GNH USA

Europe — EMA

Ilumetri

GNH USA supplies Ilumetri (tildrakizumab), a IL-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 IL-23 inhibitor presented as a 100 mg solution for subcutaneous injection use. It treats moderate-to-severe plaque psoriasis in adult patients.\n\nGNH India supplies Ilumetri as a licensed, GDP-compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

What is Tildrakizumab used for?

Ilumetri (tildrakizumab) targets the interleukin‑23 pathway, a key driver in plaque psoriasis.\n\nModerate-to-severe plaque psoriasis: reduces skin plaque formation and disease activity in adult patients.

What are the side effects of Tildrakizumab?

Common Side Effects:\n- Injection site pain or erythema\n- Upper respiratory tract infection\n- Headache\n- Fatigue\n\nSerious or Rare Side Effects:\n- Severe allergic reactions (anaphylaxis)\n- Opportunistic infections, including tuberculosis\n- Malignancies such as lymphoma or skin cancer

What precautions apply to Tildrakizumab?

Before initiating therapy, evaluate the patient for active infections and immunization status.\n\nScreen for active infections: assess and treat before starting Ilumetri\nVaccinations: update required vaccines prior to treatment\nMonitor for signs of infection: report fever, cough, or unusual symptoms promptly\nAssess for hypersensitivity: discontinue if severe allergic reaction occurs\nPregnancy and lactation: use only if potential benefit justifies potential risk\nStore at 2-8°C: keep refrigerated, protect from light, do not freeze or shake

What does Tildrakizumab interact with?

Ilumetri may interact with other agents that affect immune function.\n\nMajor Interactions (Avoid):\n- Live vaccines: contraindicated during therapy\n- Systemic immunosuppressants (e.g., cyclosporine): may increase infection risk\n- Concurrent biologics targeting IL‑12/23 (e.g., ustekinumab): avoid simultaneous use\n\nModerate Interactions (Monitor Closely):\n- Systemic corticosteroids: may augment immunosuppression\n- Antifungal agents (e.g., azoles): monitor for additive infection risk\n- Non‑live vaccines: may have reduced efficacy, assess response

Frequently asked questions

What is Ilumetri used for?+
Ilumetri is indicated for the treatment of moderate-to-severe plaque psoriasis in adult patients. By targeting a specific inflammatory pathway, it helps reduce the formation of skin plaques and improves overall disease severity.
How does tildrakizumab work?+
Tildrakizumab binds selectively to the p19 subunit of interleukin‑23, blocking the cytokine from activating its receptor. This inhibition reduces Th17‑cell activity and downstream inflammatory mediators, leading to decreased skin inflammation characteristic of plaque psoriasis.
What is the usual dose of Ilumetri?+
The exact dosing schedule for Ilumetri is determined by the prescribing healthcare professional based on the patient’s clinical condition and response. The prescriber decides the amount, frequency and duration of treatment.
Is Ilumetri safe during pregnancy or breastfeeding?+
The pregnancy safety category for tildrakizumab is unknown. It should only be used during pregnancy or lactation if the potential benefit to the mother outweighs any possible risk to the fetus or infant, and after consultation with a qualified healthcare provider.
How do I order Ilumetri from GNH USA?+
To request Ilumetri, submit an enquiry on the 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, cold‑chain shipping details and necessary import documentation.
How does Ilumetri compare with other psoriasis biologics?+
Ilumetri belongs to the IL‑23 inhibitor class, whereas alternatives such as ustekinumab target both IL‑12 and IL‑23, and agents like secukinumab inhibit IL‑17. IL‑23 inhibition offers a more selective approach, which may result in a different safety and efficacy profile compared with broader‑acting biologics.
What are the storage and handling requirements for Ilumetri?+
Ilumetri should be stored in a refrigerator at 2‑8 °C. Keep the vial in its original packaging, protect it from light, and avoid freezing or shaking the solution. Do not use the product if it has been exposed to temperatures outside the recommended range.
How is Ilumetri administered?+
Ilumetri is given as a subcutaneous injection, typically performed by a healthcare professional. The injection site should be rotated among approved areas such as the abdomen, thigh or upper arm to minimize local irritation.
What are the most serious risks associated with Ilumetri?+
Serious risks include severe infections (including tuberculosis), allergic reactions such as anaphylaxis, and the potential for malignancies. Patients should be monitored closely for signs of infection, unexpected skin changes or systemic allergic symptoms.
Who should not use Ilumetri?+
Ilumetri is contraindicated in individuals with known hypersensitivity to tildrakizumab or any excipients. It should also be avoided in patients with active serious infections, those receiving live vaccines, or anyone for whom the risk‑benefit assessment is unfavorable.
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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