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Experimental Treatment of Ebola Virus Disease with TKM-130803: A Single-Arm Phase 2 Clinical Trial

Authors :
Dunning, Jake
Sahr, Foday
Rojek, Amanda
Gannon, Fiona
Carson, Gail
Idriss, Baimba
Massaquoi, Thomas
Gandi, Regina
Joseph, Sebatu
Osman, Hassan K.
Brooks, Timothy J. G.
Simpson, Andrew J. H.
Goodfellow, Ian
Thorne, Lucy
Arias, Armando
Merson, Laura
Castle, Lyndsey
Howell-Jones, Rebecca
Pardinaz-Solis, Raul
Hope-Gill, Benjamin
Ferri, Mauricio
Grove, Jennifer
Kowalski, Mark
Stepniewska, Kasia
Lang, Trudie
Whitehead, John
Olliaro, Piero
Samai, Mohammed
Horby, Peter W.
Source :
PLoS Medicine. April 19, 2016, Vol. 13 Issue 4, e1001997
Publication Year :
2016

Abstract

Background TKM-130803, a small interfering RNA lipid nanoparticle product, has been developed for the treatment of Ebola virus disease (EVD), but its efficacy and safety in humans has not been evaluated. Methods and Findings In this single-arm phase 2 trial, adults with laboratory-confirmed EVD received 0.3 mg/kg of TKM-130803 by intravenous infusion once daily for up to 7 d. On days when trial enrolment capacity was reached, patients were enrolled into a concurrent observational cohort. The primary outcome was survival to day 14 after admission, excluding patients who died within 48 h of admission. After 14 adults with EVD had received TKM-130803, the pre-specified futility boundary was reached, indicating a probability of survival to day 14 of [less than or equal to]0.55, and enrolment was stopped. Pre-treatment geometric mean Ebola virus load in the 14 TKM-130803 recipients was 2.24 x 10.sup.9 RNA copies/ml plasma (95% CI 7.52 x 10.sup.8, 6.66 x 10.sup.9). Two of the TKM-130803 recipients died within 48 h of admission and were therefore excluded from the primary outcome analysis. Of the remaining 12 TKM-130803 recipients, nine died and three survived. The probability that a TKM-130803 recipient who survived for 48 h will subsequently survive to day 14 was estimated to be 0.27 (95% CI 0.06, 0.58). TKM-130803 infusions were well tolerated, with 56 doses administered and only one possible infusion-related reaction observed. Three patients were enrolled in the observational cohort, of whom two died. Conclusions Administration of TKM-130803 at a dose of 0.3 mg/kg/d by intravenous infusion to adult patients with severe EVD was not shown to improve survival when compared to historic controls. Trial registration Pan African Clinical Trials Registry PACTR201501000997429<br />Author(s): Jake Dunning 1, Foday Sahr 2,3, Amanda Rojek 1, Fiona Gannon 4, Gail Carson 1,5, Baimba Idriss 2, Thomas Massaquoi 2, Regina Gandi 2, Sebatu Joseph 2, Hassan K. [...]

Details

Language :
English
ISSN :
15491277
Volume :
13
Issue :
4
Database :
Gale General OneFile
Journal :
PLoS Medicine
Publication Type :
Academic Journal
Accession number :
edsgcl.476896852
Full Text :
https://doi.org/10.1371/journal.pmed.1001997