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Trials / Completed

CompletedNCT06008652

A Study to Evaluate Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of DR-0201 in Healthy Adult Volunteers

A First-in-Human Multiple Expansion Cohort Phase 1 Study Evaluating the Safety and Activity of DR-0201 as Single Ascending Dose in Healthy Volunteers

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
10 (actual)
Sponsor
Dren Bio · Industry
Sex
All
Age
18 Years – 55 Years
Healthy volunteers
Accepted

Summary

This is a randomized, double-blind, placebo-controlled dose escalation study to evaluate the safety, tolerability, PK, PD, and immunogenicity of IV administered DR-0201 in healthy volunteers.

Conditions

Interventions

TypeNameDescription
DRUGDR-0201DR-0201 is a bi-specific antibody
DRUGPlaceboPlacebo

Timeline

Start date
2023-11-26
Primary completion
2024-07-24
Completion
2024-07-24
First posted
2023-08-23
Last updated
2024-08-13

Locations

1 site across 1 country: Australia

Source: ClinicalTrials.gov record NCT06008652. Inclusion in this directory is not an endorsement.

A Study to Evaluate Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of DR-0201 in Healthy Adult Volunteers (NCT06008652) · Clinical Trials Directory