New Paediatric Formulation of Tachipirina®

NACompletedINTERVENTIONAL
Enrollment

20

Participants

Timeline

Start Date

April 9, 2022

Primary Completion Date

April 25, 2022

Study Completion Date

April 25, 2022

Conditions
Healthy
Interventions
DRUG

Tachipirina® 120 mg/5 mL oral suspension, new flavour

A single oral dose of the Tachipirina® 120 mg/5 mL oral suspension(10 mL) will be administered to healthy paediatric volunteers under fasting conditions for at least 1 h before IMP administration until completion of palatability assessment.

Trial Locations (1)

CH-6864

CROSS Research S.A. - Phase I Unit,, Arzo

All Listed Sponsors
collaborator

Cross S.A.

INDUSTRY

lead

Aziende Chimiche Riunite Angelini Francesco S.p.A

INDUSTRY