Galanthamine (galantamine), a tertiary alkaloid derived from the bulbs
of the snowdrop and various Narcissus species, is a selective, centra
lly active and reversible inhibitor of acetylcholinesterase that is su
itable for oral therapy. After a long period during which the investig
ational and clinical use of the drug was limited to anaesthesia and th
e treatment of peripheral paralysis syndromes in Eastern Europe, the m
olecule has now emerged as a promising lead substance for the treatmen
t of cognitive decline in Alzheimer's disease. Galanthamine has simila
r therapeutic potential to tacrine, but has a significantly more favou
rable pharmacokinetic and toxicity profile. A chemical synthesis proce
ss on the required industrial scale of several tons per year has becom
e available, removing a major obstacle to the development of the drug.
Clinical trials published so far are, however, rather limited in term
s of both design and patient number. The main reason for this is that
there has been a lack of strong support for the drug within the pharma
ceutical industry. However, the available data support the notion that
this molecule, if properly developed, could be a peer for any second-
generation cholinergic drug currently in clinical trials for the sympt
omatic treatment of Alzheimer's disease.