drugset / Trial / NCT04097379

Safety, Tolerability and Preliminary Efficacy of Multiple Intra-articular Injections of LRX712 in Patients With Knee OA

NCT04097379 ↗

Phase 2 Completed 45 enrolled Novartis Pharmaceuticals
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study explored the preliminary efficacy of multiple intra-articular injections of LRX712 by evaluating the ability of the drug to restore structural integrity of articular cartilage. Efficacy was evaluated in the context of the systemic safety and local tolerability of the investigational drug.

Timeline

Start
2020-07-20
Primary completion
2024-08-08
Completion
2025-01-17

Outcome

Missed primary endpoint

registry analysis (superiority test); LRX712 15 mg vs Placebo; p = 0.2366 NCT04097379 ↗

registry analysis (superiority test); LRX712 25 mg vs Placebo; p = 0.2892 NCT04097379 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject LRX712 Unknown 15 mg Other
Subject LRX712 Unknown 25 mg Other
Subject LRX712 Unknown 75 mg Other

Indications