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First in Human Study to Compare Safety Between Intravenous Bolus Versus Infusion of ApTOLL — APTABOLUS  

Stroke Clinical Trial

Official title:
First in Human Clinical Trial to Compare Safety and Tolerability Between Intravenous Infusions and Bolus Intravenous Inhection of ApTOLL in Healthy Volunteers

Clinical Trial Summary

The main objective of the study is to assess the tolerability and safety of ApTOLL administration when comparing intravenous infusion vs. bolus intravenous injection, in healthy volunteers. Pharmacokinetic profile of ApTOLL will be also analysed as secondary objective of the study.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05569720
Study type Interventional
Source aptaTargets S.L.
Contact
Status Completed
Phase Phase 1
Start date April 25, 2022
Completion date June 24, 2022
View Details
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