Drug intelligence / Profile preview

lidocaine + magnesium sulfate + sodium bicarbonate + dextrose

Development stage
Phase 3
Lead developer
Queen's University
Modality
Small Molecules
Administration
Intramuscular
01

Overview

This investigational combination therapy, developed by Queen's University, is a novel magnesium-based trigger point infiltration formulation designed to treat chronic myofascial pelvic pain. The formulation consists of four active components: lidocaine, magnesium sulfate, dextrose, and sodium bicarbonate. Lidocaine serves as a local anesthetic to provide immediate pain relief. Magnesium sulfate is included to inhibit the release of calcium, which is thought to propagate pathologic myocyte contractions in trigger points. Dextrose is utilized for prolotherapy, aiming to provoke a regenerative tissue response in painful syndromes. Sodium bicarbonate is added to the mixture to neutralize the acidity of the lidocaine, thereby decreasing the pain associated with the injection itself. The therapy is administered via intramuscular injection directly into myofascial trigger points within the pelvic floor muscles.

Other names
Magnesium-Based Trigger Point InjectionMagnesium-Based Injection FormulationMagnesium-Based Trigger Point Infiltration
02

Targets

NMDAR (Glutamate receptor ionotropic, NMDA)CaV (Voltage-gated calcium channel protein complex)SCN1A (Voltage-gated sodium channel protein type 1 subunit alpha)

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