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LRX712Wiki

Developed by Shray Alag
Clinical Trial MeSH HPO Drug Gene SNP Protein Mutation


Correlated Drug Terms (1)


Name (Synonyms) Correlation
drug1822 Placebo Wiki 0.06

Correlated MeSH Terms (1)


Name (Synonyms) Correlation
D010003 Osteoarthritis, NIH 0.50

Correlated HPO Terms (1)


Name (Synonyms) Correlation
HP:0002758 Osteoarthritis HPO 0.50

There is one clinical trial.

Clinical Trials


1 A Randomized, Placebo-controlled, Subject and Investigator Blinded Study Investigating the Safety, Tolerability and Preliminary Efficacy of 8-week Treatment With Intra-articular LRX712 to Regenerate Articular Cartilage in Patients With Mild/Moderate Knee Osteoarthritis

This study will explore 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 will be evaluated in the context of the systemic safety and local tolerability of the investigational drug.

NCT04097379 Osteoarthritis (OA) Drug: LRX712 Drug: Placebo
MeSH:Osteoarthritis
HPO:Osteoarthritis

Primary Outcomes

Description: Efficacy of multiple intra-articular injections of LRX712 in regenerating cartilage as measured with 7T MRI

Measure: Changes in articular cartilage [23Na] content from baseline compared to placebo at week 28

Time: Baseline and Week 28

Secondary Outcomes

Description: Efficacy of multiple intra-articular injections of LRX712 measured with 7T MRI

Measure: Changes in articular cartilage [23Na] content from baseline compared to placebo at Week 16 and 52

Time: Baseline, Week 16 and 52

Description: Efficacy of multiple intra-articular injections of LRX712 measured with 7T MRI

Measure: Changes from baseline in cartilage morphometrics (volume and thickness) in the medial femoral condyle at Week 16, 28 and 52

Time: Baseline, Week 16, 28 and 52

Description: The observed time to reach max (Tmax) plasma concentration following drug administration

Measure: Time to Reach the Maximum Plasma Concentration (Tmax)

Time: Pre-dose to 28 weeks

Description: The observed maximum (Cmax) plasma concentration following drug administration

Measure: Maximum Observed Plasma Concentration (Cmax)

Time: Pre-dose to 28 weeks

Description: The observed minimum (Cmin) plasma concentration following drug administration

Measure: Minimum Observed Plasma Concentration (Cmin)

Time: Pre-dose to 28 weeks

Description: The observed synovial concentration following drug administration

Measure: Concentration in synovial fluid

Time: Day 1; week 4; week 8


Related HPO nodes (Using clinical trials)