Clinical Trials Directory

Trials / Completed

CompletedNCT05406752

Pharmacokinetic Study of Paracetamol UNIFLASH (125 MG/1.25 ML)

An Open-label, Single Treatment, Single Period, Single Buccal Dose Pharmacokinetic Study of Paracetamol Uniflash (125 mg/ 1.25 mL) in Healthy, Adult, Human Subjects Under Fasting Conditions.

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
32 (actual)
Sponsor
Unither Pharmaceuticals, France · Industry
Sex
All
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

This study aims to assess the pharmacokinetic profile of a new paracetamol formulation (paracetamol Uniflash 125mg/1.25mL) for buccal use after single dose.

Conditions

Interventions

TypeNameDescription
DRUGparacetamol Uniflash (125 mg/ 1.25 mL)Oromucosal solution (125 mg/ 1.25 mL) for buccal route

Timeline

Start date
2022-07-22
Primary completion
2022-07-23
Completion
2022-07-23
First posted
2022-06-06
Last updated
2024-12-13
Results posted
2024-12-13

Locations

1 site across 1 country: India

Source: ClinicalTrials.gov record NCT05406752. Inclusion in this directory is not an endorsement.