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Clinical Trial Protocol

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Clinical Trial Protocols


VL Combination Therapy in Asia

NCT01122771 - Phase III, Study of Three Short Course Combination Regimens (Ambisome®, Miltefosine, Paromomycin) Compared With AmBisome® Alone for the Treatment of Visceral Leishmaniasis in Bangladesh
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NCT00696969 - Safety and Efficacy Study to Evaluate Different Combination Treatment Regimens for Visceral Leishmaniasis (India)
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NCT00523965 - Combination Therapy in Indian Visceral Leishmaniasis
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VL Combination Therapy in Africa

NCT01067443 - Clinical Trial to Assess the Safety and Efficacy of Sodium Stibogluconate (SSG) and AmBisome® Combination, Miltefosine and AmBisome® and Miltefosine Alone for the Treatment Visceral Leishmaniasis in Eastern Africa
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NCT00832208 - Open-Label, Sequential Step, Safety and Efficacy Study to Determine the Optimal Single Dose of Ambisome for Patients With Visceral Leishmaniasis (Ethiopia)
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NCT00255567 - Efficacy/Safety of Sodium Stibogluconate (SSG) Versus Paromomycin (PM) and SSG/PM Combination to Treat V Leishmaniasis (Ethiopia, Kenya, Sudan Uganda)
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VL in Latin America

NCT01310738- Comparison of Drugs for VL treatment in Brazil
Efficacy and Safety Study of Drugs for Treatment of Visceral Leishmaniasis in Brazil (LVBrasil)
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CL


NCT00257530 - Imiquimod for Cutaneous Leishmaniasis
Imiquimod Plus Antimony Immunochemotherapy for Cutaneous Leishmaniasis
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