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Trials / Completed

CompletedNCT04533048

A Clinical Study to Evaluate MW33 Injection

A Phase I Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetic Characteristics and Immunogenicity of a Single Dose of MW33 Injection in Healthy Subjects

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
42 (actual)
Sponsor
Mabwell (Shanghai) Bioscience Co., Ltd. · Industry
Sex
All
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

This randomized, double-blind, placebo-controlled, single-dose escalation trial will be conducted to evaluate the safety, tolerability, immunogenicity, pharmacokinetic and pharmacodynamic characteristics of a single dose of MW33 injection at different doses given to healthy subjects to provide a basis for exploration of the therapeutic and preventive effects of MW33 against neocoronavirus in human.

Conditions

Interventions

TypeNameDescription
COMBINATION_PRODUCTMW33 injectiona recombinant fully human antibody to coronavirus
COMBINATION_PRODUCTMW33 injection placeboPlacebo

Timeline

Start date
2020-08-07
Primary completion
2020-11-16
Completion
2020-12-02
First posted
2020-08-31
Last updated
2021-02-26

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT04533048. Inclusion in this directory is not an endorsement.

A Clinical Study to Evaluate MW33 Injection (NCT04533048) · Clinical Trials Directory