Copper absorption inhibitor (zinc salt)

Galzin (zinc acetate)

An approved treatment for Wilson Disease.

FDA Approved (1997)by Eton Pharmaceuticals
Preclinical
Phase 1
Phase 2
Phase 3
Approved
1997
Drug facts

The same compound appears under different names depending on the context. Here is how to identify Zinc acetate wherever you encounter it, plus the key facts at a glance.

Generic name
Zinc acetate
Brand name
Galzin
Drug class
Copper absorption inhibitor (zinc salt)
Manufacturer
Eton Pharmaceuticals
How it's taken
Capsules taken by mouth three times daily, on an empty stomach (at least 1 hour before or 2 to 3 hours after meals).

An oral zinc acetate formulation approved as maintenance therapy for Wilson disease in patients who were first treated with a chelating drug. Zinc blocks dietary copper absorption rather than chelating circulating copper, which makes it well-suited to long-term maintenance. The label also reports a study in presymptomatic patients, but its approved use is maintenance after a chelator. Galzin returned to U.S. supply through Eton Pharmaceuticals in early 2025.

Where Zinc acetate fits

First-line maintenance therapy in many centers, particularly for presymptomatic patients identified through family screening and for stable patients transitioning off chelation. The label says zinc is not recommended as the first treatment for patients who already have symptoms, because it takes time to start blocking copper; these patients start on a chelating drug, and combined chelator-then-zinc strategies are common.

How Zinc acetate works

Oral zinc that induces metallothionein in intestinal cells. Metallothionein binds dietary copper and prevents its absorption, so excess copper is shed in the feces when intestinal cells turn over. Unlike chelators, zinc does not actively remove copper that is already in the body but blocks new copper from being absorbed.

Side effects and safety

What patients report

Generally better tolerated than chelators. The most common side effect is gastric irritation and nausea, particularly with the morning dose; this can often be managed by spacing doses around meals. The label also warns about stomach ulcers with long-term use and about copper deficiency after months to years of zinc, which can cause anemia, low white blood cell or platelet counts, and nerve problems. Raised amylase, lipase, and alkaline phosphatase levels can also occur. The label advises against breastfeeding while taking zinc, because zinc passes into breast milk and can cause copper deficiency in the baby. Zinc and chelators should not be taken at the same time of day, since chelators bind zinc and reduce its effect.

This is not a complete list of side effects. Talk to your doctor or pharmacist about what to expect and when to seek medical attention.

Taking Zinc acetate

Capsules taken by mouth three times daily, on an empty stomach (at least 1 hour before or 2 to 3 hours after meals). Standard adult maintenance dose is 50 mg of elemental zinc three times daily. The label says 25 mg three times daily may be enough for children 10 and older and during pregnancy; children under 10 have not been studied.

Availability and cost

No generic available

Only available as the brand-name product.

Help paying for Galzin

Pick your insurance to see which help fits. Drugmaker copay cards can't be used with Medicare, Medicaid or TRICARE; charity funds are the usual route there.

Your insurance
From the drugmaker
Galzin (Zinc acetate)
  • Copay help

    $0 copay for eligible commercially insured patients.

    For: private insurance · source
  • Insurance and case manager help

    A Galzin prescription automatically enrolls you. Insurance specialists help verify and obtain coverage; pharmacists available 24/7 by phone.

    The official page does not say who qualifies. Ask the program. · source

Good to know: Covers brand GALZIN (Eton Pharmaceuticals), dispensed through its specialty pharmacy, Anovo (833-442-5946 or 855-813-2039). Full copay terms are not posted on the site. There is no FDA-approved generic zinc acetate.

Checked on the drugmaker's official pages on September 24, 2026. Programs change; confirm with the program before you rely on it.
Charity funds for Wilson Disease
  • From a charity · Wilson Disease Association
    WDA Patient Assistance fund
    Apply directly

    Pays for: Travel and lodging (up to 7 days) for testing or treatment, for the patient and one companion, up to $2,000 per year.

    The foundation says: “Status not shown on page”
Status as each foundation showed it on September 28, 2026.

More ways to get help paying for treatment →

How Wilson disease treatments compare

Four FDA-approved medications are available for Wilson disease, plus several investigational programs in late-stage trials. Treatment choice depends on your stage (active de-coppering versus stable maintenance), your tolerance to penicillamine, whether you have neurologic or hepatic features, and your age. This chart summarizes the practical differences between the approved options.

4 FDA-approved wilson disease treatments are available: Cuprimine / Depen (penicillamine, approved 1956); Syprine (trientine hydrochloride, approved 1985); Galzin (zinc acetate, approved 1997); Cuvrior (trientine tetrahydrochloride, approved 2022). Cuprimine / Depen is typically used as historical first-line for active de-coppering. many centers now switch patients off due to side effect burden once stable..

DrugHow it worksHow it’s givenHow oftenWhere you take itTypical useFDA approved
Cuprimine / Depen
penicillamine
Copper chelator — binds copper in the body so it can be flushed out through the urine. The original Wilson disease drug.Oral capsule or tablet, taken on an empty stomach3–4 times daily during de-coppering, lower doses for maintenanceHome (oral)Historical first-line for active de-coppering. Many centers now switch patients off due to side effect burden once stable.1956
Syprine
trientine hydrochloride
Copper chelator — binds copper for urinary excretion. Generally better tolerated than penicillamine but similar efficacy.Oral capsule, taken on an empty stomach (capsules require refrigeration)2–4 times dailyHome (oral)Alternative chelator for patients who cannot tolerate penicillamine. Generic versions widely available.1985
Galzin
zinc acetate
You are here
Copper absorption blocker — induces a protein in the gut (metallothionein) that traps dietary copper before it can be absorbed.Oral capsule, taken on an empty stomach (separated from chelators)3 times dailyHome (oral)First-line maintenance therapy in many centers, particularly for presymptomatic patients identified through family screening.1997
Cuvrior
trientine tetrahydrochloride
Copper chelator — same chelating action as Syprine, with a more chemically stable salt formulation that allows simpler storage and twice-daily dosing.Oral tablet, taken on an empty stomachTwice dailyHome (oral)Approved for adults with stable Wilson disease who are de-coppered and tolerant to penicillamine; designed as a maintenance switch option.2022
Cuprimine / Depen
penicillamine · Bausch Health (Cuprimine), Mylan (Depen); generic available
MechanismCopper chelator — binds copper in the body so it can be flushed out through the urine. The original Wilson disease drug.
RouteOral capsule or tablet, taken on an empty stomach
Frequency3–4 times daily during de-coppering, lower doses for maintenance
WhereHome (oral)
Typical useHistorical first-line for active de-coppering. Many centers now switch patients off due to side effect burden once stable.
Approved1956
Syprine
trientine hydrochloride · Aton Pharma (originally Merck); generic available
MechanismCopper chelator — binds copper for urinary excretion. Generally better tolerated than penicillamine but similar efficacy.
RouteOral capsule, taken on an empty stomach (capsules require refrigeration)
Frequency2–4 times daily
WhereHome (oral)
Typical useAlternative chelator for patients who cannot tolerate penicillamine. Generic versions widely available.
Approved1985
GalzinThis drug
zinc acetate · Eton Pharmaceuticals (Galzin); generic available
MechanismCopper absorption blocker — induces a protein in the gut (metallothionein) that traps dietary copper before it can be absorbed.
RouteOral capsule, taken on an empty stomach (separated from chelators)
Frequency3 times daily
WhereHome (oral)
Typical useFirst-line maintenance therapy in many centers, particularly for presymptomatic patients identified through family screening.
Approved1997
Cuvrior
trientine tetrahydrochloride · Orphalan
MechanismCopper chelator — same chelating action as Syprine, with a more chemically stable salt formulation that allows simpler storage and twice-daily dosing.
RouteOral tablet, taken on an empty stomach
FrequencyTwice daily
WhereHome (oral)
Typical useApproved for adults with stable Wilson disease who are de-coppered and tolerant to penicillamine; designed as a maintenance switch option.
Approved2022

This chart summarizes approved Wilson disease treatments to help you understand the landscape. It is not medical advice. Treatment decisions depend on your individual disease stage, prior therapies, tolerability, and lab values for copper control. Investigational programs (ALXN1840, VTX-801, UX701) are not included because they are not yet FDA-approved. Always discuss options with your hepatologist or metabolic specialist.

Development history

Zinc has been used in Wilson disease since George Brewer's work in the 1980s established it as effective maintenance therapy. The FDA approved Galzin (zinc acetate) in 1997 as a specifically labeled Wilson disease therapy, complementing existing over-the-counter zinc preparations. Galzin had supply interruptions in the U.S. for several years before Eton Pharmaceuticals reintroduced it in March 2025.

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Common questions about Zinc acetate

▸What is Zinc acetate (Galzin)?

An oral zinc acetate formulation approved as maintenance therapy for Wilson disease in patients who were first treated with a chelating drug. Zinc blocks dietary copper absorption rather than chelating circulating copper, which makes it well-suited to long-term maintenance. The label also reports a study in presymptomatic patients, but its approved use is maintenance after a chelator. Galzin returned to U.S. supply through Eton Pharmaceuticals in early 2025.

▸What is the mechanism of action of Zinc acetate?

Oral zinc that induces metallothionein in intestinal cells. Metallothionein binds dietary copper and prevents its absorption, so excess copper is shed in the feces when intestinal cells turn over. Unlike chelators, zinc does not actively remove copper that is already in the body but blocks new copper from being absorbed.

▸What are the side effects of Zinc acetate?

Generally better tolerated than chelators. The most common side effect is gastric irritation and nausea, particularly with the morning dose; this can often be managed by spacing doses around meals. The label also warns about stomach ulcers with long-term use and about copper deficiency after months to years of zinc, which can cause anemia, low white blood cell or platelet counts, and nerve problems. Raised amylase, lipase, and alkaline phosphatase levels can also occur. The label advises against breastfeeding while taking zinc, because zinc passes into breast milk and can cause copper deficiency in the baby. Zinc and chelators should not be taken at the same time of day, since chelators bind zinc and reduce its effect.

▸How is Zinc acetate taken?

Capsules taken by mouth three times daily, on an empty stomach (at least 1 hour before or 2 to 3 hours after meals). Standard adult maintenance dose is 50 mg of elemental zinc three times daily. The label says 25 mg three times daily may be enough for children 10 and older and during pregnancy; children under 10 have not been studied.

▸Is Zinc acetate FDA approved?

Yes, Zinc acetate (Galzin) is FDA approved (1997) for the treatment of Wilson Disease.

This page is for informational purposes only and does not constitute medical advice. Drug information is sourced from public databases and peer-reviewed literature and may not reflect the most recent updates. Always discuss treatment options with your healthcare provider. Last reviewed: September 2026.

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