Clinical Trials Directory

Trials / Terminated

TerminatedNCT05044325

A First Time in Human (FTIH) Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Single and Repeat Doses of GSK3884464 in Healthy Participants

A Two-Part First Time in Human (FTIH) Study to Evaluate Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Single and Repeat Oral Doses of GSK3884464 in a Randomized, Double Blind, Placebo-Controlled, Dose Escalation Study in Healthy Participants

Status
Terminated
Phase
Phase 1
Study type
Interventional
Enrollment
27 (actual)
Sponsor
GlaxoSmithKline · Industry
Sex
All
Age
18 Years – 50 Years
Healthy volunteers
Accepted

Summary

This will be a FTIH study which aims to evaluate safety, tolerability, pharmacokinetics (PK) and pharmacodynamics (PD) of single and repeat oral doses of GSK3884464 administered to healthy participants.

Conditions

Interventions

TypeNameDescription
DRUGGSK3884464GSK3884464 will be administered
DRUGPlaceboPlacebo to match GSK3884464 will be administered.

Timeline

Start date
2021-09-20
Primary completion
2022-08-05
Completion
2022-08-05
First posted
2021-09-14
Last updated
2024-05-02
Results posted
2024-05-02

Locations

1 site across 1 country: United Kingdom

Source: ClinicalTrials.gov record NCT05044325. Inclusion in this directory is not an endorsement.

A First Time in Human (FTIH) Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Single (NCT05044325) · Clinical Trials Directory