Product image of Metoxaleno G. L. Pharma (Methoxsalen) supplied by GNH India

Metoxaleno G. L. Pharma

Active Ingredient:
Methoxsalen
Origin:
EU

Metoxaleno G. L. Pharma (Methoxsalen)

Methoxsalen, the active ingredient in Metoxaleno, is a psoralen presented as a preparation for extracorporeal use. It is employed in photochemotherapy to treat skin disorders such as psoriasis and vitiligo, primarily in adult patients requiring PUVA therapy, and may be combined with UVA exposure under medical supervision.

GNH India supplies Metoxaleno as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides reliable logistics for global distribution. Customers benefit from consistent product availability and regulatory compliance across multiple markets.

Manufacturer / TM Owner

G.L. Pharma Gmbh

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Indications & Clinical Uses

  • Methoxsalen is employed in PUVA photochemotherapy for skin disorders that respond to UVA‑activated psoralen.
  • Psoriasis: methoxsalen, when combined with UVA exposure, slows keratinocyte proliferation and reduces inflammatory activity, leading to decreased plaque thickness, scaling, and erythema, thereby improving patient quality of life.
  • Vitiligo: the drug intercalates into DNA of melanocytes and, upon UVA activation, stimulates melanin production and migration, which can result in repigmentation of depigmented areas and better cosmetic outcomes.
  • Other photodermatoses: in specialist settings, methoxsalen may be applied for refractory skin conditions that respond to PUVA, providing an additional therapeutic option when conventional treatments have failed.

How It Works

  • Methoxsalen is a psoralen that intercalates between DNA base pairs. Upon absorption of UVA light, it forms covalent cross‑links with pyrimidine residues, inhibiting DNA synthesis and inducing apoptosis of hyperproliferative skin cells. This immunosuppressive effect reduces inflammatory pathways and normalizes keratinocyte turnover, forming the basis of PUVA therapy. The cross‑linking also alters transcription of cytokine genes, contributing to the therapeutic response.

Side Effects

Methoxsalen may cause a range of adverse reactions, varying from mild to severe, particularly when combined with UVA exposure.

Common Side Effects

  • Nausea: transient feeling of sickness, often mild.
  • Headache: dull to moderate intensity, usually resolves.
  • Skin erythema: redness at treated sites after UVA exposure.
  • Pruritus: itching of the skin during or after treatment.
  • Hyperpigmentation: darkening of skin in exposed areas.

Serious or Rare Side Effects

  • Phototoxic burns: severe skin injury with blistering after excessive UVA.
  • Erythema multiforme: target‑like skin lesions requiring medical attention.
  • Hepatic dysfunction: abnormal liver enzymes indicating possible liver injury.

Precautions & Warnings

Prior to initiating methoxsalen therapy, several precautions should be observed to ensure patient safety and optimal outcomes.

  • Dose adjustment: assess renal and hepatic function before treatment.
  • Photoprotection: advise patients to avoid excessive sunlight and use protective clothing during therapy.
  • Pregnancy: consider use only if potential benefits justify potential risks to the fetus.
  • Drug interactions: review concomitant photosensitizing or immunosuppressive medications.
  • Store at ambient temperature: keep in original container, protect from light and moisture.

Avoid Interactions

Methoxsalen can interact with other medicines, influencing its efficacy or increasing toxicity.

Major Interactions (Avoid)

  • Azathioprine: combined use may heighten bone marrow suppression risk.
  • Thiazide diuretics: can amplify photosensitivity reactions.
  • Phenobarbital: may reduce methoxsalen activation, decreasing therapeutic effect.

Moderate Interactions (Monitor Closely)

  • Acitretin: additive skin irritation may occur.
  • Systemic corticosteroids: may modify immune response and affect treatment outcome.

Frequently Asked Questions

Metoxaleno contains methoxsalen, which is used in PUVA photochemotherapy to treat chronic skin conditions such as psoriasis and vitiligo. The drug is administered under medical supervision and combined with controlled UVA exposure to achieve therapeutic skin remodeling.

Methoxsalen intercalates into DNA and, after activation by UVA light, creates covalent cross‑links with pyrimidine bases. This blocks DNA synthesis, induces apoptosis of hyperactive skin cells, and suppresses immune responses, thereby reducing inflammation and abnormal skin growth.

The prescribed dose of methoxsalen is individualized by the treating physician based on the specific skin condition, severity, patient skin type, and the planned UVA exposure schedule. Dosage is adjusted to balance efficacy with the risk of phototoxic reactions.

Safety data for methoxsalen in pregnancy and lactation are limited. It is generally classified as a drug to be used only when the potential benefits outweigh potential risks to the fetus or infant. Physicians should discuss uncertainties and consider alternative therapies.

To request Metoxaleno, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any necessary import documentation.

Compared with biologic agents for psoriasis, methoxsalen offers a non‑biologic, photochemotherapy option that can be effective for patients who prefer oral therapy or have contraindications to biologics. However, it requires careful UVA administration and carries a distinct phototoxicity profile not seen with many newer agents.

Metoxaleno should be stored at ambient temperature, below 25 °C, in its original packaging. Protect the product from direct light, moisture and extreme temperature fluctuations to maintain stability and potency throughout its shelf life.

Metoxaleno is administered orally under physician guidance, followed by a scheduled exposure to UVA light (PUVA therapy). The timing between drug intake and UVA exposure is critical to achieve optimal activation of methoxsalen and therapeutic effect.

The most serious risks include severe phototoxic burns with blistering, rare but potentially life‑threatening skin reactions such as erythema multiforme, and hepatic dysfunction indicated by abnormal liver enzymes. Prompt medical evaluation is required if any of these events occur.

Methoxsalen is contraindicated in patients with a history of porphyria, systemic lupus erythematosus, severe liver disease, known hypersensitivity to psoralens, or those who are pregnant without a clear benefit. Individuals unable to comply with strict UVA protection measures should also avoid its use.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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