Clinical Trials Directory

Trials / Completed

CompletedNCT06386211

Bioavailability Study of Magne-B6 New Formulation

Open-label, Randomized, 2-treatment, 2-sequence, 2-period, Crossover Relative Bioavailability Study of Magne-B6 New Formulation Versus Magne-B6 Solution in Healthy Male and Female Subjects in Fasting Conditions.

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
24 (actual)
Sponsor
Opella Healthcare Group SAS, a Sanofi Company · Industry
Sex
All
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

The purpose of the study is to assess the relative bioavailability of two Magne-B6 preparations, in fasting conditions.

Conditions

Interventions

TypeNameDescription
DRUGMAGNE-B6 Oral SolutionOral solution.
DRUGMAGNE-B6 New Formulation TabletNew formulation tablet.

Timeline

Start date
2024-07-03
Primary completion
2024-08-24
Completion
2024-08-24
First posted
2024-04-26
Last updated
2025-09-12

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT06386211. Inclusion in this directory is not an endorsement.