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Multiple Treatments for Ebola Virus Disease (EVD)

An Adaptive Randomized Trial Comparing Multiple Treatments for Ebola Virus (EBOV) Infected Children and Adults

Status
UNKNOWN
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02380625
Enrollment
150
Registered
2015-03-05
Start date
2015-04-30
Completion date
2016-03-31
Last updated
2015-03-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ebola Virus Disease

Keywords

Ebola, EVD, Adaptive design, therapeutics

Brief summary

The purpose of this study is to determine whether multiple therapeutic regimens are effective in the treatment of Ebola Virus Disease (EVD)

Detailed description

The ongoing epidemic of EVD has ravaged parts of West Africa, with initial cases reported in December 2013. There is no licensed specific therapy for the disease, which has a case-fatality rate of approximately 50-70%. Although anecdotal clinical data, recent studies in animal models, and in vitro screening suggest that treatment of EVD patients with anti-viral agents, immune modifying agents, and/or convalescent blood products may be effective, they have not been evaluated in clinical trials. This multi-arm clinical trial will evaluate the efficacy and safety of multiple regimens, both as mono-therapy and combination therapy. Provision of these regimens, if found effective and safe, would have a major impact on the current and future epidemics by providing effective treatment options. As described for previous adaptive trials, a randomization probability for each of the treatment regimens is created based on 14-day mortality, and is used for weighting randomization of subsequently enrolled participants. Participants will continually be preferentially assigned to regimens with better initial performance. New agents can be added or existing agents removed as the trial evolves.

Interventions

DRUGAzithromycin

Adults (\>18 yrs): 3 x 500mg tablets daily for 5 days; Children (6 months to \<18 yrs): 30mg/kg (oral suspension) daily for 5 days

DRUGSunitinib and Erlotinib

Sunitinib - Adults (\>18 yrs): 1 x 50mg tablet daily for 7 days; Children (6 months to \<18 yrs): 0.83 mg/kg (oral suspension) daily for 7 days. Erlotinib - Adults (\>18 yrs): 1 x 150mg tablet daily for 7 days; Children (8kg to \<20kg): 3.5 mg/kg daily for 7 days; Children (\>20kg to \<30kg): 3.0 mg/kg daily for 7 days; Children (\>30kg to \< 18 yrs): 25 mg/kg daily for 7 days

DRUGAtorvastatin and Irbesartan

Atorvastatin - Adults (\>18 yrs): 1 x 40mg tablet daily until discharge; Children (6 years to \<18 yrs): 1 x 40mg tablet daily until discharge; Irbesartan - Adults (\>18 yrs): 1 x 150mg tablets daily until discharge; Children (6 years to \<18 yrs): 1 x 75mg tablet daily until discharge.

OTHERIV fluids and laboratory testing

All arms will receive aggressive IV fluid rehydration and frequent laboratory tests to assist with medical management as indicated.

Sponsors

Bill and Melinda Gates Foundation
CollaboratorOTHER
Duke University
CollaboratorOTHER
University of Sierra Leone
CollaboratorOTHER
Syneos Health
CollaboratorOTHER
University of North Carolina
CollaboratorOTHER
Clinical Research Management, Inc.
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
6 Months to No maximum
Healthy volunteers
No

Inclusion criteria

* Males and females aged 6 months and \>8kg in weight * Confirmed case of EVD * Admission to the hospital \< 48 hours prior to enrollment * Participant or family member/guardian able and willing to provide signed informed consent

Exclusion criteria

* Prior treatment with any other specific experimental anti-EVD product, or expectation to receive another experimental anti-EVD product during the course of the study (this does not include general supportive care or nutritional supplements routinely administered to all hospitalized patients with EVD) * Unresponsive * In the treating physicians opinion, an inability to comply with the study treatment regimen

Design outcomes

Primary

MeasureTime frame
Death by 14 days14 days after starting treatment regimen

Secondary

MeasureTime frame
Reduction in viral load14 days after starting treatment regimen
2-week post discharge clinical sequelae, including signs and symptoms and laboratory abnormalities14 days after starting treatment

Other

MeasureTime frame
Severe adverse events that are inconsistent with EVD and are assessed as related to study agent(s) by the site principal investigator14 days after starting treatment

Contacts

Primary ContactJohn M Griffiss, MD
crapaud@loursage.org1-800-431-9640
Backup ContactChristopher W Woods, MD, MPH
chris.woods@duke.edu919-668-7174

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 2, 2026