A Two-part Proof-of-Concept Study Assessing the Safety and Efficacy of LAT8881 in Lumbar Radicular Pain

PHASE1CompletedINTERVENTIONAL
Enrollment

26

Participants

Timeline

Start Date

May 17, 2022

Primary Completion Date

May 12, 2023

Study Completion Date

June 16, 2023

Conditions
Radiculopathy Lumbar
Interventions
DRUG

LAT8881

"In Part A, LAT8881 will be given as a single intravenous infusion at doses of 0.8, 1.2 and 1.8 mg/kg.~In Part B, a single intravenous infusion of LAT8881 will be given, the dose to be determined by the results in Part A"

DRUG

Placebo

Matching placebo'given as a single intravenous infusion at all dose levels

Trial Locations (1)

5000

PARC Clinical Research, Adelaide

Sponsors
All Listed Sponsors
collaborator

Southern Star Research

INDUSTRY

lead

Lateral Pharma Pty Ltd

INDUSTRY

NCT05298306 - A Two-part Proof-of-Concept Study Assessing the Safety and Efficacy of LAT8881 in Lumbar Radicular Pain | Biotech Hunter | Biotech Hunter