Efficacy and Safety of Pafuramidine versus Pentamidine Maleate for Treatment of First Stage Sleeping Sickness in a Randomized, Comparator-Controlled, International Phase 3 Clinical Trial.

<h4>Background</h4>Sleeping sickness (human African trypanosomiasis [HAT]) is a neglected tropical disease with limited treatment options that currently require parenteral administration. In previous studies, orally administered pafuramidine was well tolerated in healthy patients (for up...

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Main Authors: Gabriele Pohlig, Sonja C Bernhard, Johannes Blum, Christian Burri, Alain Mpanya, Jean-Pierre Fina Lubaki, Alfred Mpoo Mpoto, Blaise Fungula Munungu, Patrick Mangoni N'tombe, Gratias Kambau Manesa Deo, Pierre Nsele Mutantu, Florent Mbo Kuikumbi, Alain Fukinsia Mintwo, Augustin Kayeye Munungi, Amadeu Dala, Stephen Macharia, Constantin Miaka Mia Bilenge, Victor Kande Betu Ku Mesu, Jose Ramon Franco, Ndinga Dieyi Dituvanga, Richard R Tidwell, Carol A Olson
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2016-02-01
Series:PLoS Neglected Tropical Diseases
Online Access:https://journals.plos.org/plosntds/article/file?id=10.1371/journal.pntd.0004363&type=printable
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author Gabriele Pohlig
Sonja C Bernhard
Johannes Blum
Christian Burri
Alain Mpanya
Jean-Pierre Fina Lubaki
Alfred Mpoo Mpoto
Blaise Fungula Munungu
Patrick Mangoni N'tombe
Gratias Kambau Manesa Deo
Pierre Nsele Mutantu
Florent Mbo Kuikumbi
Alain Fukinsia Mintwo
Augustin Kayeye Munungi
Amadeu Dala
Stephen Macharia
Constantin Miaka Mia Bilenge
Victor Kande Betu Ku Mesu
Jose Ramon Franco
Ndinga Dieyi Dituvanga
Richard R Tidwell
Carol A Olson
author_facet Gabriele Pohlig
Sonja C Bernhard
Johannes Blum
Christian Burri
Alain Mpanya
Jean-Pierre Fina Lubaki
Alfred Mpoo Mpoto
Blaise Fungula Munungu
Patrick Mangoni N'tombe
Gratias Kambau Manesa Deo
Pierre Nsele Mutantu
Florent Mbo Kuikumbi
Alain Fukinsia Mintwo
Augustin Kayeye Munungi
Amadeu Dala
Stephen Macharia
Constantin Miaka Mia Bilenge
Victor Kande Betu Ku Mesu
Jose Ramon Franco
Ndinga Dieyi Dituvanga
Richard R Tidwell
Carol A Olson
author_sort Gabriele Pohlig
collection DOAJ
description <h4>Background</h4>Sleeping sickness (human African trypanosomiasis [HAT]) is a neglected tropical disease with limited treatment options that currently require parenteral administration. In previous studies, orally administered pafuramidine was well tolerated in healthy patients (for up to 21 days) and stage 1 HAT patients (for up to 10 days), and demonstrated efficacy comparable to pentamidine.<h4>Methods</h4>This was a Phase 3, multi-center, randomized, open-label, parallel-group, active control study where 273 male and female patients with first stage Trypanosoma brucei gambiense HAT were treated at six sites: one trypanosomiasis reference center in Angola, one hospital in South Sudan, and four hospitals in the Democratic Republic of the Congo between August 2005 and September 2009 to support the registration of pafuramidine for treatment of first stage HAT in collaboration with the United States Food and Drug Administration. Patients were treated with either 100 mg of pafuramidine orally twice a day for 10 days or 4 mg/kg pentamidine intramuscularly once daily for 7 days to assess the efficacy and safety of pafuramidine versus pentamidine. Pregnant and lactating women as well as adolescents were included. The primary efficacy endpoint was the combined rate of clinical and parasitological cure at 12 months. The primary safety outcome was the frequency and severity of adverse events. The study was registered on the International Clinical Trials Registry Platform at www.clinicaltrials.gov with the number ISRCTN85534673.<h4>Findings/conclusions</h4>The overall cure rate at 12 months was 89% in the pafuramidine group and 95% in the pentamidine group; pafuramidine was non-inferior to pentamidine as the upper bound of the 95% confidence interval did not exceed 15%. The safety profile of pafuramidine was superior to pentamidine; however, 3 patients in the pafuramidine group had glomerulonephritis or nephropathy approximately 8 weeks post-treatment. Two of these events were judged as possibly related to pafuramidine. Despite good tolerability observed in preceding studies, the development program for pafuramidine was discontinued due to delayed post-treatment toxicity.
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spelling doaj-art-54ad4e12d63a49d885737d44dd4774db2025-08-20T03:46:24ZengPublic Library of Science (PLoS)PLoS Neglected Tropical Diseases1935-27271935-27352016-02-01102e000436310.1371/journal.pntd.0004363Efficacy and Safety of Pafuramidine versus Pentamidine Maleate for Treatment of First Stage Sleeping Sickness in a Randomized, Comparator-Controlled, International Phase 3 Clinical Trial.Gabriele PohligSonja C BernhardJohannes BlumChristian BurriAlain MpanyaJean-Pierre Fina LubakiAlfred Mpoo MpotoBlaise Fungula MununguPatrick Mangoni N'tombeGratias Kambau Manesa DeoPierre Nsele MutantuFlorent Mbo KuikumbiAlain Fukinsia MintwoAugustin Kayeye MunungiAmadeu DalaStephen MachariaConstantin Miaka Mia BilengeVictor Kande Betu Ku MesuJose Ramon FrancoNdinga Dieyi DituvangaRichard R TidwellCarol A Olson<h4>Background</h4>Sleeping sickness (human African trypanosomiasis [HAT]) is a neglected tropical disease with limited treatment options that currently require parenteral administration. In previous studies, orally administered pafuramidine was well tolerated in healthy patients (for up to 21 days) and stage 1 HAT patients (for up to 10 days), and demonstrated efficacy comparable to pentamidine.<h4>Methods</h4>This was a Phase 3, multi-center, randomized, open-label, parallel-group, active control study where 273 male and female patients with first stage Trypanosoma brucei gambiense HAT were treated at six sites: one trypanosomiasis reference center in Angola, one hospital in South Sudan, and four hospitals in the Democratic Republic of the Congo between August 2005 and September 2009 to support the registration of pafuramidine for treatment of first stage HAT in collaboration with the United States Food and Drug Administration. Patients were treated with either 100 mg of pafuramidine orally twice a day for 10 days or 4 mg/kg pentamidine intramuscularly once daily for 7 days to assess the efficacy and safety of pafuramidine versus pentamidine. Pregnant and lactating women as well as adolescents were included. The primary efficacy endpoint was the combined rate of clinical and parasitological cure at 12 months. The primary safety outcome was the frequency and severity of adverse events. The study was registered on the International Clinical Trials Registry Platform at www.clinicaltrials.gov with the number ISRCTN85534673.<h4>Findings/conclusions</h4>The overall cure rate at 12 months was 89% in the pafuramidine group and 95% in the pentamidine group; pafuramidine was non-inferior to pentamidine as the upper bound of the 95% confidence interval did not exceed 15%. The safety profile of pafuramidine was superior to pentamidine; however, 3 patients in the pafuramidine group had glomerulonephritis or nephropathy approximately 8 weeks post-treatment. Two of these events were judged as possibly related to pafuramidine. Despite good tolerability observed in preceding studies, the development program for pafuramidine was discontinued due to delayed post-treatment toxicity.https://journals.plos.org/plosntds/article/file?id=10.1371/journal.pntd.0004363&type=printable
spellingShingle Gabriele Pohlig
Sonja C Bernhard
Johannes Blum
Christian Burri
Alain Mpanya
Jean-Pierre Fina Lubaki
Alfred Mpoo Mpoto
Blaise Fungula Munungu
Patrick Mangoni N'tombe
Gratias Kambau Manesa Deo
Pierre Nsele Mutantu
Florent Mbo Kuikumbi
Alain Fukinsia Mintwo
Augustin Kayeye Munungi
Amadeu Dala
Stephen Macharia
Constantin Miaka Mia Bilenge
Victor Kande Betu Ku Mesu
Jose Ramon Franco
Ndinga Dieyi Dituvanga
Richard R Tidwell
Carol A Olson
Efficacy and Safety of Pafuramidine versus Pentamidine Maleate for Treatment of First Stage Sleeping Sickness in a Randomized, Comparator-Controlled, International Phase 3 Clinical Trial.
PLoS Neglected Tropical Diseases
title Efficacy and Safety of Pafuramidine versus Pentamidine Maleate for Treatment of First Stage Sleeping Sickness in a Randomized, Comparator-Controlled, International Phase 3 Clinical Trial.
title_full Efficacy and Safety of Pafuramidine versus Pentamidine Maleate for Treatment of First Stage Sleeping Sickness in a Randomized, Comparator-Controlled, International Phase 3 Clinical Trial.
title_fullStr Efficacy and Safety of Pafuramidine versus Pentamidine Maleate for Treatment of First Stage Sleeping Sickness in a Randomized, Comparator-Controlled, International Phase 3 Clinical Trial.
title_full_unstemmed Efficacy and Safety of Pafuramidine versus Pentamidine Maleate for Treatment of First Stage Sleeping Sickness in a Randomized, Comparator-Controlled, International Phase 3 Clinical Trial.
title_short Efficacy and Safety of Pafuramidine versus Pentamidine Maleate for Treatment of First Stage Sleeping Sickness in a Randomized, Comparator-Controlled, International Phase 3 Clinical Trial.
title_sort efficacy and safety of pafuramidine versus pentamidine maleate for treatment of first stage sleeping sickness in a randomized comparator controlled international phase 3 clinical trial
url https://journals.plos.org/plosntds/article/file?id=10.1371/journal.pntd.0004363&type=printable
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