Clinical Trials Directory

Trials / Completed

CompletedNCT05277922

Effect of C21 on Forearm Blood Flow

A Phase 1, Open-label, Single-centre Study Investigating the Effect of C21 on Forearm Blood Flow in Healthy Male Subjects by Use of Strain-gauge Venous Occlusion Plethysmography

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
5 (actual)
Sponsor
Vicore Pharma AB · Industry
Sex
Male
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to assess the effect of C21 on forearm blood flow by use of strain-gauge venous occlusion plethysmography.

Detailed description

Subject will be screened for eligibility. Eligible subjects will receive ascending doses of C21 (3, 10, 30, 100, and 200 µg/min through local intra-arterial infusions for 5 min/dose. Forearm blood flow measurements will be performed in both arms during the last 2 minutes of each dose. Infusions of sodium nitroprusside will be performed as a positive control using the same methodology.

Conditions

Interventions

TypeNameDescription
DRUGC21C21 in ascending doses of 15, 50, 150, 500 and 1000 µg
DRUGSodium NitroprussideAscending doses of 4, 8 and 16 µg sodium nitroprusside Positive control

Timeline

Start date
2022-04-28
Primary completion
2022-05-11
Completion
2022-05-18
First posted
2022-03-14
Last updated
2025-04-23
Results posted
2025-04-23

Locations

1 site across 1 country: Sweden

Source: ClinicalTrials.gov record NCT05277922. Inclusion in this directory is not an endorsement.