miltefosine has been researched along with Leishmaniasis, Cutaneous 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.
Leishmaniasis, Cutaneous: An endemic disease that is characterized by the development of single or multiple localized lesions on exposed areas of skin that typically ulcerate. The disease has been divided into Old and New World forms. Old World leishmaniasis is separated into three distinct types according to epidemiology and clinical manifestations and is caused by species of the L. tropica and L. aethiopica complexes as well as by species of the L. major genus. New World leishmaniasis, also called American leishmaniasis, occurs in South and Central America and is caused by species of the L. mexicana or L. braziliensis complexes.
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 |
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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 |
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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, Cutaneous
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, Cutaneous
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, Cutaneous
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 |