A phase IIa partial blind, placebo-controlled clinical trial to evaluate the safety and immunogenicity of the Ad5-EBOV in healthy adults aged between 18 and 60 years in Belgium.

Long title

A phase IIa partial blind, placebo-controlled clinical trial to evaluate the safety and immunogenicity of the Ad5-EBOV in healthy adults aged between 18 and 60 years in Belgium.

Date receipt dossier

EU record number

EBOVEU001

EudraCT number

2018-003912-29

Company / Sponsor

Bejing Institute of Biotechnology, CanSino Biologics Inc,

Phase

IIa

Treated organism

Humans

Indication category

Infectious disease

Disease

Ebola virus infection

Therapeutic approach

Prevention

Genetic modification

Recombinant Adenoviral vector serotype 5 expressing the envelop glycoprotein from Ebola virus (Zaïre-Makona)

Method of transfer of nucleic acid of interest

Not applicable

Administered biological material

Recombinant Adenoviral vector serotype 5 expressing the envelop glycoprotein from Ebola virus (Zaïre-Makona)

Route of administration

Intradermal & Intramuscular

Locations in Belgium

U Antwerpen

Type of procedure

Contained use only

Current status

Authorized

Pharmaceutical study code

Ad5-EBOV

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