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Active Not RecruitingNCT06604949

A Study of Single Dose of LP-003 in Healthy Adult Subjects

To Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Single Dose of LP-003 in Healthy Adult Subjects

Status
Active Not Recruiting
Phase
Phase 1
Study type
Interventional
Enrollment
12 (actual)
Sponsor
Longbio Pharma · Industry
Sex
All
Age
18 Years – 50 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to evaluate safety, tolerability, immunogenicity, pharmacokinetics, pharmacodynamics, and efficacy of LP-003 in healthy subjects.

Conditions

Interventions

TypeNameDescription
DRUGLP-003 200mgSubcutaneous injection of 200 mg LP-003
DRUGPlaceboSubcutaneous injection of placebo

Timeline

Start date
2024-10-23
Primary completion
2026-11-01
Completion
2026-12-01
First posted
2024-09-20
Last updated
2025-12-18

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT06604949. Inclusion in this directory is not an endorsement.