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 your region.

Methyl Aminolevulinate

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What is Methyl Aminolevulinate?

Methyl Aminolevulinate, the active ingredient in Metvix, is a photosensitizing agent presented as a 16% w/w cream for topical use. It treats actinic keratosis, a precancerous skin condition caused by chronic sun exposure, in adult patients with sun‑damaged skin. It is indicated for field‑directed photodynamic therapy performed by dermatologists in clinical settings.

GNH USA supplies Metvix as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, adhering to stringent quality standards and regulatory requirements, and providing reliable logistics support.

What is Methyl Aminolevulinate used for?

Metvix (methyl aminolevulinate) is used in dermatology for photodynamic therapy of precancerous skin lesions.

Actinic keratosis: provides selective destruction of dysplastic keratinocytes, leading to lesion clearance and reduced risk of progression to squamous cell carcinoma.

What are the side effects of Methyl Aminolevulinate?

Topical application of Metvix followed by light activation can cause a range of local and systemic reactions.

Common Side Effects: - Pain during illumination: transient burning or stinging sensation during light exposure. - Erythema: redness of treated skin lasting several days. - Edema: swelling around the application site. - Crusting/Scaling: formation of crusts or flaky skin as lesions heal.

Serious or Rare Side Effects: - Infection: secondary bacterial infection of treated area. - Ulceration: deep tissue breakdown requiring medical attention. - Scarring: permanent skin changes in severe cases. - Photosensitivity: exaggerated reaction to sunlight after treatment.

What precautions apply to Methyl Aminolevulinate?

Before using Metvix, clinicians should observe several safety measures to minimize adverse events. - Contraindication: avoid use in patients with known porphyria or hypersensitivity to methyl aminolevulinate. - Sunlight avoidance: advise patients to protect treated area from natural light for at least 48 hours post‑treatment. - Lesion selection: ensure lesions are suitable for photodynamic therapy and not infected or heavily hyperkeratotic. - Protective eyewear: require patients and staff to wear appropriate eye protection during illumination. - Monitoring: inspect treated sites for signs of infection or excessive inflammation during follow‑up visits. - Store at ambient temperature: keep below 25 °C in original packaging, protect from moisture and direct sunlight.

What does Methyl Aminolevulinate interact with?

Metvix may interact with other agents that influence photosensitivity or skin healing.

Major Interactions (Avoid): - Systemic photosensitizers: concurrent use of drugs such as tetracyclines, sulfonamides, or retinoids can increase phototoxic risk. - UV‑based therapies: combining with other phototherapy modalities may cause excessive skin damage. - Porphyrin‑related disorders: patients with disorders of heme synthesis should not receive methyl aminolevulinate.

Moderate Interactions (Monitor Closely): - Topical corticosteroids: may reduce efficacy if applied to the treatment area before or after PDT. - Anticoagulants: monitor for prolonged bleeding if ulceration occurs. - Herbal supplements with photosensitizing properties (e.g., St. John’s wort): advise caution and monitor skin response.

Frequently asked questions

What is Metvix used for?+
Metvix is a topical cream containing methyl aminolevulinate that is employed in photodynamic therapy to treat actinic keratosis, a precancerous skin lesion caused by chronic sun exposure. The treatment aims to selectively destroy dysplastic cells and reduce the risk of progression to squamous cell carcinoma.
How does methyl aminolevulinate work?+
Methyl aminolevulinate acts as a prodrug that is taken up by abnormal skin cells and converted into protoporphyrin IX. When the area is illuminated with red light, the accumulated protoporphyrin IX generates reactive oxygen species, causing localized oxidative damage that selectively kills the targeted dysplastic cells while sparing surrounding healthy tissue.
What determines the usual dose of Metvix?+
The dosage and application schedule of Metvix are determined by the prescribing dermatologist based on the extent and location of the actinic keratosis lesions, the patient’s skin type, and the specific photodynamic therapy protocol used. No fixed regimen can be provided without a medical prescription.
Is Metvix safe during pregnancy or breastfeeding?+
The safety of methyl aminolevulinate in pregnancy and lactation has not been established. Because the drug is classified as a photosensitizing agent and systemic absorption is possible, it should be used only if the potential benefit justifies any potential risk to the fetus or infant.
How do I order Metvix from GNH USA?+
To request Metvix, submit an enquiry on the product page at gnh-usa.com, specifying the required quantity. GNH USA supplies hospitals, pharmacies and procurement teams across international markets. After the enquiry, the sales team will verify trade or institutional credentials and respond with pricing, availability, shipping details and any required import documentation.
How does Metvix compare with the main alternative drug or class?+
The most common alternative for topical photodynamic therapy is 5‑aminolevulinic acid (ALA) cream, such as Levulan. Both agents generate protoporphyrin IX, but methyl aminolevulinate typically provides deeper penetration and higher lesion‑clearance rates, especially for thicker or field‑directed treatments, while ALA may be preferred for thinner lesions or when a shorter incubation time is needed.
What are the storage and handling requirements for Metvix?+
Metvix should be stored at ambient temperature, below 25 °C, in its original container. The packaging must be kept closed to protect the cream from moisture and direct sunlight. Do not freeze the product, and avoid exposing it to extreme temperatures that could compromise its stability.
How is Metvix administered?+
A dermatologist applies a thin layer of Metvix cream to the affected skin area, typically covering the lesion and a small margin of surrounding tissue. After a prescribed incubation period (usually 3 hours), the area is illuminated with a red light source (approximately 635 nm) for a defined duration to activate the photosensitizer and achieve lesion clearance.
What are the most serious risks to watch for with Metvix?+
Serious adverse events include severe ulceration, secondary bacterial infection of the treated site, significant scarring, and extensive photosensitivity reactions that may persist after illumination. Patients should be monitored closely for signs of infection, excessive pain, or unexpected tissue breakdown, and any such events should be reported to a healthcare professional promptly.
Who should not use Metvix?+
Metvix is contraindicated in individuals with known porphyria, hypersensitivity to methyl aminolevulinate or any component of the formulation, and in patients with active skin infections at the treatment site. Caution is also advised for patients taking systemic photosensitizing medications or those with disorders of heme synthesis.
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
Galderma International
Origin
EU

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