Clinical Trials Directory

Trials / Completed

CompletedNCT04449939

A Study of Subcutaneous KY1005 in Healthy Volunteers

A Phase I, Open-label Study to Assess the Pharmacokinetics of KY1005 After Single Dose Administration by Subcutaneous and Intravenous Route in Healthy Volunteers

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
24 (actual)
Sponsor
Kymab Limited · Industry
Sex
Male
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

Single centre, open-label, single dose, parallel group study to investigate the PK, safety and tolerability of KY1005 after subcutaneous (s.c.) and intravenous (i.v.) administration, with i.v. KY1005 as a reference treatment.

Conditions

Interventions

TypeNameDescription
DRUGKY1005A human anti-OX40 ligand monoclonal antibody

Timeline

Start date
2020-07-07
Primary completion
2020-11-30
Completion
2020-11-30
First posted
2020-06-29
Last updated
2021-09-30

Locations

1 site across 1 country: United Kingdom

Source: ClinicalTrials.gov record NCT04449939. Inclusion in this directory is not an endorsement.

A Study of Subcutaneous KY1005 in Healthy Volunteers (NCT04449939) · Clinical Trials Directory