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ILUMYA (TILDRAKIZUMAB-ASMN)

SUN PHARMA GLOBAL · FDA-approved approved Under review Quality 10/100

ILUMYA (generic name: TILDRAKIZUMAB-ASMN) is a Interleukin-23 Antagonist [EPC] drug developed by SUN PHARMA GLOBAL. It is currently FDA-approved for Plaque psoriasis.

ILUMYA is a monoclonal antibody that targets Interleukin-23, classified as an inhibitor. It is used to treat conditions such as Psoriasis Vulgaris, Plaque-type Psoriasis, and Moderate to Severe Nail Psoriasis.

At a glance

Generic nameTILDRAKIZUMAB-ASMN
SponsorSUN PHARMA GLOBAL
Drug classInterleukin-23 Antagonist [EPC]
TargetInterleukin-23
Therapeutic areaImmunology
PhaseFDA-approved

Approved indications

Common side effects

Serious adverse events

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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Frequently asked questions about ILUMYA

What is ILUMYA?

ILUMYA (TILDRAKIZUMAB-ASMN) is a Interleukin-23 Antagonist [EPC] drug developed by SUN PHARMA GLOBAL, indicated for Plaque psoriasis.

What is ILUMYA used for?

ILUMYA is indicated for Plaque psoriasis.

Who makes ILUMYA?

ILUMYA is developed and marketed by SUN PHARMA GLOBAL (see full SUN PHARMA GLOBAL pipeline at /company/sun-pharma-global).

What is the generic name of ILUMYA?

TILDRAKIZUMAB-ASMN is the generic (nonproprietary) name of ILUMYA.

What drug class is ILUMYA in?

ILUMYA belongs to the Interleukin-23 Antagonist [EPC] class. See all Interleukin-23 Antagonist [EPC] drugs at /class/interleukin-23-antagonist-epc.

What development phase is ILUMYA in?

ILUMYA is FDA-approved (marketed).

What are the side effects of ILUMYA?

Common side effects of ILUMYA include Upper respiratory infections, Injection site reactions, Diarrhea, Dizziness, Pain in extremity. Serious adverse events: Angioedema, Urticaria.

What does ILUMYA target?

ILUMYA targets Interleukin-23 and is a Interleukin-23 Antagonist [EPC].

Related

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing