Overview

A Phase III Study to Evaluate Analgesic Efficacy and Safety of PRF-110 for Post-surgical Pain

Status:
Recruiting
Trial end date:
2024-01-30
Target enrollment:
Participant gender:
Summary
PRF-110 is a viscous, yellowish clear oily solution of ropivacaine intended for administration into surgical sites to provide post-operative analgesia. The pharmacokinetic profile for PRF-110 suggests that its effect could last up to 72 hours. This is A Phase 3, Randomized, Double-Blind, Saline Placebo- and Active-Controlled, Multicenter Study to Evaluate the Analgesic Efficacy and Safety of Intra-operative Administration of PRF-110 Following Unilateral Bunionectomy
Phase:
Phase 3
Details
Lead Sponsor:
PainReform LTD
Collaborator:
Lotus Clinical Research, LLC
Treatments:
Ropivacaine