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SELARSDI (USTEKINUMAB-AEKN)

ALVOTECH USA INC · FDA-approved approved ✓ Verified May 2026 Quality 16/100

SELARSDI (generic name: USTEKINUMAB-AEKN) is a drug developed by ALVOTECH USA INC. It is currently FDA-approved for Moderate to Severe Plaque Psoriasis, Active Psoriatic Arthritis, Moderately to Severely Active Crohn’s Disease.

SELARSDI is an interleukin-12 inhibitor, classified as an antibody drug. It is also known by other names, including STELARA and STELERA.

At a glance

Generic nameUSTEKINUMAB-AEKN
SponsorALVOTECH USA INC
Therapeutic areaOther
PhaseFDA-approved

Approved indications

Common side effects

Serious adverse events

Competitive intelligence

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Frequently asked questions about SELARSDI

What is SELARSDI?

SELARSDI (USTEKINUMAB-AEKN) is a pharmaceutical drug developed by ALVOTECH USA INC, indicated for Moderate to Severe Plaque Psoriasis, Active Psoriatic Arthritis, Moderately to Severely Active Crohn’s Disease.

What is SELARSDI used for?

SELARSDI is indicated for Moderate to Severe Plaque Psoriasis, Active Psoriatic Arthritis, Moderately to Severely Active Crohn’s Disease, Moderately to Severely Active Ulcerative Colitis.

Who makes SELARSDI?

SELARSDI is developed and marketed by ALVOTECH USA INC (see full ALVOTECH USA INC pipeline at /company/alvotech-usa-inc).

What is the generic name of SELARSDI?

USTEKINUMAB-AEKN is the generic (nonproprietary) name of SELARSDI.

What development phase is SELARSDI in?

SELARSDI is FDA-approved (marketed).

What are the side effects of SELARSDI?

Common side effects of SELARSDI include Nasopharyngitis, Upper respiratory tract infection, Headache, Fatigue, Back pain, Dizziness. Serious adverse events: Serious infections, Malignancies (excluding non-melanoma skin cancer), Non-melanoma skin cancer, Posterior reversible encephalopathy syndrome (PRES).

Related

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