Overview

Ibuprofen Bioavailability Study

Status:
Completed
Trial end date:
2017-06-13
Target enrollment:
Participant gender:
Summary
This project is the in-house development of a 200 mg ibuprofen acid orodispersable tablet (ODT; meltlet). It is designed to appeal to consumers who want a dosage form that may be taken without water and can be used 'on the go'. Vanquish has an improved organoleptic profile compared to the currently marketed meltet by the Sponsor. ODTs are also considered as a suitable dosage form for children who may be reluctant to swallow tablets. This product has the potential for application in both adults and children due to the convenience of the format and the ease of administration for both groups. This will be the first pharmacokinetic (PK) assessment of the ibuprofen acid ODT formulation.
Phase:
Phase 1
Details
Lead Sponsor:
Reckitt Benckiser Healthcare (UK) Limited
Collaborator:
Simbec Research
Treatments:
Ibuprofen