Trial Profile

A Phase 1 Randomized, Double-Blind, Placebo-Controlled, Dose-Escalation Study to Evaluate the Safety, Tolerability, and Immunogenicity of the Human Cytomegalovirus Vaccine (V160) in Healthy Adults

Status: Completed

Phase of Trial: Phase I

Latest Information Update: 13 May 2022

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At a glance

Drugs V 160 (Primary) ; V 160 (Primary) ; Aluminium phosphate
Indications Cytomegalovirus infections
Focus Adverse reactions; Pharmacodynamics
Sponsors Merck Sharp & Dohme Corp.

Most Recent Events

08 Oct 2017 Results presented at the IDWeek 2017
21 Mar 2017 Status changed from active, no longer recruiting to completed.
22 Feb 2016 Planned End Date changed from 1 Apr 2016 to 1 Mar 2017, according to ClinicalTrials.gov record.

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