LB-9. Broad Spectrum Investigational Agent GS-5734 for the Treatment of Ebola, MERS Coronavirus and Other Pathogenic Viral Infections with High Outbreak Potential
Session: Oral Abstract Session: Late Breaker Oral Abstracts
Saturday, October 7, 2017: 11:50 AM
Room: 02
Background:Recent viral outbreaks with significant mortality such as Ebola virus (EBOV), SARS-coronavirus (CoV) and MERS-CoV reinforced the need for effective antiviral therapeutics to control future epidemics. GS-5734 is a novel nucleotide analog prodrug in development for treatment of EBOV.

Method:Antiviral activity of GS-5734 has been established in vitro against a wide range of pathogenic RNA virus families including filoviruses, coronaviruses and paramyxoviruses (EC50 = 37 to 200 nM) (Warren et al, Nature 2016; Sheahan et al, Sci Transl Med 2017; Lo et al, Sci Rep 2017). Herein, we describe the in vivo translation of the broad spectrum activity of GS-5734 in relevant animal disease models for Ebola, Marburg, MERS-CoV and Nipah.

Result:Therapeutic efficacy against multiple filoviruses with 80-100% survival was observed in rhesus monkeys infected with lethal doses of EBOV (Kikwit/1995 or Makona/2014) or Marburg virus and treated with once daily intravenous (IV) administration of 5 to 10 mg/kg GS-5734 beginning 3 to 5 days post-infection (p.i.). In all rhesus monkey filovirus infection models, GS-5734 significantly reduced systemic viremia and ameliorated severe clinical disease signs and anatomic pathology. In mice infected with MERS-CoV, twice daily subcutaneous administration of 25 mg/kg GS-5734 beginning 1 day p.i. significantly reduced lung viral load and improved respiratory function. In rhesus monkeys, once-daily IV administration of 5 mg/kg GS-5734 initiated 1 day prior to MERS-CoV infection reduced lung viral load, improved clinical disease signs, and ameliorated severe lung pathology. Finally, in African green monkeys infected with a lethal dose of Nipah virus therapeutic once-daily IV administration of 10 mg/kg GS-5734, starting 1 day p.i. resulted in 100% survival to at least day 35 without any major respiratory or CNS symptoms.


GS-5734 is currently being tested in a phase 2 study in male Ebola survivors with persistent viral RNA in semen. Lyophilized drug formulation has been developed that can be administered to humans via a 30-min IV infusion and does not require cold chain storage. Together, these results support further development of GS-5734 as a broad spectrum antiviral to treat viral infections with high mortality and significant outbreak potential.

Robert Jordan, Ph.D.1, Alison Hogg, PhD2, Travis Warren, Ph.D.3, Emmie De Wit, PhD4, Timothy Sheahan, PhD5, Michael Lo, Ph.D.6, Veronica Soloveva, Ph.D.3, Jessica Weidner, PhD3, Laura Gomba, MBA3, Friederike Feldmann, BS4, Jacqueline Cronin, BS4, Amy Sims, PhD5, Adam Cockrell, PhD5, Joy Feng, Ph.D.2, Iva Trantcheva, FPD2, Darius Babusis, MS2, Danielle Porter-Poulin, PhD2, Roy Bannister, Ph.D.2, Richard Mackman, Ph.D.2, Dustin Siegel, PhD2, Adrian Ray, Ph.D.2, Mark Denison, MD7, Christina Spiropoulou, PhD8, Stuart Nichol, PhD6, Tomas Cihlar, PhD9, Ralph Baric, PhD5, Heinrich Feldmann, MD, PhD4 and Sina Bavari, PhD3, (1)Gilead Sciences, Inc., Foster City, CA, (2)Gilead Sciences, Inc, Foster City, CA, (3)United States Army Medical Research Institute of Infectious Diseases, Frederick, MD, (4)Laboratory of Virology, Division of Intramural Research, National Institute for Allergy and Infectious Diseases, National Institutes of Health, Rocky Mountain Laboratories, Hamilton, MT, (5)Department of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, NC, (6)Centers for Disease Control and Prevention, Atlanta, GA, (7)Pediatrics, Vanderbilt University Medical Center, Nashville, TN, (8)US CDC, Atlanta, GA, (9)Biology, Gilead Sciences, Inc., Foster City, CA


R. Jordan, Gilead: Employee , Salary

A. Hogg, None

T. Warren, None

E. De Wit, None

T. Sheahan, None

M. Lo, None

V. Soloveva, None

J. Weidner, None

L. Gomba, None

F. Feldmann, None

J. Cronin, None

A. Sims, None

A. Cockrell, None

J. Feng, Gilead: Employee , Salary

I. Trantcheva, Gilead: Employee , Salary

D. Babusis, Gilead: Employee , Salary

D. Porter-Poulin, Gilead: Employee , Salary

R. Bannister, Gilead: Employee , Salary

R. Mackman, Gilead: Employee , Salary

D. Siegel, Gilead: Employee , Salary

A. Ray, Gilead: Employee , Salary

M. Denison, None

C. Spiropoulou, None

S. Nichol, None

T. Cihlar, Gilead: Employee , Salary

R. Baric, None

H. Feldmann, None

S. Bavari, None

<< Previous Abstract | Next Abstract

Findings in the abstracts are embargoed until 12:01 a.m. PDT, Wednesday Oct. 4th with the exception of research findings presented at the IDWeek press conferences.