GNH USA

Europe — EMA

Ilumetri

GNH USA supplies Ilumetri (Tildrakizumab), an IL-23 inhibitor for moderate-to-severe plaque psoriasis. Request a quote for worldwide supply via supply chain.

Tildrakizumab

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What is Tildrakizumab?

Tildrakizumab, the active ingredient in Ilumetri, is a IL-23 inhibitor presented as a subcutaneous formulation for subcutaneous use. It is indicated for the treatment of moderate-to-severe plaque psoriasis in adult patients. GNH USA supplies Ilumetri as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

What is Tildrakizumab used for?

Ilumetri targets the IL‑23 pathway, a key driver of inflammatory skin disease. - Moderate-to-severe plaque psoriasis: reduces the severity and extent of psoriatic plaques, improving skin clearance and quality of life.

What are the side effects of Tildrakizumab?

Common Side Effects: - Injection site pain: mild to moderate discomfort at the injection site. - Upper respiratory tract infection: symptoms such as sore throat or nasal congestion. - Headache: transient, usually mild. - Diarrhea: occasional loose stools. - Fatigue: feeling of tiredness without exertion. - Nausea: mild stomach upset.

Serious or Rare Side Effects: - Severe allergic reaction: rash, swelling, or difficulty breathing. - Opportunistic infections: signs of fungal or bacterial infection. - New onset or worsening inflammatory bowel disease. - Hepatic abnormalities: elevated liver enzymes. - Malignancies: rare reports of skin or lymphoid cancers. - Cardiovascular events: rare cases of myocardial infarction or stroke.

What precautions apply to Tildrakizumab?

Before initiating therapy, clinicians should assess patient history and monitor for specific risks. - Infection screening: evaluate for active or latent infections, especially tuberculosis. - Vaccination status: administer required vaccines before treatment; avoid live vaccines during therapy. - Pregnancy and lactation: discuss potential risks; use only if benefits outweigh risks. - Concomitant immunosuppression: consider increased infection risk when combined with other immunosuppressants. - Monitoring: regular laboratory tests for liver function and complete blood count. - Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

What does Tildrakizumab interact with?

Tildrakizumab may interact with other agents that affect immune function. Major Interactions (Avoid): - Live vaccines: may cause uncontrolled infection. - Other biologic immunomodulators: increased risk of severe infections.

Moderate Interactions (Monitor Closely): - Systemic immunosuppressants (e.g., methotrexate): monitor infection signs. - Antifungal agents: watch for additive immunosuppression. - Cytokine‑targeting therapies: assess overlapping immune effects.

Frequently asked questions

What is Ilumetri used for?+
Ilumetri is prescribed for adults with moderate-to-severe plaque psoriasis. It works by targeting the interleukin‑23 pathway, which helps reduce skin inflammation, plaque thickness, and overall disease severity, leading to clearer skin and improved quality of life.
How does tildrakizumab work?+
Tildrakizumab is a monoclonal antibody that binds specifically to the p19 subunit of interleukin‑23. By blocking IL‑23 from activating its receptor, the drug interrupts the downstream inflammatory cascade that drives the formation of psoriatic plaques.
What is the usual dose of Ilumetri?+
The dosing regimen for Ilumetri is determined by the prescribing healthcare professional based on the patient’s clinical condition, weight, and treatment response. The prescriber will decide the appropriate dose and administration schedule.
Is Ilumetri safe during pregnancy or breastfeeding?+
Safety data for tildrakizumab in pregnancy and lactation are limited. It should only be used if the potential benefit justifies the potential risk to the fetus or infant, and the decision should be made in consultation with a qualified healthcare provider.
How do I order Ilumetri from GNH USA?+
To place an order, submit an enquiry on the Ilumetri product page at gnh-usa.com, specifying the required quantity. GNH USA works with hospitals, pharmacies, and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain logistics), and necessary import documentation.
How does Ilumetri compare with other psoriasis biologics?+
Ilumetri belongs to the IL‑23 inhibitor class, offering a targeted mechanism distinct from TNF‑α or IL‑17 inhibitors. Compared with some alternatives, it may have a favorable dosing interval and a safety profile focused on fewer systemic infections, but individual response varies and should be evaluated by the treating physician.
What are the storage and handling requirements for Ilumetri?+
Ilumetri must be stored refrigerated at 2‑8 °C. Keep the product in its original packaging, protect it from light, and avoid freezing or shaking the vial. If temporary storage at room temperature is unavoidable, limit exposure to no more than 24 hours.
How is Ilumetri administered?+
Ilumetri is given by subcutaneous injection, typically in the thigh, abdomen, or upper arm. The injection is performed by a healthcare professional or a trained patient following the prescriber’s instructions and using aseptic technique.
What are the most serious risks associated with Ilumetri?+
Serious risks include severe allergic reactions, opportunistic infections, new or worsening inflammatory bowel disease, hepatic abnormalities, and rare reports of malignancies. Patients should be monitored regularly for signs of infection, liver dysfunction, or unexpected skin changes.
Who should not use Ilumetri?+
Ilumetri is contraindicated in patients with known hypersensitivity to tildrakizumab or any excipients. It should be avoided in individuals with active serious infections, uncontrolled tuberculosis, or those receiving live vaccines. Caution is also advised for pregnant or nursing women and patients with a history of malignancy.
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
Tildrakizumab
Route
Subcutaneous Use
Manufacturer
Almirall, S.A.
Origin
EU

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