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Trials / Completed

CompletedNCT05396235

A Clinical Pharmacology Study of MT-3921 in Healthy Adult Males

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
10 (actual)
Sponsor
Tanabe Pharma Corporation · Industry
Sex
Male
Age
18 Years – 55 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to investigate the safety, tolerability, and pharmacokinetics when MT-3921 or a placebo is intravenously given to Japanese healthy adult male subjects

Conditions

Interventions

TypeNameDescription
BIOLOGICALMT-3921Solution for infusion; Intravenous (IV)
BIOLOGICALPlaceboSolution for infusion; Intravenous (IV)

Timeline

Start date
2022-08-03
Primary completion
2022-12-24
Completion
2022-12-24
First posted
2022-05-31
Last updated
2023-01-18

Locations

1 site across 1 country: Japan

Regulatory

Source: ClinicalTrials.gov record NCT05396235. Inclusion in this directory is not an endorsement.

A Clinical Pharmacology Study of MT-3921 in Healthy Adult Males (NCT05396235) · Clinical Trials Directory