tremfya

tremfya Uses, Dosage, Side Effects, Food Interaction and all others data.

tremfya is a human immunoglobulin G1 lambda (IgG1λ) monoclonal antibody that selectively blocks interleukin-23. IL-23 is an inflammatory cytokine that activates the CD4+ T-helper (Th17) cell pathway to mediate the inflammatory cascade that induces psoriatic plaque formation . In clinical trials, guselkumab demonstrated improved skin clearance and symptomatic improvements in dermatological manifestations of psoriasis.

Developed by Janssen, the subcutenous injection form of guselkumab was approved in July 2017 under the market name Tremfya for the treatment of adult patients with moderate-to-severe plaque psoriasis.

tremfya is shown to reduce serum levels of IL-17A, IL-17F and IL-22 .

Trade Name tremfya
Availability Prescription only
Generic Guselkumab
Guselkumab Other Names Guselkumab
Related Drugs Skyrizi, Tremfya, Humira, Otezla, Cosentyx, prednisone, methotrexate, Enbrel, Remicade, Stelara
Weight 100mg/ml,
Type Injection, Solution, Subcutaneous Solution
Formula C6402H9864N1676O1994S42
Weight 143.6 Da (units in kg/mol)
Groups Approved, Investigational
Therapeutic Class
Manufacturer Janssen-cilag, Janssen-cilag Ltd
Available Country Saudi Arabia, Australia, Canada, United Kingdom, United States,
Last Updated: September 19, 2023 at 7:00 am
tremfya
tremfya

Uses

tremfya is a monoclonal antibody used to treat moderate to severe plaque psoriasis.

Indicated for the treatment of adults with moderate-to-severe plaque psoriasis who are candidates for systemic therapy or phototherapy.

tremfya is also used to associated treatment for these conditions: Severe Plaque psoriasis, Moderate Plaque psoriasis

How tremfya works

tremfya targets the p19 alpha subunit of IL-23. While IL-23 promotes the normal inflammatory and immune responses, the p19 and p40 subunits of IL-23 are found to be over-expressed in the condition of psoriasis and other autoimmune inflammatory skin diseases . tremfya selectively binds to the p19 subunit of IL-23 in dendritic cells and keratinocytes and blocks its interaction with IL-23 receptor, which further prevents the release of other pro-inflammatory cytokines and chemokines via stimulation of immune cells such as Th17 cells . Thus, guselkumab blocks the abnormally-heightened signalling of inflammatory cascades that promote epidermal abnormalities including keratinocyte hyperproliferation and psoriatic plaque formation .

Toxicity

Animal studies to assess the effect of guselkumab on carcinogenesis, mutagenesis and impairment on fertility have not been conducted. When subcutaneously injected into guinea pigs, the doses of guselkumab up to 100mg/kg twice-weekly demonstrated no effects on fertility parameters .

Food Interaction

No interactions found.

Volume of Distribution

The apparent volume of distribution is 13.5 L .

Elimination Route

Following a 100mg subcutaneous administration, the peak plasma concentration (Cmax) of guselkumab is 8.09 ± 3.68 mcg/mL which is reached after approximately 5.5 days .

Half Life

Mean half-life of guselkumab is approximately 15 to 18 days in subjects with plaque psoriasis .

Clearance

Apparent clearance in subjects with plaque psoriasis is 0.516 L/day .

Elimination Route

Like other human IgG monoclonal antibodies, guselkumab is expected to be both renally and fecally excreted as smaller peptide units.

Innovators Monograph

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