GNH USA

Europe — EMA

Ilumetri

GNH USA supplies Ilumetri (tildrakizumab), a interleukin‑23 inhibitor for moderate‑to‑severe plaque psoriasis. Request a quote for global supply.

Tildrakizumab

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What is Tildrakizumab?

Tildrakizumab, the active ingredient in Ilumetri, is a selective humanized IgG1κ monoclonal antibody classified as an interleukin‑23 (IL‑23) inhibitor, presented as a 100 mg subcutaneous injection 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. The company ensures product integrity through cold‑chain logistics and adheres to stringent quality standards across global markets.

What is Tildrakizumab used for?

Ilumetri (tildrakizumab) targets the interleukin‑23 pathway and is used in the management of psoriasis.

- Plaque psoriasis (moderate‑to‑severe): reduces skin lesions and improves quality of life. - Chronic plaque psoriasis: lowers PASI scores and achieves sustained skin clearance. - Adult psoriasis patients: provides long‑term disease control when topical therapies are insufficient.

What are the side effects of Tildrakizumab?

Ilumetri may cause a range of adverse reactions, most of which are mild to moderate.

Common Side Effects: - Injection site pain or erythema. - Upper respiratory tract infection. - Headache. - Nasopharyngitis. - Fungal skin infection. - Mild fatigue.

Serious or Rare Side Effects: - Severe hypersensitivity reactions, including anaphylaxis. - Opportunistic infections such as tuberculosis reactivation. - Malignancies, including lymphoma and skin cancer. - Neutropenia or other hematologic abnormalities. - Cardiovascular events (rare).

What precautions apply to Tildrakizumab?

Before initiating Ilumetri, clinicians should evaluate patient history and monitor for potential risks.

- Screen for active infections: assess and treat before starting therapy. - Update vaccination status: administer required vaccines prior to treatment. - Monitor for signs of infection: report fever, chills, or persistent cough. - Assess for hypersensitivity: discontinue if severe allergic reaction occurs. - Pregnancy and lactation: use only if potential benefit justifies potential risk (category unknown). - Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

What does Tildrakizumab interact with?

Ilumetri has a limited interaction profile, but certain agents require caution.

Major Interactions (Avoid): - Live vaccines: contraindicated during therapy due to immunosuppression. - Concurrent use of other biologics targeting the same pathway.

Moderate Interactions (Monitor Closely): - Systemic corticosteroids: may increase infection risk, monitor closely. - Other immunosuppressants (e.g., methotrexate): assess cumulative immunosuppression. - Cytochrome P450 substrates: minimal interaction, but monitor drug levels if clinically relevant.

Frequently asked questions

What is Ilumetri used for?+
Ilumetri is a biologic medication indicated for the treatment of moderate‑to‑severe plaque psoriasis in adult patients. It works by targeting a specific immune pathway that drives the formation of psoriatic plaques, helping to reduce skin redness, scaling, and thickness when conventional topical therapies are inadequate.
How does tildrakizumab work?+
Tildrakizumab is a selective humanized IgG1κ monoclonal antibody that binds to the p19 subunit of interleukin‑23. By blocking IL‑23 from interacting with its receptor, the drug suppresses downstream Th17‑driven inflammation, which is a key driver of the excessive skin cell growth seen in plaque psoriasis.
What is the usual dose of Ilumetri?+
The prescribed dose of Ilumetri is determined by the treating physician based on the patient’s clinical condition and response. Typically, the medication is supplied as a 100 mg prefilled syringe for subcutaneous injection, and the prescriber decides the dosing interval and any subsequent adjustments.
Is Ilumetri safe in pregnancy or breastfeeding?+
The safety of Ilumetri during pregnancy and lactation has not been fully established, and it is classified as having an unknown pregnancy category. It should only be used if the potential benefit to the mother outweighs any possible risk to the fetus or infant, and the decision should be made in consultation with a healthcare professional.
How do I order Ilumetri from GNH USA?+
To order Ilumetri, submit an enquiry on the product page at gnh-usa.com, specifying the required quantity. GNH USA supplies hospitals, pharmacies, and procurement teams worldwide. After receiving the request, the sales team will verify trade or institutional credentials, then provide pricing, availability, shipping details (including cold‑chain handling), and any necessary import documentation.
How does Ilumetri compare with other IL‑23 inhibitors?+
Ilumetri (tildrakizumab) belongs to the same IL‑23 inhibitor class as guselkumab and risankizumab. All three target the p19 subunit of IL‑23, but they differ in dosing frequency, molecular structure, and clinical trial outcomes. Ilumetri is typically administered every 12 weeks after the initial loading phase, offering a convenient schedule compared with some alternatives.
What are the storage and handling requirements for Ilumetri?+
Ilumetri must be stored refrigerated at 2‑8 °C (36‑46 °F). The prefilled syringes should be kept in their original packaging, protected from light, and must not be frozen or shaken. If temporary storage at room temperature is unavoidable, the product may remain out of the refrigerator for no longer than 14 days, after which it should be discarded.
How is Ilumetri administered?+
Ilumetri is given as a subcutaneous injection using a prefilled syringe. The injection is typically performed in the thigh, abdomen, or upper arm, rotating sites to reduce local irritation. Healthcare professionals should follow aseptic technique, and patients may be taught self‑administration after appropriate training.
What are the most serious risks associated with Ilumetri?+
The most serious risks include severe infections (such as tuberculosis or opportunistic fungal infections), hypersensitivity reactions including anaphylaxis, and the potential for malignancies like lymphoma or skin cancer. Patients should be monitored regularly for signs of infection, unexplained weight loss, or new skin lesions, and therapy should be discontinued if serious adverse events occur.
Who should not use Ilumetri?+
Ilumetri is contraindicated in individuals with known hypersensitivity to tildrakizumab or any of its excipients. It should also be avoided in patients with active, uncontrolled infections, and it is not recommended for use with live vaccines. Clinicians should assess each patient’s medical history before initiating therapy.
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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