Overview

Assess the Efficacy and Safety in Volunteers of DCF100, TIB200 and SPR300 vs. Placebo and Control(s) in a UV Pain Model

Status:
Completed
Trial end date:
2015-05-01
Target enrollment:
Participant gender:
Summary
This is a randomised, double blind, cross over clinical study in healthy human volunteers (including pharmacokinetic [PK] sampling and laser Doppler assessment of local blood flow in a subset of up to 6 subjects per cohort of 20) to assess the efficacy and safety of three different topical analgesics (DCF100, TIB200 and SPR300) versus placebo and active control(s) in a model of UV-induced inflammatory pain.
Phase:
Phase 1
Details
Lead Sponsor:
Futura Medical Developments Ltd.
Collaborator:
Parexel
Treatments:
Diclofenac
Ibuprofen
Menthol
Methyl salicylate
Salicylates