Clinical Trials Directory

Trials / Recruiting

RecruitingNCT07453784

Study to Evaluate Pharmacokinetics, Relative Bioavailability, Palatability of Obefazimod Minitablet Formulation

Two-Part, Open-Label Study to Evaluate Single Dose Pharmacokinetics of an Obefazimod Minitablet Formulation, Estimate the Relative Bioavailability of the Minitablet Formulation and to Evaluate Minitablet Palatability in Healthy Participants

Status
Recruiting
Phase
Phase 1
Study type
Interventional
Enrollment
44 (estimated)
Sponsor
Abivax S.A. · Industry
Sex
All
Age
18 Years – 55 Years
Healthy volunteers
Accepted

Summary

The sponsor is developing a pediatric minitablet formulation as part of the overall pharmaceutical development strategy. In vitro dissolution and physiological-based bio-pharmaceutics modelling and simulation have been used to guide the development of the mini-tablet formulation to match the PK exposure of the adult capsule formulation. The study aims to investigate the relative bioavailability of the 50mg minitablet compared to the adult obefazimod 50 mg capsule in adult healthy volunteers.

Detailed description

This is a single center, open-label, two-part study in healthy male and female participants. Part 1 of this study aims to investigate the PK properties of single dose of obefazimod 50 mg minitablet formulation and to identify a dose that provides systemic exposures (Cmax and AUC) comparable to that of the adult clinical obefazimod 50 mg capsule formulation. In part 2, the minitablet formulation will be administered with a soft food vehicle (applesauce, yogurt or chocolate pudding or water) to investigate the relative bioavailability of the 50mg minitablet mixed with water or soft foods compared to the adult obefazimod 50 mg capsule administered with no vehicle.

Conditions

Interventions

TypeNameDescription
DRUGObefazimod 50 mg CapsuleAdult formulation
DRUGObefazimod Minitablet 50 mgPediatric formulation

Timeline

Start date
2026-03-03
Primary completion
2026-09-01
Completion
2026-10-01
First posted
2026-03-06
Last updated
2026-04-06

Locations

1 site across 1 country: United Kingdom

Source: ClinicalTrials.gov record NCT07453784. Inclusion in this directory is not an endorsement.