GNH USA

Europe — EMA

Metvix

GNH USA supplies Metvix (Methyl aminolevulinate), a photosensitizing agent for actinic keratosis treatment. Request a quote for global supply to clinics.

Methyl Aminolevulinate

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What is Methyl Aminolevulinate?

Methyl aminolevulinate, the active ingredient in Metvix, is a photosensitizing agent presented as a 5% w/w cream for topical use. It is applied to areas of sun‑damaged skin to treat actinic keratosis, a precancerous lesion, in adult patients by enabling targeted photodynamic therapy that selectively destroys dysplastic cells.

GNH USA supplies Metvix as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, providing reliable sourcing, regulatory support and logistics for this EU‑approved photodynamic therapy product to meet clinical demand.

What is Methyl Aminolevulinate used for?

Metvix is employed in photodynamic therapy for actinic keratosis, a field cancerization of sun‑damaged skin that can progress to squamous cell carcinoma, providing a non‑surgical option for lesion clearance. - Actinic keratosis (multiple lesions): reduces the number of visible lesions across the treated area. - Actinic keratosis (individual lesions): achieves complete clinical clearance of targeted lesions. - Field cancerization of sun‑damaged skin: treats subclinical dysplastic cells to prevent future lesion development. - Prevention of new actinic lesions: diminishes emergence of new lesions in treated area over several months.

What are the side effects of Methyl Aminolevulinate?

Methyl aminolevulinate cream may cause local and systemic reactions after application and light activation.

Common Side Effects: - Application site pain: mild to moderate discomfort during illumination. - Erythema: redness of the treated skin. - Edema: swelling around the application area. - Scaling or crusting: skin flaking as lesions resolve.

Serious or Rare Side Effects: - Severe phototoxic reaction: intense pain, blistering, or ulceration requiring medical attention. - Infection: secondary bacterial infection of treated sites. - Allergic contact dermatitis: widespread rash or swelling. - Ulceration: deep tissue damage that may lead to scarring.

What precautions apply to Methyl Aminolevulinate?

When using Metvix, careful patient management and site care are essential. - Patient selection: use in adults with diagnosed actinic keratosis. - Sun exposure: avoid direct sunlight on treated area for at least 48 hours after illumination. - Concurrent photosensitizers: discontinue systemic photosensitizing drugs such as tetracyclines during treatment. - Pregnancy and lactation: safety not established; avoid unless benefit outweighs risk. - Application site care: keep area clean and avoid trauma during healing. - Store below 25°C: keep in original packaging, protect from moisture and light.

What does Methyl Aminolevulinate interact with?

Methyl aminolevulinate may interact with other agents that affect photosensitivity or wound healing.

Major Interactions (Avoid): - Systemic photosensitizing agents (e.g., tetracyclines, retinoids): may increase phototoxicity. - Topical irritants (e.g., benzoyl peroxide, salicylic acid) applied to same area: may exacerbate skin reactions.

Moderate Interactions (Monitor Closely): - Topical corticosteroids applied after treatment: may reduce efficacy of photodynamic effect. - Oral anticoagulants: monitor for bleeding if ulceration occurs. - Immunosuppressive therapy: may diminish treatment response.

Frequently asked questions

What is Metvix used for?+
Metvix is a prescription topical cream indicated for the treatment of actinic keratosis, a precancerous skin condition caused by chronic sun exposure. It is applied to the affected area and activated by red light, providing a non‑surgical option to remove dysplastic cells and reduce the risk of progression to squamous cell carcinoma.
How does methyl aminolevulinate work?+
Methyl aminolevulinate is a prodrug that is taken up by skin cells and converted inside the mitochondria to protoporphyrin IX. When the treated skin is exposed to red light, protoporphyrin IX produces reactive oxygen species that cause selective oxidative damage, destroying abnormal keratinocytes while sparing normal tissue.
What is the usual dose of Metvix?+
The exact dosing regimen for Metvix is determined by the prescribing clinician. Typically, a thin layer of the 5% cream is applied to the target area once daily for a prescribed number of days before illumination with red light, but the frequency, amount and duration are individualized based on lesion size and treatment protocol.
Is Metvix safe to use during pregnancy or breastfeeding?+
The safety of Metvix in pregnancy and lactation has not been established. Because the drug is a photosensitizing agent, it is generally avoided in pregnant or nursing women unless the potential therapeutic benefit justifies the potential risk to the fetus or infant.
How do I order Metvix from GNH USA?+
To order Metvix, submit an enquiry on the product page at gnh-usa.com, specifying the required quantity. GNH USA supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including any cold‑chain requirements) and the necessary import documentation.
How does Metvix compare with other treatments for actinic keratosis?+
Metvix offers a photodynamic approach that targets dysplastic cells after light activation, whereas topical agents such as 5‑fluorouracil or imiquimod rely on chemical cytotoxicity. Compared with these creams, Metvix can treat larger fields of subclinical disease in a single session, but it requires specialized illumination equipment and careful post‑treatment skin care.
What are the storage and handling requirements for Metvix?+
Metvix should be stored below 25 °C in its original container, protected from moisture and direct light. Keep the cream tightly sealed when not in use and avoid freezing. Follow any additional handling instructions provided by the supplier to maintain product stability.
How is Metvix administered?+
Metvix is applied as a thin layer of the 5% cream to the affected skin area, usually once daily for a defined pre‑treatment period. After the application window, the treated region is illuminated with a red light source (approximately 630 nm) for a prescribed duration, which activates the drug and initiates the therapeutic effect.
What are the most serious risks associated with Metvix?+
The most serious risks include severe phototoxic reactions such as intense pain, blistering or ulceration, secondary bacterial infection of the treated sites, and allergic contact dermatitis. Patients should be monitored closely for these events, and any severe reaction should prompt immediate medical evaluation.
Who should not use Metvix?+
Metvix should not be used by individuals with known hypersensitivity to methyl aminolevulinate or any component of the formulation, by patients taking systemic photosensitizing medications, by pregnant or breastfeeding women unless clearly indicated, and by children or adolescents unless specifically prescribed by a qualified dermatologist.
Information provided on this page is for educational use by procurement and clinical professionals. Always consult a licensed healthcare provider for medical advice and prescribing decisions. GNH USA supplies this product subject to applicable regulatory and licensing requirements.

Product details

Drug
Methyl Aminolevulinate
Route
Cutaneous Use
Manufacturer
Laboratorios Galderma S.A. - Sucursal Em Portugal
Origin
EU

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