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Secukinumab 300 mg

GWT-TUD GmbH · FDA-approved active Small molecule ✓ Verified May 2026 Quality 5/100

Secukinumab 300 mg is a Small molecule drug developed by GWT-TUD GmbH. It is currently FDA-approved. Also known as: COSENTYX ®, AIN457, AIN457 300 mg.

Secukinumab 300 mg is an interleukin 17A inhibitor, classified as an INHIBITOR drug modality, which targets Interleukin-17A. It is used to treat conditions such as moderate to severe plaque-type psoriasis, dermatitis, atopic eczema, and pyoderma gangrenosum, among others.

At a glance

Generic nameSecukinumab 300 mg
Also known asCOSENTYX ®, AIN457, AIN457 300 mg
SponsorGWT-TUD GmbH
ModalitySmall molecule
PhaseFDA-approved

Approved indications

No approved indications tracked.

Common side effects

No common side effects on file.

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 Secukinumab 300 mg

What is Secukinumab 300 mg?

Secukinumab 300 mg is a Small molecule drug developed by GWT-TUD GmbH.

Who makes Secukinumab 300 mg?

Secukinumab 300 mg is developed and marketed by GWT-TUD GmbH (see full GWT-TUD GmbH pipeline at /company/gwt-tud-gmbh).

Is Secukinumab 300 mg also known as anything else?

Secukinumab 300 mg is also known as COSENTYX ®, AIN457, AIN457 300 mg.

What development phase is Secukinumab 300 mg in?

Secukinumab 300 mg is FDA-approved (marketed).

Related

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