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NCT03445897

Miltefosine Plus IL Pentamidine for Bolivian CL

Completed Phase 2 Last updated 27 February 2018
What this trial tests

Phase 2 trial testing miltefosine plus intralesional pentamidine in Leishmaniasis, Cutaneous in 50 participants. Completed in 21 February 2018.

Timeline
31 January 2016
Primary endpoint
31 January 2018
21 February 2018

Quick facts

Lead sponsorJonathan Berman
PhasePhase 2
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment50
Start date31 January 2016
Primary completion31 January 2018
Estimated completion21 February 2018

Drugs / interventions tested

Conditions studied

Sponsor

Jonathan Berman — full company profile →

Who can join

12 and older, any sex, with Leishmaniasis, Cutaneous. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Bolivian cutaneous leishmaniasis due to Leishmania braziliensis was treated with the combination of miltefosine (150 mg/day for 28 days) plus intralesional pentamidine (120 ug/mm2 lesion area on days 1, 3, and 5).

Publications & conference data

2 peer-reviewed publications reference this trial (live from Europe PMC):

  1. Nanotechnological approaches for pentamidine delivery.
    Andreana I, Bincoletto V, Milla P, Dosio F, et al · · 2022 · cited 14× · PMID 35217992 · DOI 10.1007/s13346-022-01127-4
  2. Miltefosine Combined with Intralesional Pentamidine for <i>Leishmania braziliensis</i> Cutaneous Leishmaniasis in Bolivia.
    Soto J, Soto P, Ajata A, Rivero D, et al · · 2018 · cited 9× · PMID 30255833 · DOI 10.4269/ajtmh.18-0183

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Other recruiting trials for Leishmaniasis, Cutaneous

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