Trial intelligence / Profile preview

Safety and PK of SP-8356 in Healthy Volunteers

NCT05574166Phase 1Terminated

Sponsor
Shinpoong Pharma
Start
Jan 2021
Primary completion
Oct 2021
Modality
Classical Binding Small Molecules
Countries
1
01

Overview

Phase 1, randomised, double-blind trial in atherosclerosis and ischemic stroke comparing SP-8356 with Placebo (2 arms). Primary endpoint: Safety and tolerability of single oral doses of SP-8356 up to 3 days. Started Jan 2021; status: terminated.

02

Drugs

SP-8356
03

Conditions

atherosclerosisischemic stroke

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