Drug intelligence / Profile preview

lidocaine + heparin

Development stage
Unknown
Lead developer
Urigen Pharmaceuticals
Modality
Small Molecules
Administration
Intravesical
01

Overview

Lidocaine + heparin is a **combination drug** administered primarily by intravesical instillation (directly into the bladder) as a compounded, non-commercial pharmaceutical for the treatment of bladder pain, urgency, and frequency, especially in patients with interstitial cystitis/bladder pain syndrome (IC/BPS)[1][3][6]. Lidocaine is a local anesthetic that blocks sodium channel protein type 1 subunit alpha on sensory nerve fibers, producing rapid and reversible local anesthesia to reduce pain, while heparin is a glycosaminoglycan that forms a protective coating on the bladder epithelium, restoring the mucosal permeability barrier disrupted in IC, and may additionally stabilize lidocaine in solution[1][5][6]. This combination has demonstrated greater and more rapid symptom improvement—bladder pain reduction (up to 42%), decreased urgency, and extended relief (up to 12 hours)—than lidocaine alone in randomized control trials for IC patients[3][4][5][6]. Formulations typically include 50,000 units heparin and 200 mg alkalinized lidocaine hydrochloride in 15 mL water, buffered to pH ~7.2 with sodium bicarbonate[5][6].

Other names
heparin-lidocaineheparin + lidocainealkalinized lidocaine + heparin
02

Targets

NaV (Voltage-gated sodium channels)

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