Drug intelligence / Profile preview

levoflunarizine

Development stage
Phase 2
Lead developer
Beijing Four Rings Biopharmaceutical
Modality
Small Molecules
Administration
Oral
01

Overview

Levoflunarizine is the levo-enantiomer (S-isomer) of flunarizine, a selective calcium channel blocker. Developed by Beijing Fourth Ring Pharmaceutical, it is an investigational small molecule being evaluated for the treatment of vertigo associated with posterior circulation ischemic stroke. Like its parent compound flunarizine, levoflunarizine acts as an antagonist of voltage-gated calcium channels, which is thought to reduce vestibular excitability and improve cerebral microcirculation. The drug is currently in Phase 2 clinical development in China, where it is being studied in a tablet formulation to assess its efficacy, safety, and pharmacokinetic profile in adult patients.

Other names
levo flunarizinelevo flunarizine hydrochloride(S)-flunarizine
02

Targets

CACNA1C (Voltage-dependent L-type calcium channel subunit alpha-1C)CACNA1D (Voltage-dependent L-type calcium channel subunit alpha-1D)CACNA1A (P-type Calcium Channel)CACNA1B (Voltage-dependent N-type calcium channel subunit alpha-1B)CACNA1H (T-type voltage-gated calcium channel 3.2)DRD2 (Dopamine D2 Receptor)HRH1 (Histamine H1 Receptor)HTR2A (Serotonin receptor 5-HT2A)

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