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A First-in-human Trial to Evaluate Safety, Tolerability, and Pharmacokinetics of APC148 in Healthy Adults

Healthy Subjects Clinical Trial

Official title:
A First-in-human, Randomised, Double-blind, Placebo-controlled, Single Ascending Dose Trial to Evaluate Safety, Tolerability, and Pharmacokinetics of APC148 in Healthy Adults

Clinical Trial Summary

The purpose of this first-in-human trial is to investigate the safety, tolerability, and pharmacokinetics of APC148 after intravenous (IV) infusion of single ascending doses in healthy adults.

Clinical Trial Description

Participants will receive a single 3-hours IV infusion of APC148 or placebo. 6 sequential cohorts are planned. The first 2 subjects in each cohort will be dosed in a sentinel fashion. The subjects will be followed for 7 days. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06360640
Study type Interventional
Source AdjuTec Pharma AS
Contact Caroline Hammarström, MSc
Phone 0046 (0) 705292158
Email caroline.hammarstrom@ctc-ab.se
Status Not yet recruiting
Phase Phase 1
Start date June 2024
Completion date March 2025
View Details
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