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UnknownNCT05912049

A Study to Evaluate the Safety, Tolerability, Pharmacokinetic Properties and Immunogenicity of 9MW3811 in Healthy Subjects

A Phase 1, Randomized, Double-blind,Placebo-controlled, Single Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetic, Pharmacodynamics and Immunogenicity of 9MW3811 in Healthy Participants

Status
Unknown
Phase
Phase 1
Study type
Interventional
Enrollment
24 (estimated)
Sponsor
Mabwell (Shanghai) Bioscience Co., Ltd. · Industry
Sex
All
Age
18 Years – 55 Years
Healthy volunteers
Accepted

Summary

This is a single ascending dose study of 9MW3811, the primary objective of which is to evaluate the safety and tolerability of 9MW3811 in healthy adult participants.

Conditions

Interventions

TypeNameDescription
DRUG9MW3811 InjectionSingle dose intravenously infused on day 1
DRUGPlaceboSingle dose of matching placebo intravenously infused on day 1

Timeline

Start date
2023-07-26
Primary completion
2023-12-01
Completion
2023-12-01
First posted
2023-06-22
Last updated
2023-09-01

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT05912049. Inclusion in this directory is not an endorsement.