3-year, Open-Label Study Evaluating Safety, Tolerability, and Efficacy of Lorecivivint in Subjects With Osteoarthritis of the Knee

PHASE3TerminatedINTERVENTIONAL
Enrollment

73

Participants

Timeline

Start Date

July 15, 2021

Primary Completion Date

December 13, 2021

Study Completion Date

December 13, 2021

Conditions
Osteoarthritis of the Knee
Interventions
DRUG

Lorecivivint

Healthcare professional-administered intra-articular (IA) injection into one or both knees as clinically indicated. Bilateral injections of 0.07 mg of LOR are allowed. IA injection performed on Day 1. Additional IA injections of LOR to same knee (with at least a 6 month separation) between Day 1 and Month 33.

Trial Locations (4)

32789

Research Site, Winter Park

60523

Research Site, Oak Brook

75231

Research Site, Dallas

85712

Research Site, Tucson

Sponsors
All Listed Sponsors
lead

Biosplice Therapeutics, Inc.

INDUSTRY