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Placebo/Galantamine (Reminyl®)

Ludwig-Maximilians - University of Munich · FDA-approved active Small molecule

Placebo/Galantamine (Reminyl®) is a Acetylcholinesterase inhibitor Small molecule drug developed by Ludwig-Maximilians - University of Munich. It is currently FDA-approved for Mild to moderate Alzheimer's disease.

Galantamine inhibits acetylcholinesterase to increase acetylcholine levels in the brain, improving cognitive function in Alzheimer's disease.

Galantamine inhibits acetylcholinesterase to increase acetylcholine levels in the brain, improving cognitive function in Alzheimer's disease. Used for Mild to moderate Alzheimer's disease.

At a glance

Generic namePlacebo/Galantamine (Reminyl®)
SponsorLudwig-Maximilians - University of Munich
Drug classAcetylcholinesterase inhibitor
TargetAcetylcholinesterase; nicotinic acetylcholine receptors
ModalitySmall molecule
Therapeutic areaNeurology
PhaseFDA-approved

Mechanism of action

Galantamine is a reversible inhibitor of the enzyme acetylcholinesterase, which breaks down the neurotransmitter acetylcholine. By inhibiting this enzyme, galantamine increases acetylcholine concentration in the synaptic cleft, enhancing cholinergic neurotransmission. Additionally, galantamine acts as an allosteric modulator of nicotinic receptors, further potentiating cholinergic signaling and potentially providing neuroprotective effects.

Approved indications

Common side effects

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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Frequently asked questions about Placebo/Galantamine (Reminyl®)

What is Placebo/Galantamine (Reminyl®)?

Placebo/Galantamine (Reminyl®) is a Acetylcholinesterase inhibitor drug developed by Ludwig-Maximilians - University of Munich, indicated for Mild to moderate Alzheimer's disease.

How does Placebo/Galantamine (Reminyl®) work?

Galantamine inhibits acetylcholinesterase to increase acetylcholine levels in the brain, improving cognitive function in Alzheimer's disease.

What is Placebo/Galantamine (Reminyl®) used for?

Placebo/Galantamine (Reminyl®) is indicated for Mild to moderate Alzheimer's disease.

Who makes Placebo/Galantamine (Reminyl®)?

Placebo/Galantamine (Reminyl®) is developed and marketed by Ludwig-Maximilians - University of Munich (see full Ludwig-Maximilians - University of Munich pipeline at /company/ludwig-maximilians-university-of-munich).

What drug class is Placebo/Galantamine (Reminyl®) in?

Placebo/Galantamine (Reminyl®) belongs to the Acetylcholinesterase inhibitor class. See all Acetylcholinesterase inhibitor drugs at /class/acetylcholinesterase-inhibitor.

What development phase is Placebo/Galantamine (Reminyl®) in?

Placebo/Galantamine (Reminyl®) is FDA-approved (marketed).

What are the side effects of Placebo/Galantamine (Reminyl®)?

Common side effects of Placebo/Galantamine (Reminyl®) include Nausea, Vomiting, Diarrhea, Dizziness, Headache, Abdominal pain.

What does Placebo/Galantamine (Reminyl®) target?

Placebo/Galantamine (Reminyl®) targets Acetylcholinesterase; nicotinic acetylcholine receptors and is a Acetylcholinesterase inhibitor.

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