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Tildrakizumab

Generic Name
Tildrakizumab
Brand Names
Ilumya, Ilumetri
Drug Type
Biotech
CAS Number
1326244-10-3
Unique Ingredient Identifier
DEW6X41BEK
Background

Tildrakizumab is a high-affinity, humanized, IgG1 κ antibody targeting interleukin 23 p19 that shows promise in the evolution of treatment strategy in chronic plaque psoriasis .

The Food and Drug Administration (FDA) approved ILUMYA (tildrakizumab-asmn) for the treatment of adults with moderate-to-severe plaque psoriasis who are candidates for systemic therapy or phototherapy in March 2018. The approved recommended dosage of ILUMYA is a subcutaneous injection of 100 mg at Weeks 0, 4, and every 12 weeks thereafter .

A study was performed on the pharmacokinetics of this drug on various ethnicities. The pharmacokinetics of tildrakizumab were similar in Japanese, Caucasian, and Chinese subjects .

Indication

Moderate-severe plaque psoriasis , .

Associated Conditions
Moderate to Severe Plaque Psoriasis

A Real World Study Evaluating the Long-Term Quality of Life of Tildrakizumab in Adult Patients With Psoriasis

Phase 4
Completed
Conditions
Psoriasis
Interventions
First Posted Date
2018-10-24
Last Posted Date
2023-02-23
Lead Sponsor
Sun Pharmaceutical Industries Limited
Target Recruit Count
55
Registration Number
NCT03718299
Locations
🇺🇸

Therapeutics Clinical Research, San Diego, California, United States

🇺🇸

Site 02, Grandville, Michigan, United States

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