Single Ascending Dose Study of Two Liquidia Bupivacaine Formulations

PHASE1CompletedINTERVENTIONAL
Enrollment

29

Participants

Timeline

Start Date

December 5, 2016

Primary Completion Date

March 23, 2017

Study Completion Date

April 26, 2017

Conditions
Acute Pain
Interventions
DRUG

LIQ865A bupivacaine formulation

single subcutaneous injection in medial calf

DRUG

LIQ865B bupivacaine formulation

single subcutaneous injection in medial calf

DRUG

Diluent for LIQ865

Sterile diluent composed of 12.5mg/g sodium hyaluronate, 5.8mg/g sodium chloride, 1mg/g polysorbate 80, 6.1mg/g Tris base, in sterile water for injection - single subcutaneous injection

DRUG

0.5% bupivacaine hydrochoride

single subcutaneous injection

Trial Locations (1)

2400

DanTrial Aps, Copenhagen

Sponsors
All Listed Sponsors
collaborator

Premier Research Group plc

UNKNOWN

lead

Liquidia Technologies, Inc.

INDUSTRY