Drug intelligence / Profile preview

triamcinolone + lidocaine (University of California, San Francisco)

Development stage
Unknown
Lead developer
University of California, San Francisco
Modality
Small Molecules
Administration
Intraarticular, Subcutaneous
01

Overview

This combination therapy is utilized as the standard care (SOC) treatment component in a Phase 4 randomized controlled trial (NCT07278323) conducted by the University of California, San Francisco (UCSF) for adhesive capsulitis of the shoulder (frozen shoulder). The treatment protocol involves ultrasound-guided glenohumeral joint injections. The corticosteroid component, specifically triamcinolone acetonide, serves as a potent anti-inflammatory agent that targets inflammatory pathways by acting as a glucocorticoid receptor agonist. Lidocaine and ropivacaine are local anesthetics that provide immediate and short-term pain relief by blocking voltage-gated sodium channels. In the context of the UCSF study, this combination is used alongside physical therapy to establish a baseline for evaluating the efficacy of Hormone Replacement Therapy (HRT) as an adjunct treatment in peri- and postmenopausal women.

Other names
Corticosteroid and 1%lidocaintriamcinolone + lidocaine + ropivacaine
02

Targets

GR (Glucocorticoid receptor)NaV (Voltage-gated sodium channels)

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