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Trials / Completed

CompletedNCT02643901

Tolerability and Pharmacokinetics(PK)/Pharmacodynamics(PD) Study of GW003 in Healthy Subjects

The Single-Dose Tolerability and PK/PD Study of Recombinant (Expressed by Pichia Pastoris) Human Serum Albumin/Human Granulocyte-Colony Stimulating Factor(I) Fusion Protein for Injection (GW003) in Healthy Subjects

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
26 (actual)
Sponsor
Jiangsu T-Mab Biopharma Co.,Ltd · Industry
Sex
All
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

This study is designed to access the tolerability and Pharmacokinetic/Pharmacodynamic (PK/PD) of single subcutaneous (SC) injection of GW003 in healthy subjects.

Conditions

Interventions

TypeNameDescription
BIOLOGICALGW003single SC injection

Timeline

Start date
2015-09-01
Primary completion
2016-10-10
Completion
2016-10-10
First posted
2015-12-31
Last updated
2017-08-18

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT02643901. Inclusion in this directory is not an endorsement.

Tolerability and Pharmacokinetics(PK)/Pharmacodynamics(PD) Study of GW003 in Healthy Subjects (NCT02643901) · Clinical Trials Directory