Drug intelligence / Profile preview

galantamine + nimodipine

Development stage
Phase 4
Lead developer
Synaptech
Modality
Small Molecules
Administration
Oral
01

Overview

Galantamine + nimodipine is a combination of two approved drugs: galantamine, a reversible, competitive acetylcholinesterase inhibitor and allosteric modulator of neuronal nicotinic acetylcholine receptors, and nimodipine, a calcium channel blocker selective for cerebral circulation. This combination has been studied for the treatment of mild to moderate mixed dementia (Alzheimer's disease with cerebrovascular disease) to evaluate additive benefits on cognitive speed and quality of life. A clinical trial found the combination to be not advantageous compared to galantamine monotherapy, indicating no significant improvement in primary efficacy measures. Both drugs are small molecules, administered orally. Galantamine increases acetylcholine levels and enhances cholinergic transmission; nimodipine blocks L-type calcium channels, improving cerebral blood flow and potentially contributing neuroprotection[1][3][6][4][5].

02

Targets

AcetylcholinesteraseCACNA1C (Voltage-dependent L-type calcium channel subunit alpha-1C)CHRNA7 (α7 nicotinic receptor)CACNA1D (Voltage-dependent L-type calcium channel subunit alpha-1D)CACNA1F (CaV1.4)CACNA1S (Voltage-dependent L-type calcium channel subunit alpha-1S)CACNB1 (L-type voltage-gated calcium channel β1-subunit)CACNB2 (Voltage-gated calcium channel β2 subunit)CACNB3 (Calcium voltage-gated channel auxiliary subunit beta 3)CACNB4 (Voltage-dependent L-type calcium channel subunit beta-4)

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