Antiprotozoal Agents; Bolivia; Child; Female; Humans; Leishmania brazili | 2008 |
Efficacy of miltefosine for Bolivian cutaneous leishmaniasis.
Topics: Adolescent; Adult; Animals; Antiprotozoal Agents; Bolivia; Child; Female; Humans; Leishmania brazili | 2008 |
Treatment of American cutaneous leishmaniasis with miltefosine, an oral agent.
Topics: Administration, Oral; Adult; Antiprotozoal Agents; Colombia; Humans; Leishmaniasis, Cutaneous; Male; | 2001 |
124 other studies available for miltefosine and Leishmaniasis, American
Article | Year |
---|---|
Miltefosine efficiently eliminates Leishmania major amastigotes from infected murine dendritic cells without altering their immune functions.
Topics: Animals; Antiprotozoal Agents; Apoptosis; CD4-Positive T-Lymphocytes; CD8-Positive T-Lymphocytes; Ce | 2010 |
Effect of 1,2,3-triazole salts, non-classical bioisosteres of miltefosine, on Leishmania amazonensis.
Topics: Animals; Antiprotozoal Agents; Apoptosis; Cell Line; Erythrocytes; Humans; Leishmania mexicana; Leis | 2017 |
Anti-leishmanial click modifiable thiosemicarbazones: Design, synthesis, biological evaluation and in silico studies.
Topics: Animals; Chlorocebus aethiops; Click Chemistry; Drug Design; Humans; Leishmania major; Leishmaniasis | 2018 |
Efficacy of Apigenin and Miltefosine Combination Therapy against Experimental Cutaneous Leishmaniasis.
Topics: Animals; Antiprotozoal Agents; Apigenin; Biomarkers; Drug Combinations; Female; Leishmania mexicana; | 2018 |
Post-kala-azar dermal leishmaniasis due to Leishmania infantum in an HIV-negative patient treated with miltefosine.
Topics: Antiprotozoal Agents; HIV Infections; Humans; Leishmania infantum; Leishmaniasis, Cutaneous; Leishma | 2022 |
Miltefosine to Treat Childhood Cutaneous Leishmaniasis.
Topics: Antiprotozoal Agents; Child; Humans; Leishmaniasis, Cutaneous; Phosphorylcholine | 2022 |
Anti-leishmanial physalins-Phytochemical investigation, in vitro evaluation against clinical and MIL-resistant L. tropica strains and in silico studies.
Topics: Antiprotozoal Agents; Humans; Leishmania major; Leishmaniasis, Cutaneous; Molecular Docking Simulati | 2022 |
Anti-leishmanial physalins-Phytochemical investigation, in vitro evaluation against clinical and MIL-resistant L. tropica strains and in silico studies.
Topics: Antiprotozoal Agents; Humans; Leishmania major; Leishmaniasis, Cutaneous; Molecular Docking Simulati | 2022 |
Anti-leishmanial physalins-Phytochemical investigation, in vitro evaluation against clinical and MIL-resistant L. tropica strains and in silico studies.
Topics: Antiprotozoal Agents; Humans; Leishmania major; Leishmaniasis, Cutaneous; Molecular Docking Simulati | 2022 |
Anti-leishmanial physalins-Phytochemical investigation, in vitro evaluation against clinical and MIL-resistant L. tropica strains and in silico studies.
Topics: Antiprotozoal Agents; Humans; Leishmania major; Leishmaniasis, Cutaneous; Molecular Docking Simulati | 2022 |
In vitro miltefosine and amphotericin B susceptibility of strains and clinical isolates of Leishmania species endemic in Brazil that cause tegumentary leishmaniasis.
Topics: Amphotericin B; Antiprotozoal Agents; Brazil; Humans; Leishmania; Leishmaniasis; Leishmaniasis, Cuta | 2023 |
Efficacy of oleylphosphocholine in experimental cutaneous leishmaniasis.
Topics: Animals; Antiprotozoal Agents; Leishmania major; Leishmaniasis, Cutaneous; Leishmaniasis, Visceral; | 2023 |
Combination oral therapy against Leishmania amazonensis infection in BALB/c mice using nanoassemblies made from amphiphilic antimony(V) complex incorporating miltefosine.
Topics: Administration, Oral; Animals; Antimony; Antiprotozoal Agents; Disease Models, Animal; Female; Leish | 2019 |
Novel functionalized 1,2,3-triazole derivatives exhibit antileishmanial activity, increase in total and mitochondrial-ROS and depolarization of mitochondrial membrane potential of Leishmania amazonensis.
Topics: Animals; Antiprotozoal Agents; Leishmania mexicana; Leishmaniasis, Cutaneous; Macrophages, Peritonea | 2020 |
Topical treatment of cutaneous leishmaniasis with novel amphotericin B-miltefosine co-incorporated second generation ultra-deformable liposomes.
Topics: Administration, Cutaneous; Amphotericin B; Animals; Antiprotozoal Agents; Disease Models, Animal; Dr | 2020 |
Assessing the Efficacy and Safety of Liposomal Amphotericin B and Miltefosine in Combination for Treatment of Post Kala-Azar Dermal Leishmaniasis.
Topics: Adolescent; Adult; Amphotericin B; Antiprotozoal Agents; Child; DNA, Protozoan; Drug Therapy, Combin | 2020 |
Advanced case of PKDL due to delayed treatment: A rare case report.
Topics: Antiprotozoal Agents; Humans; India; Leishmania donovani; Leishmaniasis, Cutaneous; Leishmaniasis, V | 2020 |
Comparison of
Topics: Amphotericin B; Animals; Antimony Sodium Gluconate; Antiprotozoal Agents; Drug Resistance; Female; G | 2020 |
Case Report: Cutaneous Leishmaniasis due to
Topics: Administration, Oral; Adult; Antiprotozoal Agents; Biopsy; Central America; Female; Humans; Leishman | 2020 |
Computationally designed synthetic peptides for transporter proteins imparts allostericity in Miltefosine resistant L. major.
Topics: Allosteric Regulation; Animals; Antiprotozoal Agents; ATP Binding Cassette Transporter, Subfamily B, | 2020 |
Evaluation of the Ability of Miltefosine Associated with Topical GM-CSF in Modulating the Immune Response of Patients with Cutaneous Leishmaniasis.
Topics: Administration, Topical; Antiprotozoal Agents; Cytokines; Cytotoxicity, Immunologic; Female; Granulo | 2020 |
Keratitis occurring in patients treated with miltefosine for post-kala-azar dermal leishmaniasis.
Topics: Adolescent; Adult; Antiprotozoal Agents; Female; Glucocorticoids; Humans; Keratitis; Leishmaniasis, | 2021 |
Overcoming the Challenge; In Vivo Efficacy of Miltefosine for Chronic Cutaneous Leishmaniasis.
Topics: Animals; Antiprotozoal Agents; Humans; Leishmaniasis, Cutaneous; Male; Meglumine Antimoniate; Mice; | 2021 |
Cutaneous Leishmaniasis Treated with Miltefosine: A Case Series of 10 Paediatric Patients.
Topics: Adolescent; Antiprotozoal Agents; Child; Child, Preschool; Humans; Israel; Leishmaniasis, Cutaneous; | 2020 |
Efficacy and Tolerability of Miltefosine in the Treatment of Cutaneous Leishmaniasis.
Topics: Antiprotozoal Agents; Humans; Leishmania infantum; Leishmaniasis, Cutaneous; Phosphorylcholine | 2021 |
Miltefosine Treatment of Cutaneous Leishmaniasis.
Topics: Humans; Leishmaniasis, Cutaneous; Phosphorylcholine | 2021 |
Cutaneous leishmaniasis successfully treated with miltefosine.
Topics: Adult; Antiprotozoal Agents; Female; Humans; Leishmaniasis, Cutaneous; Male; Middle Aged; Phosphoryl | 2020 |
Cutaneous Leishmaniasis Treated with Miltefosine: A Case Series of 10 Paediatric Patients.
Topics: Adolescent; Antiprotozoal Agents; Child; Child, Preschool; Humans; Israel; Leishmaniasis, Cutaneous; | 2020 |
Case Report: Erysipeloid Cutaneous Leishmaniasis Treated with Oral Miltefosine.
Topics: Administration, Oral; Aged; Antibodies, Protozoan; Antiprotozoal Agents; Erysipeloid; Humans; Leishm | 2020 |
Development, in vitro and in vivo evaluation of miltefosine loaded nanostructured lipid carriers for the treatment of Cutaneous Leishmaniasis.
Topics: Drug Carriers; Humans; Leishmaniasis, Cutaneous; Lipids; Nanostructures; Particle Size; Phosphorylch | 2021 |
Acute uveitis: A rare adverse effect of miltefosine in the treatment of post-kala-azar dermal leishmaniasis.
Topics: Antiprotozoal Agents; Humans; Leishmaniasis, Cutaneous; Leishmaniasis, Visceral; Phosphorylcholine; | 2020 |
Efficacy of topical Miltefosine formulations in an experimental model of cutaneous leishmaniasis.
Topics: Animals; Leishmania; Leishmaniasis, Cutaneous; Mice; Mice, Inbred BALB C; Models, Theoretical; Phosp | 2022 |
Effectiveness of miltefosine in cutaneous leishmaniasis caused by Leishmania tropica in Pakistan after antimonial treatment failure or contraindications to first line therapy-A retrospective analysis.
Topics: Adolescent; Adult; Aged; Antimony; Antiprotozoal Agents; Child; Female; Humans; Leishmania tropica; | 2021 |
Macrophage targeting with the novel carbopol-based miltefosine-loaded transfersomal gel for the treatment of cutaneous leishmaniasis:
Topics: Acrylic Resins; Animals; Leishmaniasis, Cutaneous; Macrophages; Mice; Mice, Inbred BALB C; Phosphory | 2021 |
The effect of oral miltefosine in treatment of antimoniate resistant anthroponotic cutaneous leishmaniasis: An uncontrolled clinical trial.
Topics: Administration, Oral; Adolescent; Adult; Antiprotozoal Agents; Child; Child, Preschool; Drug Resista | 2021 |
Investigating the Aggregation of Imported Cutaneous Leishmaniasis in Henan, Central China.
Topics: Amphotericin B; Animals; Antimony Sodium Gluconate; Antiprotozoal Agents; China; Communicable Diseas | 2021 |
Case Report: An Atypical Erysipeloid Presentation of Cutaneous Leishmaniasis from the Hilly Region of Nepal.
Topics: Antifungal Agents; Antiprotozoal Agents; Fluconazole; Humans; Leishmaniasis, Cutaneous; Male; Middle | 2021 |
Case Report: Miltefosine Failure and Spontaneous Resolution of Cutaneous Leishmaniasis braziliensis.
Topics: Antiprotozoal Agents; Female; Humans; Leishmania braziliensis; Leishmaniasis, Cutaneous; Peru; Phosp | 2021 |
Miltefosine for the treatment of cutaneous leishmaniasis-A pilot study from Ethiopia.
Topics: Administration, Oral; Adolescent; Adult; Antiprotozoal Agents; Cohort Studies; Ethiopia; Female; Hum | 2021 |
Risk factors for therapeutic failure to meglumine antimoniate and miltefosine in adults and children with cutaneous leishmaniasis in Colombia: A cohort study.
Topics: Adolescent; Adult; Antiprotozoal Agents; Child; Child, Preschool; Cohort Studies; Colombia; Female; | 2017 |
Risk factors for therapeutic failure to meglumine antimoniate and miltefosine in adults and children with cutaneous leishmaniasis in Colombia: A cohort study.
Topics: Adolescent; Adult; Antiprotozoal Agents; Child; Child, Preschool; Cohort Studies; Colombia; Female; | 2017 |
Risk factors for therapeutic failure to meglumine antimoniate and miltefosine in adults and children with cutaneous leishmaniasis in Colombia: A cohort study.
Topics: Adolescent; Adult; Antiprotozoal Agents; Child; Child, Preschool; Cohort Studies; Colombia; Female; | 2017 |
Risk factors for therapeutic failure to meglumine antimoniate and miltefosine in adults and children with cutaneous leishmaniasis in Colombia: A cohort study.
Topics: Adolescent; Adult; Antiprotozoal Agents; Child; Child, Preschool; Cohort Studies; Colombia; Female; | 2017 |
Risk factors for therapeutic failure to meglumine antimoniate and miltefosine in adults and children with cutaneous leishmaniasis in Colombia: A cohort study.
Topics: Adolescent; Adult; Antiprotozoal Agents; Child; Child, Preschool; Cohort Studies; Colombia; Female; | 2017 |
Risk factors for therapeutic failure to meglumine antimoniate and miltefosine in adults and children with cutaneous leishmaniasis in Colombia: A cohort study.
Topics: Adolescent; Adult; Antiprotozoal Agents; Child; Child, Preschool; Cohort Studies; Colombia; Female; | 2017 |
Risk factors for therapeutic failure to meglumine antimoniate and miltefosine in adults and children with cutaneous leishmaniasis in Colombia: A cohort study.
Topics: Adolescent; Adult; Antiprotozoal Agents; Child; Child, Preschool; Cohort Studies; Colombia; Female; | 2017 |
Risk factors for therapeutic failure to meglumine antimoniate and miltefosine in adults and children with cutaneous leishmaniasis in Colombia: A cohort study.
Topics: Adolescent; Adult; Antiprotozoal Agents; Child; Child, Preschool; Cohort Studies; Colombia; Female; | 2017 |
Risk factors for therapeutic failure to meglumine antimoniate and miltefosine in adults and children with cutaneous leishmaniasis in Colombia: A cohort study.
Topics: Adolescent; Adult; Antiprotozoal Agents; Child; Child, Preschool; Cohort Studies; Colombia; Female; | 2017 |
Cost-effectiveness of meglumine antimoniate versus miltefosine caregiver DOT for the treatment of pediatric cutaneous leishmaniasis.
Topics: Administration, Oral; Antiprotozoal Agents; Caregivers; Child; Child, Preschool; Cost-Benefit Analys | 2017 |
Efficacy of Paromomycin-Chloroquine Combination Therapy in Experimental Cutaneous Leishmaniasis.
Topics: Amphotericin B; Animals; Antiprotozoal Agents; Chloroquine; Disease Models, Animal; Drug Combination | 2017 |
Recurrence of visceral and muco-cutaneous leishmaniasis in a patient under immunosuppressive therapy.
Topics: Amphotericin B; Antiprotozoal Agents; Biopsy; Female; Humans; Immunocompromised Host; Leishmania; Le | 2017 |
Epidemiology of Cutaneous Leishmaniasis in a Colombian Municipality.
Topics: Adolescent; Antimony Sodium Gluconate; Antiprotozoal Agents; Child; Child, Preschool; Colombia; Fema | 2017 |
Monitoring of Parasite Kinetics in Indian Post-Kala-azar Dermal Leishmaniasis.
Topics: Adolescent; Adult; Amphotericin B; Antiprotozoal Agents; Asymptomatic Infections; Biopsy; DNA, Inter | 2018 |
In vitro activity of new N-benzyl-1H-benzimidazol-2-amine derivatives against cutaneous, mucocutaneous and visceral Leishmania species.
Topics: Amino Acid Sequence; Amphotericin B; Animals; Antiprotozoal Agents; Arginase; Benzimidazoles; Cell L | 2018 |
Perichondritis of the ear in an Afghan immigrant.
Topics: Adult; Afghanistan; Animals; Biopsy; Cartilage Diseases; Diagnosis, Differential; Ear Diseases; Ear, | 2018 |
Successful Treatment of Disseminated Cutaneous Leishmaniasis With Liposomal Amphotericin B and Miltefosine in an Eight-year-old Girl.
Topics: Amphotericin B; Antiprotozoal Agents; Child; Female; Humans; Iran; Leishmaniasis, Cutaneous; Phospho | 2018 |
Effects of nanoemulsions prepared with essential oils of copaiba- and andiroba against Leishmania infantum and Leishmania amazonensis infections.
Topics: Animals; Antiprotozoal Agents; Emulsions; Fabaceae; Female; Gas Chromatography-Mass Spectrometry; In | 2018 |
Investigation of anti-leishmanial efficacy of miltefosine and ketoconazole loaded on nanoniosomes.
Topics: Animals; Antiprotozoal Agents; Ketoconazole; Leishmania major; Leishmaniasis, Cutaneous; Nanostructu | 2018 |
Using focused pharmacovigilance for ensuring patient safety against antileishmanial drugs in Bangladesh's National Kala-azar Elimination Programme.
Topics: Acute Kidney Injury; Adolescent; Adult; Aged; Amphotericin B; Antiprotozoal Agents; Bangladesh; Fema | 2018 |
Corneal complications following Post Kala-azar Dermal Leishmaniasis treatment.
Topics: Adolescent; Adult; Antiprotozoal Agents; Bangladesh; Humans; Keratitis; Leishmaniasis, Cutaneous; Le | 2018 |
Case Report: Squamous Cell Carcinoma Referred for Mohs Surgery Found to be Cutaneous Leishmaniasis.
Topics: Antibodies, Protozoan; Antiprotozoal Agents; Carcinoma, Squamous Cell; Diagnosis, Differential; Fema | 2018 |
Case Reports: Late Emergence of Cutaneous Leishmaniasis in an Immunocompromised Patient in a Non-Endemic Setting.
Topics: Adult; Afghanistan; Antiprotozoal Agents; Australia; Biopsy; DNA, Ribosomal Spacer; Humans; Immunoco | 2019 |
[Refractory cutaneous leishmaniasis: Benefit of miltefosine].
Topics: Aged; Antiprotozoal Agents; Drug Resistance; Humans; Leishmaniasis, Cutaneous; Male; Phosphorylcholi | 2019 |
Resistance of
Topics: Animals; Antiprotozoal Agents; Cells, Cultured; Drug Resistance; Extracellular Traps; Humans; Leishm | 2018 |
Anti-leishmanial effect of spiro dihydroquinoline-oxindoles on volume regulation decrease and sterol biosynthesis of Leishmania braziliensis.
Topics: Animals; Antiprotozoal Agents; Inhibitory Concentration 50; Leishmania braziliensis; Leishmaniasis, | 2019 |
Severe post-kala-azar dermal leishmaniasis successfully treated with miltefosine in an Ethiopian HIV patient.
Topics: Administration, Oral; Adult; Antiprotozoal Agents; Ethiopia; HIV Infections; Humans; Leishmania dono | 2019 |
Anti-leishmanial activity of a topical miltefosine gel in experimental models of New World cutaneous leishmaniasis.
Topics: Administration, Topical; Animals; Antiprotozoal Agents; Biopsy; Disease Models, Animal; Drug Stabili | 2019 |
Investigation of the pathways related to intrinsic miltefosine tolerance in Leishmania (Viannia) braziliensis clinical isolates reveals differences in drug uptake.
Topics: Biological Transport; Drug Resistance; Gene Expression Profiling; Humans; Leishmania braziliensis; L | 2019 |
Semicarbazone derivatives as promising therapeutic alternatives in leishmaniasis.
Topics: Analysis of Variance; Animals; Antiprotozoal Agents; Caspases; Cell Cycle; Cell Line; Cell Membrane; | 2019 |
Miltefosine Induced Reduced Male Fertility Capacity after Treatment of Post Kala-azar Dermal Leishmaniasis, Bangladesh.
Topics: Adolescent; Antiprotozoal Agents; Bangladesh; Fertility; Humans; Infertility, Male; Leishmaniasis, C | 2019 |
Development of topical liposomes containing miltefosine for the treatment of Leishmania major infection in susceptible BALB/c mice.
Topics: Administration, Topical; Animals; Antiprotozoal Agents; Leishmania major; Leishmaniasis, Cutaneous; | 2019 |
Susceptibility of clinical isolates of Leishmania aethiopica to miltefosine, paromomycin, amphotericin B and sodium stibogluconate using amastigote-macrophage in vitro model.
Topics: Amphotericin B; Animals; Antimony Sodium Gluconate; Antiprotozoal Agents; Cells, Cultured; Ethiopia; | 2013 |
Clinical complexity of Leishmania (Viannia) braziliensis infections amongst travelers.
Topics: Adult; Aged; Amphotericin B; Antiprotozoal Agents; Humans; Leishmania braziliensis; Leishmaniasis, C | 2013 |
Cutaneous leishmaniasis in Switzerland: first experience with species-specific treatment.
Topics: Adolescent; Adult; Aged; Aged, 80 and over; Antiprotozoal Agents; Child; Child, Preschool; Female; H | 2013 |
Post-kala-azar dermal leishmaniasis with mucosal involvement: an unusual case presentation including successful treatment with miltefosine.
Topics: Adult; Antiprotozoal Agents; Bangladesh; Humans; Leishmaniasis, Cutaneous; Leishmaniasis, Visceral; | 2013 |
Combination therapy with amphotericin-B and miltefosine for post-kala-azar dermal leishmaniasis: a preliminary report.
Topics: Amphotericin B; Antiprotozoal Agents; DNA, Protozoan; Drug Therapy, Combination; Humans; Leishmanias | 2014 |
Treatment failure and miltefosine susceptibility in dermal leishmaniasis caused by Leishmania subgenus Viannia species.
Topics: Adolescent; Adult; ATP Binding Cassette Transporter, Subfamily G; ATP-Binding Cassette Transporters; | 2014 |
In vivo antileishmanial efficacy of miltefosine against Leishmania (Leishmania) amazonensis.
Topics: Animals; Antiprotozoal Agents; Leishmania mexicana; Leishmaniasis, Cutaneous; Male; Meglumine; Meglu | 2014 |
Direct comparison of the efficacy and safety of oral treatments with oleylphosphocholine (OlPC) and miltefosine in a mouse model of L. major cutaneous leishmaniasis.
Topics: Administration, Oral; Animals; Antiprotozoal Agents; Disease Models, Animal; Leishmania major; Leish | 2014 |
Effectiveness of miltefosine-pentoxifylline compared to miltefosine in the treatment of cutaneous leishmaniasis in C57Bl/6 mice.
Topics: Administration, Oral; Animals; Antiprotozoal Agents; Disease Models, Animal; Drug Evaluation, Precli | 2014 |
[Cutaneous leishmaniasis in a patient with ulcerative colitis under treatment with infliximab].
Topics: Antiprotozoal Agents; Azathioprine; Colitis, Ulcerative; Diagnosis, Differential; Humans; Immunocomp | 2015 |
Evaluation of the efficacy of systemic miltefosine associated with photodynamic therapy with liposomal chloroaluminium phthalocyanine in the treatment of cutaneous leishmaniasis caused by Leishmania (L.) amazonensis in C57BL/6 mice.
Topics: Animals; Antifungal Agents; Female; Indoles; Leishmania; Leishmaniasis, Cutaneous; Liposomes; Mice; | 2016 |
Combined suboptimal schedules of topical paromomycin, meglumine antimoniate and miltefosine to treat experimental infection caused by Leishmania (Viannia) braziliensis.
Topics: Administration, Oral; Administration, Topical; Animals; Antiprotozoal Agents; Appointments and Sched | 2015 |
PKDL--A Silent Parasite Pool for Transmission of Leishmaniasis in Kala-azar Endemic Areas of Malda District, West Bengal, India.
Topics: Administration, Oral; Adolescent; Adult; Animals; Antimony Sodium Gluconate; Antiprotozoal Agents; C | 2015 |
Decline in Clinical Efficacy of Oral Miltefosine in Treatment of Post Kala-azar Dermal Leishmaniasis (PKDL) in India.
Topics: Adult; Antiprotozoal Agents; Child; Female; Histocytochemistry; Humans; India; Leishmaniasis, Cutane | 2015 |
A male preponderance in patients with Indian post kala-azar dermal leishmaniasis is associated with increased circulating levels of testosterone.
Topics: Adolescent; Adult; Amphotericin B; Antibodies, Protozoan; Antimony Sodium Gluconate; Antiprotozoal A | 2016 |
Two cases of cutaneous leishmaniasis in Dutch military personnel treated with oral miltefosine.
Topics: Administration, Oral; Adult; Antiprotozoal Agents; Humans; Leishmaniasis, Cutaneous; Male; Military | 2017 |
Efficacy of tamoxifen and miltefosine combined therapy for cutaneous leishmaniasis in the murine model of infection with Leishmania amazonensis.
Topics: Administration, Oral; Animals; Antiprotozoal Agents; Disease Models, Animal; Drug Interactions; Drug | 2016 |
A Luciferase-Expressing Leishmania braziliensis Line That Leads to Sustained Skin Lesions in BALB/c Mice and Allows Monitoring of Miltefosine Treatment Outcome.
Topics: Amphotericin B; Animals; Antifungal Agents; Antiprotozoal Agents; Cricetinae; Deoxycholic Acid; Drug | 2016 |
Study on the safety and efficacy of miltefosine for the treatment of children and adolescents with post-kala-azar dermal leishmaniasis in Bangladesh, and an association of serum vitamin E and exposure to arsenic with post-kala-azar dermal leishmaniasis: a
Topics: Adolescent; Antiprotozoal Agents; Arsenic; Bangladesh; Case-Control Studies; Child; Child, Preschool | 2016 |
Topical formulations of miltefosine for cutaneous leishmaniasis in a BALB/c mouse model.
Topics: Administration, Topical; Animals; Cells, Cultured; Disease Models, Animal; Drug Compounding; Female; | 2016 |
In Vitro and In Vivo Miltefosine Susceptibility of a Leishmania amazonensis Isolate from a Patient with Diffuse Cutaneous Leishmaniasis: Follow-Up.
Topics: Animals; Antiprotozoal Agents; Drug Resistance; Humans; Leishmania; Leishmaniasis, Cutaneous; Mice; | 2016 |
Post-Kala-Azar Dermal Leishmaniasis Without Previous History of Visceral Leishmaniasis.
Topics: Adolescent; Adult; Antiprotozoal Agents; DNA, Protozoan; Female; Humans; Leishmania donovani; Leishm | 2016 |
Immune response following miltefosine therapy in a patient with post-kala-azar dermal leishmaniasis.
Topics: Adolescent; Animals; Antiprotozoal Agents; Clofazimine; Diagnosis, Differential; Humans; Hypopigment | 2008 |
Isolation of Leishmania tropica from a patient with visceral leishmaniasis and disseminated cutaneous leishmaniasis, southern Iran.
Topics: Adolescent; Amphotericin B; Animals; Antiprotozoal Agents; Female; Humans; Interferon-gamma; Iran; L | 2008 |
In vivo activity of perifosine against Leishmania amazonensis.
Topics: Administration, Oral; Animals; Antiprotozoal Agents; Female; Leishmania mexicana; Leishmaniasis, Cut | 2008 |
Post-Kala-Azar dermal leishmaniasis in an HIV-1-infected woman: recovery after amphotericin B following failure of oral miltefosine.
Topics: Administration, Oral; Adult; AIDS-Related Opportunistic Infections; Amphotericin B; Antiparasitic Ag | 2008 |
Cutaneous leishmaniasis with lymphadenopathy due to Leishmania donovani.
Topics: Animals; Antiprotozoal Agents; Facial Dermatoses; Female; Humans; Leishmania donovani; Leishmaniasis | 2009 |
Cutaneous leishmaniasis with boggy induration and simultaneous mucosal disease.
Topics: Amphotericin B; Antimony; Antiprotozoal Agents; Biopsy; Bolivia; Drug Therapy, Combination; Female; | 2009 |
Miltefosine to treat cutaneous leishmaniasis caused by Leishmania tropica.
Topics: Animals; Antiprotozoal Agents; Child; Humans; Leishmania tropica; Leishmaniasis, Cutaneous; Male; Ph | 2009 |
Short report: Development of post-kala-azar dermal leishmaniasis (PKDL) in miltefosine-treated visceral leishmaniasis.
Topics: Adult; Amphotericin B; Antiprotozoal Agents; Dermatitis; Humans; Leishmaniasis, Cutaneous; Leishmani | 2009 |
[Mucosal complication of cutaneous leishmaniasis].
Topics: Aged; Anemia; Antiprotozoal Agents; Contraindications; Eyelid Diseases; Humans; Hypertension; Kidney | 2009 |
Amiodarone and miltefosine act synergistically against Leishmania mexicana and can induce parasitological cure in a murine model of cutaneous leishmaniasis.
Topics: Amiodarone; Animals; Antiprotozoal Agents; Cricetinae; Disease Models, Animal; Drug Synergism; Femal | 2009 |
Combined topical paromomycin and oral miltefosine treatment of mice experimentally infected with Leishmania (Leishmania) major leads to reduction in both lesion size and systemic parasite burdens.
Topics: Administration, Oral; Administration, Topical; Animals; Disease Models, Animal; Drug Therapy, Combin | 2009 |
Miltefosine treatment of Leishmania major infection: an observational study involving Dutch military personnel returning from northern Afghanistan.
Topics: Adult; Afghanistan; Female; Humans; Leishmania major; Leishmaniasis, Cutaneous; Male; Middle Aged; M | 2010 |
Post-kala-azar dermal leishmaniasis (PKDL) developing after treatment of visceral leishmaniasis with amphotericin B and miltefosine.
Topics: Adult; Amphotericin B; Antimony Sodium Gluconate; Antiprotozoal Agents; Biopsy; Female; Humans; Leis | 2009 |
Resolution of cutaneous old world and new world leishmaniasis after oral miltefosine treatment.
Topics: Administration, Oral; Antiprotozoal Agents; Female; Humans; Leishmaniasis, Cutaneous; Male; Phosphor | 2010 |
Visceral Leishmaniasis treated with antimonials/paromomycin followed by itraconazole/miltefosine after standard therapy failures in a human immunodeficiency virus-infected patient.
Topics: AIDS-Related Opportunistic Infections; HIV; HIV Infections; HIV-1; Humans; Itraconazole; Leishmanias | 2010 |
A species-specific approach to the use of non-antimony treatments for cutaneous leishmaniasis.
Topics: Adult; Aged; Amphotericin B; Antiprotozoal Agents; Child; Female; Humans; Ketoconazole; Leishmania; | 2011 |
Cutaneous leishmaniasis after travel to Cyprus and successful treatment with miltefosine.
Topics: Antiprotozoal Agents; Austria; Cyprus; Female; Humans; Leishmaniasis, Cutaneous; Middle Aged; Phosph | 2011 |
Miltefosine-induced apoptotic cell death on Leishmania major and L. tropica strains.
Topics: Animals; Apoptosis; Cell Cycle; Cell Line; DNA Fragmentation; Humans; Leishmania major; Leishmania t | 2011 |
Miltefosine as an effective choice in the treatment of post-kala-azar dermal leishmaniasis.
Topics: Administration, Oral; Adolescent; Adult; Antiprotozoal Agents; Dose-Response Relationship, Drug; Dru | 2011 |
Miltefosine effectively modulates the cytokine milieu in Indian post kala-azar dermal leishmaniasis.
Topics: Adolescent; Adult; Aged; Antiprotozoal Agents; B7-1 Antigen; B7-2 Antigen; Child; Cytokines; Female; | 2011 |
Treatment of imported New World cutaneous leishmaniasis in Germany.
Topics: Adolescent; Adult; Aged; Amphotericin B; Animals; Antiprotozoal Agents; Female; Germany; Humans; Lei | 2011 |
Dynamics of parasite clearance in cutaneous leishmaniasis patients treated with miltefosine.
Topics: Antiprotozoal Agents; Female; Humans; Leishmania infantum; Leishmania major; Leishmaniasis, Cutaneou | 2011 |
Efficacy of miltefosine treatment in Leishmania amazonensis-infected BALB/c mice.
Topics: Animals; Antiprotozoal Agents; Azure Stains; DNA, Protozoan; Dose-Response Relationship, Drug; Drug | 2012 |
Cutaneous leishmaniasis acquired in Jura, France.
Topics: Antiprotozoal Agents; France; Humans; Leishmaniasis, Cutaneous; Male; Middle Aged; Phosphorylcholine | 2012 |
Leishmania strains causing self-healing cutaneous leishmaniasis have greater susceptibility towards oxidative stress.
Topics: Antimony; Free Radicals; Humans; Leishmania major; Leishmaniasis, Cutaneous; Leishmaniasis, Visceral | 2012 |
Drug susceptibility in Leishmania isolates following miltefosine treatment in cases of visceral leishmaniasis and post kala-azar dermal leishmaniasis.
Topics: Adolescent; Adult; Animals; Antiprotozoal Agents; Child; Female; Humans; India; Inhibitory Concentra | 2012 |
Leishmania major infection in humanized mice induces systemic infection and provokes a nonprotective human immune response.
Topics: Animals; Antiprotozoal Agents; Disease Models, Animal; Humans; Immune Evasion; Leishmania major; Lei | 2012 |
[Leishmaniasis--oral treatment with hexadecylphosphocholine].
Topics: Administration, Oral; Adult; Antiprotozoal Agents; Child; Clinical Trials as Topic; Drug Resistance; | 2004 |
The sensitivity of clinical isolates of Leishmania from Peru and Nepal to miltefosine.
Topics: Animals; Antiprotozoal Agents; Cells, Cultured; Humans; Leishmania; Leishmaniasis, Cutaneous; Leishm | 2005 |
Successful treatment of post-kala-azar dermal leishmaniasis (PKDL) in a HIV infected patient with multiple relapsing leishmaniasis from Western Europe.
Topics: Adult; Amphotericin B; Animals; Antimony Sodium Gluconate; Antiprotozoal Agents; Europe; Germany; HI | 2006 |
Cure of antimony-unresponsive Indian post-kala-azar dermal leishmaniasis with oral miltefosine.
Topics: Administration, Oral; Adult; Antimony Sodium Gluconate; Antiprotozoal Agents; Humans; Injections, In | 2006 |
Successful miltefosine treatment of post-kala-azar dermal leishmaniasis occurring during antiretroviral therapy.
Topics: Administration, Oral; Adult; Anti-Retroviral Agents; Antiprotozoal Agents; Drug Therapy, Combination | 2006 |
Quantification of the response to miltefosine treatment for visceral leishmaniasis by QT-NASBA.
Topics: Administration, Oral; Antiprotozoal Agents; Humans; Leishmaniasis, Cutaneous; Leishmaniasis, Viscera | 2006 |
Treatment of diffuse cutaneous leishmaniasis with miltefosine: a case report.
Topics: Adult; Antiprotozoal Agents; Humans; Leishmaniasis, Cutaneous; Male; Phosphorylcholine; Treatment Ou | 2006 |
Relapse of new world diffuse cutaneous leishmaniasis caused by Leishmania (Leishmania) mexicana after miltefosine treatment.
Topics: Adult; Animals; Antiprotozoal Agents; Humans; Leishmania mexicana; Leishmaniasis, Cutaneous; Male; P | 2006 |
Hexadecyl-phosphorylcholine ointment for treatment of cutaneous leishmaniasis: an animal trial.
Topics: Administration, Cutaneous; Analysis of Variance; Animals; Anti-Infective Agents, Local; Antiprotozoa | 2006 |
First case of typical Old World cutaneous leishmaniasis treated with miltefosine.
Topics: Administration, Oral; Adult; Animals; Antiprotozoal Agents; Diagnosis, Differential; DNA, Protozoan; | 2007 |
[Cutaneous leishmaniasis].
Topics: Animals; Biopsy; Cross-Sectional Studies; Diagnosis, Differential; Humans; Leishmania; Leishmaniasis | 2007 |
Chronic cutaneous leishmaniasis in an immunocompetent patient: response to miltefosine.
Topics: Administration, Oral; Antiprotozoal Agents; Humans; Leishmaniasis, Cutaneous; Male; Middle Aged; Pho | 2007 |
Glucantime-resistant Leishmania tropica isolated from Iranian patients with cutaneous leishmaniasis are sensitive to alternative antileishmania drugs.
Topics: Amphotericin B; Animals; Antimony Sodium Gluconate; Antiprotozoal Agents; Drug Resistance; Humans; I | 2007 |
Oral miltefosine in the treatment of post-kala-azar dermal leishmaniasis.
Topics: Adult; Antiprotozoal Agents; Humans; Leishmaniasis, Cutaneous; Leishmaniasis, Visceral; Male; Phosph | 2008 |
Successful treatment of a married couple for American leishmaniasis with miltefosine.
Topics: Animals; Antiprotozoal Agents; Female; Humans; Leishmania; Leishmaniasis, Cutaneous; Male; Middle Ag | 2008 |